Micellar SN2 reaction of methyl naphthalene-2-sulfonate and its 6-sulfonalte derivative:: Effect of the negative charge

被引:17
作者
Brinchi, L
Di Profio, P
Germani, R
Marte, L
Savelli, G
Bunton, CA
机构
[1] Univ Perugia, Dipartimento Chim, I-06123 Perugia, Italy
[2] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
关键词
micelles; anionic substrates; bimolecular nucleophilic substitution;
D O I
10.1006/jcis.2001.7834
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Comparison of reactivities of methyl naphthalene-2-sulfonate, MeONs, and its 6-sulfonate derivative, MeONsS(-), toward H2O, OH-, and Br- in water and in cationic micelles of cetyl trialkylammonium surfactants, n-C16H33N+R3X-, R = Me, n-Pr, n-Bu, CTA(+), CTPA(+), CTBA(+), X = OH, Br, and CH3SO3 has been investigated. For reactions in water, the introduction of the negative charge accelerates hydrolysis by a factor of ca. 2, but does not affect reactivity of OH- and Br-. For reactions in micelles, the negative charge decreases values of km for reactions with water, with OH- and Br- by a factor of ca. 2; differences for the two substrates decrease with bulking the surfactant head group for a reaction with Br- but not for a reaction with OH-. (C) 2001 Academic Press.
引用
收藏
页码:469 / 475
页数:7
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