Synthesis and Characterization of para‐Nitrophenoxides of Zirconium(IV)

S. C. Chaudhry, C. Verma, S. S. Bhatt, N. Sharma
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引用次数: 2

Abstract

Abstract Compounds of the composition ZrCl3(OC6H4NO2‐p) and ZrCl2(OC6H4NO2‐p)2 have been synthesized from the reaction of ZrCl4 with equimolar and bimolar amounts of the trimethylsilyl derivative of p‐nitrophenol in benzene under reflux. Attempts to isolate the tetrakis derivative, Zr(OC6H4NO2‐p)4, even by heating the components in high‐boiling solvents were unsuccessful. Based upon analytical data, conductance, cryoscopic, IR and 1H NMR studies, dimeric structures with bridging through phenoxo groups have been proposed for these compounds. The thermal decomposition of these complexes is a combination of both exothermic and endothermic processes, as is inferred from TG/DT studies. Reactions of these compounds with nitrogen bases viz., pyridine, 1,10‐phenanthroline and 2,2′‐bipyridyl results in breakdown of the bridged structure and formation of simple addition compounds, which have been assigned octahedral structures.
对硝基苯氧化锆(IV)的合成与表征
摘要以ZrCl4与对硝基苯酚的三甲基硅基衍生物等摩尔和双摩尔量的ZrCl3(OC6H4NO2‐p)为原料,在回流条件下合成了ZrCl3(OC6H4NO2‐p)和ZrCl2(OC6H4NO2‐p)2。试图分离四系衍生物Zr(OC6H4NO2‐p)4,即使在高沸点溶剂中加热也不成功。根据分析数据、电导、低温、红外和核磁共振氢谱研究,这些化合物的二聚体结构通过苯氧基桥接。从TG/DT研究中可以推断,这些配合物的热分解是放热和吸热过程的结合。这些化合物与氮碱(如吡啶、1,10‐菲罗啉和2,2′‐联吡啶)的反应导致桥接结构的破坏和简单加成化合物的形成,这些化合物被指定为八面体结构。
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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