CALIBRATION OF A NEW HOROLOGERY OF FAST RADICAL CLOCKS - RING-OPENING RATES FOR RING-ALKYL-SUBSTITUTED AND ALPHA-ALKYL-SUBSTITUTED CYCLOPROPYLCARBINYL RADICALS AND FOR THE BICYCLO[2.1.0]PENT-2-YL RADICAL

Bowry, VW; Lusztyk, J; Ingold, KU

HERO ID

4854549

Reference Type

Journal Article

Year

1991

HERO ID 4854549
In Press No
Year 1991
Title CALIBRATION OF A NEW HOROLOGERY OF FAST RADICAL CLOCKS - RING-OPENING RATES FOR RING-ALKYL-SUBSTITUTED AND ALPHA-ALKYL-SUBSTITUTED CYCLOPROPYLCARBINYL RADICALS AND FOR THE BICYCLO[2.1.0]PENT-2-YL RADICAL
Authors Bowry, VW; Lusztyk, J; Ingold, KU
Journal Journal of the American Chemical Society
Volume 113
Issue 15
Page Numbers 5687-5698
Abstract Rate constants have been determined at 37-degrees-C for the ring opening of a variety of alkyl-substituted cyclopropylcarbinyl radical ''clocks'' by nitroxide radical trapping (NRT) using TEMPO. Relative yields of unrearranged and rearranged trialkylhydroxylamines were measured at various TEMPO concentrations, and these data were then combined with absolute rate constants for the reactions of structurally appropriate alkyl radicals with TEMPO as determined by laser flash photolysis. Cyclopropylcarbinyl radicals, including the bicyclo[2.1.0]pent-2-yl radical, were generated by H-atom abstraction from the parent hydrocarbon and, in a few cases, also from the appropriate diacyl peroxide. Twelve substrates yielded sixteen clock reactions because some cyclopropylcarbinyls can undergo two different ring-opening reactions. For six methyl-substituted cyclopropylcarbinyls rate constants ranged from 0.8 x 10(8) s-1 for 1-methylcyclopropylcarbinyl to 47 x 10(8) s-1 for pentamethylcyclopropylcarbinyl. Rate constants for the ring opening of cyclopropylcarbinyl, alpha-methyl- and alpha,alpha-dimethylcyclopropylcarbinyl are 1.2, 0.70, and 0.88 x 10(8) s-1, respectively. Rate constants for H-atom ion by tert-butoxyl from various positions in the 12 cyclopropane substrates relative to the rate of H-atom ion from cyclopentane have also been determined by using competitive NRT.
Doi 10.1021/ja00015a024
Wosid WOS:A1991FX87800024
Is Certified Translation No
Dupe Override No
Is Public Yes