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双核钼(V)草酸配合物的热稳定性研究

A Study on Thermal Stabilities of Dinuclear Molybdenum(V) Oxalate Complexes

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【作者】 陈汉文贝自英焦厚生戴寰

【Author】 Chen Han-wen Bei Zi-ying Jiao Hou-sheng Dai Huan(Department of Chemistry of University Nanjing)

【机构】 南京大学化学系南京中医学院南京大学化学系

【摘要】 <正> 单核和双核钼(V)配合物与钼在酶中所起的作用的密切关系,在固氮酶模拟物的研究中颇引人注目。钼(V)的草酸配合物是以双氧桥连的双核配合物,其草酸配阴离子结构为

【Abstract】 A number of coordination compounds having general formula M1or2 [Mo2O4(C2O42]. nH2O (where M=divalent or univalent metals) were prepared and their thermal stabilies in the solid state were studied with gas chromatographic method in a helium and a hydrogen atmosphere. The results indicated that the products are H2O, CO and CO2 in both atmospheres, but in case of Ni and Cd salts a smaller amour of CH4 were produced in Hydrogen atmosphere. The sources of H2O formed arised from 3 parts: crystallized, coordinated and reduced. The temperature of losing crystallized H2O of coordinating salts is lower than that of their decomposition, and the temperature of losing coodihating H2O was in the range of starting decomposition of coordinating salts. The reduced water was formed only in hydrogen atmosphere. From gas chromatographic diagrams, the thermal decomposition of complexes had 2 temperature ranges, in the lower one, Co and CO2 appeared with the quantity of the latter bigger than that of the former in peak area, while in the higher one, there appeared only CO except in Ba salts in a He atmosphere and in Ba and Cd salts in a H2 atmosphere. The results from gas chromatography indicated that the thermal stability of complexes decreases approximately with the increase in the ionic potential of the central metal ion.

  • 【文献出处】 内蒙古大学学报(自然科学版) ,Acta Scientiarum Naturalium Universitatis Neimongol , 编辑部邮箱 ,1983年04期
  • 【被引频次】2
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