| Literature DB >> 29053274 |
Huayan Yang1, Juanzhu Yan1, Yu Wang1, Guocheng Deng1, Haifeng Su1, Xiaojing Zhao1, Chaofa Xu1, Boon K Teo1, Nanfeng Zheng1.
Abstract
A general strategy, using mixed ligands, is utilized to synthesize atomically precise, intrinsically chiral nanocluster [Ag78(DPPP)6(SR)42] (Ag78) where DPPP is the achiral 1,3-bis(diphenyphosphino)propane and SR = SPhCF3. Ag78 crystallizes as racemates in a centric space group. Using chiral diphosphines BDPP = 2,4-bis(diphenylphosphino)pentane, the enantiomeric pair [Ag78(R/S-BDPP)6(SR)42] can be prepared with 100% optical purity. The chiral diphosphines gives rise to, separately, two asymmetric surface coordination motifs composed of tetrahedral R3PAg(SR)3 moieties. The flexible nature of C-C-C angles between the two phosphorus atoms restricts the relative orientation of the tetrahedral R3PAg(SR)3 moieties, thereby resulting in the enantiomeric selection of the intrinsic chiral metal core. This proof-of-concept strategy raises the prospect of enantioselectively synthesizing optically pure, atomically precise chiral noble metal nanoclusters for specific applications.Entities:
Year: 2017 PMID: 29053274 DOI: 10.1021/jacs.7b10448
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419