Abstract
The reaction of closo-2,4-C2B5H7with BX3 (X = Cl, Br, I, C6H5) at elevated temperatures (270 °C for BC13, 160 °C for BBr3, 120 °C for BI3, 160 °C for B(C6H5)3) results in halogen, or phenyl, substitution primarily at the 3-position of the carborane (i.e. 3-X-closo-2,4-C2B5H6). closo-2,4-C2B5H7also reacts with (CH3)3CC1 at 270 °C to give 3-C1-Closo-2,4-C2B5H6. A closo carborane containing a trigonal boron σ-bonded to a cage carborane, 2-Br2B-closo-l,6-C2B4H5, is prepared from closo- 1,6-C2B4H6and BBr3 at 265 °C.
| Original language | English |
|---|---|
| Pages (from-to) | 48-52 |
| Number of pages | 5 |
| Journal | Inorganic Chemistry |
| Volume | 26 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1987 |
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Dive into the research topics of 'Reaction of the Small Closo Carboranes 1,6-C2B4H6 and 2,4-C2B5H7 with BX3 (X = Halogen, Phenyl): A Method of Preparing “3”-Substituted 2,4-C2B5H7 Derivatives and Preparation of 2-Br2B-closo-l,6-C2B4H5'. Together they form a unique fingerprint.Cite this
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