Oligomerization of N-vinylpyrroles under the action of iodine View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2016-11

AUTHORS

M. V. Markova, I. V. Tatarinova, T. I. Vakul’skaya, S. S. Khutsishvili, A. V. Yakimanskii, G. F. Prozorova, B. A. Trofimov

ABSTRACT

The oligomerization of N-vinylpyrroles (N-vinyl-4,5,6,7-tetrahydroindole, N-vinyl-2-[1-(1-4,5,6,7-tetrahydroindole)ethyl]-4,5,6,7-tetrahydroindole, N-vinyl-2-phenylpyrrole, N-vinyl-3-heptyl-2-phenylpyrrole, N-vinyl-2,3-diphenylpyrrole, and N-vinyl-2-(2-naphthyl)pyrrole) under the action of iodine vapor leads to the formation of iodine-containing oligomers with an iodine content of 17–52% and a yield of up to 99%. The oligomers are paramagnetic and possess conductivity; they are readily soluble in organic solvents (benzene, dioxane, and chloroform) and are stable up to 110–260°C. More... »

PAGES

681-688

References to SciGraph publications

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http://scigraph.springernature.com/pub.10.1134/s1560090416060117

DOI

http://dx.doi.org/10.1134/s1560090416060117

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https://app.dimensions.ai/details/publication/pub.1050048475


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