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3%;
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><span
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nyl </span></span><span
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 <div v:shape=3D"_x0000_s6147" class=3DT style=3D'position:absolute;top:3.0=
%;
 left:8.42%;width:83.14%;height:9.25%'><span style=3D'color:#FAFD00'>Experi=
mental</span></div>
 <div v:shape=3D"_x0000_s6146" class=3DB><span style=3D'position:absolute;t=
op:16.5%;
 left:8.42%;width:94.0%;height:5.25%'><span style=3D'mso-special-format:nob=
ullet;
 display:none;color:black;mso-color-index:3;font-family:"Monotype Sorts";
 font-size:75%'>n</span><span style=3D'font-size:75%;color:#FAFD00'><span
 style=3D'mso-tab-count:1;width:3.98%'> </span>The cyclopentadienylmanganese
 tricarbonyl derivatives </span></span><span style=3D'position:absolute;
 top:21.75%;left:12.17%;width:87.07%;height:5.25%'><span style=3D'font-size=
:75%;
 color:#FAFD00'>were synthesized by published<span
 style=3D'mso-spacerun:yes'>&nbsp; </span>methods.</span><span style=3D'fon=
t-size:
 50%;color:#FAFD00;position:relative;top:-.45em;mso-text-raise:30%'>2,3<span
 style=3D'mso-spacerun:yes'>&nbsp; </span></span><span style=3D'font-size:7=
5%;
 color:#FAFD00'>The cyclic </span></span><span style=3D'position:absolute;
 top:27.25%;left:12.17%;width:95.31%;height:5.25%'><span style=3D'font-size=
:75%;
 color:#FAFD00'>voltammograms were collected with a Bioanalytical CV-27 </s=
pan></span><span
 style=3D'position:absolute;top:32.5%;left:12.17%;width:90.82%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>and recorded by a Hewlett Packard 70=
90A
 Measurement </span></span><span style=3D'position:absolute;top:37.75%;
 left:12.17%;width:88.95%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>Plotting
 System.<span style=3D'mso-spacerun:yes'>&nbsp; </span>The samples were sca=
nned
 at six scan </span></span><span style=3D'position:absolute;top:43.0%;left:=
12.17%;
 width:88.2%;height:5.25%'><span style=3D'font-size:75%;color:#FAFD00'>rate=
s, 30,
 60, 100, 400, 700 and 1000 mV/s.<span style=3D'mso-spacerun:yes'>&nbsp;
 </span>Ferrocene </span></span><span style=3D'position:absolute;top:48.5%;
 left:12.17%;width:90.07%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>was
 used as a reference and all data was normalized to a </span></span><span
 style=3D'position:absolute;top:53.75%;left:12.17%;width:81.27%;height:5.25=
%'><span
 style=3D'font-size:75%;color:#FAFD00'>ferrocene E </span><span style=3D'fo=
nt-size:
 50%;color:#FAFD00;position:relative;top:.37em;mso-text-raise:-25%'>1/2 </s=
pan><span
 style=3D'font-size:75%;color:#FAFD00'>=3D 0.4V.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span>The initial voltammograms </span>=
</span><span
 style=3D'position:absolute;top:59.0%;left:12.17%;width:86.14%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>indicated a steady increase in Epa v=
alues
 after several </span></span><span style=3D'position:absolute;top:64.5%;
 left:12.17%;width:93.44%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>scans.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span>The formation of a deposit on the
 working eletrode </span></span><span style=3D'position:absolute;top:69.75%;
 left:12.17%;width:85.2%;height:5.25%'><span style=3D'font-size:75%;color:#=
FAFD00'>was
 indicated as the cause of this shift.<span style=3D'mso-spacerun:yes'>&nbs=
p;
 </span>Therefore, to </span></span><span style=3D'position:absolute;top:75=
.0%;
 left:12.17%;width:89.13%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>eliminate
 this error, the working electrode was polished </span></span><span
 style=3D'position:absolute;top:80.25%;left:12.17%;width:79.4%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>following each scan to remove the
 deposit.<span style=3D'mso-spacerun:yes'>&nbsp; </span></span></span></div>
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butyl)4BF4 vs. Ag/AgCl at 100mV/s.a  A platinum disk working electrode and =
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op:1.5%;
 left:.93%;width:98.12%;height:5.25%'><span style=3D'font-size:55%;color:#F=
AFD00'>Table
 1. Values of Avg E</span><span style=3D'font-size:36%;color:#FAFD00;positi=
on:
 relative;top:.37em;mso-text-raise:-25%'>p</span><span style=3D'font-size:5=
5%;
 color:#FAFD00'>-E</span><span style=3D'font-size:36%;color:#FAFD00;positio=
n:
 relative;top:.37em;mso-text-raise:-25%'>p/2 </span><span style=3D'font-siz=
e:
 55%;color:#FAFD00'>and E</span><span style=3D'font-size:36%;color:#FAFD00;
 position:relative;top:.37em;mso-text-raise:-25%'>pa</span><span
 style=3D'font-size:55%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp;</span>during oxidation for 5 </span></sp=
an><span
 style=3D'position:absolute;top:6.75%;left:5.05%;width:90.07%;height:5.25%'=
><span
 style=3D'font-size:55%;color:#FAFD00'>mmolar solutions of A1-A5 and acyl in
 acetonitrile/0.01 </span></span><span style=3D'position:absolute;top:12.0%;
 left:.93%;width:98.12%;height:5.25%'><span style=3D'font-size:55%;color:#F=
AFD00'>molar
 N(n-butyl)</span><span style=3D'font-size:36%;color:#FAFD00;position:relat=
ive;
 top:.37em;mso-text-raise:-25%'>4</span><span style=3D'font-size:55%;color:=
#FAFD00'>BF</span><span
 style=3D'font-size:36%;color:#FAFD00;position:relative;top:.37em;mso-text-=
raise:
 -25%'>4</span><span style=3D'font-size:55%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp;</span>vs. Ag/AgCl at 100mV/s.</span><span
 style=3D'font-size:36%;color:#FAFD00;position:relative;top:-.45em;mso-text=
-raise:
 30%'>a</span><span style=3D'font-size:55%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp; </span>A platinum </span></span><span
 style=3D'position:absolute;top:17.5%;left:1.31%;width:97.75%;height:5.25%'=
><span
 style=3D'font-size:55%;color:#FAFD00'>disk working electrode and platinum =
wire
 auxillary electrode </span></span><span style=3D'position:absolute;top:22.=
75%;
 left:8.42%;width:83.14%;height:5.25%'><span style=3D'font-size:55%;color:#=
FAFD00'>were
 used.<span style=3D'mso-spacerun:yes'>&nbsp; </span></span></span></div>
 <div v:shape=3D"_x0000_s7170" class=3DB>
 <div style=3D'position:absolute;top:27.5%;left:8.42%;width:83.14%;height:4=
.0%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 56%;color:#FAFD00;display:none'>&#13;</span></div>
 <div style=3D'position:absolute;top:32.5%;left:8.42%;width:83.14%;height:4=
.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>Sample<span style=3D'mso-tab-count:2;width:14.07%'> </s=
pan>Avg
 E</span><span style=3D'font-size:41%;color:#FAFD00;position:relative;top:.=
37em;
 mso-text-raise:-25%'>p</span><span style=3D'font-size:63%;color:#FAFD00'>-=
E</span><span
 style=3D'font-size:41%;color:#FAFD00;position:relative;top:.37em;mso-text-=
raise:
 -25%'>p/2 </span><span style=3D'font-size:63%;color:#FAFD00'>(mV)</span><s=
pan
 style=3D'font-size:41%;color:#FAFD00;position:relative;top:-.45em;mso-text=
-raise:
 30%'>b</span><span style=3D'font-size:63%;color:#FAFD00'><span style=3D'ms=
o-tab-count:
 1;width:11.58%'> </span>mean E</span><span style=3D'font-size:41%;color:#F=
AFD00;
 position:relative;top:.37em;mso-text-raise:-25%'>pa</span><span
 style=3D'font-size:63%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp;</span>(mV)</span><span style=3D'font-siz=
e:41%;
 color:#FAFD00;position:relative;top:-.45em;mso-text-raise:30%'>b</span><sp=
an
 style=3D'font-size:63%;color:#FAFD00;display:none'>&#13;</span></div>
 <div style=3D'position:absolute;top:37.75%;left:8.42%;width:83.14%;height:=
4.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>Acyl<span style=3D'mso-tab-count:2;width:17.51%'> </spa=
n>94(3)<span
 style=3D'mso-tab-count:3;width:28.85%'> </span>1390(10)&#13;</span></div>
 <div style=3D'position:absolute;top:43.0%;left:8.42%;width:83.14%;height:4=
.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>A1<span style=3D'mso-tab-count:3;width:19.96%'> </span>=
95(2)<span
 style=3D'mso-tab-count:3;width:28.85%'> </span>1410(19)&#13;</span></div>
 <div style=3D'position:absolute;top:48.5%;left:8.42%;width:83.14%;height:4=
.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>A2<span style=3D'mso-tab-count:3;width:19.96%'> </span>=
82(8)<span
 style=3D'mso-tab-count:3;width:28.85%'> </span>1350(14)&#13;</span></div>
 <div style=3D'position:absolute;top:53.75%;left:8.42%;width:83.14%;height:=
4.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>A3<span style=3D'mso-tab-count:3;width:19.96%'> </span>=
102(4)<span
 style=3D'mso-tab-count:3;width:27.18%'> </span>1400(5)&#13;</span></div>
 <div style=3D'position:absolute;top:59.0%;left:8.42%;width:83.14%;height:4=
.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>A4<span style=3D'mso-tab-count:3;width:19.96%'> </span>=
92(2)<span
 style=3D'mso-tab-count:3;width:28.85%'> </span>1250(38)&#13;</span></div>
 <div style=3D'position:absolute;top:64.5%;left:8.42%;width:83.14%;height:4=
.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>A5<span style=3D'mso-tab-count:3;width:19.96%'> </span>=
91(4)<span
 style=3D'mso-tab-count:3;width:28.85%'> </span>1240(6)&#13;</span></div>
 <span style=3D'position:absolute;top:69.75%;left:8.42%;width:95.88%;height=
:4.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>a. All potentials are normalized to a ferrocene E1/2 of=
 0.4
 V.<span style=3D'mso-spacerun:yes'>&nbsp; </span>Ferrocene </span></span><=
span
 style=3D'position:absolute;top:74.25%;left:12.17%;width:79.4%;height:4.5%'=
><span
 style=3D'font-size:63%;color:#FAFD00'>oxidation wave had a Avg
 Ep-Ep/2=3D60mV.&#13;</span></span>
 <div style=3D'position:absolute;top:79.5%;left:8.42%;width:83.14%;height:4=
.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>b. Standard deviations are given in parenthesis.&#13;</=
span></div>
 <div style=3D'position:absolute;top:84.75%;left:8.42%;width:83.14%;height:=
4.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
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<title>Cyclic Voltammetric Investigation in the Oxidative Processes of
Cyclopentadienyl Manganese Tricarbonyl Derivatives</title>
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 <div v:shape=3D"_x0000_s8195" class=3DT><span style=3D'position:absolute;t=
op:3.0%;
 left:.93%;width:98.12%;height:5.25%'><span style=3D'font-size:55%;color:#F=
AFD00'>Table
 2. Values of Avg E</span><span style=3D'font-size:36%;color:#FAFD00;positi=
on:
 relative;top:.37em;mso-text-raise:-25%'>p</span><span style=3D'font-size:5=
5%;
 color:#FAFD00'>-E</span><span style=3D'font-size:36%;color:#FAFD00;positio=
n:
 relative;top:.37em;mso-text-raise:-25%'>p/2 </span><span style=3D'font-siz=
e:
 55%;color:#FAFD00'>and E</span><span style=3D'font-size:36%;color:#FAFD00;
 position:relative;top:.37em;mso-text-raise:-25%'>pa</span><span
 style=3D'font-size:55%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp;</span>during oxidation for 5 </span></sp=
an><span
 style=3D'position:absolute;top:8.5%;left:4.3%;width:91.57%;height:5.25%'><=
span
 style=3D'font-size:55%;color:#FAFD00'>mmolar solutions of A2Chelate, A2PPh=
3,
 A3Chelate and </span></span><span style=3D'position:absolute;top:13.75%;
 left:6.92%;width:86.32%;height:5.25%'><span style=3D'font-size:55%;color:#=
FAFD00'>A3PPh3
 in acetonitrile/0.01 molar N(n-butyl)</span><span style=3D'font-size:36%;
 color:#FAFD00;position:relative;top:.37em;mso-text-raise:-25%'>4</span><sp=
an
 style=3D'font-size:55%;color:#FAFD00'>BF</span><span style=3D'font-size:36=
%;
 color:#FAFD00;position:relative;top:.37em;mso-text-raise:-25%'>4</span><sp=
an
 style=3D'font-size:55%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp;</span>vs. </span></span><span
 style=3D'position:absolute;top:19.0%;left:.18%;width:99.62%;height:5.25%'>=
<span
 style=3D'font-size:55%;color:#FAFD00'>Ag/AgCl at 100mV/s.</span><span
 style=3D'font-size:36%;color:#FAFD00;position:relative;top:-.45em;mso-text=
-raise:
 30%'>a </span><span style=3D'font-size:55%;color:#FAFD00'>A platinum disk
 working electrode and </span></span><span style=3D'position:absolute;top:2=
4.5%;
 left:8.42%;width:83.14%;height:5.25%'><span style=3D'font-size:55%;color:#=
FAFD00'>platinum
 wire auxillary electrode were used. </span></span></div>
 <div v:shape=3D"_x0000_s8194" class=3DB>
 <div style=3D'position:absolute;top:33.0%;left:8.42%;width:83.14%;height:4=
.0%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 56%;color:#FAFD00;display:none'>&#13;</span></div>
 <div style=3D'position:absolute;top:38.0%;left:8.42%;width:83.14%;height:4=
.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>Sample<span style=3D'mso-tab-count:2;width:14.07%'> </s=
