Polymerizable mesoions, 2. Radical polymerization and 1,4-dipolar polycycloaddition of a 4-vinylphenyl-modified mesoionic 4,6-dioxo-1,3-diazine
✍ Scribed by Helmut Ritter; Rolf Sperber
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 339 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Abstract
Mesoionic 5‐methyl‐4,6‐dioxo‐3‐phenyl‐1‐(4‐vinylphenyl)‐1,3‐diazine (5) was obtained by condensation of 3‐phenyl‐1‐(4‐vinylphenyl)formamidine (3) with methylmalonic acid (4). This vinyl‐substituted mesoionic heterocyclic compound was polymerized by usual radical initiation and, additionally, by thermally controlled polycycloaddition in solution, yielding two different types of polymers, 6, 7. According to the X‐ray diffraction analysis, the structure of a low molecular weight model proves the regioselectivity of the polycycloaddition.
📜 SIMILAR VOLUMES
## Abstract Mesoionic 5‐alkyl‐4,6‐dioxo‐1,3‐diphenyl‐2‐(3‐vinylbenzylthio)‐1,3‐diazine (6) was prepared by condensation of alkylmalonic acid (5) with 1,3‐diphenyl‐2‐(3‐vinylbenzyl)isothiourea (4) by use of dicyclohexylcarbodiimide (DCC). Homopolymerization of 6 led to new polystyrene derivatives (7
## Abstract The reaction of the 6‐chloro‐2‐(1‐methyl‐2‐thiocarbamoylhydrazino)quinoxaline 4‐oxides 3a‐d with trifluoroacetic anhydride gave the 2‐(__N__‐aryl)trifluoroacetamido‐8‐chloro‐4‐methyl‐4__H__‐1,3,4‐thiadiazino‐[5,6‐__b__]quinoxalines 7a‐d, respectively, while the reflux of compounds 3a‐c