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Spontaneous Transition of Alkyl Carbocations to Unsaturated Vinyl-Type Carbocations in Organic Solutions
It was found that alkyl carbocations, when their salts are dissolved in common organochlorine solvents, decompose to unsaturated vinyl-type carbocations that are stabler in solutions. This is a convenient method for obtaining salts of vinyl cations and their solutions for further research.
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860910/ https://www.ncbi.nlm.nih.gov/pubmed/36675316 http://dx.doi.org/10.3390/ijms24021802 |
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author | Stoyanov, Evgenii S. Stoyanova, Irina V. |
author_facet | Stoyanov, Evgenii S. Stoyanova, Irina V. |
author_sort | Stoyanov, Evgenii S. |
collection | PubMed |
description | It was found that alkyl carbocations, when their salts are dissolved in common organochlorine solvents, decompose to unsaturated vinyl-type carbocations that are stabler in solutions. This is a convenient method for obtaining salts of vinyl cations and their solutions for further research. |
format | Online Article Text |
id | pubmed-9860910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98609102023-01-22 Spontaneous Transition of Alkyl Carbocations to Unsaturated Vinyl-Type Carbocations in Organic Solutions Stoyanov, Evgenii S. Stoyanova, Irina V. Int J Mol Sci Communication It was found that alkyl carbocations, when their salts are dissolved in common organochlorine solvents, decompose to unsaturated vinyl-type carbocations that are stabler in solutions. This is a convenient method for obtaining salts of vinyl cations and their solutions for further research. MDPI 2023-01-16 /pmc/articles/PMC9860910/ /pubmed/36675316 http://dx.doi.org/10.3390/ijms24021802 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Stoyanov, Evgenii S. Stoyanova, Irina V. Spontaneous Transition of Alkyl Carbocations to Unsaturated Vinyl-Type Carbocations in Organic Solutions |
title | Spontaneous Transition of Alkyl Carbocations to Unsaturated Vinyl-Type Carbocations in Organic Solutions |
title_full | Spontaneous Transition of Alkyl Carbocations to Unsaturated Vinyl-Type Carbocations in Organic Solutions |
title_fullStr | Spontaneous Transition of Alkyl Carbocations to Unsaturated Vinyl-Type Carbocations in Organic Solutions |
title_full_unstemmed | Spontaneous Transition of Alkyl Carbocations to Unsaturated Vinyl-Type Carbocations in Organic Solutions |
title_short | Spontaneous Transition of Alkyl Carbocations to Unsaturated Vinyl-Type Carbocations in Organic Solutions |
title_sort | spontaneous transition of alkyl carbocations to unsaturated vinyl-type carbocations in organic solutions |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860910/ https://www.ncbi.nlm.nih.gov/pubmed/36675316 http://dx.doi.org/10.3390/ijms24021802 |
work_keys_str_mv | AT stoyanovevgeniis spontaneoustransitionofalkylcarbocationstounsaturatedvinyltypecarbocationsinorganicsolutions AT stoyanovairinav spontaneoustransitionofalkylcarbocationstounsaturatedvinyltypecarbocationsinorganicsolutions |