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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...

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Autores principales: Press, David J., Gendy, Chris, Pasalkar, Samruddhi, Schechtel, Shauna, Heyne, Belinda, Sutherland, Todd C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
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.
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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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