Temperature-dependent acid dissociation constants (Ka, .DELTA.Ha, .DELTA.Sa) for a series of nitrogen-substituted hydroxamic acids in aqueous solution

1982 ◽  
Vol 47 (7) ◽  
pp. 1171-1176 ◽  
Author(s):  
Christina Poth Brink ◽  
Alvin L. Crumbliss

2009 ◽  
Vol 13 (08n09) ◽  
pp. 849-853 ◽  
Author(s):  
Takuya Shimomura ◽  
Masaaki Tabata ◽  
Jun Nishimoto

A water-soluble octabromoporphyrin 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetrakis(1-methylpyridinium-4-yl)porphyrin (H2(OBTMPyP)4+), H2P4+) and its lithium complex, Li(OBTMPyP)3+ , (LiP3+) , transferred quantitatively to an ionic liquid (IL), 1-butyl-3-methylimidazolium hexafluorophosphate (BMIM+PF6-) with no addition of other counter ions. The acid-dissociation constants of H2(OBTMPyP)4+ between aqueous and BMIM+PF6- phases were determined spectrophotometrically and found to be 10-7.67 and 10-11.33 at I = 0.1 for K a1,IL = [H+]aq[HP3+]IL/[H2P4+]IL and K a2,IL = [H+]aq[P2+]IL/[HP3+]IL , respectively. Since the acid-dissociation constants involve the partition of H2(OBTMPyP)4+ between aqueous and IL phases, the determined values are ten times as low as those observed in aqueous solution. The transfer equilibrium constants of LiP3+ and NaP3+ to IL defined by K MP,IL = [MP3+]IL/[M+]aq[P2+]IL (M = Li+ or Na+) were found to be 104.83 and 101.31 for K LiP,IL and KNaP,IL , respectively. LiP3+ transferred selectively in the presence of Na+ (K LiP,IL /K NaP,IL = 103.52) to IL phase through an ion-exchange mechanism between BMIM+PF6- and Li(OBTMPyP)3+ .



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