pH-Potentiometric Investigation towards Chelating Tendencies of <svg style="vertical-align:-4.626pt;width:13.4125px;" id="M1" height="17.5" version="1.1" viewBox="0 0 13.4125 17.5" width="13.4125" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns="http://www.w3.org/2000/svg"><g transform="matrix(.022,-0,0,-.022,.062,11.675)"><path id="x1D45D" d="M570 304q0 -108 -87 -199q-40 -42 -94.5 -74t-105.5 -43q-41 0 -65 11l-29 -141q-9 -45 -1.5 -58t45.5 -16l26 -2l-5 -29l-241 -10l4 26q51 10 67.5 24t26.5 60l113 520q-54 -20 -89 -41l-7 26q38 28 105 53l11 49q20 25 77 58l8 -7l-17 -77q39 14 102 14q82 0 119 -36
t37 -108zM482 289q0 114 -113 114q-26 0 -66 -7l-70 -327q12 -14 32 -25t39 -11q59 0 118.5 81.5t59.5 174.5z" /></g></svg>-Hydroquinone and Phenol Iminodiacetate Copper(II) Complexes

<table>Iminodiacetic derivatives of phenol/<i>p</i>-hydroquinone ligands with their abbreviations. The ligands referred to the potentiometric/stability studies are denoted in parentheses.</table>

Bioinorganic Chemistry and Applications

sch1

Scheme 1

Scheme 1: pH-Potentiometric Investigation towards Chelating Tendencies of <svg style="vertical-align:-4.626pt;width:13.4125px;" id="M1" height="17.5" version="1.1" viewBox="0 0 13.4125 17.5" width="13.4125" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns="http://www.w3.org/2000/svg"><g transform="matrix(.022,-0,0,-.022,.062,11.675)"><path id="x1D45D" d="M570 304q0 -108 -87 -199q-40 -42 -94.5 -74t-105.5 -43q-41 0 -65 11l-29 -141q-9 -45 -1.5 -58t45.5 -16l26 -2l-5 -29l-241 -10l4 26q51 10 67.5 24t26.5 60l113 520q-54 -20 -89 -41l-7 26q38 28 105 53l11 49q20 25 77 58l8 -7l-17 -77q39 14 102 14q82 0 119 -36
t37 -108zM482 289q0 114 -113 114q-26 0 -66 -7l-70 -327q12 -14 32 -25t39 -11q59 0 118.5 81.5t59.5 174.5z" /></g></svg>-Hydroquinone and Phenol Iminodiacetate Copper(II) Complexes 

Bioinorganic Chemistry and Applications

pH-Potentiometric Investigation towards Chelating Tendencies of -Hydroquinone and Phenol Iminodiacetate Copper(II) Complexes

Scheme 1