pan>Avg
 E</span><span style=3D'font-size:41%;color:#FAFD00;position:relative;top:.=
37em;
 mso-text-raise:-25%'>p</span><span style=3D'font-size:63%;color:#FAFD00'>-=
E</span><span
 style=3D'font-size:41%;color:#FAFD00;position:relative;top:.37em;mso-text-=
raise:
 -25%'>p/2<span style=3D'mso-spacerun:yes'>&nbsp;&nbsp; </span></span><span
 style=3D'font-size:63%;color:#FAFD00'>(mV)</span><span style=3D'font-size:=
41%;
 color:#FAFD00;position:relative;top:-.45em;mso-text-raise:30%'>b</span><sp=
an
 style=3D'font-size:63%;color:#FAFD00'><span style=3D'mso-tab-count:1;width=
:10.5%'>
 </span>mean E</span><span style=3D'font-size:41%;color:#FAFD00;position:re=
lative;
 top:.37em;mso-text-raise:-25%'>pa</span><span style=3D'font-size:63%;color=
:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp;</span>(mV)</span><span style=3D'font-siz=
e:41%;
 color:#FAFD00;position:relative;top:-.45em;mso-text-raise:30%'>b</span><sp=
an
 style=3D'font-size:63%;color:#FAFD00;display:none'>&#13;</span></div>
 <div style=3D'position:absolute;top:43.25%;left:8.42%;width:83.14%;height:=
4.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>A2Chelate<span style=3D'mso-tab-count:1;width:9.77%'> <=
/span>76(3)<span
 style=3D'mso-tab-count:3;width:28.85%'> </span>540(6)&#13;</span></div>
 <div style=3D'position:absolute;top:48.75%;left:8.42%;width:83.14%;height:=
4.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>A2PPh3<span style=3D'mso-tab-count:2;width:12.9%'> </sp=
an>48(3)<span
 style=3D'mso-tab-count:3;width:28.85%'> </span>830(5)&#13;</span></div>
 <div style=3D'position:absolute;top:54.0%;left:8.42%;width:83.14%;height:4=
.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>A3Chelate<span style=3D'mso-tab-count:1;width:9.77%'> <=
/span>71(5)<span
 style=3D'mso-tab-count:3;width:28.85%'> </span>580(9)&#13;</span></div>
 <div style=3D'position:absolute;top:59.25%;left:8.42%;width:83.14%;height:=
4.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>A3PPh3<span style=3D'mso-tab-count:2;width:12.9%'> </sp=
an>53(2)<span
 style=3D'mso-tab-count:3;width:28.85%'> </span>830(4)&#13;</span></div>
 <span style=3D'position:absolute;top:64.5%;left:8.42%;width:98.5%;height:4=
.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>a. All potentials are normalized to a ferrocene E1/2 of=
 0.4
 mV.<span style=3D'mso-spacerun:yes'>&nbsp; </span>Ferrocene </span></span>=
<span
 style=3D'position:absolute;top:69.0%;left:12.17%;width:79.4%;height:4.5%'>=
<span
 style=3D'font-size:63%;color:#FAFD00'>oxidation wave had a Avg
 Ep-Ep/2=3D60mV.&#13;</span></span>
 <div style=3D'position:absolute;top:74.5%;left:8.42%;width:83.14%;height:4=
.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 63%;color:#FAFD00'>b.<span style=3D'mso-spacerun:yes'>&nbsp; </span>Standa=
rd
 deviations are given in parenthesis.</span><span style=3D'font-size:113%;
 display:none'>&#13;</span></div>
 <div style=3D'position:absolute;top:80.75%;left:8.42%;width:83.14%;height:=
7.5%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 113%;mso-special-format:lastCR;display:none'>&#13;</span></div>
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uction</span></div>
 <div v:shape=3D"_x0000_s9218" class=3DB><span style=3D'position:absolute;t=
op:14.24%;
 left:8.42%;width:93.82%;height:5.25%'><span style=3D'mso-special-format:no=
bullet;
 display:none;color:black;mso-color-index:3;font-family:"Monotype Sorts";
 font-size:75%'>n</span><span style=3D'font-size:75%;color:#FAFD00'><span
 style=3D'mso-tab-count:1;width:3.99%'> </span>Previous research concludes =
that
 intermediates found in </span></span><span style=3D'position:absolute;
 top:19.5%;left:12.17%;width:94.19%;height:5.25%'><span style=3D'font-size:=
75%;
 color:#FAFD00'>electrochemical studies of manganese carbonyl derivatives <=
/span></span><span
 style=3D'position:absolute;top:25.0%;left:12.17%;width:79.4%;height:5.25%'=
><span
 style=3D'font-size:75%;color:#FAFD00'>could be useful as catalysis in synt=
hesis
 of other </span></span><span style=3D'position:absolute;top:30.25%;left:12=
.17%;
 width:80.89%;height:5.25%'><span style=3D'font-size:75%;color:#FAFD00'>org=
anometallic
 compounds.</span><span style=3D'font-size:50%;color:#FAFD00;position:relat=
ive;
 top:-.45em;mso-text-raise:30%'>1</span><span style=3D'font-size:75%;color:=
#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp; </span>The possiblity of the </span></sp=
an><span
 style=3D'position:absolute;top:35.5%;left:12.17%;width:92.69%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>electrochemical formation of these
 catalytic intermediates </span></span><span style=3D'position:absolute;
 top:41.0%;left:12.17%;width:94.75%;height:5.25%'><span style=3D'font-size:=
75%;
 color:#FAFD00'>from cyclopentadienylmanganese tricarbonyl derivatives is <=
/span></span><span
 style=3D'position:absolute;top:46.25%;left:12.17%;width:87.45%;height:5.25=
%'><span
 style=3D'font-size:75%;color:#FAFD00'>explored in this study. The photoche=
mical
 chelation of </span></span><span style=3D'position:absolute;top:51.5%;
 left:12.17%;width:90.44%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>cyclopentadienylmanganese
 tricarbonyl derivatives (See </span></span><span style=3D'position:absolut=
e;
 top:56.75%;left:12.17%;width:87.26%;height:5.25%'><span style=3D'font-size=
:75%;
 color:#FAFD00'>Figure 1) is evident in the literature and occurs in high <=
/span></span><span
 style=3D'position:absolute;top:62.25%;left:12.17%;width:90.26%;height:5.25=
%'><span
 style=3D'font-size:75%;color:#FAFD00'>yields of the chelate derivatives.</=
span><span
 style=3D'font-size:50%;color:#FAFD00;position:relative;top:-.45em;mso-text=
-raise:
 30%'>2</span><span style=3D'font-size:75%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp; </span>Thus, it was proposed </span></sp=
an><span
 style=3D'position:absolute;top:67.5%;left:12.17%;width:82.58%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>that a cyclic voltammetric oxidation=
 would
 produce </span></span><span style=3D'position:absolute;top:72.75%;left:12.=
17%;
 width:91.19%;height:5.25%'><span style=3D'font-size:75%;color:#FAFD00'>che=
lates
 of the species.<span style=3D'mso-spacerun:yes'>&nbsp; </span>This study
 included two types of </span></span><span style=3D'position:absolute;top:7=
8.25%;
 left:12.17%;width:95.13%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>cyclopentadienylmanganese
 tricarbonyl derivatives that are </span></span><span style=3D'position:abs=
olute;
 top:83.5%;left:12.17%;width:79.4%;height:5.25%'><span style=3D'font-size:7=
5%;
 color:#FAFD00'>illustrated in Figure 2.<span style=3D'mso-spacerun:yes'>&n=
bsp;
 </span></span></span></div>
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 <div v:shape=3D"_x0000_s10243" class=3DT style=3D'text-align:left'><span
 style=3D'position:absolute;top:79.75%;left:8.42%;width:83.14%;height:6.0%'=
><span
 style=3D'font-size:64%;color:#FAFD00'>Figure 2.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span>Formulas and Abbreviations for </=
span></span><span
 style=3D'position:absolute;top:86.0%;left:8.42%;width:97.19%;height:6.0%'>=
<span
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 derivatives.</span></span></div>
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<title>Cyclic Voltammetric Investigation in the Oxidative Processes of
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l-format:
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Sorts";
 font-size:75%'>n</span><span style=3D'font-size:88%;color:#FAFD00'>Figure
 1.<span style=3D'mso-spacerun:yes'>&nbsp; </span>The photochemical chelati=
on of
 a </span></span><span style=3D'position:absolute;top:65.0%;left:16.47%;
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opentadienylmanganese
 tricarbonyl </span></span><span style=3D'position:absolute;top:71.25%;
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FAFD00'>derivative.
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 <div v:shape=3D"_x0000_s11266" class=3DT style=3D'position:absolute;top:3.=
0%;
 left:8.42%;width:83.14%;height:9.25%'><span style=3D'color:#FAFD00'>Result=
s</span></div>
 <div v:shape=3D"_x0000_s11267" class=3DB>
 <div style=3D'position:absolute;top:13.25%;left:8.42%;width:83.14%;height:=
6.0%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 88%;color:#FAFD00'><u><span style=3D'mso-tab-count:1;width:4.51%'> </span>=
</u></span><span
 style=3D'font-size:75%;color:#FAFD00'><u>Oxidation of A1-A5 and ACYL&#13;<=
/u></span></div>
 <span style=3D'position:absolute;top:20.5%;left:8.42%;width:99.25%;height:=
5.25%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 75%;color:#FAFD00'><span style=3D'mso-tab-count:1;width:3.77%'> </span>A s=
ingle
 oxidation wave was observed for each compound.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span></span></span><span style=3D'posi=
tion:
 absolute;top:25.75%;left:12.17%;width:89.13%;height:5.25%'><span
 style=3D'font-size:75%;color:#FAFD00'>This is evident in the cyclic voltam=
mogram
 in Figure 3.<span style=3D'mso-spacerun:yes'>&nbsp; </span></span></span><=
span
 style=3D'position:absolute;top:31.0%;left:12.17%;width:95.31%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>The average E</span><span
 style=3D'font-size:50%;color:#FAFD00;position:relative;top:.37em;mso-text-=
raise:
 -25%'>pa</span><span style=3D'font-size:75%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp;</span>and E</span><span style=3D'font-si=
ze:50%;
 color:#FAFD00;position:relative;top:.37em;mso-text-raise:-25%'>p</span><sp=
an
 style=3D'font-size:75%;color:#FAFD00'>-E</span><span style=3D'font-size:50=
%;
 color:#FAFD00;position:relative;top:.37em;mso-text-raise:-25%'>p/2 </span>=
<span
 style=3D'font-size:75%;color:#FAFD00'>values can be found in Table 1.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span></span></span><span style=3D'posi=
tion:
 absolute;top:36.5%;left:12.17%;width:95.31%;height:5.25%'><span
 style=3D'font-size:75%;color:#FAFD00'>The ratio of I</span><span
 style=3D'font-size:50%;color:#FAFD00;position:relative;top:.37em;mso-text-=
raise:
 -25%'>pa</span><span style=3D'font-size:75%;color:#FAFD00'>/v</span><span
 style=3D'font-size:50%;color:#FAFD00;position:relative;top:-.45em;mso-text=
-raise:
 30%'>1/2<span style=3D'mso-spacerun:yes'>&nbsp; </span></span><span
 style=3D'font-size:75%;color:#FAFD00'>remained fairly constant.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span>The values of </span></span><span
 style=3D'position:absolute;top:41.75%;left:12.17%;width:79.4%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>E</span><span style=3D'font-size:50%;
 color:#FAFD00;position:relative;top:.37em;mso-text-raise:-25%'>p</span><sp=
an
 style=3D'font-size:75%;color:#FAFD00'>-E</span><span style=3D'font-size:50=
%;
 color:#FAFD00;position:relative;top:.37em;mso-text-raise:-25%'>p/2 </span>=
<span
 style=3D'font-size:75%;color:#FAFD00'>indicate a single electron process.<=
span
 style=3D'mso-spacerun:yes'>&nbsp; </span>This is </span></span><span
 style=3D'position:absolute;top:47.0%;left:12.17%;width:92.69%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>consistent with other literature. </=
span><span
 style=3D'font-size:50%;color:#FAFD00;position:relative;top:-.45em;mso-text=
-raise:
 30%'>4</span><span style=3D'font-size:75%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp; </span>There was no indication </span></=
span><span
 style=3D'position:absolute;top:52.5%;left:12.17%;width:79.4%;height:5.25%'=
><span
 style=3D'font-size:75%;color:#FAFD00'>of a return reduction wave.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span>&#13;</span></span>
 <div style=3D'position:absolute;top:58.75%;left:8.42%;width:97.37%;height:=
5.25%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 75%;color:#FAFD00'><u><span style=3D'mso-tab-count:1;width:3.85%'> </span>=
Oxidation
 of A2Chelate, A2PPh</u></span><span style=3D'font-size:50%;color:#FAFD00;
 position:relative;top:.37em;mso-text-raise:-25%'><u>3</u></span><span
 style=3D'font-size:75%;color:#FAFD00'><u>, A3Chelate and A3PPh</u></span><=
span
 style=3D'font-size:50%;color:#FAFD00;position:relative;top:.37em;mso-text-=
raise:
 -25%'><u>3</u></span><span style=3D'font-size:75%;color:#FAFD00;display:no=
ne'>&#13;</span></div>
 <span style=3D'position:absolute;top:65.25%;left:8.42%;width:98.12%;height=
:5.25%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 75%;color:#FAFD00'><span style=3D'mso-tab-count:1;width:3.82%'> </span>A s=
ingle
 oxidation was also observed for these compound.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span></span></span><span style=3D'posi=
