TY - JOUR
T1 - Reaction of the Small Closo Carboranes 1,6-C2B4H6 and 2,4-C2B5H7 with BX3 (X = Halogen, Phenyl)
T2 - A Method of Preparing “3”-Substituted 2,4-C2B5H7 Derivatives and Preparation of 2-Br2B-closo-l,6-C2B4H5
AU - Nam, Wonwoo
AU - Onak, Thomas
PY - 1987
Y1 - 1987
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=0344359684&partnerID=8YFLogxK
U2 - 10.1021/ic00248a011
DO - 10.1021/ic00248a011
M3 - Article
AN - SCOPUS:0344359684
SN - 0020-1669
VL - 26
SP - 48
EP - 52
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 1
ER -