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Reactivity of a coordinated inorganic acetylene unit, HBNH, and the azidoborane cation [HB(N(3))](+)
A donor–acceptor complex of HBNH was prepared via thermolysis of a carbene-stabilized azidoborane. The reactivity of the fundamentally important HBNH unit (inorganic alkyne analogue) was explored in detail, including attempts to convert this species and related hydrido(azido)borane cations into mole...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365008/ https://www.ncbi.nlm.nih.gov/pubmed/28451338 http://dx.doi.org/10.1039/c6sc04893e |
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author | Swarnakar, Anindya K. Hering-Junghans, Christian Ferguson, Michael J. McDonald, Robert Rivard, Eric |
author_facet | Swarnakar, Anindya K. Hering-Junghans, Christian Ferguson, Michael J. McDonald, Robert Rivard, Eric |
author_sort | Swarnakar, Anindya K. |
collection | PubMed |
description | A donor–acceptor complex of HBNH was prepared via thermolysis of a carbene-stabilized azidoborane. The reactivity of the fundamentally important HBNH unit (inorganic alkyne analogue) was explored in detail, including attempts to convert this species and related hydrido(azido)borane cations into molecular complexes of BN. This work provides added impetus for the development of molecular precursors that can release bulk boron nitride (a desirable insulator and thermal conductor) under mild conditions, and from solution. |
format | Online Article Text |
id | pubmed-5365008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-53650082017-04-27 Reactivity of a coordinated inorganic acetylene unit, HBNH, and the azidoborane cation [HB(N(3))](+) Swarnakar, Anindya K. Hering-Junghans, Christian Ferguson, Michael J. McDonald, Robert Rivard, Eric Chem Sci Chemistry A donor–acceptor complex of HBNH was prepared via thermolysis of a carbene-stabilized azidoborane. The reactivity of the fundamentally important HBNH unit (inorganic alkyne analogue) was explored in detail, including attempts to convert this species and related hydrido(azido)borane cations into molecular complexes of BN. This work provides added impetus for the development of molecular precursors that can release bulk boron nitride (a desirable insulator and thermal conductor) under mild conditions, and from solution. Royal Society of Chemistry 2017-03-01 2016-12-19 /pmc/articles/PMC5365008/ /pubmed/28451338 http://dx.doi.org/10.1039/c6sc04893e Text en This journal is © The Royal Society of Chemistry 2017 https://creativecommons.org/licenses/by-nc/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Swarnakar, Anindya K. Hering-Junghans, Christian Ferguson, Michael J. McDonald, Robert Rivard, Eric Reactivity of a coordinated inorganic acetylene unit, HBNH, and the azidoborane cation [HB(N(3))](+) |
title | Reactivity of a coordinated inorganic acetylene unit, HBNH, and the azidoborane cation [HB(N(3))](+)
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title_full | Reactivity of a coordinated inorganic acetylene unit, HBNH, and the azidoborane cation [HB(N(3))](+)
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title_fullStr | Reactivity of a coordinated inorganic acetylene unit, HBNH, and the azidoborane cation [HB(N(3))](+)
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title_full_unstemmed | Reactivity of a coordinated inorganic acetylene unit, HBNH, and the azidoborane cation [HB(N(3))](+)
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title_short | Reactivity of a coordinated inorganic acetylene unit, HBNH, and the azidoborane cation [HB(N(3))](+)
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title_sort | reactivity of a coordinated inorganic acetylene unit, hbnh, and the azidoborane cation [hb(n(3))](+) |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365008/ https://www.ncbi.nlm.nih.gov/pubmed/28451338 http://dx.doi.org/10.1039/c6sc04893e |
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