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具有咔唑骨架的非手性和手性 PNP-夹式配体:与 d8 过渡金属的配位化学。

Achiral and chiral PNP-pincer ligands with a carbazole backbone: coordination chemistry with d8 transition metals.

机构信息

Anorganisch-Chemisches Institut, Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany.

出版信息

Inorg Chem. 2013 Feb 18;52(4):2050-9. doi: 10.1021/ic302454n. Epub 2013 Jan 30.

DOI:10.1021/ic302454n
PMID:23363395
Abstract

Two new monoanionic PNP pincer type ligands have been synthesized, the achiral 3,6-di-tert-butyl-1,8-bis((diphenyl-phosphino)methyl)-9H-carbazole CbzdiphosH (5) and the chiral 3,6-di-tert-butyl-1,8-bis(((2R,5R)-2,5-diphenylphospholan-1-yl)methyl)-9H-carbazole CbzdipholH (7), both of which were initially prepared as their borane complexes. The synthesis of CbzdiphosH is based on the reaction between the key intermediate 1,8-bis(bromomethyl)-3,6-di-tert-butyl-9H-carbazole (3) and lithium diphenylphosphide-borane complex. The chiral ligand CbzdipholH was prepared by treating 3 with lithium (2R,5R)-2,5-diphenylphospholanide-borane complex and subsequent deprotection with diethylamine. The complexation of the two ligands with nickel, palladium and rhodium was investigated, for which the conformational behavior of the ligands was found to be different. Although the arrangement of the donor atoms in all crystallographically characterized complexes is approximately square planar, the carbazole plane in Cbzdiphos complexes is inclined relative to the coordination plane. On the other hand, a helical twist is observed in Cbzdiphol complexes.

摘要

两种新的单核阴离子 PNP 型钳式配体已被合成,非手性的 3,6-二叔丁基-1,8-双((二苯基膦基)甲基)-9H-咔唑 CbzdiphosH(5)和手性的 3,6-二叔丁基-1,8-双(((2R,5R)-2,5-二苯基膦基)甲基)-9H-咔唑 CbzdipholH(7),它们最初均以硼烷络合物的形式制备。CbzdiphosH 的合成基于关键中间体 1,8-双(溴甲基)-3,6-二叔丁基-9H-咔唑(3)与二苯基膦基硼锂络合物之间的反应。手性配体 CbzdipholH 通过用(2R,5R)-2,5-二苯基膦基硼锂络合物处理 3 并随后用二乙胺脱保护来制备。研究了两种配体与镍、钯和铑的络合,发现配体的构象行为不同。尽管所有晶体结构表征的配合物中供体原子的排列大致为正方形平面,但 Cbzdiphos 配合物中咔唑平面相对于配位平面倾斜。另一方面,在 Cbzdiphol 配合物中观察到螺旋扭曲。

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