Syntheses of lipophilic tetraarylborate ions substituted with many perfluoroalkyl groups and their stability under acid conditions

被引:13
作者
Fujiki, K
Ichikawa, J
Kobayashi, H
Sonoda, A
Sonoda, T [1 ]
机构
[1] Kyushu Univ, Inst Adv Mat Study, Kasuga, Fukuoka 816, Japan
[2] Kyushu Univ, Grad Sch Engn Sci, Kasuga, Fukuoka 816, Japan
关键词
weakly coordinating anions; perfluoroalkyl-substituted tetraarylborate ions; syntheses; lipophilicity; stability;
D O I
10.1016/S0022-1139(99)00291-2
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Syntheses are investigated on several new kinds of perfluoroalkyl-substituted tetraarylborate ions such as tetrakis(3,5-bis(nonafluorobutyl)phenyl)borate, tetrakis(3,5-bis(heptafluoro-2-propyl)phenyl)borate (PFPB), tetrakis(3-(heptafluoro-2-propyl)-1-(trifluoromethyl)phenyl)borate, and tetrakis(3-(heptafluoro-2-propyl)phenyl))borate. Solubilities of tetramethylammonium tetraarylborates in some hydrophobic halocarbon solvents and rate constants of acid-catalyzed decomposition of the tetraarylborate ions in methanolic sulfuric acid solutions and in dichloromethane/aqueous sulfuric acid two-phase system are determined. Trifluoromethyl- and perfluoroalkyl-substituent effects on the lipophilicity and chemical stability of the tetraarylborate ions are discussed in comparisons with a range of those described previously. (C) 2000 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:293 / 300
页数:8
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