tion:
 absolute;top:70.5%;left:12.17%;width:95.31%;height:5.25%'><span
 style=3D'font-size:75%;color:#FAFD00'>The specific E</span><span
 style=3D'font-size:50%;color:#FAFD00;position:relative;top:.37em;mso-text-=
raise:
 -25%'>pa</span><span style=3D'font-size:75%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp;</span>and E</span><span style=3D'font-si=
ze:50%;
 color:#FAFD00;position:relative;top:.37em;mso-text-raise:-25%'>p</span><sp=
an
 style=3D'font-size:75%;color:#FAFD00'>-E</span><span style=3D'font-size:50=
%;
 color:#FAFD00;position:relative;top:.37em;mso-text-raise:-25%'>p/2 </span>=
<span
 style=3D'font-size:75%;color:#FAFD00'>values can be found in Table 2.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span></span></span><span style=3D'posi=
tion:
 absolute;top:75.75%;left:12.17%;width:88.01%;height:5.25%'><span
 style=3D'font-size:75%;color:#FAFD00'>The compounds were similar to the ot=
hers
 with a fairly </span></span><span style=3D'position:absolute;top:81.25%;
 left:12.17%;width:91.01%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>constant
 I</span><span style=3D'font-size:50%;color:#FAFD00;position:relative;top:.=
37em;
 mso-text-raise:-25%'>pa</span><span style=3D'font-size:75%;color:#FAFD00'>=
/v</span><span
 style=3D'font-size:50%;color:#FAFD00;position:relative;top:-.45em;mso-text=
-raise:
 30%'>1/2 </span><span style=3D'font-size:75%;color:#FAFD00'>and a single
 electron process.<span style=3D'mso-spacerun:yes'>&nbsp; </span>There was =
</span></span><span
 style=3D'position:absolute;top:86.5%;left:12.17%;width:79.4%;height:5.25%'=
><span
 style=3D'font-size:75%;color:#FAFD00'>no indication of a return reduction
 wave.<span style=3D'mso-spacerun:yes'>&nbsp; </span></span><span
 style=3D'font-size:75%;color:#FAFD00;display:none'><u>&#13;</u></span></sp=
an>
 <div style=3D'position:absolute;top:92.75%;left:8.42%;width:83.14%;height:=
5.25%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 75%;color:#FAFD00;mso-special-format:lastCR;display:none'><u>&#13;</u></sp=
an></div>
 </div>
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5%;
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sions</span></div>
 <div v:shape=3D"_x0000_s13314" class=3DB><span style=3D'position:absolute;
 top:13.25%;left:8.42%;width:85.39%;height:5.25%'><span style=3D'mso-specia=
l-format:
 nobullet;display:none;color:black;mso-color-index:3;font-family:"Monotype =
Sorts";
 font-size:75%'>n</span><span style=3D'font-size:75%;color:#FAFD00'><span
 style=3D'mso-tab-count:2;width:11.7%'> </span>During the oxidation of the
 cyclopentadienyl-</span></span><span style=3D'position:absolute;top:18.5%;
 left:12.17%;width:94.75%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>manganese
 tricarbonyl derivatives, a deposit formed on the </span></span><span
 style=3D'position:absolute;top:23.75%;left:12.17%;width:92.69%;height:5.25=
%'><span
 style=3D'font-size:75%;color:#FAFD00'>working electrode.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span>This was presented in the experim=
etal </span></span><span
 style=3D'position:absolute;top:28.99%;left:12.17%;width:92.5%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>section.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span>This deposit is a indication of a
 chemical formed </span></span><span style=3D'position:absolute;top:34.5%;
 left:12.17%;width:94.75%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>as
 a result of the oxidation of the compounds studied.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span>This </span></span><span
 style=3D'position:absolute;top:39.75%;left:12.17%;width:92.69%;height:5.25=
%'><span
 style=3D'font-size:75%;color:#FAFD00'>deposit and the absence of return
 reduction waves implies </span></span><span style=3D'position:absolute;
 top:45.0%;left:12.17%;width:86.14%;height:5.25%'><span style=3D'font-size:=
75%;
 color:#FAFD00'>that the compounds undergo an EC mechanism.</span><span
 style=3D'font-size:50%;color:#FAFD00;position:relative;top:-.45em;mso-text=
-raise:
 30%'>5</span><span style=3D'font-size:75%;color:#FAFD00'><span
 style=3D'mso-spacerun:yes'>&nbsp; </span>The </span></span><span
 style=3D'position:absolute;top:50.5%;left:12.17%;width:89.51%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>deposit on the electrode was not
 identified in this study. &#13;</span></span><span style=3D'position:absol=
ute;
 top:56.75%;left:8.42%;width:96.81%;height:5.25%'><span style=3D'mso-specia=
l-format:
 nobullet;display:none;color:black;mso-color-index:3;font-family:"Monotype =
Sorts";
 font-size:75%'>n</span><span style=3D'font-size:75%;color:#FAFD00'><span
 style=3D'mso-tab-count:2;width:10.32%'> </span>The intent of this research=
 was
 to attempt to form the </span></span><span style=3D'position:absolute;
 top:62.25%;left:12.17%;width:92.69%;height:5.25%'><span style=3D'font-size=
:75%;
 color:#FAFD00'>chelate derivatives.<span style=3D'mso-spacerun:yes'>&nbsp;
 </span>When compounds A1-A5 and ACYL </span></span><span style=3D'position=
:absolute;
 top:67.5%;left:12.17%;width:89.51%;height:5.25%'><span style=3D'font-size:=
75%;
 color:#FAFD00'>did not show return reduction waves, the chelates of A2 </s=
pan></span><span
 style=3D'position:absolute;top:72.75%;left:12.17%;width:88.01%;height:5.25=
%'><span
 style=3D'font-size:75%;color:#FAFD00'>and A3 were studied
 electrochemically.<span style=3D'mso-spacerun:yes'>&nbsp; </span>If the ch=
elates
 </span></span><span style=3D'position:absolute;top:78.0%;left:12.17%;width=
:89.88%;
 height:5.25%'><span style=3D'font-size:75%;color:#FAFD00'>indicated a retu=
rn
 reduction wave, it could be concluded </span></span><span style=3D'positio=
n:
 absolute;top:83.5%;left:12.17%;width:86.7%;height:5.25%'><span
 style=3D'font-size:75%;color:#FAFD00'>that A1-A5 and ACYL did not form the
 chelates upon </span></span><span style=3D'position:absolute;top:88.75%;
 left:12.17%;width:89.51%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>electrochemical
 oxidation.<span style=3D'mso-spacerun:yes'>&nbsp; </span>However, a return
 reduction</span></span></div>
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<title>Cyclic Voltammetric Investigation in the Oxidative Processes of
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 <div v:shape=3D"_x0000_s14338" class=3DB><span style=3D'position:absolute;
 top:9.75%;left:8.42%;width:92.5%;height:5.25%'><span style=3D'mso-special-=
format:
 nobullet;display:none;color:black;mso-color-index:3;font-family:"Monotype =
Sorts";
 font-size:75%'>n</span><span style=3D'font-size:75%;color:#FAFD00'><span
 style=3D'mso-tab-count:1;width:4.05%'> </span>wave was not evident for the=
se
 chelates. Therefore, the </span></span><span style=3D'position:absolute;
 top:15.25%;left:12.17%;width:93.07%;height:5.25%'><span style=3D'font-size=
:75%;
 color:#FAFD00'>electrochemical formation of the chelate derivatives could =
</span></span><span
 style=3D'position:absolute;top:20.5%;left:12.17%;width:79.4%;height:5.25%'=
><span
 style=3D'font-size:75%;color:#FAFD00'>not be confirmed or denied.&#13;</sp=
an></span><span
 style=3D'position:absolute;top:26.75%;left:8.42%;width:99.62%;height:5.25%=
'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 75%;color:#FAFD00'><span style=3D'mso-tab-count:2;width:10.03%'> </span>Ul=
timately,
 although evidence to prove or disprove the </span></span><span
 style=3D'position:absolute;top:32.25%;left:12.17%;width:79.4%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>electrochemical formation of the che=
lates
 of the </span></span><span style=3D'position:absolute;top:37.5%;left:12.17=
%;
 width:89.13%;height:5.25%'><span style=3D'font-size:75%;color:#FAFD00'>cyc=
lopentadienylmanganese
 tricarbonyl derivatives, the </span></span><span style=3D'position:absolut=
e;
 top:42.75%;left:12.17%;width:94.56%;height:5.25%'><span style=3D'font-size=
:75%;
 color:#FAFD00'>oxidation of these derivatives leads to interesting questio=
ns </span></span><span
 style=3D'position:absolute;top:48.25%;left:12.17%;width:93.44%;height:5.25=
%'><span
 style=3D'font-size:75%;color:#FAFD00'>and study.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span>Continued study could lead to dis=
covery
 of the </span></span><span style=3D'position:absolute;top:53.5%;left:12.17=
%;
 width:94.56%;height:5.25%'><span style=3D'font-size:75%;color:#FAFD00'>che=
mical
 species formed on the electrode during oxidation.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span></span></span><span style=3D'posi=
tion:
 absolute;top:58.75%;left:12.17%;width:83.14%;height:5.25%'><span
 style=3D'font-size:75%;color:#FAFD00'>It may also result in information th=
at
 could prove or </span></span><span style=3D'position:absolute;top:64.0%;
 left:12.17%;width:86.89%;height:5.25%'><span style=3D'font-size:75%;color:=
#FAFD00'>disprove
 the electrochemical formation of the chelates </span></span><span
 style=3D'position:absolute;top:69.5%;left:12.17%;width:79.4%;height:5.25%'=
><span
 style=3D'font-size:75%;color:#FAFD00'>from the cyclopentadienylmanganese
 tricarbonyl </span></span><span style=3D'position:absolute;top:74.75%;
 left:12.17%;width:79.4%;height:5.25%'><span style=3D'font-size:75%;color:#=
FAFD00'>derivatives.<span
 style=3D'mso-spacerun:yes'>&nbsp; </span></span></span></div>
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ay:
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phis
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0%;
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nces</span></div>
 <div v:shape=3D"_x0000_s21506" class=3DB>
 <div style=3D'position:absolute;top:17.5%;left:8.42%;width:86.14%;height:5=
.25%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 75%;color:#FAFD00'>1<span style=3D'mso-spacerun:yes'>&nbsp; </span>Pickett,
 C.J.; Pletcher, D. </span><span style=3D'font-size:75%;color:#FAFD00'><i>J=
.C.S.
 Dalton</i></span><span style=3D'font-size:75%;color:#FAFD00'>. </span><span
 style=3D'font-size:75%;color:#FAFD00'><b>1975</b></span><span style=3D'fon=
t-size:
 75%;color:#FAFD00'>, 879.&#13;</span></div>
 <span style=3D'position:absolute;top:24.0%;left:8.42%;width:95.5%;height:5=
.25%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 75%;color:#FAFD00'>2<span style=3D'mso-spacerun:yes'>&nbsp; </span>Pang, Z=
. </span><span
 style=3D'font-size:75%;color:#FAFD00'><i>The Synthesis and the Chemistry of
 Cymantrene </i></span></span><span style=3D'position:absolute;top:29.25%;
 left:12.17%;width:79.4%;height:5.25%'><span style=3D'font-size:75%;color:#=
FAFD00'><i>Derivatives
 with Chelatable Substituent on the </i></span></span><span style=3D'positi=
on:
 absolute;top:34.75%;left:12.17%;width:79.4%;height:5.25%'><span
 style=3D'font-size:75%;color:#FAFD00'><i>Cyclopentadienyl Ring</i></span><=
span
 style=3D'font-size:75%;color:#FAFD00'>; Ph.D. Dissertation, UM.&#13;</span=
></span><span
 style=3D'position:absolute;top:41.0%;left:8.42%;width:91.94%;height:5.25%'=
><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 75%;color:#FAFD00'>3<span style=3D'mso-spacerun:yes'>&nbsp; </span>Pang, Z;
 Johnston, R.F.; VanDerVeer. Submitted for J. </span></span><span
 style=3D'position:absolute;top:46.25%;left:12.17%;width:79.4%;height:5.25%=
'><span
 style=3D'font-size:75%;color:#FAFD00'>Organometallic Chem. &#13;</span></s=
pan>
 <div style=3D'position:absolute;top:52.75%;left:8.42%;width:96.25%;height:=
5.25%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 75%;color:#FAFD00'>4<span style=3D'mso-spacerun:yes'>&nbsp; </span>Connell=
y,
 N.G.; Kitchen, M. D. J.C.S. Dalton. </span><span style=3D'font-size:75%;
 color:#FAFD00'><b>1975</b></span><span style=3D'font-size:75%;color:#FAFD0=
0'>,
 931.&#13;</span></div>
 <span style=3D'position:absolute;top:59.0%;left:8.42%;width:88.2%;height:5=
.25%'><span
 style=3D'mso-special-format:nobullet;display:none;color:black;mso-color-in=
dex:
 3;font-family:"Monotype Sorts";font-size:75%'>n</span><span style=3D'font-=
size:
 75%;color:#FAFD00'>5<span style=3D'mso-spacerun:yes'>&nbsp; </span>Crabtre=
e,
 R.H. </span><span style=3D'font-size:75%;color:#FAFD00'><i>The Organometal=
lic
 Chemistry of the </i></span></span><span style=3D'position:absolute;top:64=
.5%;
 left:12.17%;width:80.52%;height:5.25%'><span style=3D'font-size:75%;color:=
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------=_NextPart_01C4FE1D.DEC8E130
Content-Location: file:///C:/2B3AA291/ddbslidessummerpres1_files/script.js
Content-Transfer-Encoding: quoted-printable
Content-Type: application/javascript; charset="us-ascii"

