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Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work
The combination of singly or doubly bidentate halogen‐bond donors with double bidentate acceptors was investigated as a supramolecular synthon in crystal engineering. The crystal topologies obtained feature novel halogen‐bonding motifs like double two‐point recognition and infinite chains or network...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028063/ https://www.ncbi.nlm.nih.gov/pubmed/31638284 http://dx.doi.org/10.1002/chem.201904322 |
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author | Bulfield, David Engelage, Elric Mancheski, Lucas Stoesser, Julian Huber, Stefan M. |
author_facet | Bulfield, David Engelage, Elric Mancheski, Lucas Stoesser, Julian Huber, Stefan M. |
author_sort | Bulfield, David |
collection | PubMed |
description | The combination of singly or doubly bidentate halogen‐bond donors with double bidentate acceptors was investigated as a supramolecular synthon in crystal engineering. The crystal topologies obtained feature novel halogen‐bonding motifs like double two‐point recognition and infinite chains or networks based on two‐point interactions. Induced conformational changes in the double bidentate halogen‐bond donors could be exploited to obtain different 1D and 2D networks. All solid‐state studies were accompanied by DFT calculations to predict and rationalize the outcome. |
format | Online Article Text |
id | pubmed-7028063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70280632020-02-25 Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work Bulfield, David Engelage, Elric Mancheski, Lucas Stoesser, Julian Huber, Stefan M. Chemistry Full Papers The combination of singly or doubly bidentate halogen‐bond donors with double bidentate acceptors was investigated as a supramolecular synthon in crystal engineering. The crystal topologies obtained feature novel halogen‐bonding motifs like double two‐point recognition and infinite chains or networks based on two‐point interactions. Induced conformational changes in the double bidentate halogen‐bond donors could be exploited to obtain different 1D and 2D networks. All solid‐state studies were accompanied by DFT calculations to predict and rationalize the outcome. John Wiley and Sons Inc. 2020-02-03 2020-02-03 /pmc/articles/PMC7028063/ /pubmed/31638284 http://dx.doi.org/10.1002/chem.201904322 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Full Papers Bulfield, David Engelage, Elric Mancheski, Lucas Stoesser, Julian Huber, Stefan M. Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work |
title | Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work |
title_full | Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work |
title_fullStr | Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work |
title_full_unstemmed | Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work |
title_short | Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work |
title_sort | crystal engineering with multipoint halogen bonding: double two‐point donors and acceptors at work |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028063/ https://www.ncbi.nlm.nih.gov/pubmed/31638284 http://dx.doi.org/10.1002/chem.201904322 |
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