Electrochemical synthesis of copper (II) based metal organic frameworks: Determination of structure by Single X-ray diffraction crystallography and other supportive techniques

Kalawati Saini
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Abstract

The copper (II) extended metal organic frameworks with oxalic acid ( ox = oxalate ) [Na 2 ( Cu ( ox) 2 ].H2O and [ (NH4)2 ({ Cu ( ox)2(H2O)2}{ Cu( ox)2 }] .H2O have been synthesized using electrochemical route at room temperature and applied potential at 12.5 V. Herein copper rod has taken as a working electrode and platinum wire as a reference electrode. The single crystal X-ray diffraction (SXRD) and other supportive techniques like as PXRD, TGA/DTA, FT-IR have been used for structural characterizations. Metal organic frameworks (MOFs) are crystalline in nature where the ligands and metal ions are assembled infinitely resulting in one, two or three-dimensional networks having direct metalligand coordination. The growth of the solids has been explained corresponding to the mechanistic approach proposed by Ramanan and Whittingham. The crystal packing has been influenced by the supporting electrolyte. The electrolytic method is a simple process, low energy consumption, high yield, easy control and no environmental pollution. Copyright © 2018 VBRI Press.
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铜(II)基金属有机骨架的电化学合成:用单x射线衍射晶体学和其他辅助技术测定结构
含草酸(ox =草酸)的铜(II)扩展金属有机骨架[Na 2 (Cu (ox) 2]。在室温和12.5 V电势下,采用电化学路线合成了H2O和[(NH4)2 ({Cu(ox)2(H2O)2}{Cu(ox)2}] .H2O。本文以铜棒为工作电极,铂丝为参比电极。单晶x射线衍射(SXRD)和其他支持技术如PXRD、TGA/DTA、FT-IR等被用于结构表征。金属有机骨架(MOFs)本质上是结晶的,其中配体和金属离子无限地组装在一起,形成具有直接金属配位的一维、二维或三维网络。固体的生长已经用Ramanan和Whittingham提出的力学方法来解释。晶体填充物受到支撑电解质的影响。电解法工艺简单,能耗低,收率高,易控制,无环境污染。版权所有©2018 VBRI出版社。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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