Abstract
The compound [(CH3)C(NH2)2]4 [Re6Se8(CN)6] has been synthesized by the reaction at 200°C for 3 days of Re4Te4(TeCl2)4Cl8, KSeCN, and NH4Cl in superheated acetonitrile. This compound crystallizes in the space group C2/c of the monoclinic system with four formula units in a cell of dimensions a = 20.3113(14) Å, b = 10.1332(7) Å, c = 19.9981(14) Å, β = 106.754(1)°, V = 3941.3(5) Å3 (T = 153 K). The [Re6Se8(CN)6]4- anion comprises an Re6 octahedron face capped by μ3-Se atoms, with each Re atom liganded by a CN group. The anions and cations are connected by an extensive network of hydrogen bonds. The conversion of a Re(IV) tetrahedral cluster to a Re(III) octahedral cluster appears to be unprecedented.
Original language | English (US) |
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Pages (from-to) | 6170-6171 |
Number of pages | 2 |
Journal | Inorganic chemistry |
Volume | 41 |
Issue number | 24 |
DOIs | |
State | Published - Dec 2 2002 |
ASJC Scopus subject areas
- Inorganic Chemistry
- Physical and Theoretical Chemistry
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Dive into the research topics of 'Conversion of a Re(IV) tetrahedral cluster to.a Re(III) octahedral cluster: Synthesis of [(CH3)C(NH2)2]4 [Re6Se8(CN)6] by a solvothermal route'. Together they form a unique fingerprint.Datasets
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CCDC 201091: Experimental Crystal Structure Determination
Emirdag-Eanes, M. (Creator) & Ibers, J. A. (Creator), Cambridge Crystallographic Data Centre, 2003
DOI: 10.5517/cc6r7tz, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/cc6r7tz&sid=DataCite
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