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Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles
Conjugation between a 3-D icosahedral carborane and a fused 2-D π-ring system is ambiguous. To address this issue, we prepared several carborane-fused carbo- and heterocycles. Detailed studies on their molecular structures, NMR data, and NICS (nucleus-independent chemical shift) and ISE (isomerizati...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897843/ https://www.ncbi.nlm.nih.gov/pubmed/29719701 http://dx.doi.org/10.1039/c7sc04722c |
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author | Chan, Tek Long Xie, Zuowei |
author_facet | Chan, Tek Long Xie, Zuowei |
author_sort | Chan, Tek Long |
collection | PubMed |
description | Conjugation between a 3-D icosahedral carborane and a fused 2-D π-ring system is ambiguous. To address this issue, we prepared several carborane-fused carbo- and heterocycles. Detailed studies on their molecular structures, NMR data, and NICS (nucleus-independent chemical shift) and ISE (isomerization stabilization energy) values as well as molecular orbital analyses clearly suggest the presence of (1) considerable aromatic character in the exo five-membered ring of carborane-fused carbo- and heterocycles and (2) considerable conjugation between a 3-D carborane and a fused 2-D π-ring system. These results will shed some light on the design of new carborane-based materials. |
format | Online Article Text |
id | pubmed-5897843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-58978432018-05-01 Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles Chan, Tek Long Xie, Zuowei Chem Sci Chemistry Conjugation between a 3-D icosahedral carborane and a fused 2-D π-ring system is ambiguous. To address this issue, we prepared several carborane-fused carbo- and heterocycles. Detailed studies on their molecular structures, NMR data, and NICS (nucleus-independent chemical shift) and ISE (isomerization stabilization energy) values as well as molecular orbital analyses clearly suggest the presence of (1) considerable aromatic character in the exo five-membered ring of carborane-fused carbo- and heterocycles and (2) considerable conjugation between a 3-D carborane and a fused 2-D π-ring system. These results will shed some light on the design of new carborane-based materials. Royal Society of Chemistry 2018-01-16 /pmc/articles/PMC5897843/ /pubmed/29719701 http://dx.doi.org/10.1039/c7sc04722c Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Chan, Tek Long Xie, Zuowei Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles |
title | Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles
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title_full | Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles
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title_fullStr | Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles
|
title_full_unstemmed | Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles
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title_short | Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles
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title_sort | synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897843/ https://www.ncbi.nlm.nih.gov/pubmed/29719701 http://dx.doi.org/10.1039/c7sc04722c |
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