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Preparation of the 1-Methylimidazole Borane/Tetrazole System for Hypergolic Fuels
Based on the acid–base neutralization, the (1-methylimidazolium)(tetrazol-1-yl)borane was successfully synthesized by taking advantage of the acidity of the tetrazole and the basicity of the 1-methylimidazole borane complex. Through HRMS, NMR, and FT−IR, the structure of synthetic compounds was char...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9323667/ https://www.ncbi.nlm.nih.gov/pubmed/35889339 http://dx.doi.org/10.3390/molecules27144466 |
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author | Li, Xue Wu, Jun Fang, Fan Li, Hongping Wang, Lei Wan, Hui Guan, Guofeng |
author_facet | Li, Xue Wu, Jun Fang, Fan Li, Hongping Wang, Lei Wan, Hui Guan, Guofeng |
author_sort | Li, Xue |
collection | PubMed |
description | Based on the acid–base neutralization, the (1-methylimidazolium)(tetrazol-1-yl)borane was successfully synthesized by taking advantage of the acidity of the tetrazole and the basicity of the 1-methylimidazole borane complex. Through HRMS, NMR, and FT−IR, the structure of synthetic compounds was characterized in detail. Concerning about the (1-methylimidazolium)(tetrazol-1-yl)borane, it had an ignition−delay time of about 25 ms and a density specific impulse over 351 s·g/cm(3), making it a suitable candidate for green hypergolic fuels. Moreover, it also demonstrated that introducing tetrazole into the borane could be an appropriate strategy to adjust the performance of the energy of those borane compounds. |
format | Online Article Text |
id | pubmed-9323667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93236672022-07-27 Preparation of the 1-Methylimidazole Borane/Tetrazole System for Hypergolic Fuels Li, Xue Wu, Jun Fang, Fan Li, Hongping Wang, Lei Wan, Hui Guan, Guofeng Molecules Article Based on the acid–base neutralization, the (1-methylimidazolium)(tetrazol-1-yl)borane was successfully synthesized by taking advantage of the acidity of the tetrazole and the basicity of the 1-methylimidazole borane complex. Through HRMS, NMR, and FT−IR, the structure of synthetic compounds was characterized in detail. Concerning about the (1-methylimidazolium)(tetrazol-1-yl)borane, it had an ignition−delay time of about 25 ms and a density specific impulse over 351 s·g/cm(3), making it a suitable candidate for green hypergolic fuels. Moreover, it also demonstrated that introducing tetrazole into the borane could be an appropriate strategy to adjust the performance of the energy of those borane compounds. MDPI 2022-07-13 /pmc/articles/PMC9323667/ /pubmed/35889339 http://dx.doi.org/10.3390/molecules27144466 Text en © 2022 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 | Article Li, Xue Wu, Jun Fang, Fan Li, Hongping Wang, Lei Wan, Hui Guan, Guofeng Preparation of the 1-Methylimidazole Borane/Tetrazole System for Hypergolic Fuels |
title | Preparation of the 1-Methylimidazole Borane/Tetrazole System for Hypergolic Fuels |
title_full | Preparation of the 1-Methylimidazole Borane/Tetrazole System for Hypergolic Fuels |
title_fullStr | Preparation of the 1-Methylimidazole Borane/Tetrazole System for Hypergolic Fuels |
title_full_unstemmed | Preparation of the 1-Methylimidazole Borane/Tetrazole System for Hypergolic Fuels |
title_short | Preparation of the 1-Methylimidazole Borane/Tetrazole System for Hypergolic Fuels |
title_sort | preparation of the 1-methylimidazole borane/tetrazole system for hypergolic fuels |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9323667/ https://www.ncbi.nlm.nih.gov/pubmed/35889339 http://dx.doi.org/10.3390/molecules27144466 |
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