摘要
采用NMR方法考察了室温和低温(-78~-60℃)下Pd2X2(dpm)2(X=NCO-,CH3CO,SCN-和NO,dpm=Ph2PCH2PPh2)与H2S在CD2Cl2或CDCl3中的反应。结果表明,在X=NCO-和CH3CO的情况下,H2S优先与这些Pd配合物的阴离子作用生成相应的共轭酸HX和Pd2(SH)2(dpm)2,后者在H2S存在下又进一步转化为Pd2(SH)2(dpm)2(μ-S);当X=SCN-和NO时,反应则生成结构可能为[Pd2(H)(SH)(μ-SH)(dpm)2]+的双核Pd配合物。
The reactions of Pd2X2(dpm)2(X=NCO-,CH3CO,SCN-and NO;dpm = Ph2PCH2PPh2)with H2S in CD2Cl2 or CDCl3 were studied by NMR at room and low temperature (-78--60 ℃).In the case of X = NCO-and CH3CO, H2S at first reacted with the anions of the palladium complexes and generated HX and Pd2(SH)2(dpm)_2 that was subsequently converted to Pd2(SH)2(dpm)2(μ-S)in the presence of excess amount of H2S.In the case of X=SCN- and NO,the reactions resulted in the formation of a dinuclear palladium complex with a possible structure of[Pd2(H)(SH)(μ-SH)(dpm)2]+.
出处
《高等学校化学学报》
CSCD
北大核心
1994年第2期173-177,共5页
Chemical Journal of Chinese Universities
关键词
钯络合物
双二苯膦基
甲烷
硫化氢
Palladium complex
Bis(diphenylphosphino)methane
Hydrogen sulfide