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Synthesis of Tetrathia–Oligothiophene Macrocycles
[Image: see text] The synthesis of six tetrathia–oligothiophene macrocycles is described with modest ring-closing yields between 21 and 55%. Single-crystal X-ray studies of four of the macrocycles indicated that encapsulated solvent or guest molecules were possible. A variety of guest molecules were...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648883/ https://www.ncbi.nlm.nih.gov/pubmed/31459556 http://dx.doi.org/10.1021/acsomega.8b03444 |
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author | Press, David J. Gendy, Chris Pasalkar, Samruddhi Schechtel, Shauna Heyne, Belinda Sutherland, Todd C. |
author_facet | Press, David J. Gendy, Chris Pasalkar, Samruddhi Schechtel, Shauna Heyne, Belinda Sutherland, Todd C. |
author_sort | Press, David J. |
collection | PubMed |
description | [Image: see text] The synthesis of six tetrathia–oligothiophene macrocycles is described with modest ring-closing yields between 21 and 55%. Single-crystal X-ray studies of four of the macrocycles indicated that encapsulated solvent or guest molecules were possible. A variety of guest molecules were explored for inclusion complexes via NMR, absorption, emission, and X-ray techniques. The solution-phase inclusion complexes were uninformative; yet the solid-state experiments revealed that solvent exchangeable channels exist through the macrocyclic pores. |
format | Online Article Text |
id | pubmed-6648883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66488832019-08-27 Synthesis of Tetrathia–Oligothiophene Macrocycles Press, David J. Gendy, Chris Pasalkar, Samruddhi Schechtel, Shauna Heyne, Belinda Sutherland, Todd C. ACS Omega [Image: see text] The synthesis of six tetrathia–oligothiophene macrocycles is described with modest ring-closing yields between 21 and 55%. Single-crystal X-ray studies of four of the macrocycles indicated that encapsulated solvent or guest molecules were possible. A variety of guest molecules were explored for inclusion complexes via NMR, absorption, emission, and X-ray techniques. The solution-phase inclusion complexes were uninformative; yet the solid-state experiments revealed that solvent exchangeable channels exist through the macrocyclic pores. American Chemical Society 2019-02-15 /pmc/articles/PMC6648883/ /pubmed/31459556 http://dx.doi.org/10.1021/acsomega.8b03444 Text en Copyright © 2019 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 | Press, David J. Gendy, Chris Pasalkar, Samruddhi Schechtel, Shauna Heyne, Belinda Sutherland, Todd C. Synthesis of Tetrathia–Oligothiophene Macrocycles |
title | Synthesis of Tetrathia–Oligothiophene Macrocycles |
title_full | Synthesis of Tetrathia–Oligothiophene Macrocycles |
title_fullStr | Synthesis of Tetrathia–Oligothiophene Macrocycles |
title_full_unstemmed | Synthesis of Tetrathia–Oligothiophene Macrocycles |
title_short | Synthesis of Tetrathia–Oligothiophene Macrocycles |
title_sort | synthesis of tetrathia–oligothiophene macrocycles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648883/ https://www.ncbi.nlm.nih.gov/pubmed/31459556 http://dx.doi.org/10.1021/acsomega.8b03444 |
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