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Advances in the Chemistry of 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine

Heterocyclic systems are now considered to be an integral part of material chemistry. Thiophene, selenophene, furan, pyrrole, carbazole, triazine and others are some such examples worth mentioning. 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine is a C (3h )‐symmetric system with thiophene as the donor unit...

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Detalles Bibliográficos
Autores principales: Rani Kumar, Neha, Agrawal, Abhijeet R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812756/
https://www.ncbi.nlm.nih.gov/pubmed/36599693
http://dx.doi.org/10.1002/open.202200203
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author Rani Kumar, Neha
Agrawal, Abhijeet R.
author_facet Rani Kumar, Neha
Agrawal, Abhijeet R.
author_sort Rani Kumar, Neha
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description Heterocyclic systems are now considered to be an integral part of material chemistry. Thiophene, selenophene, furan, pyrrole, carbazole, triazine and others are some such examples worth mentioning. 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine is a C (3h )‐symmetric system with thiophene as the donor unit and s‐triazine as the acceptor unit. This review gives an insight into the advances made in the thienyl‐triazine chemistry over the past two to three decades. The synthetic pathways for arriving at this system and all its important derivatives are provided. The major focus is on the materials synthesized using the thienyl‐triazine system, including star molecules, linear and hyperbranched polymers, porous materials and their diverse applications. This review will play a catalytic role for new dimensions to be explored in thienyl‐triazine chemistry.
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spelling pubmed-98127562023-01-05 Advances in the Chemistry of 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine Rani Kumar, Neha Agrawal, Abhijeet R. ChemistryOpen Reviews Heterocyclic systems are now considered to be an integral part of material chemistry. Thiophene, selenophene, furan, pyrrole, carbazole, triazine and others are some such examples worth mentioning. 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine is a C (3h )‐symmetric system with thiophene as the donor unit and s‐triazine as the acceptor unit. This review gives an insight into the advances made in the thienyl‐triazine chemistry over the past two to three decades. The synthetic pathways for arriving at this system and all its important derivatives are provided. The major focus is on the materials synthesized using the thienyl‐triazine system, including star molecules, linear and hyperbranched polymers, porous materials and their diverse applications. This review will play a catalytic role for new dimensions to be explored in thienyl‐triazine chemistry. John Wiley and Sons Inc. 2023-01-04 /pmc/articles/PMC9812756/ /pubmed/36599693 http://dx.doi.org/10.1002/open.202200203 Text en © 2023 The Authors. Published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://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 Reviews
Rani Kumar, Neha
Agrawal, Abhijeet R.
Advances in the Chemistry of 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine
title Advances in the Chemistry of 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine
title_full Advances in the Chemistry of 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine
title_fullStr Advances in the Chemistry of 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine
title_full_unstemmed Advances in the Chemistry of 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine
title_short Advances in the Chemistry of 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine
title_sort advances in the chemistry of 2,4,6‐tri(thiophen‐2‐yl)‐1,3,5‐triazine
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812756/
https://www.ncbi.nlm.nih.gov/pubmed/36599693
http://dx.doi.org/10.1002/open.202200203
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