| Literature DB >> 24803070 |
Alison J Edwards1, Rajendra S Dhayal, Ping-Kuei Liao, Jian-Hong Liao, Ming-Hsi Chiang, Ross O Piltz, Samia Kahlal, Jean-Yves Saillard, C W Liu.
Abstract
The syntheses of the first rhombicuboctahedral copper polyhydride complexes [Cu28 (H)15 (S2 CNR)12 ]PF6 (NR=N(n) Pr2 or aza-15-crown-5) are reported. These complexes were analyzed by single-crystal X-ray and one by neutron diffraction. The core of each copper hydride nanoparticle comprises one central interstitial hydride and eight outer-triangular-face-capping hydrides. A further six face-truncating hydrides form an unprecedented bridge between the inner and outer copper atom arrays. The irregular inner Cu4 tetrahedron is encapsulated within the Cu24 rhombicuboctahedral cage, which is further enclosed by an array of twelve dithiocarbamate ligands that subtends the truncated octahedron of 24 sulfur atoms, which is concentric with the Cu24 rhombicuboctahedron and Cu4 tetrahedron about the innermost hydride. For these compounds, an intriguing, albeit limited, H2 evolution was observed at room temperature, which is accompanied by formation of the known ion [Cu8 (H)(S2 CNR)6 ](+) upon exposure of solutions to sunlight, under mild thermolytic conditions, and on reaction with weak (or strong) acids.Entities:
Keywords: copper; hydride; hydrogen evolution; nanocluster; rhombicuboctahedron
Year: 2014 PMID: 24803070 DOI: 10.1002/anie.201403324
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336