function LoadSld()
{
	var sld=3DGetObj("SlideObj")
	if( !g_supportsPPTHTML ) {	=09
		sld.style.visibility=3D"visible"
		return
	}

	if( MakeNotesVis() ) return

	runAnimations =3D _InitAnimations();
=09
	if( IsWin("PPTSld") )
		parent.SldUpdated(GetSldId())
	g_origSz=3DparseInt(SlideObj.style.fontSize)
	g_origH=3Dsld.style.posHeight
	g_origW=3Dsld.style.posWidth
	g_scaleHyperlinks=3D(document.all.tags("AREA").length>0)
	if( g_scaleHyperlinks )
		InitHLinkArray()
	if( g_scaleInFrame||(IsWin("PPTSld") && parent.IsFullScrMode() ) )
		document.body.scroll=3D"no"
	_RSW()
	if( IsWin("PPTSld") && parent.IsFullScrMode() )
		FullScrInit();
=09
	MakeSldVis();
	ChkAutoAdv()

	if( runAnimations )
	{
		if( document.all("NSPlay") )
			document.all("NSPlay").autoStart =3D false;

		if( sld.filters && sld.filters.revealtrans )
			setTimeout( "document.body.start()", sld.filters.revealtrans.duration * =
1000 );
		else
			document.body.start();
	}
}

function MakeSldVis()=20
{
	var fTrans=3Dg_showAnimation && SldHasTrans()
	if( fTrans )=09
	{
		if( g_bgSound ) {
			idx=3Dg_bgSound.indexOf(",");
			pptSound.src=3Dg_bgSound.substr( 0, idx );
			pptSound.loop=3D -(parseInt(g_bgSound.substr(idx+1)));
		}
		SlideObj.filters.revealtrans.Apply()=09
    }
	SlideObj.style.visibility=3D"visible"
	if( fTrans )
		SlideObj.filters.revealtrans.Play()
}
function MakeNotesVis()=20
{
	if( !IsNts() ) return false=20
	SlideObj.style.display=3D"none"
	nObj =3D document.all.item("NotesObj")
	parent.SetHasNts(0)
	if( nObj ) {=20
		nObj.style.display=3D""
		parent.SetHasNts(1)
	}
	return 1
}
function ChkAutoAdv()
{
	if(SldHasTrans())
		SlideObj.onfilterchange=3DAutoAdv
	else
		AutoAdv()
}
function AutoAdv()
{
	if(!IsWin("PPTSld") || !gUseSldTimings )return
	var sld=3DGetCurSld()
	if( (sld.mAdvDelay>0) && !parent.IsFramesMode() )
		setTimeout("parent.GoToNextSld()",sld.mAdvDelay)
}
function GetObj(id)
{
	if(g_supportsPPTHTML) return document.all(id);
	else return document.getElementById(id);
}
function SldHasTrans() { return SlideObj.style.filter !=3D ""; }
function GetSldId() { return sId=3Dlocation.href.substring(location.href.la=
stIndexOf('/')+1) }
function HideMenu() { if( frames["PPTSld"] && PPTSld.document.all.item("ctx=
tmenu") && PPTSld.ctxtmenu.style.display!=3D"none" ) { PPTSld.ctxtmenu.styl=
e.display=3D'none'; return true } return false }
function IsWin( name ) { return window.name =3D=3D name }
function IsNts() { return IsWin("PPTNts") }
function IsSldOrNts() { return( IsWin("PPTSld")||IsWin("PPTNts") ) }
function SupportsPPTAnimation() { return( navigator.platform =3D=3D "Win32"=
 && navigator.appVersion.indexOf("Windows")>0 ) }
function SupportsPPTHTML()
{
	var appVer=3Dnavigator.appVersion, msie=3DappVer.indexOf("MSIE "), ver=3D0
	if( msie >=3D 0 )
		ver=3DparseFloat( appVer.substring( msie+5, appVer.indexOf(";",msie) ) )
	else
		ver=3DparseInt(appVer)

	return( ver >=3D 4 && msie >=3D 0 )
}
function _RSW()
{
	if( !g_supportsPPTHTML || IsNts() ||
	  ( !g_scaleInFrame && (!IsWin("PPTSld") || !parent.IsFullScrMode()) ) )
		return

        var padding=3D0;
        if( IsWin("PPTSld") && parent.IsFramesMode() ) padding=3D6

	cltWidth=3Ddocument.body.clientWidth-padding
	cltHeight=3Ddocument.body.clientHeight-padding
	factor=3D(1.0*cltWidth)/g_origW
	if( cltHeight < g_origH*factor )
		factor=3D(1.0*cltHeight)/g_origH

	newSize =3D g_origSz * factor
	if( newSize < 1 ) newSize=3D1

	s=3DSlideObj.style
	s.fontSize=3DnewSize+"px"
	s.posWidth=3Dg_origW*factor
	s.posHeight=3Dg_origH*factor
	s.posLeft=3D(cltWidth-s.posWidth+padding)/2
	s.posTop=3D(cltHeight-s.posHeight+padding)/2

