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Influence of N-Base and O-Base Hybridization on Triel Bonds

[Image: see text] The complexes of TrR(3) (Tr = B and Al; R = H, F, Cl, and Br) with three N-bases (NH(3), CH(2)NH, and HCN) and three O-bases (CH(3)OH, H(2)CO, and CO) are utilized to explore the hybridization effect of N and O atoms on the strength, properties, and nature of the triel bond. The sp...

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Autores principales: Yang, Qingqing, Yao, Xin, Yang, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450710/
https://www.ncbi.nlm.nih.gov/pubmed/32875266
http://dx.doi.org/10.1021/acsomega.0c03394
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author Yang, Qingqing
Yao, Xin
Yang, Xin
author_facet Yang, Qingqing
Yao, Xin
Yang, Xin
author_sort Yang, Qingqing
collection PubMed
description [Image: see text] The complexes of TrR(3) (Tr = B and Al; R = H, F, Cl, and Br) with three N-bases (NH(3), CH(2)NH, and HCN) and three O-bases (CH(3)OH, H(2)CO, and CO) are utilized to explore the hybridization effect of N and O atoms on the strength, properties, and nature of the triel bond. The sp-hybridized O and N atoms form the weakest triel bond, followed by the sp(2)-hybridized O atom or the sp(3)-hybridized N atom, and the sp(3)-hybridized O atom or the sp(2)-hybridized N atom engages in the strongest triel bond. The hybridization effect is also related to the substituent of TrR(3). Most complexes are dominated by electrostatic, with increasing polarization contribution from sp to sp(2) to sp(3). Although the CO oxygen engages in a weaker triel bond, its carbon atom is a better electron donor and the interaction energy even amounts to −37 kcal/mol in the BH(3) complex.
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spelling pubmed-74507102020-08-31 Influence of N-Base and O-Base Hybridization on Triel Bonds Yang, Qingqing Yao, Xin Yang, Xin ACS Omega [Image: see text] The complexes of TrR(3) (Tr = B and Al; R = H, F, Cl, and Br) with three N-bases (NH(3), CH(2)NH, and HCN) and three O-bases (CH(3)OH, H(2)CO, and CO) are utilized to explore the hybridization effect of N and O atoms on the strength, properties, and nature of the triel bond. The sp-hybridized O and N atoms form the weakest triel bond, followed by the sp(2)-hybridized O atom or the sp(3)-hybridized N atom, and the sp(3)-hybridized O atom or the sp(2)-hybridized N atom engages in the strongest triel bond. The hybridization effect is also related to the substituent of TrR(3). Most complexes are dominated by electrostatic, with increasing polarization contribution from sp to sp(2) to sp(3). Although the CO oxygen engages in a weaker triel bond, its carbon atom is a better electron donor and the interaction energy even amounts to −37 kcal/mol in the BH(3) complex. American Chemical Society 2020-08-14 /pmc/articles/PMC7450710/ /pubmed/32875266 http://dx.doi.org/10.1021/acsomega.0c03394 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Yang, Qingqing
Yao, Xin
Yang, Xin
Influence of N-Base and O-Base Hybridization on Triel Bonds
title Influence of N-Base and O-Base Hybridization on Triel Bonds
title_full Influence of N-Base and O-Base Hybridization on Triel Bonds
title_fullStr Influence of N-Base and O-Base Hybridization on Triel Bonds
title_full_unstemmed Influence of N-Base and O-Base Hybridization on Triel Bonds
title_short Influence of N-Base and O-Base Hybridization on Triel Bonds
title_sort influence of n-base and o-base hybridization on triel bonds
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450710/
https://www.ncbi.nlm.nih.gov/pubmed/32875266
http://dx.doi.org/10.1021/acsomega.0c03394
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