ABSOLUTE KINETICS OF ALPHA-METHOXY RADICAL REACTIONS - A FOUNDATION FOR A KINETIC SCALE FOR ALPHA-ALKOXY RADICAL REACTIONS

Citation
Cc. Johnson et al., ABSOLUTE KINETICS OF ALPHA-METHOXY RADICAL REACTIONS - A FOUNDATION FOR A KINETIC SCALE FOR ALPHA-ALKOXY RADICAL REACTIONS, Journal of the American Chemical Society, 117(6), 1995, pp. 1684-1687
Citations number
29
Categorie Soggetti
Chemistry
ISSN journal
00027863
Volume
117
Issue
6
Year of publication
1995
Pages
1684 - 1687
Database
ISI
SICI code
0002-7863(1995)117:6<1684:AKOARR>2.0.ZU;2-B
Abstract
Rate constants for cyclization of the 1-methoxy-6,6-diphenyl-5-hexenyl radical (2a) and the 1-methoxy-7,7-diphenyl-6-heptenyl radical (2b) w ere measured directly. The 5-exo cyclization of 2a in THF and in CH3CN displays no solvent effect; it is described by log(k(c).s) = 9.3 - 2. 3/2.3RT, and the rate constant for the cyclization at 25 degrees C is 3.8 x 10(7) s(-1). Radical 2b cyclizes in a 6-exo fashion with rate co nstants approximately 2 orders of magnitude smaller than those of 2a; log (k(c).s) = 8.8 - 4.9/2.3RT, and k(c) at 25 degrees C is 1.5 x 10(5 ) s(-1). The kinetics of bimolecular hydrogen atom transfer trapping o f 2a by t-BuSH (log (k(T).M.s)j = 8.4 - 2.1/2.3RT) and 2b by Bu(3)SnH (log (k(T).M.s) = 8.4 - 3.8/2.3RT) also were measured. The polarity-ma tched thiol reacts with 2a with rate constants similar to those for re action with a primary alkyl radical, but the polarity-mismatched Bu(3) SnH reacts with 2b about an order of magnitude less rapidly than with an alkyl radical.