	if( g_scaleHyperlinks )
		ScaleHyperlinks( factor )
}
function _InitAnimations()
{
	animRuntimeInstalled =3D ''+document.body.localTime !=3D 'undefined';
	isFullScreen =3D (window.name =3D=3D "PPTSld") && !parent.IsFramesMode();
	g_animUseRuntime =3D g_showAnimation && animRuntimeInstalled && !(isFullSc=
reen && parent.IsSldVisited());
	if( g_animUseRuntime ) {
		collSeq =3D document.all.tags("seq");
		if( collSeq !=3D null ) {
			for(ii=3D0;ii<collSeq.length;ii++) {
				if( collSeq[ii].getAttribute( "p:nodeType" ) =3D=3D "mainSeq" ) {
					g_animMainSequence =3D collSeq[ii];
					break;
				}
			}
		}
=09
		if( g_animItemsToHide && document.body.playAnimations !=3D false ) {
			for(jj =3D 0; jj < g_animItemsToHide.length; jj++) {
				if( hideObj =3D GetObj(g_animItemsToHide[jj]) )
					hideObj.runtimeStyle.visibility=3D"hidden";
			}
		}

		if( g_animInteractiveItems ){
			for(jj =3D 0; jj < g_animInteractiveItems.length; jj++) {
				if( triggerObj =3D GetObj(g_animInteractiveItems[jj]) )
					triggerObj.runtimeStyle.cursor=3D"hand";
			}
		}
	=09
		if( gUseSldTimings && ''+g_animSlideTime !=3D 'undefined' ) {
			adjustedTime =3D document.body.calculateAutoAdvanceTimes( g_animSlideTim=
e, g_animEffectTimings );
			if( IsWin("PPTSld") && adjustedTime !=3D g_animSlideTime ) {
			   var sld =3D GetCurSld();
			   sld.mAdvDelay =3D adjustedTime * 1000;
			}
		}
	}

	return g_animUseRuntime;
}

gSldJump =3D 0, gSldJumpTrack =3D 0, gSldJumpIdx =3D "";

function _KPH()
{=20
	if( IsNts() ) return;

	if( !parent.IsFramesMode() && event.keyCode =3D=3D 27 && !HideMenu() )
		parent.window.close( self );
	else if( event.keyCode =3D=3D 32 ) {
		if( window.name =3D=3D "PPTSld" )
			parent.PPTSld.DocumentOnClick();
		else
			parent.GoToNextSld();
	}

	CatchNumKeys( parent, event );
}

function CatchNumKeys( win, event ) {
	if( win.IsFullScrMode() && (48<=3Devent.keyCode) && (event.keyCode<=3D57) =
) {
		gSldJump =3D 1;
		gSldJumpIdx +=3D (event.keyCode-48).toString();
	}
	if( win.IsFullScrMode() && gSldJump && event.keyCode =3D=3D 13 ) {
		var numSlds =3D parent.GetSldList().mList.length
		if ( gSldJumpIdx > numSlds )
			gSldJumpIdx =3D numSlds;
		if ( gSldJumpIdx >=3D 0 ) {
			if ( gSldJumpIdx =3D=3D 0 )
				gSldJumpIdx =3D 1;
			var jumpTo =3D parseInt(gSldJumpIdx);
			gSldJump =3D 0; gSldJumpIdx =3D "";
			win.GoToSld( parent.GetSldList().mList[jumpTo-1].mSldHref )
		}
	}
}

function _KDH()
{
	if( event.keyCode =3D=3D 8 ) {
		event.returnValue =3D 0;
		parent.GoToPrevSld();
	}
}
function DocumentOnClick()
{
	if( IsNts() || parent.HideMenu() ) return;
	if( ( g_allowAdvOnClick && !parent.IsFramesMode() ) ||
	    (event && (event.keyCode=3D=3D32) ) )
		parent.GoToNextSld();
}



var g_supportsPPTHTML =3D SupportsPPTHTML(), g_scaleInFrame =3D 1, gId=3D""=
, g_bgSound=3D"",
    g_scaleHyperlinks =3D false, g_allowAdvOnClick =3D 1, g_showInBrowser =
=3D 0, gLoopCont =3D 0, gUseSldTimings =3D 0;
var g_showAnimation =3D g_supportsPPTHTML && SupportsPPTAnimation() && ( (w=
indow.name=3D=3D"PPTSld" && !parent.IsFramesMode()) || g_showInBrowser );va=
r g_animManager =3D null;
var g_animUseRuntime =3D false;
var g_animItemsToHide, g_animInteractiveItems, g_animSlideTime;
var g_animMainSequence =3D null;

var ENDSHOW_MESG=3D"End of slide show, click to exit.", SCREEN_MODE=3D"Fram=
es", gIsEndShow=3D0, NUM_VIS_SLDS=3D13, SCRIPT_HREF=3D"script.js", FULLSCR_=
HREF=3D"fullscreen.htm";
var gCurSld =3D gPrevSld =3D 1, g_offset =3D 0, gNtsOpen =3D gHasNts =3D gO=
tlTxtExp =3D 0, gHasNarration =3D 0, gOtlOpen =3D true
window.gPPTHTML=3DSupportsPPTHTML()
var gMainDoc=3Dnew Array(new hrefList("slide0001.htm",1,-1,1),new hrefList(=
"slide0002.htm",1,-1,1),new hrefList("slide0003.htm",1,-1,1),new hrefList("=
slide0004.htm",1,-1,1),new hrefList("slide0005.htm",1,-1,1),new hrefList("s=
lide0006.htm",1,-1,1),new hrefList("slide0007.htm",1,-1,1),new hrefList("sl=
ide0008.htm",1,-1,1),new hrefList("slide0009.htm",1,-1,1),new hrefList("sli=
de0010.htm",1,-1,1),new hrefList("slide0011.htm",1,-1,1),new hrefList("slid=
e0012.htm",1,-1,1),new hrefList("slide0013.htm",1,-1,1));

/*********************************************
 Frameset functions

 These functions control slide navigation
 and state of the frameset.
**********************************************/

function FullScrInit()
{
	g_allowAdvOnClick =3D GetCurSld().mAdvOnClk
	document.body.style.backgroundColor=3D"black"
	document.oncontextmenu=3Dparent._CM;
	document.onkeydown =3D _KDH;
	document.ondragstart=3DCancel
	document.onselectstart=3DCancel
	self.focus()
}

function Redirect( frmId )
{=09
	var str=3Ddocument.location.hash,idx=3Dstr.indexOf('#'), sId=3DGetSldId()
	if(idx>=3D0) str=3Dstr.substr(1);
	if( window.name !=3D frmId && ( sId !=3D str) ) {
		obj =3D GetObj("Main-File")
		window.location.href=3Dobj.href+"#"+sId
		return 1
	}
	return 0
}

var MHTMLPrefix =3D CalculateMHTMLPrefix();=20
function CalculateMHTMLPrefix()
{
	if ( document.location.protocol =3D=3D 'mhtml:') {=20
		href=3Dnew String(document.location.href)=20
		Start=3Dhref.indexOf('!')+1=20
		End=3Dhref.lastIndexOf('/')+1=20
		if (End < Start)=20
			return href.substring(0, Start)=20
		else=20
		return href.substring(0, End)=20
	}
	return '';
}

function GetTags(base,tag)
{
	if(g_supportsPPTHTML) return base.all.tags(tag);
	else return base.getElementsByTagName(tag);
}


function UpdNtsPane(){ if(frames["PPTNts"]) PPTNts.location.replace( MHTMLP=
refix+GetHrefObj( gCurSld ).mNtsHref ) }

function UpdNavPane( sldIndex ){ if(gNavLoaded) PPTNav.UpdNav() }

function UpdOtNavPane(){ if(gOtlNavLoaded) PPTOtlNav.UpdOtlNav() }

function UpdOtlPane(){ if(gOtlLoaded) PPTOtl.UpdOtl() }

function SetHasNts( fVal )
{
	if( gHasNts !=3D fVal ) {
		gHasNts=3DfVal
		UpdNavPane()
	}
}

function ToggleOtlText()
{
	gOtlTxtExp=3D!gOtlTxtExp
	UpdOtlPane()
}

function ClearMedia()
{
	// Clear any sounds playing before launching another browser window. Other=
wise,
	// in fullscreen mode, you'll continue to hear the sound in the frames mod=
e.
	if (PPTSld.pptSound) PPTSld.pptSound.loop =3D 0;
}

function FullScreen()
{=20
	if ( PPTSld.g_animUseRuntime )
		PPTSld.document.body.pause();
	ClearMedia();
	var href =3D ( document.location.protocol =3D=3D 'mhtml:') ? FULLSCR_HREF =
: FULLSCR_HREF+"#"+GetHrefObj(gCurSld).mSldHref;
	if(PPTNav.event.ctrlKey) {
		var w =3D (window.screen.availWidth * 1.0) / 2.0
		var h =3D w * (PPTSld.g_origH * 1.0) / PPTSld.g_origW
		win =3D window.open( MHTMLPrefix+href,null,"toolbar=3D0,resizable=3D1,top=
=3D0,left=3D0," + "width=3D"+ w + ",height=3D" + h );
		if( win.document.body && PPTSld.g_animUseRuntime )
			win.document.body.PPTSldFrameset=3Dwindow;
	}
	else
	{
		win =3D window.open( MHTMLPrefix+href,null,"fullscreen=3Dyes" );
		if( win.document.body && PPTSld.g_animUseRuntime )
			win.document.body.PPTSldFrameset=3Dwindow;
	}
}

function ToggleVNarration()
{
	rObj=3DPPTSld.document.all("NSPlay")
	if( rObj && !PPTSld.g_animUseRuntime ) {
		if( (rObj.playState =3D=3D 1)||(rObj.playState =3D=3D 0) )
			rObj.Play()
		else if( rObj.playState =3D=3D 2 )
			rObj.Pause()
		else
			return;
	}
	else if( PPTSld.g_animUseRuntime )
	{
		narObj =3D PPTSld.document.all("narrationID")
		if( narObj )
			narObj.togglePause()
	}
}

function GetCurSldNum()
{  =20
	obj=3DGetHrefObj(gCurSld)
	if( obj.mOrigVis =3D=3D 1 )
		return obj.mSldIdx
	else  =20
		return gCurSld
}

function GetNumSlds()
{  =20
	if( GetHrefObj(gCurSld).mOrigVis =3D=3D 1 )
		return GetSldList().mNumVisSlds;
	else
		return GetSldList().mList.length
}

function GetSldNum( href )
{
	for(ii=3D0; ii<GetSldList().mList.length; ii++) {
		if ( GetSldList().mList[ii].mSldHref =3D=3D href )
			return ii+1
	}
	return 1
}

function GetHrefObj( sldIdx ){ return GetSldList().mList[sldIdx-1] }

function IsFramesMode(){ return ( SCREEN_MODE =3D=3D "Frames" ) }

function IsFullScrMode(){ return ( SCREEN_MODE =3D=3D "FullScreen" ) }

function GoToNextSld()
{
	ii=3DgCurSld + 1
	if( GetHrefObj( ii-1 ).mOrigVis =3D=3D 0 ) {
		if( ii<=3DGetSldList().mList.length ) {
			obj=3DGetHrefObj(ii)
			obj.mVis=3D1
			GoToSldNum(ii)
			return
		}
	}
	else {
		obj=3DGetHrefObj( ii )
		while ( obj && ( obj.mOrigVis =3D=3D 0 ) )
			obj=3DGetHrefObj(++ii)
		if( obj && obj.mOrigVis ) {
			GoToSldNum(ii)
			return
		}
	}
	if( gSldStack.length > 1 )
		PopSldList();
	else if( !IsFramesMode() ) {
                if( gLoopCont )
			GoToFirst()
                else
			EndShow()
	}
}

