The role of bridged structures in the mechanism of the reaction between chlorine atom and ethylene

[1]  D. Feller,et al.  A CCSDT study of the effects of higher order correlation on spectroscopic constants. I. First row diatomic hydrides , 2000 .

[2]  H. Valdés,et al.  On the violation of Legon–Millen's rules for predicting angular geometries of hydrogen-bonded dimers: an ab initio study , 1999 .

[3]  P. Vogel,et al.  Sulfur dioxide promotes its hetero-Diels-Alder and cheletropic additions to 1,2-dimethylidenecyclohexane , 1998 .

[4]  E. Bernstein,et al.  Aromatic van der Waals Clusters: Structure and Nonrigidity , 1996 .

[5]  M. Guerra.  A theoretical investigation of the structures and properties of classical and bridged .beta.-substituted ethyl radicals , 1992 .

[6]  H. Bernhard Schlegel,et al.  Reaction Path Following in Mass-Weighted Internal Coordinates , 1990 .

[7]  B. Engels,et al.  Theoretical study of the potential energy surface governing the stereochemistry in chloroethyl radical reactions , 1990 .

[8]  D. J. Stevens,et al.  Kinetics and mechanism of recoil chlorine atom reactions with ethylene , 1977 .

[9]  R. Lloyd,et al.  Free radicals in an Adamantane matrix. XI. Electron paramagnetic resonance study of conformations in the $beta$-halo-tert-butyl radicals , 1975 .

[10]  J. Kochi,et al.  Bridging in .beta.-chloroalkyl radicals by electron spin resonance , 1973 .

[11]  W. Thaler.  Photobromination of Alkyl Halides, an Unusual Orienting Effect in the Bromination of Alkyl Bromides , 1963 .

[12]  B. F. Aycock,et al.  The Stereochemistry of the Free Radical Addition of Hydrogen Bromide to 1-Bromocyclohexene and 1-Methylcyclohexene , 1952 .