Kinetics of C6H5 radical reactions with 2-methylpropane, 2,3-dimethylbutane and 2,3,4-trimethylpentane
β Scribed by J. Park; S. I. Gheyas; M. C. Lin
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 180 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
The absolute bimolecular rate constants for the reactions of C 6 H 5 with 2-methylpropane, 2,3-dimethylbutane and 2,3,4-trimethylpentane have been measured by cavity ringdown spectrometry at temperatures between 290 and 500 K. For 2-methylpropane, additional measurements were performed with the pulsed laser photolysis/mass spectrometry, extending the temperature range to 972 K. The reactions were found to be dominated by the abstraction of a tertiary C-H bond from the molecular reactant, resulting in the production of a tertiary alkyl radical:
6 5 3 3 6 6 4 9 C H Ο© (CH ) CHCH(CH ) !: C H Ο© t-C H (2)
π SIMILAR VOLUMES
Reaction of elemental antimony with sulfur under mild hydrothermal conditions yielded different polysulfidoclusters of antimony. These were isolated as tetraphenylphosphonium salts [P(C 6 H 5 ) 4 ] 3 Sb 3 S 25 and [P(C 6 H 5 ) 4 ] 2 Sb 2 S 15 2(C 3 N 2 H 6 ) and their crystal structures were determi
Two new 1,2,3,5-dithiadiazoles, [4-(4Π-C 5 H 4 N)CN 2 S 2 ] (L 1 ) and [4-(3Π-C 5 H 4 N)CN 2 S 2 ] (L 2 ), with different pyridyl groups at the 4-position were prepared. As Lewis bases, the dithiadiazoles reacted with Lewis acids via their pyridyl groups to form acid-base adducts with retention of t