Abstract
A series of 2-aryl derivatives of B5H9 have been prepared via aluminum chloride catalyzed electrophilic substitution by 2-ClB5H8 on various alkylbenzenes. Analyses of 1H NMR spectra suggest that the site of attack of the B5H8 moiety is controlled by steric interactions.
Original language | English |
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Pages (from-to) | 4117-4121 |
Number of pages | 5 |
Journal | Inorganic Chemistry |
Volume | 21 |
Issue number | 12 |
DOIs | |
State | Published - 1982 |