Reactions of the phenyl (m-carboran-9-yl) chloronium cation with nucleophiles. Influence of the nature of the onium halogen atom on the reactivity and the reaction …
VV Grushin, II Demkina, TP Tolstaya
Index: Grushin, Vladimir V.; Demkina, Iraida I.; Tolstaya, Tat'yana P. Inorganic Chemistry, 1991 , vol. 30, p. 1760 - 1765
Full Text: HTML
Citation Number: 15
Abstract
Comparing reactions of 1 with analogous reactions of phenyl (m-carboran-9-yl) bromonium and phenyl (m-carboran-9-yl) iodonium cations revealed the following pattern. For the sequence [C2BloH, lI-Ph]+,[C2BIoHll-Br-Ph] t,[C2BIOHIICI-Ph]+, degradation of the carborane ligand occurs with increasing ease, one-electron reduction reactions lead to only halogen-phenyl bond cleavage regardless of the halogen atom of the halonium cation, ...
Related Articles:
[Journal of the American Chemical Society, , vol. 105, # 24 p. 7175 - 7176]
[Applied Catalysis A: General, , vol. 469, p. 146 - 152]
[Li, Jian; Liu, Li; Ding, Dong; Sun, Jiang-Tao Letters in Organic Chemistry, 2013 , vol. 10, # 8 p. 541 - 548]
[Li, Jian; Liu, Li; Ding, Dong; Sun, Jiang-Tao Letters in Organic Chemistry, 2013 , vol. 10, # 8 p. 541 - 548]
[Li, Jian; Liu, Li; Ding, Dong; Sun, Jiang-Tao Letters in Organic Chemistry, 2013 , vol. 10, # 8 p. 541 - 548]