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Borohydride-containing coordination polymers: synthesis, air stability and dehydrogenation
Control of the reactivity of hydride (H(–)) in crystal structures has been a challenge because of its strong electron-donating ability and reactivity with protic species. For metal borohydrides, the dehydrogenation activity and air stability are in a trade-off, and control of the reactivity of BH(4)...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585883/ https://www.ncbi.nlm.nih.gov/pubmed/31360426 http://dx.doi.org/10.1039/c9sc00731h |
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author | Kadota, Kentaro Duong, Nghia Tuan Nishiyama, Yusuke Sivaniah, Easan Kitagawa, Susumu Horike, Satoshi |
author_facet | Kadota, Kentaro Duong, Nghia Tuan Nishiyama, Yusuke Sivaniah, Easan Kitagawa, Susumu Horike, Satoshi |
author_sort | Kadota, Kentaro |
collection | PubMed |
description | Control of the reactivity of hydride (H(–)) in crystal structures has been a challenge because of its strong electron-donating ability and reactivity with protic species. For metal borohydrides, the dehydrogenation activity and air stability are in a trade-off, and control of the reactivity of BH(4)(–) has been demanded. For this purpose, we synthesize a series of BH(4)(–)-based coordination polymers/metal–organic frameworks. The reactivity of BH(4)(–) in the structures is regulated by coordination geometry and neighboring ligands, and one of the compounds [Zn(BH(4))(2)(dipyridylpropane)] exhibits both high dehydrogenation reactivity (1.4 wt% at 179 °C) and high air stability (50 RH% at 25 °C, 7 days). Single crystal X-ray diffraction analysis reveals that H(δ+)···H(δ–) dihydrogen interactions and close packing of hydrophobic ligands are the key for the reactivity and stability. The dehydrogenation mechanism is investigated by temperature-programmed desorption, in situ synchrotron PXRD and solid-state NMR. |
format | Online Article Text |
id | pubmed-6585883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-65858832019-07-29 Borohydride-containing coordination polymers: synthesis, air stability and dehydrogenation Kadota, Kentaro Duong, Nghia Tuan Nishiyama, Yusuke Sivaniah, Easan Kitagawa, Susumu Horike, Satoshi Chem Sci Chemistry Control of the reactivity of hydride (H(–)) in crystal structures has been a challenge because of its strong electron-donating ability and reactivity with protic species. For metal borohydrides, the dehydrogenation activity and air stability are in a trade-off, and control of the reactivity of BH(4)(–) has been demanded. For this purpose, we synthesize a series of BH(4)(–)-based coordination polymers/metal–organic frameworks. The reactivity of BH(4)(–) in the structures is regulated by coordination geometry and neighboring ligands, and one of the compounds [Zn(BH(4))(2)(dipyridylpropane)] exhibits both high dehydrogenation reactivity (1.4 wt% at 179 °C) and high air stability (50 RH% at 25 °C, 7 days). Single crystal X-ray diffraction analysis reveals that H(δ+)···H(δ–) dihydrogen interactions and close packing of hydrophobic ligands are the key for the reactivity and stability. The dehydrogenation mechanism is investigated by temperature-programmed desorption, in situ synchrotron PXRD and solid-state NMR. Royal Society of Chemistry 2019-05-13 /pmc/articles/PMC6585883/ /pubmed/31360426 http://dx.doi.org/10.1039/c9sc00731h Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Kadota, Kentaro Duong, Nghia Tuan Nishiyama, Yusuke Sivaniah, Easan Kitagawa, Susumu Horike, Satoshi Borohydride-containing coordination polymers: synthesis, air stability and dehydrogenation |
title | Borohydride-containing coordination polymers: synthesis, air stability and dehydrogenation
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title_full | Borohydride-containing coordination polymers: synthesis, air stability and dehydrogenation
|
title_fullStr | Borohydride-containing coordination polymers: synthesis, air stability and dehydrogenation
|
title_full_unstemmed | Borohydride-containing coordination polymers: synthesis, air stability and dehydrogenation
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title_short | Borohydride-containing coordination polymers: synthesis, air stability and dehydrogenation
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title_sort | borohydride-containing coordination polymers: synthesis, air stability and dehydrogenation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585883/ https://www.ncbi.nlm.nih.gov/pubmed/31360426 http://dx.doi.org/10.1039/c9sc00731h |
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