A Chiral Gold Nanocluster Au20 Protected by Tetradentate Phosphine Ligands

The chirality of a gold nanocluster can be generated from either an intrinsically chiral inorganic core or an achiral inorganic core in a chiral environment. The first structural determination of a gold nanocluster containing an intrinsic chiral inorganic core is reported. The chiral gold nanocluste...

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Published inAngewandte Chemie International Edition Vol. 53; no. 11; pp. 2923 - 2926
Main Authors Wan, Xian-Kai, Yuan, Shang-Fu, Lin, Zhi-Wei, Wang, Quan-Ming
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 10.03.2014
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
EditionInternational ed. in English
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Online AccessGet full text
ISSN1433-7851
1521-3773
1521-3773
DOI10.1002/anie.201308599

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Summary:The chirality of a gold nanocluster can be generated from either an intrinsically chiral inorganic core or an achiral inorganic core in a chiral environment. The first structural determination of a gold nanocluster containing an intrinsic chiral inorganic core is reported. The chiral gold nanocluster [Au20(PP3)4]Cl4 (PP3=tris(2‐(diphenylphosphino)ethyl)phosphine) has been prepared by the reduction of a gold(I)–tetraphosphine precursor in dichloromethane solution. Single‐crystal structural determination reveals that the cluster molecular structure has C3 symmetry. It consists of a Au20 core consolidated by four peripheral tetraphosphines. The Au20 core can be viewed as the combination of an icosahedral Au13 and a helical Y‐shaped Au7 motif. The identity of this Au20 cluster is confirmed by ESI‐MS. The chelation of multidentate phosphines enhances the stability of this Au20 cluster. Gold with a twist: A chiral Au20 nanocluster has been prepared by the reduction of a gold(I)–tetraphosphine complex. The C3 Au20 core can be viewed as the combination of an icosahedral Au13 (see picture, orange) and a helical Y‐shaped Au7 motif (green). This is the first structural determination of a gold nanocluster containing an intrinsic chiral inorganic core.
Bibliography:Natural Science Foundation of China - No. 21125102
This work was supported by the Natural Science Foundation of China (21125102) and the 973 program (2014CB845603).
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ArticleID:ANIE201308599
973 program - No. 2014CB845603
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SourceType-Scholarly Journals-1
ObjectType-Feature-2
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ISSN:1433-7851
1521-3773
1521-3773
DOI:10.1002/anie.201308599