Supramolecular macrocycles reversibly assembled by Te…O chalcogen bonding

Supramolecular macrocycles reversibly assembled by Te…O chalcogen bonding

Similarly to halogen bonding, the heavier chalcogens are capable of forming supramolecular links with electron rich sites. Here, the authors show that these forces can allow the formation of well-defined cyclic structures that are stable in solution and are capable of forming host-guest complexes.

Bibliographic Details
Main Authors: Peter C. Ho, Patrick Szydlowski, Jocelyn Sinclair, Philip J. W. Elder, Joachim Kübel, Chris Gendy, Lucia Myongwon Lee, Hilary Jenkins, James F. Britten, Derek R. Morim, Ignacio Vargas-Baca
Format: Article
Language:English
Published: Nature Publishing Group 2016-04-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/ncomms11299
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spelling doaj-cf1ebf0553e54ae4936f6e679632a9a12021-05-11T11:16:33ZengNature Publishing GroupNature Communications2041-17232016-04-017111010.1038/ncomms11299Supramolecular macrocycles reversibly assembled by Te…O chalcogen bondingPeter C. Ho0Patrick Szydlowski1Jocelyn Sinclair2Philip J. W. Elder3Joachim Kübel4Chris Gendy5Lucia Myongwon Lee6Hilary Jenkins7James F. Britten8Derek R. Morim9Ignacio Vargas-Baca10Department of Chemistry and Chemical Biology, McMaster UniversityDepartment of Chemistry and Chemical Biology, McMaster UniversityDepartment of Chemistry and Chemical Biology, McMaster UniversityDepartment of Chemistry and Chemical Biology, McMaster UniversityDepartment of Chemistry and Chemical Biology, McMaster UniversityDepartment of Chemistry and Chemical Biology, McMaster UniversityDepartment of Chemistry and Chemical Biology, McMaster UniversityDepartment of Chemistry and Chemical Biology, McMaster UniversityDepartment of Chemistry and Chemical Biology, McMaster UniversityDepartment of Chemistry and Chemical Biology, McMaster UniversityDepartment of Chemistry and Chemical Biology, McMaster UniversitySimilarly to halogen bonding, the heavier chalcogens are capable of forming supramolecular links with electron rich sites. Here, the authors show that these forces can allow the formation of well-defined cyclic structures that are stable in solution and are capable of forming host-guest complexes.https://doi.org/10.1038/ncomms11299
collection DOAJ
language English
format Article
sources DOAJ
author Peter C. Ho
Patrick Szydlowski
Jocelyn Sinclair
Philip J. W. Elder
Joachim Kübel
Chris Gendy
Lucia Myongwon Lee
Hilary Jenkins
James F. Britten
Derek R. Morim
Ignacio Vargas-Baca
spellingShingle Peter C. Ho
Patrick Szydlowski
Jocelyn Sinclair
Philip J. W. Elder
Joachim Kübel
Chris Gendy
Lucia Myongwon Lee
Hilary Jenkins
James F. Britten
Derek R. Morim
Ignacio Vargas-Baca
Supramolecular macrocycles reversibly assembled by Te…O chalcogen bonding
Nature Communications
author_facet Peter C. Ho
Patrick Szydlowski
Jocelyn Sinclair
Philip J. W. Elder
Joachim Kübel
Chris Gendy
Lucia Myongwon Lee
Hilary Jenkins
James F. Britten
Derek R. Morim
Ignacio Vargas-Baca
author_sort Peter C. Ho
title Supramolecular macrocycles reversibly assembled by Te…O chalcogen bonding
title_short Supramolecular macrocycles reversibly assembled by Te…O chalcogen bonding
title_full Supramolecular macrocycles reversibly assembled by Te…O chalcogen bonding
title_fullStr Supramolecular macrocycles reversibly assembled by Te…O chalcogen bonding
title_full_unstemmed Supramolecular macrocycles reversibly assembled by Te…O chalcogen bonding
title_sort supramolecular macrocycles reversibly assembled by te…o chalcogen bonding
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2016-04-01
description Similarly to halogen bonding, the heavier chalcogens are capable of forming supramolecular links with electron rich sites. Here, the authors show that these forces can allow the formation of well-defined cyclic structures that are stable in solution and are capable of forming host-guest complexes.
url https://doi.org/10.1038/ncomms11299
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