Electron Spin Resonance and Laser Flash Photolysis Study of Radical Addition to Vinyl Acrylate and Related Alkenes†

2002 ◽  
Vol 106 (10) ◽  
pp. 1938-1945 ◽  
Author(s):  
Matthias Weber ◽  
Igor V. Khudyakov ◽  
Nicholas J. Turro
1999 ◽  
Vol 77 (5-6) ◽  
pp. 1066-1076
Author(s):  
Hideo Tomioka ◽  
Junichi Nakajima ◽  
Hidehiko Mizuno ◽  
Eiji Iiba ◽  
Katsuyuki Hirai

A series of triplet 9-triptycyl(aryl)carbenes, where aryl groups are phenyl, 1- and 2-naphthyl, and 9-anthryl, is generated by photolysis of the corresponding diazomethanes and observed directly by spectroscopic means. Their structures are characterized by electron spin resonance (ESR) spectroscopy in a 2-methyltetrahydrofuran matrix at 77 K, and the reactivities are investigated by laser flash photolysis in degassed benzene solution at room temperature. Comparison of the data with other arylcarbenes bearing a series of substituents, i.e., hydrogen, phenyl, naphthyl, and anthryl groups, revealed an interesting relationship between structures and reactivities of triplet arylcarbenes.Key words: steric protection, stability of triplet carbenes, electron spin resonance, laser flash photolysis, structure-reactivity relationship.


1984 ◽  
Vol 78 ◽  
pp. 257 ◽  
Author(s):  
Christopher D. Buckley ◽  
Andrew I. Grant ◽  
Keith A. McLauchlan ◽  
Andrew J. D. Ritchie

1973 ◽  
Vol 44 (2) ◽  
pp. 197-199 ◽  
Author(s):  
Edward S. P. Hsi ◽  
Leonard Fabes ◽  
James R. Bolton

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