Journal
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES
Volume 66, Issue 1, Pages 65-68Publisher
WALTER DE GRUYTER GMBH
DOI: 10.5560/ZNB.2011.66b0065
Keywords
Diphenyldiselenide; o-Carborane; Synthesis; Crystal Structure; Photoluminescence
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Funding
- NSFC [20702020]
- SRF for ROCS, SEM [SQT0804]
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The reaction of dithio-o-carborane with diphenyldiselenide (PhSeSePh) affords the title compound, closo-1,2-(PhSe)(2)C2B10H10 (1), which has been characterized by IR and NMR (H-1, B-11) spectroscopy and by single-crystal X-ray diffraction. The phenylselenyl groups are bonded to the cage carbon atoms of the o-carborane cluster with a C-cage-C-cage distance of 1.751(6) angstrom and an Se-C-cage-C-cage-Se torsion angle of 10.1(3)degrees. Compound 1 displays a violet emission on excitation with UV light. For comparison the photoluminescence of the known analog closo-1,2-(PhS)(2)C2B10H10 (2) was also studied.
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