A TRIPOD LIGAND WITH 3 DIFFERENT LEGS AND SOME CHIRAL ZINC-COMPLEXES THEREOF

被引:40
作者
ABUFARAG, A [1 ]
VAHRENKAMP, H [1 ]
机构
[1] UNIV FREIBURG,INST ANORGAN & ANALYT CHEM,D-79104 FREIBURG,GERMANY
关键词
D O I
10.1021/ic00116a021
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Stepwise alkylation of 2-picolylamine has yielded the unsymmetrical tripodal amine ligand (2-picolyl)(N-pyrrolidinylethyl)(2-hydroxy-3,5-di-tert-butylbenzyl) (L). In the presence of diethylzinc, L is deprotonated at the phenolic OH function with formation of the unstable complex L . Zn-Et (1). 1 can be used as an intermediate for the synthesis of chiral L . Zn-X complexes by protolysis. Thus, with 2,4-dibromophenol, L . Zn-OC6H3Br2 (2) is obtained, and with diphenylphosphoric acid, L . Zn-OPO(OPh)(2) (3) is formed. The low symmetry of the ligand L allows detailed NMR assignments. Complex 2 was subjected to a crystal structure determination
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收藏
页码:3279 / 3284
页数:6
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