Chemistry Research Laboratory, Department of Chemistry, University of Oxford, 12 Mansfield Road, Oxford, United Kingdom OX1 3TA.
Dalton Trans. 2010 Feb 14;39(6):1576-85. doi: 10.1039/b913463h. Epub 2009 Nov 5.
A series of copper complexes have been synthesised as potential agents for the catalytic reduction of nitrite anions. The ligands and corresponding copper complexes have been characterised by using a range of techniques including X-ray crystallography, NMR, microanalysis, mass spectrometry, infra-red spectroscopy, electrochemical studies and density functional theory calculations. For complexes with simple aliphatic substituents bonded to the equatorial donor nitrogen atoms, catalytic studies on the conversion of NO(2)(-) anions into NO and N(2)O gases revealed an excellent correlation between the initial rate of conversion and the experimental reduction potential as measured by cyclic voltammetry. Initial catalytic investigations reveal that these simple model complexes display a wide range of catalytic turnover rates, conversion yields and product gas compositions. Overall the results suggest that further investigations into the design and use of copper complexes as nitrite reduction catalysts are warranted.
已经合成了一系列铜配合物,作为催化还原亚硝酸盐阴离子的潜在试剂。通过使用一系列技术,包括 X 射线晶体学、NMR、微量分析、质谱、红外光谱、电化学研究和密度泛函理论计算,对配体和相应的铜配合物进行了表征。对于与赤道供氮原子键合的简单脂肪族取代基的配合物,对将 NO(2)(-)阴离子转化为 NO 和 N(2)O 气体的催化研究表明,转化率的初始速率与通过循环伏安法测量的实验还原电势之间存在极好的相关性。初步的催化研究表明,这些简单的模型配合物显示出广泛的催化周转率、转化率和产物气体组成。总的来说,结果表明,有必要进一步研究铜配合物作为亚硝酸盐还原催化剂的设计和应用。