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Correction: Chemistry of group 9 dimetallaborane analogues of octaborane(12)
Subrat Kumar
Barik
,
Dipak Kumar
Roy
and
Sundargopal
Ghosh
*
Department of Chemistry, Indian Institute of Technology Madras, Chennai 600 036, India. E-mail: sghosh@iitm.ac.in; Fax: (+91) 44 2257 4202; Tel: (+91) 44 2257 4230
First published on 20th March 2015
Abstract
Correction for ‘Chemistry of group 9 dimetallaborane analogues of octaborane(12)’ by Subrat Kumar Barik, et al., Dalton Trans., 2015, 44, 669–676.
The authors wish to add the following references to their manuscript:
1 V. R. Miller, R. Weiss and R. N. Grimes, Polyhedral cobaltaboranes. Versatile replacement of BH groups by Co(η5-C5H5) units in boron hydride frameworks. Borane–metal cluster hybrid molecules, J. Am. Chem. Soc., 1977, 99, 5646–5651.
2 J. R. Pipal and R. N. Grimes, Crystal and molecular structure of 5-(η5-C5H5)CoB9H13, a cobaltaborane analogue of B10H14, Inorg. Chem., 1977, 16, 3251–3255.
3 T. L. Venable, W. C. Hutton and R. N. Grimes, Two-dimensional boron-11-boron-11 nuclear magnetic resonance spectroscopy as a probe of polyhedral structure: application to boron hydrides, carboranes, metallaboranes, and metallacarboranes, J. Am. Chem. Soc., 1984, 106, 29–37.
4 T. L. Venable and R. N. Grimes, (Pentamethylcyclopentadienyl)cobaltaboranes derived from the B5H8− and B9H14− ions: studies in synthesis and structure, Inorg. Chem., 1982, 21, 887–895.
5 T. L. Venable, E. Sinn and R. N. Grimes, Cobaltaborane analogues of B10H14. Crystal and molecular structures of 6-[η5-C5(CH3)5]CoB9H13, 6,9-[η5-C5(CH3)5]2Co2B8H12, 5,7-[η5-C5(CH3)5]2Co2B8H12, and 6-C1-5,7-[η5-C5(CH3)5]2Co2B8H11, Inorg. Chem., 1982, 21, 895–904.
6 C. T. Brewer and R. N. Grimes, Metal-promoted fusion and linkage of B5H8−, 1-XB5H7− (X = D, CH3), B10H13−, and (η5-C5H5)CoB4H7−. Facile routes to B10H14 and (η5-C5H5)2Co2B8H10 isomers, J. Am. Chem. Soc., 1985, 107, 3552–3557.
As a result the authors also wish to include the following in their results and discussion section:
Note that, compound 1 has been synthesized and structurally characterized by Grimes and co-workers in a different synthetic pathway (J. Am. Chem. Soc., 1977, 99, 5646; Inorg. Chem., 1977, 16, 3251).
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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