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Modes of Neighbouring Group Participation by the Methyl Selenyl Substituent in β-Methylselenylmethyl-substituted 1-Phenylethyl Carbenium Ions
Selenium substituents which are disposed β to an electron deficient centre, such as a carbocation p-orbital, or the π* orbital of an electron deficient p-system, interact in a stabilising way by a combination of C-Se hyperconjugation (σ(Se-C)–π* interaction), and a through-space homoconjugative n(Se...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270508/ https://www.ncbi.nlm.nih.gov/pubmed/24071979 http://dx.doi.org/10.3390/molecules181011705 |
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author | Harris, Benjamin L. White, Jonathan M. |
author_facet | Harris, Benjamin L. White, Jonathan M. |
author_sort | Harris, Benjamin L. |
collection | PubMed |
description | Selenium substituents which are disposed β to an electron deficient centre, such as a carbocation p-orbital, or the π* orbital of an electron deficient p-system, interact in a stabilising way by a combination of C-Se hyperconjugation (σ(Se-C)–π* interaction), and a through-space homoconjugative n(Se)–π* interaction. The relative importance of these two modes of interaction is dependant on the electron demand of the cation, with hyperconjugation predominating for low electron demand systems, and the n(Se)–π* interaction predominating for high electron demand cations. |
format | Online Article Text |
id | pubmed-6270508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62705082018-12-18 Modes of Neighbouring Group Participation by the Methyl Selenyl Substituent in β-Methylselenylmethyl-substituted 1-Phenylethyl Carbenium Ions Harris, Benjamin L. White, Jonathan M. Molecules Article Selenium substituents which are disposed β to an electron deficient centre, such as a carbocation p-orbital, or the π* orbital of an electron deficient p-system, interact in a stabilising way by a combination of C-Se hyperconjugation (σ(Se-C)–π* interaction), and a through-space homoconjugative n(Se)–π* interaction. The relative importance of these two modes of interaction is dependant on the electron demand of the cation, with hyperconjugation predominating for low electron demand systems, and the n(Se)–π* interaction predominating for high electron demand cations. MDPI 2013-09-25 /pmc/articles/PMC6270508/ /pubmed/24071979 http://dx.doi.org/10.3390/molecules181011705 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Harris, Benjamin L. White, Jonathan M. Modes of Neighbouring Group Participation by the Methyl Selenyl Substituent in β-Methylselenylmethyl-substituted 1-Phenylethyl Carbenium Ions |
title | Modes of Neighbouring Group Participation by the Methyl Selenyl Substituent in β-Methylselenylmethyl-substituted 1-Phenylethyl Carbenium Ions |
title_full | Modes of Neighbouring Group Participation by the Methyl Selenyl Substituent in β-Methylselenylmethyl-substituted 1-Phenylethyl Carbenium Ions |
title_fullStr | Modes of Neighbouring Group Participation by the Methyl Selenyl Substituent in β-Methylselenylmethyl-substituted 1-Phenylethyl Carbenium Ions |
title_full_unstemmed | Modes of Neighbouring Group Participation by the Methyl Selenyl Substituent in β-Methylselenylmethyl-substituted 1-Phenylethyl Carbenium Ions |
title_short | Modes of Neighbouring Group Participation by the Methyl Selenyl Substituent in β-Methylselenylmethyl-substituted 1-Phenylethyl Carbenium Ions |
title_sort | modes of neighbouring group participation by the methyl selenyl substituent in β-methylselenylmethyl-substituted 1-phenylethyl carbenium ions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270508/ https://www.ncbi.nlm.nih.gov/pubmed/24071979 http://dx.doi.org/10.3390/molecules181011705 |
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