Configurationally homogeneous diastereomers of a linear hexa(tertiary phosphine):: Enantioselective self-assembly of a double-stranded parallel helicate of the type (P)-[Cu3(hexaphos)2](PF6)3

被引:44
作者
Bowyer, PK [1 ]
Cook, VC [1 ]
Gharib-Naseri, N [1 ]
Gugger, PA [1 ]
Rae, AD [1 ]
Swiegers, GF [1 ]
Willis, AC [1 ]
Zank, J [1 ]
Wild, SB [1 ]
机构
[1] Australian Natl Univ, Res Sch Chem, Canberra, ACT 0200, Australia
关键词
D O I
10.1073/pnas.072640699
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Three configurationally homogeneous diastereomers of the linear hexa(tertiary phosphine) Ph2PCH2CH2P(Ph)CH2CH2P(Ph)CH2CH2P(Ph)CH2CH2P(Ph)CH2CH2PPh2 (hexaphos) have been isolated in enantiomerically pure form, namely (R,S,S,R)-, (R,S,S,S)-, and (S,S,S,S)hexaphos. The strongly helicating (R,S,S,R)-(-) form of the ligand combines with copper(l) ions to generate by stereoselective self-assembly the P enantiomer of a parallel helicate of the type [CU3(hexaphos)(2)](PF6)(3), which has been characterized by x-ray crystallography. Theoretical modeling of the cation indicates that it is the relationship between the helicities of the two 10-membered rings containing the three copper ions, each of which has the twist-boat-chair-boat conformation, and the configurations of the three chiral, tetrahedral copper stereocenters of Pconfiguration that determines the stereochemistry of the parallel and double alpha-helix conformers of the double-stranded trinuclear metal helicate.
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页码:4877 / 4882
页数:6
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