Synthesis, Spectroscopic Characterization, and Biological Activities of Metal Complexes of 4-((4-Chlorophenyl)diazenyl)-2-((<i>p-</i>tolylimino)methyl)phenol

<table class="table-group" id="tab6"><tr><td><table class="table"><tr><td class="thead-hr" colspan="5"><hr/></td></tr><tr class="thead"><td align="left">Compound</td><td align="center">Scan rate (mV)</td><td align="center"><svg height="18.112499" id="M98" style="vertical-align:-5.56921pt" version="1.1" viewbox="0 0 22.862499 18.112499" width="22.862499" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
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</svg> (V)</td><td align="center"><svg height="18.112499" id="M99" style="vertical-align:-5.56921pt" version="1.1" viewbox="0 0 23.012501 18.112499" width="23.012501" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
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l14 20.5t15 23.5t13.5 21.5l29 -10q-52 -129 -71 -163h-500l6 28q66 4 83 17.5t28 73.5l77 409q11 61 -0.5 75.5t-78.5 18.5l10 28h467z" id="x1D438"></path></g>
<g transform="matrix(.012,-0,0,-.012,10.8,15.187)"><path d="M169 380l92 53q26 16 49 16q80 0 128.5 -56t48.5 -133q0 -108 -72.5 -180.5t-176.5 -91.5q-38 1 -69 18v-131q0 -57 13 -70t71 -18v-27h-236v27q49 5 61 17t12 61v452q0 48 -9.5 58.5t-56.5 16.5v24q66 11 145 43v-79zM169 346v-270q37 -39 94 -39q63 0 101.5 50
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</svg> (V)</td><td align="center">Δ<svg height="18.3125" id="M100" style="vertical-align:-5.73167pt" version="1.1" viewbox="0 0 18.549999 18.3125" width="18.549999" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
<g transform="matrix(.017,-0,0,-.017,.062,11.113)"><path d="M609 650l-19 -162l-30 -2q2 69 -14 94q-9 18 -28.5 26t-74.5 8h-88q-30 0 -37 -6.5t-12 -36.5l-41 -212h103q48 0 69 5.5t32 19t26 50.5h29l-40 -198h-30q2 58 -11.5 70.5t-85.5 12.5h-99l-30 -167q-17 -87 3 -101q18 -15 111 -15q59 0 89 7t54 27q8 7 15.5 16t16 21.5
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</svg> (V)</td></tr><tr><td class="thead-hr" colspan="5"><hr/></td></tr><tr><td align="left" rowspan="3"><svg height="14.85" id="M101" style="vertical-align:-2.22495pt" version="1.1" viewbox="0 0 5.9875002 14.85" width="5.9875002" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
<g transform="matrix(.017,-0,0,-.017,.062,12.012)"><path d="M290 -163h-170v866h170v-28q-79 -7 -94 -19.5t-15 -72.5v-627q0 -59 14.5 -71.5t94.5 -19.5v-28z" id="x5B"></path></g>
</svg>Cu(CDTMP)<sub>2</sub>] (<svg height="15.7" id="M102" style="vertical-align:-3.27605pt" version="1.1" viewbox="0 0 26.5375 15.7" width="26.5375" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
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<g transform="matrix(.012,-0,0,-.012,11.4,15.637)"><path d="M441 24v-24h-373v24q75 2 96 20q22 19 22 85v378q0 70 -36 70q-26 0 -65 -16l-20 -8v26l251 109h18v-570q0 -57 19 -75q19 -17 88 -19z" id="x1D7CF"></path></g>
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						)</td><td align="center">100</td><td align="center">0.122</td><td align="center">0.812<br/>0.352</td><td align="center">0.690</td></tr><tr><td align="center">150</td><td align="center">0.105</td><td align="center">0.862<br/>0.409</td><td align="center">0.757</td></tr><tr><td align="center">200</td><td align="center">0.092</td><td align="center">0.871</td><td align="center">0.779</td></tr><tr class="table-tr"><td colspan="5"><hr class="tbody-hr"/></td></tr></table></td></tr></table>

Redox potential of [Cu(CDTMP)<sub>2</sub>] at different scan rates.

Journal of Chemistry

tab6

Table 6

Table 6: Synthesis, Spectroscopic Characterization, and Biological Activities of Metal Complexes of 4-((4-Chlorophenyl)diazenyl)-2-((<i>p-</i>tolylimino)methyl)phenol 

Table 6 | Synthesis, Spectroscopic Characterization, and Biological Activities of Metal Complexes of 4-((4-Chlorophenyl)diazenyl)-2-((p-tolylimino)methyl)phenol 