function GoToPrevSld()
{
	ii=3DgCurSld-1
	if( ii > 0 ) {
		obj=3DGetHrefObj(ii)
		while ( obj && ( obj.mVis =3D=3D 0 ) && ( ii>0 ) )
			obj=3DGetHrefObj(--ii)
        if( ii =3D=3D 0 ) ii=3D1
		GoToSldNum(ii)
	}
}

function GoToFirst(){ GoToSld( GetHrefObj(1).mSldHref ) }

function GoToLast()
{
	ii=3DGetSldList().mList.length
	if( ii !=3D gCurSld )
		GoToSld( GetHrefObj(ii).mSldHref )
}

function GoToSldNum( num )
{
	if( PPTSld.event ) PPTSld.event.cancelBubble=3Dtrue
	obj =3D GetHrefObj( num )
	obj.mVis=3D1
	gPrevSld=3DgCurSld
	gCurSld =3D num;
	PPTSld.location.replace(MHTMLPrefix+obj.mSldHref)
	if( IsFramesMode() ) {
		UpdNavPane(); UpdOtlPane(); UpdNtsPane()
	}
}

function GoToSld( href )
{
	if( PPTSld.event ) PPTSld.event.cancelBubble=3Dtrue
	GetHrefObj( GetSldNum(href) ).mVis=3D1
	PPTSld.location.replace(MHTMLPrefix+href)
}

function SldUpdated( id )
{
	if( id =3D=3D GetHrefObj(gCurSld).mSldHref ) return
	gPrevSld=3DgCurSld
	gCurSld=3DGetSldNum(id)
	if( IsFramesMode() ) {
		UpdNavPane(); UpdOtlPane(); UpdNtsPane()
	}
}

function PrevSldViewed(){ GoToSld( GetHrefObj(gPrevSld).mSldHref ) }
function HasPrevSld() { return ( gIsEndShow || ( gCurSld !=3D 1 && GetHrefO=
bj( gCurSld-1 ).mVis =3D=3D 1 )||( GetCurSldNum() > 1 ) ) }
function HasNextSld() { return (GetCurSldNum() !=3D GetNumSlds()) }

function CloseWindow() {
	if( HideMenu() ) return;
=09
	var event =3D PPTSld.event;
	if( !IsFramesMode() && event && (event.keyCode=3D=3D27 || event.keyCode=3D=
=3D32 || event.type=3D=3D"click" ) )
		window.close( self );
	CatchNumKeys( self, event );
}

function Unload() { gIsEndShow=3D0; }

function SetupEndShow() {
	gIsEndShow=3D1;
	PPTSld.document.body.scroll=3D"no";
	PPTSld.document.onkeypress=3DCloseWindow;
	PPTSld.document.onclick=3DCloseWindow;
	PPTSld.document.oncontextmenu=3D_CM;
}

function EndShow()
{
	if( IsFramesMode() ) return
	if( PPTSld.event ) PPTSld.event.cancelBubble=3Dtrue

	doc=3DPPTSld.document
	var dir =3D doc.body.dir
	if( dir !=3D "rtl" ) dir =3D "ltr";
	doc.open()
	doc.writeln('<html><body dir=3D' + dir + ' bgcolor=3Dblack onload=3Dparent=
.SetupEndShow() onunload=3Dparent.Unload()><center><p><font face=3DTahoma c=
olor=3Dwhite size=3D2><br><b>' + ENDSHOW_MESG + '</b></font></p></center></=
body></html>')
	doc.close()
}

function SetSldVisited(){ GetSldList().mList[gCurSld-1].mVisited=3Dtrue }

function IsSldVisited(){ return GetSldList().mList[gCurSld-1].mVisited }

function hrefList( sldHref, visible, advDelay, advClk )
{
	this.mSldHref=3D this.mNtsHref =3D sldHref
	this.mOrigVis=3D this.mVis =3D visible
	this.mVisited=3D false
	this.mAdvDelay=3D advDelay
	this.mAdvOnClk=3D advClk
}

function SldList(arr,curSld,fEnd)
{
	this.mCurSld =3D curSld;
	this.mList =3D new Array();

	var idx =3D 1;
	for(ii=3D0;ii<arr.length;ii++) {
		this.mList[ii] =3D new hrefList( arr[ii].mSldHref, arr[ii].mOrigVis, arr[=
ii].mAdvDelay, arr[ii].mAdvOnClk );
		if( arr[ii].mOrigVis )
			this.mList[ii].mSldIdx =3D idx++;
	}
	this.mNumVisSlds =3D idx-1;
	this.fEndShow =3D fEnd;
}

function GetSldList() {	return gSldStack[gSldStack.length-1] }
function GetCurSld() { return parent.GetSldList().mList[parent.gCurSld - 1]=
 }

gSldStack =3D new Array();
gSldStack[0] =3D new SldList(gMainDoc,gCurSld,1)
function ToggleOtlPane()
{
	frmset=3Ddocument.all("PPTHorizAdjust")
	frm=3Ddocument.all("PPTOtl")

	if( gOtlOpen )
		frmset.cols=3D"*,100%"
	else
		frmset.cols=3D"25%,*"

	gOtlOpen=3D!gOtlOpen
	frm.noResize=3D!frm.noResize
	UpdOtNavPane()
}

function ToggleNtsPane()
{
	frmset=3Ddocument.all("PPTVertAdjust")
	frm=3Ddocument.all("PPTNts")

	if( gNtsOpen )
		frmset.rows=3D"100%,*"
	else
		frmset.rows=3D"*,20%"

	gNtsOpen=3D!gNtsOpen
	UpdNtsPane()
}

/*********************************************
Custom Shows implementation

When ViewCustomShow() is called, we create
a new array that is a subset of the slides in=20
the main doc. This list pushed on a stack so
we can return after the end of the custom
show.
*********************************************/
function ViewCustomShow(idx,fEnd)
{
	if( !IsFullScrMode() ) return;
	var sldList =3D new Array();
	var custShow =3D custShowList[idx-1];
	var jj =3D 0;
	for( ii=3D0;ii<custShow.length;ii++ ) {
		if( custShow[ii] <=3D gMainDoc.length )
			sldList[jj++] =3D gMainDoc[custShow[ii]-1];
	}
	if (sldList.length > 0) {
	PushSldList(sldList,fEnd);
	gCurSld =3D 1;
	}
	else
		if( PPTSld.event ) PPTSld.event.cancelBubble=3Dtrue
}

function PushSldList(arr,fEnd) {
	var ii =3D gSldStack.length;
	gSldStack[ii] =3D new SldList(arr,gCurSld,fEnd);
	GoToSld( gSldStack[ii].mList[0].mSldHref );
}

function PopSldList() {
	if (gSldStack[gSldStack.length-1].fEndShow)
		EndShow()
	else {
	gCurSld =3D gSldStack[gSldStack.length-1].mCurSld;
	gSldStack[gSldStack.length-1] =3D null;
	gSldStack.length--;
	var sldList =3D gSldStack[gSldStack.length-1];
	GoToSld( sldList.mList[gCurSld - 1].mSldHref );
	}
}
var custShowList=3Dnew Array();

/*********************************************
 Navigation button implementation

 There are 2 types of buttons: ImgBtn, TxtBtn
 implemented as function objects. They share
 a similiar interface so the event handlers
 can call SetActive, for example, on a button=20
 object without needing to know exactly=20
 what type of button it is.
**********************************************/

//----------------------------------
function ImgBtn( oId,bId,w,action )
//----------------------------------
{
	var t=3Dthis
	t.Perform    =3D _IBP
	t.SetActive  =3D _IBSetA
	t.SetInactive=3D _IBSetI
	t.SetPressed =3D _IBSetP
	t.SetDisabled=3D _IBSetD
	t.Enabled    =3D _IBSetE
	t.ChangeIcon =3D null
	t.UserAction =3D action
	t.ChgState   =3D _IBUI
	t.mObjId   =3D oId
	t.mBorderId=3D bId
	t.mWidth   =3D w
	t.mIsOn    =3D t.mCurState =3D 0
}

function _IBSetA()
{
	if( this.mIsOn ) {
		obj=3Dthis.ChgState( gHiliteClr,gShadowClr,2 )
		obj.style.posTop=3D0
	}
}

function _IBSetI()
{
	if( this.mIsOn ) {
		obj=3Dthis.ChgState( gFaceClr,gFaceClr,1 )
		obj.style.posTop=3D0=20
	}
}

function _IBSetP()
{
	if( this.mIsOn ) {
		obj=3Dthis.ChgState( gShadowClr,gHiliteClr,2 )
		obj.style.posLeft+=3D1; obj.style.posTop+=3D1
	}
}

function _IBSetD()
{ =20
	obj=3Dthis.ChgState( gFaceClr,gFaceClr,0 )
	obj.style.posTop=3D0=20
}

function _IBSetE( state )
{
	var t=3Dthis
	GetObj( t.mBorderId ).style.visibility=3D"visible"
	if( state !=3D t.mIsOn ) {
		t.mIsOn=3Dstate
		if( state )
			t.SetInactive()
		else
			t.SetDisabled()
	}
}

function _IBP()
{
	var t=3Dthis
	if( t.mIsOn ) {
		if( t.UserAction !=3D null )
			t.UserAction()
		if( t.ChangeIcon ) {
			obj=3DGetObj(t.mObjId)
			if( t.ChangeIcon() )
				obj.style.posLeft=3Dobj.style.posLeft+(t.mCurState-4)*t.mWidth
			else
				obj.style.posLeft=3Dobj.style.posLeft+(t.mCurState-0)*t.mWidth
		}
		t.SetActive()
	} =20
}

function _IBUI( clr1,clr2,nextState )
{
	var t=3Dthis
	SetBorder( GetObj( t.mBorderId ),clr1,clr2 )
	obj=3DGetObj( t.mObjId )
	obj.style.posLeft=3Dobj.style.posLeft+(t.mCurState-nextState)*t.mWidth-obj=
.style.posTop
	t.mCurState=3DnextState
	return obj
}

//-----------------------------------------
function TxtBtn( oId,oeId,action,chkState )
//-----------------------------------------
{
	var t=3Dthis
	t.Perform    =3D _TBP
	t.SetActive  =3D _TBSetA
	t.SetInactive=3D _TBSetI
	t.SetPressed =3D _TBSetP
	t.SetDisabled=3D _TBSetD
	t.SetEnabled =3D _TBSetE
	t.GetState   =3D chkState
	t.UserAction =3D action
	t.ChgState   =3D _TBUI
	t.mObjId      =3D oId
	t.m_elementsId=3D oeId
	t.mIsOn       =3D 1
}

function _TBSetA()
{
	var t=3Dthis
	if( t.mIsOn && !t.GetState() )
		t.ChgState( gHiliteClr,gShadowClr,0,0 )
}

function _TBSetI()
{
	var t=3Dthis
	if( t.mIsOn && !t.GetState() )
		t.ChgState( gFaceClr,gFaceClr,0,0 )
}

function _TBSetP()
{
	if( this.mIsOn )
		this.ChgState( gShadowClr,gHiliteClr,1,1 )
}

function _TBSetD()
{  =20
	this.ChgState( gFaceClr,gFaceClr,0,0 )
	this.mIsOn =3D 0
}

function _TBSetE()
{
	var t=3Dthis
	if( !t.GetState() )
		t.ChgState( gFaceClr,gFaceClr,0,0 )
	else
		t.ChgState( gShadowClr,gHiliteClr,1,1 )
	t.mIsOn =3D 1
}

function _TBP()
{
	var t=3Dthis
	if( t.mIsOn ) {=20
		if( t.UserAction !=3D null )
			t.UserAction()
        if( !t.GetState )
            return
		if( t.GetState() )
			t.SetPressed()
		else
			t.SetActive()
	} =20
}

