Synthesis, structure, and catalytic activity of titanium complexes with new chiral 11,12-diamino-9,10-dihydro-9,10-ethanoanthracene-based ligands

被引:33
|
作者
Zhang, Furen [1 ]
Song, Haibin [2 ]
Zi, Guofu [1 ]
机构
[1] Beijing Normal Univ, Dept Chem, Beijing 100875, Peoples R China
[2] Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
11,12-Diamino-9,10-dihydro-9,10-ethanoanthracene; Chiral titanium complexes; Synthesis; Crystal structure; Polymerization of rac-lactide; DIELS-ALDER REACTIONS; X-RAY STRUCTURES; ENANTIOSELECTIVE ADDITION; AG(I) COMPLEXES; DIETHYLZINC; REACTIVITY; ALDEHYDES; AMIDES;
D O I
10.1016/j.jorganchem.2010.05.003
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A new series of organo-titanium complexes have been prepared from the reaction between Ti(NMe2)(4) and C-2-symmetric ligands, (R,R)-11,12-bis(pyrrol-2-ylmethyleneamino)-9,10-dihydro-9,10-ethanoanthracene (1H(2)), and (R, R)-bis(diphenylthiophosphoramino)-9,10-dihydro-9,10-ethanoanthracene (2H(2)), (R,R)-11,12-bis(mesitylenesulphonylamino)-9,10-dihydro-9,10-ethanoanthracene (3H(2)) and (R,R)-bis (diphenylthiophosphoramino)-1,2-cyclohexane (4H(2)). Treatment of Ti(NMe2)(4) with 1 equiv of 1H(2) gives, after recrystallization from a benzene solution, the binuclear double helicate titanium amide (1) 2[ Ti (NMe2)(2)](2)center dot(5) in 71% yield. While under similar reaction conditions, reaction of Ti(NMe2)(4) with 1 equiv of 2H(2), 3H(2) or 4H(2) gives, after recrystallization from a toluene or benzene solution, the mononuclear single helicate titanium amides (2) Ti(NMe2)(2) (6), (3) Ti(NMe2)(2) (7) and (4) Ti(NMe2)(2) (8), respectively, in good yields. All new compounds have been characterized by various spectroscopic techniques, and elemental analyses. The solid-state structures of complexes 5-8 have further been confirmed by X-ray diffraction analyses. The titanium amides are active catalysts for the polymerization of rac-lactide, leading to the isotactic-rich polylactides. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1993 / 1999
页数:7
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