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Spectral kinetics of 3 + 3 dipolar thermal dimerization in some carbanion monosubstituted 3-(p-halo-phenyl)-pyridazinium ylid solutions

✍ Scribed by Dana Dorohoi; M. Cotlet; I. Mangalagiu


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
194 KB
Volume
34
Category
Article
ISSN
0538-8066

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✦ Synopsis


Abstract

The visible intramolecular charge transfer band of some carbanion monosubstituted 3‐(p‐halo‐phenyl)‐pyridazinium ylids in benzene solutions has been considered as an indicator of the ylid stability. The catalytic effect of light on 3 + 3 dipolar thermal dimerization reaction was revealed. The dimerization reaction was found to be of the second order in the ylid concentration. The rate of dimerization was found to be promoted by increasing the electronegativity of the substituents on the ylid carbanion. The associated intramolecular charge transfer band oscillator strength has been correlated with the rate constant. © 2002 Wiley Periodicals, Inc. Int J Chem Kinet 34: 613–619, 2002


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## Abstract 3‐(__p__‐Bromo‐phenyl)‐pyridazinium‐benzoyl methylid (BPPBM) participates in solution at 3 + 3 dipolar thermal dimerization that can be spectrally monitored by the extinction in its visible intramolecular charge transfer (ICT) band. The attenuation of ICT band intensity shows the decrea