function _TBUI( clr1,clr2,lOffset,tOffset )
{
	SetBorder( GetObj( this.mObjId ),clr1,clr2 )
	Offset( GetObj( this.m_elementsId ),lOffset,tOffset )
}

function Offset( obj, top, left ){ obj.style.top=3Dtop; obj.style.left=3Dle=
ft }

function SetBorder( obj, upperLeft, lowerRight )
{
	s=3Dobj.style;
	s.borderStyle      =3D "solid"
	s.borderWidth      =3D 1=20
	s.borderLeftColor  =3D s.borderTopColor =3D upperLeft
	s.borderBottomColor=3D s.borderRightColor =3D lowerRight
}

function GetBtnObj(){ return gBtnArr[window.event.srcElement.id] }

function BtnOnOver(){ b=3DGetBtnObj(); if( b !=3D null ) b.SetActive() }

function BtnOnDown(){ b=3DGetBtnObj(); if( b !=3D null ) b.SetPressed() }

function BtnOnOut(){ b=3DGetBtnObj(); if( b !=3D null ) b.SetInactive() }

function BtnOnUp()
{
	b=3DGetBtnObj()
	if( b !=3D null )
		b.Perform()
	else
		Upd()
}
function GetNtsState(){ return parent.gNtsOpen }

function GetOtlState(){ return parent.gOtlOpen }

function GetOtlTxtState(){ return parent.gOtlTxtExp }

function NtsBtnSetFlag( fVal )
{
	s=3Ddocument.all.item( this.m_flagId ).style
	s.display=3D"none"
	if( fVal )
		s.display=3D""
	else
		s.display=3D"none"
}

function _BSetA_Border(){ b =3D gBtnArr[this.mObjId]; if( b !=3D null ) b.S=
etActive() }

function _BSetI_Border(){ b =3D gBtnArr[this.mObjId]; if( b !=3D null ) b.S=
etInactive() }

function _BSetP_Border(){ b =3D gBtnArr[this.mObjId]; if( b !=3D null ) b.S=
etPressed() }

function _BSetA_BorderImg()
{=20
	b =3D gBtnArr[this.mBorderId]=20
	if( b !=3D null && this.mIsOn && !b.GetState() ) {
		obj=3Dthis.ChgState( gHiliteClr,gShadowClr,2 )
		obj.style.posTop=3D0
	}
}

function _BSetI_BorderImg()
{=20
	b =3D gBtnArr[this.mBorderId]
	if( b !=3D null && this.mIsOn && !b.GetState() ) {
		obj=3Dthis.ChgState( gFaceClr,gFaceClr,1 )
		obj.style.posTop=3D0
	}
}


var gHiliteClr=3D"THREEDHIGHLIGHT",gShadowClr=3D"THREEDSHADOW",gFaceClr=3D"=
THREEDFACE"
var gBtnArr =3D new Array()
gBtnArr["nb_otl"] =3D new TxtBtn( "nb_otl","nb_otlElem",parent.ToggleOtlPan=
e,GetOtlState )
gBtnArr["nb_otlElem"] =3D new TxtBtn( "nb_otl","nb_otlElem",parent.ToggleOt=
lPane,GetOtlState )
gBtnArr["nb_nts"] =3D new ImgBtn( "nb_nts","nb_ntsBorder",10,parent.ToggleN=
tsPane )
gBtnArr["nb_nts"].SetActive =3D _BSetA_BorderImg;
gBtnArr["nb_nts"].SetInactive =3D _BSetI_BorderImg;
gBtnArr["nb_ntsBorder"] =3D new TxtBtn( "nb_ntsBorder","nb_ntsElem",parent.=
ToggleNtsPane,GetNtsState )
gBtnArr["nb_ntsElem"] =3D new TxtBtn( "nb_ntsBorder","nb_ntsElem",parent.To=
ggleNtsPane,GetNtsState )
gBtnArr["nb_prevBorder"] =3D gBtnArr["nb_prev"]=3D new ImgBtn( "nb_prev","n=
b_prevBorder",30,parent.GoToPrevSld )
gBtnArr["nb_nextBorder"] =3D gBtnArr["nb_next"]=3D new ImgBtn( "nb_next","n=
b_nextBorder",30,parent.GoToNextSld )
gBtnArr["nb_sldshw"]=3D new ImgBtn( "nb_sldshw","nb_sldshwBorder",18,parent=
.FullScreen )
gBtnArr["nb_sldshwBorder"] =3D new TxtBtn( "nb_sldshw","nb_sldshwBorder",pa=
rent.FullScreen,null )
gBtnArr["nb_sldshwBorder"].SetActive =3D _BSetA_Border;
gBtnArr["nb_sldshwBorder"].SetInactive =3D _BSetI_Border;
gBtnArr["nb_sldshwText"] =3D new TxtBtn( "nb_sldshw","nb_sldshwText",parent=
.FullScreen,null )
gBtnArr["nb_sldshwText"].SetActive =3D _BSetA_Border;
gBtnArr["nb_sldshwText"].SetInactive =3D _BSetI_Border;
gBtnArr["nb_voice"] =3D gBtnArr["nb_voiceBorder"] =3D new ImgBtn( "nb_voice=
","nb_voiceBorder",18,parent.ToggleVNarration )
gBtnArr["nb_otlTxtBorder"] =3D gBtnArr["nb_otlTxt"]=3D new ImgBtn( "nb_otlT=
xt","nb_otlTxtBorder",23,parent.ToggleOtlText )
gBtnArr["nb_ntsBorder"].m_flagId=3D "nb_nts"
gBtnArr["nb_ntsBorder"].SetFlag =3D NtsBtnSetFlag
gBtnArr["nb_otlTxt"].ChangeIcon=3D GetOtlTxtState

/*********************************************
 Context menu implementation

 _CM() is the function that's hooked up to
 the oncontextmenu event. Once we're asked to
 show the menu, we first build it by creating
 DIVs on-the-fly. Then we position it=20
 within the screen area so it doesn't get
 clipped.

 Creating the DIVs using createElement() means
 we don't have to write out any extra HTML
 into the slide HTML files.
**********************************************/
var sNext=3D"Next",sPrev=3D"Previous",sEnd=3D"End Show",sFont=3D"Arial",sAr=
row=3D"Arrow",sFreeform=3D"Freeform",sRect=3D"Rectangle",sOval=3D"Oval"

function ShowMenu()
{
	BuildMenu();
	var doc=3DPPTSld.document.body,x=3DPPTSld.event.clientX+doc.scrollLeft,y=
=3DPPTSld.event.clientY+doc.scrollTop
	m =3D PPTSld.document.all.item("ctxtmenu")
	m.style.pixelLeft=3Dx
	if( (x+m.scrollWidth > doc.clientWidth)&&(x-m.scrollWidth > 0) )
		m.style.pixelLeft=3Dx-m.scrollWidth

	m.style.pixelTop=3Dy
	if( (y+m.scrollHeight > doc.clientHeight)&&(y-m.scrollHeight > 0) )
		m.style.pixelTop=3Dy-m.scrollHeight

	m.style.display=3D""
}

function _CM()
{
	if( !parent.IsFullScrMode() ) return;
	if(!PPTSld.event.ctrlKey) {
		ShowMenu()
		return false
	} else
		HideMenu()
}

function BuildMenu()
{
	if( PPTSld.document.all.item("ctxtmenu") ) return

	var mObj=3DCreateItem( PPTSld.document.body )
	mObj.id=3D"ctxtmenu"
	mObj.style.visibility=3D"hidden"
	var s=3DmObj.style
	s.position=3D"absolute"
	s.cursor=3D"default"
	s.width=3D"120px"
	SetCMBorder(mObj,"menu","black")

