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氨膦配体 R(2)P(CH(2))(n)NH(2)和钌氢化催化剂 RuCl(2)(R(2)P(CH(2))(n)NH(2))(2)。

Aminophosphine ligands R(2)P(CH(2))(n)NH(2) and ruthenium hydrogenation catalysts RuCl(2)(R(2)P(CH(2))(n)NH(2))(2).

机构信息

Kanata Chemical Technologies Inc., 101 College Street, Office 230, MaRS Centre, South Tower, Toronto, ON M5G 1L7, Canada.

出版信息

Dalton Trans. 2009 Oct 21(39):8301-7. doi: 10.1039/b911459a. Epub 2009 Aug 12.

Abstract

The aminophosphine ligands R(2)P(CH(2))(2)NH(2) and R(2)P(CH(2))(3)NH(2) (R = Ph, (i)Pr, (t)Bu) were isolated in good to excellent yields from the reaction of LiPR(2) with Cl(CH(2))(2)N(TMS)(2) and Cl(CH(2))(3)N(TMS)(2), respectively, followed by hydrolysis. This approach allows fine tuning of the ligands' stereoelectronic properties through the variation of the substituents on the phosphine. The aminophosphine ligands were used to prepare the ruthenium complexes RuCl(2)(R(2)P(CH(2))(2)NH(2))(2) and RuCl(2)(R(2)P(CH(2))(3)NH(2))(2) by reacting a 2:1 mixture of the respective ligand and RuCl(2)(cod) in an appropriate solvent. The resulting complexes were found to be excellent catalysts for the hydrogenation of ketones and imines.

摘要

氨基膦配体 R(2)P(CH(2))(2)NH(2) 和 R(2)P(CH(2))(3)NH(2)(R = Ph,(i)Pr,(t)Bu)可通过 LiPR(2)与 Cl(CH(2))(2)N(TMS)(2)和 Cl(CH(2))(3)N(TMS)(2)反应,然后水解,以良好到优异的产率分离得到。这种方法可以通过改变膦上的取代基来精细调整配体的立体电子性质。氨基膦配体用于通过反应来制备钌配合物 RuCl(2)(R(2)P(CH(2))(2)NH(2))(2)和 RuCl(2)(R(2)P(CH(2))(3)NH(2))(2),反应中使用了相应配体与RuCl(2)(cod)的 2:1 混合物,在适当的溶剂中。发现所得配合物是酮和亚胺加氢的优异催化剂。

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