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Intra- and inter-molecular carboranyl C-H center dot center dot center dot N hydrogen bonds in pyridyl-containing ortho-carboranes

Alekseyeva, E. S.; Batsanov, A. S.; Boyd, L. A.; Fox, M. A.; Hibbert, T. G.; Howard, J. A. K.; MacBride, J. A. H.; Mackinnon, A.; Wade, K.

Authors

E. S. Alekseyeva

L. A. Boyd

T. G. Hibbert

J. A. H. MacBride

A. Mackinnon

K. Wade



Abstract

Four C-substituted derivatives of ortho-carborane, 1-R-1,2-C2B10H11, where R = 2'-pyridyl (1), 2'-picolyl (2), 5'-bromo-2'-pyridyl (3) or 3'-pyridyl (4) have been prepared using adaptations of standard procedures, and structurally characterised by single crystal X-ray diffraction studies in an exploration of C-H...N hydrogen bonding effects involving their carborane CH units. Calculations at the MP2/6-31G* level of theory were used to assess the strength of the hydrogen bonding detected, and calculated NMR shifts at the GIAO-B3LYP/6-311G* level were compared with measured C-H shifts to show that intramolecular C-H...N hydrogen bonding persisted in solution in the case of compound 1. The value of IR C-H stretching frequencies for probing hydrogen bonding in these systems was also studied. An unsuccessful attempt to convert compound 3 into a macrocyclic species (C2B10H10C5H3N)(3) in which three ortho-carborane units are linked through 2,5-disubstituted pyridine rings is also described.

Citation

Alekseyeva, E. S., Batsanov, A. S., Boyd, L. A., Fox, M. A., Hibbert, T. G., Howard, J. A. K., MacBride, J. A. H., Mackinnon, A., & Wade, K. (2003). Intra- and inter-molecular carboranyl C-H center dot center dot center dot N hydrogen bonds in pyridyl-containing ortho-carboranes. Dalton Transactions, 2003(3), 475-482. https://doi.org/10.1039/B209931D

Journal Article Type Article
Online Publication Date Dec 24, 2002
Publication Date 2003
Journal Dalton Transactions
Print ISSN 1477-9226
Electronic ISSN 1477-9234
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 2003
Issue 3
Pages 475-482
DOI https://doi.org/10.1039/B209931D
Public URL https://durham-repository.worktribe.com/output/1572176