	var iObj=3DCreateItem( mObj )
	SetCMBorder( iObj, "threedhighlight","threedshadow" )
	iObj.style.padding=3D2
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  </td>
  <td width=3D"100%">
  <div id=3DPPTP1 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0001.htm');" id=3DPPTL1>Cyclic Voltammet=
ric
  Investigation in the Oxidative Processes of Cyclopentadienyl Manganese
  Tricarbonyl Derivatives</a></font></div>
  <div id=3DPPTC1 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>Dartha D. Babcock and Randy F. Johnston</li>
   <li>Union University</li>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>2</font></div>
  </td>
  <td>
  <div id=3DPPTP2 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0002.htm');" id=3DPPTL2>Experimental</a>=
</font></div>
  <div id=3DPPTC2 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>	The cyclopentadienylmanganese tricarbonyl derivatives were synthesi=
zed
       by published<span style=3D'mso-spacerun:yes'>&nbsp; </span>methods.<=
sup>2,3<span
       style=3D'mso-spacerun:yes'>&nbsp; </span></sup>The cyclic voltammogr=
ams
       were collected with a Bioanalytical CV-27 and recorded by a Hewlett
       Packard 7090A Measurement Plotting System.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>The samples were scanned at=
 six
       scan rates, 30, 60, 100, 400, 700 and 1000 mV/s.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>Ferrocene was used as a ref=
erence
       and all data was normalized to a ferrocene E <sub>1/2 </sub>=3D 0.4V=
.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>The initial voltammograms
       indicated a steady increase in Epa values after several scans.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>The formation of a deposit =
on the
       working eletrode was indicated as the cause of this shift.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>Therefore, to eliminate this
       error, the working electrode was polished following each scan to rem=
ove
       the deposit.</li>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>3</font></div>
  </td>
  <td>
  <div id=3DPPTP3 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0003.htm');" id=3DPPTL3>Table 1. Values =
of Avg E<sub>p</sub>-E<sub>p/2
  </sub>and E<sub>pa</sub> during oxidation for 5 mmolar solutions of A1-A5=
 and
  acyl in acetonitrile/0.01 molar N(n-butyl)<sub>4</sub>BF<sub>4</sub> vs.
  Ag/AgCl at 100mV/s.<sup>a</sup><span style=3D'mso-spacerun:yes'>&nbsp; </=
span>A
  platinum disk working electrode and platinum wire auxillary electrode were
  used.</a></font></div>
  <div id=3DPPTC3 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <br>
   <li>Sample		Avg E<sub>p</sub>-E<sub>p/2 </sub>(mV)<sup>b</sup>	mean E<su=
b>pa</sub>
       (mV)<sup>b</sup></li>
   <li>Acyl		94(3)			1390(10)</li>
   <li>A1			95(2)			1410(19)</li>
   <li>A2			82(8)			1350(14)</li>
   <li>A3			102(4)			1400(5)</li>
   <li>A4			92(2)			1250(38)</li>
   <li>A5			91(4)			1240(6)</li>
   <li>a. All potentials are normalized to a ferrocene E1/2 of 0.4 V.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>Ferrocene oxidation wave ha=
d a
       Avg Ep-Ep/2=3D60mV.</li>
   <li>b. Standard deviations are given in parenthesis.</li>
   <br>
   <br>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>4</font></div>
  </td>
  <td>
  <div id=3DPPTP4 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0004.htm');" id=3DPPTL4>Table 2. Values =
of Avg E<sub>p</sub>-E<sub>p/2
  </sub>and E<sub>pa</sub> during oxidation for 5 mmolar solutions of
  A2Chelate, A2PPh3, A3Chelate and A3PPh3 in acetonitrile/0.01 molar N(n-bu=
tyl)<sub>4</sub>BF<sub>4</sub>
  vs. Ag/AgCl at 100mV/s.<sup>a </sup>A platinum disk working electrode and
  platinum wire auxillary electrode were used.</a></font></div>
  <div id=3DPPTC4 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <br>
   <li>Sample		Avg E<sub>p</sub>-E<sub>p/2<span
       style=3D'mso-spacerun:yes'>&nbsp;&nbsp; </span></sub>(mV)<sup>b</sup=
>	mean
       E<sub>pa</sub> (mV)<sup>b</sup></li>
   <li>A2Chelate	76(3)			540(6)</li>
   <li>A2PPh3		48(3)			830(5)</li>
   <li>A3Chelate	71(5)			580(9)</li>
   <li>A3PPh3		53(2)			830(4)</li>
   <li>a. All potentials are normalized to a ferrocene E1/2 of 0.4 mV.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>Ferrocene oxidation wave ha=
d a
       Avg Ep-Ep/2=3D60mV.</li>
   <li>b.<span style=3D'mso-spacerun:yes'>&nbsp; </span>Standard deviations=
 are
       given in parenthesis.</li>
   <br>
   <br>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>5</font></div>
  </td>
  <td>
  <div id=3DPPTP5 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0005.htm');" id=3DPPTL5>Introduction</a>=
</font></div>
  <div id=3DPPTC5 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>	Previous research concludes that intermediates found in electrochem=
ical
       studies of manganese carbonyl derivatives could be useful as catalys=
is
       in synthesis of other organometallic compounds.<sup>1</sup><span
       style=3D'mso-spacerun:yes'>&nbsp; </span>The possiblity of the
       electrochemical formation of these catalytic intermediates from
       cyclopentadienylmanganese tricarbonyl derivatives is explored in this
       study. The photochemical chelation of cyclopentadienylmanganese
       tricarbonyl derivatives (See Figure 1) is evident in the literature =
and
       occurs in high yields of the chelate derivatives.<sup>2</sup><span
       style=3D'mso-spacerun:yes'>&nbsp; </span>Thus, it was proposed that a
       cyclic voltammetric oxidation would produce chelates of the
       species.<span style=3D'mso-spacerun:yes'>&nbsp; </span>This study in=
cluded
       two types of cyclopentadienylmanganese tricarbonyl derivatives that =
are
       illustrated in Figure 2.</li>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>6</font></div>
  </td>
  <td>
  <div id=3DPPTP6 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0006.htm');" id=3DPPTL6>Figure 2.<span
  style=3D'mso-spacerun:yes'>&nbsp; </span>Formulas and Abbreviations for
  cyclopentadienylmanganese tricarbonyl derivatives.</a></font></div>
  <div id=3DPPTC6 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>Abbreviation		Formula</li>
   <br>
   <br>
   <li>ACYL			C<sub>5</sub>H<sub>4</sub>C(O)CH<sub>3</sub>Mn(CO)<sub>3</sub=
></li>
   <li>A1				C<sub>5</sub>H<sub>4</sub>C(O)CH<sub>2</sub>OCH<sub>3</sub>Mn(=
CO)<sub>3</sub></li>
   <li>A2				C<sub>5</sub>H<sub>4</sub>C(O)CH<sub>2</sub>SCH<sub>3</sub>Mn(=
CO)<sub>3</sub></li>
   <li>A3				C<sub>5</sub>H<sub>4</sub>C(O)CH<sub>2</sub>CH<sub>2</sub>SCH<=
sub>3</sub>Mn(CO)<sub>3</sub></li>
   <li>A4				C<sub>5</sub>H<sub>4</sub>CH<sub>2</sub>CO<sub>2</sub>CH<sub>3=
</sub>Mn(CO)<sub>3</sub></li>
   <li>A5				C<sub>5</sub>H<sub>4</sub>CH<sub>2</sub>CH<sub>2</sub>CO<sub>2=
</sub>CH<sub>3</sub>Mn(CO)<sub>3</sub></li>
   <li>A2Chelate		C<sub>5</sub>H<sub>4</sub>C(O)CH<sub>2</sub>SCH<sub>3</su=
b>Mn(CO)<sub>2</sub></li>
   <li>A2PPh<sub>3			</sub>C<sub>5</sub>H<sub>4</sub>C(O)CH<sub>2</sub>SCH<=
sub>3</sub>Mn(CO)<sub>2
       </sub>PPh<sub>3</sub></li>
   <li>A3Chelate		C<sub>5</sub>H<sub>4</sub>C(O)CH<sub>2</sub>CH<sub>2</sub=
>SCH<sub>3</sub>Mn(CO)<sub>2</sub></li>
   <li>A3PPh<sub>3			</sub>C<sub>5</sub>H<sub>4</sub>C(O)CH<sub>2</sub>CH<s=
ub>2</sub>SCH<sub>3</sub>Mn(CO)<sub>2
       </sub>PPh<sub>3</sub></li>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>7</font></div>
  </td>
  <td>
  <div id=3DPPTP7 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0007.htm');" id=3DPPTL7>&quot;Figure 1&q=
uot;</a></font></div>
  <div id=3DPPTC7 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>Figure 1.<span style=3D'mso-spacerun:yes'>&nbsp; </span>The photoche=
mical
       chelation of a cyclopentadienylmanganese tricarbonyl derivative.</li>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>8</font></div>
  </td>
  <td>
  <div id=3DPPTP8 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0008.htm');" id=3DPPTL8>Results</a></fon=
t></div>
  <div id=3DPPTC8 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>	Oxidation of A1-A5 and ACYL</li>
   <li>	A single oxidation wave was observed for each compound.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>This is evident in the cycl=
ic
       voltammogram in Figure 3.<span style=3D'mso-spacerun:yes'>&nbsp;
       </span>The average E<sub>pa</sub> and E<sub>p</sub>-E<sub>p/2 </sub>=
values
       can be found in Table 1.<span style=3D'mso-spacerun:yes'>&nbsp; </sp=
an>The
       ratio of I<sub>pa</sub>/v<sup>1/2<span style=3D'mso-spacerun:yes'>&n=
bsp;
       </span></sup>remained fairly constant.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>The values of E<sub>p</sub>=
-E<sub>p/2
       </sub>indicate a single electron process.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>This is consistent with oth=
er
       literature. <sup>4</sup><span style=3D'mso-spacerun:yes'>&nbsp;
       </span>There was no indication of a return reduction wave.</li>
   <li>	Oxidation of A2Chelate, A2PPh<sub>3</sub>, A3Chelate and A3PPh<sub>=
3</sub></li>
   <li>	A single oxidation was also observed for these compound.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>The specific E<sub>pa</sub>=
 and E<sub>p</sub>-E<sub>p/2
       </sub>values can be found in Table 2.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>The compounds were similar =
to the
       others with a fairly constant I<sub>pa</sub>/v<sup>1/2 </sup>and a
       single electron process.<span style=3D'mso-spacerun:yes'>&nbsp;
       </span>There was no indication of a return reduction wave.</li>
   <br>
   <br>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>9</font></div>
  </td>
  <td>
  <div id=3DPPTP9 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0009.htm');" id=3DPPTL9>Conclusions</a><=
/font></div>
  <div id=3DPPTC9 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>		During the oxidation of the cyclopentadienyl-manganese tricarbonyl
       derivatives, a deposit formed on the working electrode.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>This was presented in the
       experimetal section.<span style=3D'mso-spacerun:yes'>&nbsp; </span>T=
his
       deposit is a indication of a chemical formed as a result of the
       oxidation of the compounds studied.<span style=3D'mso-spacerun:yes'>=
&nbsp;
       </span>This deposit and the absence of return reduction waves implies
       that the compounds undergo an EC mechanism.<sup>5</sup><span
       style=3D'mso-spacerun:yes'>&nbsp; </span>The deposit on the electrod=
e was
       not identified in this study.</li>
   <li>		The intent of this research was to attempt to form the chelate
       derivatives.<span style=3D'mso-spacerun:yes'>&nbsp; </span>When comp=
ounds
       A1-A5 and ACYL did not show return reduction waves, the chelates of =
A2
       and A3 were studied electrochemically.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>If the chelates indicated a
       return reduction wave, it could be concluded that A1-A5 and ACYL did=
 not
       form the chelates upon electrochemical oxidation.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>However, a return reduction=
</li>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>10</font></div>
  </td>
  <td>
  <div id=3DPPTP10 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0010.htm');" id=3DPPTL10>&quot;wave was =
not
  evident for...&quot;</a></font></div>
  <div id=3DPPTC10 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>	wave was not evident for these chelates. Therefore, the electrochem=
ical
       formation of the chelate derivatives could not be confirmed or denie=
d.</li>
   <li>		Ultimately, although evidence to prove or disprove the electrochem=
ical
       formation of the chelates of the cyclopentadienylmanganese tricarbon=
yl
       derivatives, the oxidation of these derivatives leads to interesting
       questions and study.<span style=3D'mso-spacerun:yes'>&nbsp;
       </span>Continued study could lead to discovery of the chemical speci=
es
       formed on the electrode during oxidation.<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>It may also result in infor=
mation
       that could prove or disprove the electrochemical formation of the
       chelates from the cyclopentadienylmanganese tricarbonyl derivatives.=
</li>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>11</font></div>
  </td>
  <td>
  <div id=3DPPTP11 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0011.htm');" id=3DPPTL11>Acknowledgement=
s</a></font></div>
  <div id=3DPPTC11 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>Union University Chemistry Department</li>
   <li>University of Memphis Chemistry Department</li>
   <li>Dr. T. Burkey, Associate Professor, UM</li>
   <br>
   <br>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>12</font></div>
  </td>
  <td>
  <div id=3DPPTP12 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0012.htm');" id=3DPPTL12>References</a><=
/font></div>
  <div id=3DPPTC12 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>1<span style=3D'mso-spacerun:yes'>&nbsp; </span>Pickett, C.J.; Pletc=
her,
       D. J.C.S. Dalton. 1975, 879.</li>
   <li>2<span style=3D'mso-spacerun:yes'>&nbsp; </span>Pang, Z. The Synthes=
is and
       the Chemistry of Cymantrene Derivatives with Chelatable Substituent =
on
       the Cyclopentadienyl Ring; Ph.D. Dissertation, UM.</li>
   <li>3<span style=3D'mso-spacerun:yes'>&nbsp; </span>Pang, Z; Johnston, R=
.F.;
       VanDerVeer. Submitted for J. Organometallic Chem.</li>
   <li>4<span style=3D'mso-spacerun:yes'>&nbsp; </span>Connelly, N.G.; Kitc=
hen,
       M. D. J.C.S. Dalton. 1975, 931.</li>
   <li>5<span style=3D'mso-spacerun:yes'>&nbsp; </span>Crabtree, R.H. The
       Organometallic Chemistry of the Transition Metals; Wiley:<span
       style=3D'mso-spacerun:yes'>&nbsp; </span>New York, 1988, p 74.</li>
   <br>
   <br>
  </ul>
  </font></div>
  </td>
 </tr>
 <tr onmouseover=3D"Over(this)" onmouseout=3D"Out(this)" onclick=3D"Follow(=
this)"
  style=3D'cursor:hand'>
  <td align=3Dright valign=3Dtop>
  <div class=3DsldNum><font size=3D2>13</font></div>
  </td>
  <td>
  <div id=3DPPTP13 class=3DPTxt><font size=3D2><a
  href=3D"javascript:GoToSld('slide0013.htm');" id=3DPPTL13>&quot;Figure 3&=
quot;</a></font></div>
  <div id=3DPPTC13 class=3DCTxt style=3D'display:none'><font size=3D2>
  <ul>
   <li>Figure 3. Cyclic voltammagram of<span style=3D'mso-spacerun:yes'>&nb=
sp;
       </span>5 mmolar ACYL<span style=3D'mso-spacerun:yes'>&nbsp; </span>a=
nd
       ferrocene in acetonitrile/0.1 molar N(n-butyl)<sub>4</sub>BF<sub>4</=
sub>
       vs. Ag/AgCl at 100mV/s.</li>
  </ul>
  </font></div>
  </td>
 </tr>
</table>



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