摘要
RuCl2(Ph3P)4或RuCl2(DMSO)4在甲苯中直接与等摩尔的亚胺膦配体N,N-双-[邻-(二苯基膦苯亚甲基)]乙二胺(P2N2)在甲苯中回流反应,高产率地合成了反式配位的双亚胺双膦钌配合物trans-RuCl2P2N2.在温和条件下,该配合物作为新型催化剂有效地催化α,β-不饱和酸和几种功能团烯烃的选择加氢反应.讨论了可能的催化活性物种.
The trans form of the title complex was synthesized in high yield by interaction of equimole RuCl 2(Ph 3P) 4 or RuCl 2(DMSO) 4 (DMSO=dimethylsulfoxide) with P 2N 2 (i.e.= N,N bis[ o (diphenylphosphine benzylidene)]ethylene diamine) in refluxing toluene. The complex has been investigated as catalyst for selective hydrogenation of α,β unsaturated acids and some functionalized olefins. The hydrogenation catalytic activity was observed as follows: styrene>acrylic acid>benzaldehyde>salicyl aldehyde>cyclohexanone>furfural>methylacrylic acidacetophenone. The effect of addition of NH 4PF 6 or AgNO 3 as promotor has also been studied.
出处
《应用化学》
CAS
CSCD
北大核心
1997年第3期58-61,共4页
Chinese Journal of Applied Chemistry
基金
国家教育委员会留学回国人员资助
关键词
亚胺膦配体
钌配合物
氢化
催化活性
催化剂
diiminodiphosphine ligand,ruthenium complex,synthesis, hydrogenation,catalytic activity