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Mesolytic Cleavage of CC Bonds. Comparison with Homolytic and Heterolytic Processes in the Same Substrate
Author(s) -
Maslak Przemyslaw,
Narvaez Javier N.
Publication year - 1990
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.199002831
Subject(s) - heterolysis , homolysis , chemistry , bond cleavage , fragmentation (computing) , ion , photochemistry , cleavage (geology) , radical ion , radical , stereochemistry , materials science , organic chemistry , catalysis , composite material , fracture (geology) , computer science , operating system
The fragmentation of 1 is up to 10 20 times faster if it is present as radical ion and not as neutral compound. This acceleration has thermodynamic reasons, which surprisingly lead almost exclusively to a lowering of the energy of the transition state, even for weakly endergonic processes. The term (catio‐/anio) mesolytic is proposed for the fragmentations of radical ions.

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