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Asymmetric hydrogenation of aromatic ketones by chiral (1S,2S)-DPEN-Ru(II)Cl2(TPP)2 encapsulated in SBA-16

机译:SBA-16中封装的手性(1S,2S)-DPEN-Ru(II)Cl2(TPP)2不对称氢化芳族酮

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摘要

Chiral complex (1S,2S)-DPEN-RuC12(TPP)2 (DPEN = 1,2-diphenylethylenediamine; TPP = triphenylphos-phine) was successfully encapsulated in the mesoporous cage of SBA-16 modified with phenyltrimethox-ysilane. This was verified by ICP, powder XRD, N2 adsorption, FT1R, DRS and TEM analysis. The encapsulated chiral Ru complex gave high catalytic activity and excellent enantioselectivity like its homogeneous counterpart in asymmetric hydrogenation of various aromatic ketones. The encapsulated complex also showed high stability and could be recycled without significant loss of activity and enantioselectivity.
机译:将手性配合物(1S,2S)-DPEN-RuC12(TPP)2(DPEN = 1,2-二苯基乙二胺; TPP =三苯基膦)成功地封装在SBA-16的经苯基三甲氧基乙硅烷改性的介孔笼中。 ICP,粉末XRD,N2吸附,FT1R,DRS和TEM分析证实了这一点。包封的手性Ru络合物具有高催化活性和出色的对映选择性,就像在各种芳族酮的不对称氢化反应中的均相对应物一样。包封的复合物还显示出高稳定性,并且可以再循环而没有显着的活性和对映选择性损失。

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