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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Thermodynamic studies of the binding of bidentate nitrogen donors with methyltrioxorhenium(MTO)in CHCl_3 solution
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Thermodynamic studies of the binding of bidentate nitrogen donors with methyltrioxorhenium(MTO)in CHCl_3 solution

机译:CHCl_3溶液中双齿氮供体与甲基三氧or(MTO)结合的热力学研究

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摘要

Methyltrioxorhenium(MTO)adduct formation with bidentate nitrogen donors 2,2'-bipyridine(bpy),4,4'-dimethyl-2,2'-bipyridine(Me_2bpy),4,4'-di-tert-butyl-2,2'-bipyridine('Bu2bpy),1,10-phenanthroline(phen),5-methyl-l,10-phenanthroline(5-Mephen),5-chloro-1,10-phenanthroline(5-Clphen),4,7-dimethyl-1,10-phenanthroline(Me_2phen)has been studied at different temperatures in CHC1_3 solution.Spectrophotometeric measurements have been carried out to obtain the thermodynamic parameters.All complexes are enthalpy stabilized whereas the entropy changes counteract the adduct formation.The results are discussed in terms of different basicities of the bidentate N-donors.
机译:与二齿氮供体2,3'-联吡啶(bpy),4,4'-二甲基-2,2'-联吡啶(Me_2bpy),4,4'-二叔丁基-2, 2'-联吡啶('Bu2bpy),1,10-菲咯啉(phen),5-甲基-1,10-菲咯啉(5-Mephen),5-氯-1,10-菲咯啉(5-Clphen),4,在CHC1_3溶液中于不同温度下研究了7-二甲基-1,10-菲咯啉(Me_2phen),通过分光光度法测定了热力学参数,所有配合物均稳定了焓,但熵变抵消了加合物的形成。将根据双齿N供体的不同基础进行讨论。

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