Journal
JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 798, Issue -, Pages 171-181Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2015.05.053
Keywords
Carboranes; Iodination; Acidity; Solvent free
Categories
Funding
- MEC [CTQ2013-44670-R]
- Generalitat de Catalunya [2014/SGR/149]
- MICINN
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The preparation of Cc-monosubstituted closo and nido carborane derivatives, mono-, di and tetraiodinated is reported. Some of these mono-to poly-iodinated nido carboranes are studied in terms of the acidity of the open face bridging proton, their chemical shift position in the H-1 NMR, and the lesser tendency to eta(5)-coordination in parallel to a larger number of iodo groups. (C) 2015 Elsevier B.V. All rights reserved.
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