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

Citation
K. Fujiki et al., Syntheses of lipophilic tetraarylborate ions substituted with many perfluoroalkyl groups and their stability under acid conditions, J FLUORINE, 102(1-2), 2000, pp. 293-300
Citations number
19
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF FLUORINE CHEMISTRY
ISSN journal
00221139 → ACNP
Volume
102
Issue
1-2
Year of publication
2000
Pages
293 - 300
Database
ISI
SICI code
0022-1139(200003)102:1-2<293:SOLTIS>2.0.ZU;2-4
Abstract
Syntheses are investigated on several new kinds of perfluoroalkyl-substitut ed tetraarylborate ions such as tetrakis(3,5-bis(nonafluorobutyl)phenyl)bor ate, tetrakis(3,5-bis(heptafluoro-2-propyl)phenyl)borate (PFPB), tetrakis(3 -(heptafluoro-2-propyl)-1-(trifluoromethyl)phenyl)borate, and tetrakis(3-(h eptafluoro-2-propyl)phenyl))borate. Solubilities of tetramethylammonium tet raarylborates in some hydrophobic halocarbon solvents and rate constants of acid-catalyzed decomposition of the tetraarylborate ions in methanolic sul furic acid solutions and in dichloromethane/aqueous sulfuric acid two-phase system are determined. Trifluoromethyl- and perfluoroalkyl-substituent eff ects on the lipophilicity and chemical stability of the tetraarylborate ion s are discussed in comparisons with a range of those described previously. (C) 2000 Elsevier Science S.A. All rights reserved.