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首页> 外文期刊>Inorganica Chimica Acta >Supported organometallic complexes part 39: cationic diamine(ether-phosphine)ruthenium(II) complexes as precursors for the hydrogenation of trans-4-phenyl-3-butene-2-one
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Supported organometallic complexes part 39: cationic diamine(ether-phosphine)ruthenium(II) complexes as precursors for the hydrogenation of trans-4-phenyl-3-butene-2-one

机译:负载的有机金属配合物第39部分:阳离子二胺(醚-膦)钌(II)配合物作为反式-4-苯基-3-丁烯-2-一氢化反应的前体

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摘要

Treatment of RuCl2(eta(1)-Ph2PCH2CH2OCH3)(2)(diamine) (1L(1)-1L(7)) with one equivalent of AgX (X = OTf, BF4) in CH2Cl2 results in the formation of the monocationic ruthenium(H) complexes [RuCl(eta(1)-Ph2PCH2CH2OCH3)(eta(2)-Ph2PCH2CH2OCH3)(diamine)]X-+(-) (2L(1)-2L(7)). These complexes were characterized by NMR, and mass spectroscopy as well as by elemental analyses, 2L(1) additionally by an X-ray structural analysis. Complex 2L(1) crystallizes in the monoclinic space group C2/c with Z = 8. The monocationic and neutral complexes were applied as catalysts in the selective hydrogenation of trans-4-phenyl-3-butene-2-one. With the exception of 1L(3)/1L(7) and 2L(3)/2L(7) all catalysts showed high activities and selectivities toward the hydrogenation of the carbonyl group under mild conditions. However, the activity of the cationic catalysts is only half of that of their neutral congeners. (C) 2003 Elsevier B.V. All rights reserved.
机译:用一当量的AgX(X = OTf,BF4)在CH2Cl2中处理RuCl2(eta(1)-Ph2PCH2CH2OCH3)(2)(二胺)(1L(1)-1L(7))导致单阳离子钌的形成(H)络合物[RuCl(eta(1)-Ph2PCH2CH2OCH3)(eta(2)-Ph2PCH2CH2OCH3)(二胺)] X-+(-)(2L(1)-2L(7))。这些配合物的特征在于NMR,质谱以及元素分析,此外还通过X射线结构分析确定了2L(1)。配合物2L(1)在Z = 8的单斜空间群C2 / c中结晶。单阳离子和中性配合物用作反式-4-苯基-3-丁烯-2-一的选择性加氢的催化剂。除1L(3)/ 1L(7)和2L(3)/ 2L(7)外,所有催化剂在温和条件下均表现出高活性和对羰基氢化的选择性。然而,阳离子催化剂的活性仅为其中性同类物的一半。 (C)2003 Elsevier B.V.保留所有权利。

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