期刊
JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 747, 期 -, 页码 174-177出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2013.03.016
关键词
Boron; Carboranes; Borylation; Weak hydrogen-hydrogen interaction
资金
- Deutsche Forschungsgemeinschaft (DFG)
- Fonds der Chemischen Industrie
- National Science Foundation of China [20702020]
- Natural Science Foundation of Shandong Province [ZR2010BM020]
- Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry [SQT0804]
Reactions of dilithio-o-carborane Li2C2B10H10 (generated in situ from o-carborane 1 and butyllithium) with aminodichloroboranes R2NBCl2 (R = Et, iPr) led to the corresponding mono- and/or bis-C-amino-boryl-o-carboranes. The molecular compositions of the new o-carborane derivatives follow from NMR and MS data as well as from X-ray diffraction analyses. The structures of the new carborane compounds feature combined weak intramolecular C-H center dot center dot center dot H-B hydrogen-hydrogen and C-H center dot center dot center dot Cl hydrogen-chlorine bonding in the solid state. (C) 2013 Elsevier B. V. All rights reserved.
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