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A comparison of experimental and theoretical studies of benzoquinone modified poly(thiophene): effect of polymerization techniques on the structure and properties

The present manuscript reports the synthesis of benzoquinone (BQ) modified polythiophene (PTh) by chemical and microwave-assisted polymerization techniques. The synthesized oligomers were investigated for their spectral, morphological and thermal properties via FTIR, UV-visible, scanning electron mi...

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Detalles Bibliográficos
Autores principales: Singh, Neetika, Singh, Sumit, Kumar, Prabhat, Riaz, Ufana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057122/
https://www.ncbi.nlm.nih.gov/pubmed/35521288
http://dx.doi.org/10.1039/d0ra07714c
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author Singh, Neetika
Singh, Sumit
Kumar, Prabhat
Riaz, Ufana
author_facet Singh, Neetika
Singh, Sumit
Kumar, Prabhat
Riaz, Ufana
author_sort Singh, Neetika
collection PubMed
description The present manuscript reports the synthesis of benzoquinone (BQ) modified polythiophene (PTh) by chemical and microwave-assisted polymerization techniques. The synthesized oligomers were investigated for their spectral, morphological and thermal properties via FTIR, UV-visible, scanning electron microscopy (SEM) and thermogravimetric (TGA) analyses. Theoretical calculations were performed by using Gaussian 09 software via the DFT/B3LYP method with the 6-311G basis set. FTIR confirmed the formation of hydroquinone modified PTh when the polymerization was carried out by magnetic stirring and ultrasonication, while the formation of BQ modified PTh was obtained by microwave irradiation. The electronic transitions obtained via experimental UV-visible studies were also found to be in close agreement with the theoretical spectra. SEM revealed a well-formed morphology comprising needle shaped rods for the oligomer synthesized under microwave irradiation. The TGA-DTA studies revealed low char content for the above oligomer, while the florescence studies revealed intense emission around 450 nm. The highest quantum yield was found to be 0.024, which also showed high singlet oxygen generation tendency as well as a high single oxygen quantum yield of 0.30 and could be utilized to design imaging probes applicable in photodynamic therapy.
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spelling pubmed-90571222022-05-04 A comparison of experimental and theoretical studies of benzoquinone modified poly(thiophene): effect of polymerization techniques on the structure and properties Singh, Neetika Singh, Sumit Kumar, Prabhat Riaz, Ufana RSC Adv Chemistry The present manuscript reports the synthesis of benzoquinone (BQ) modified polythiophene (PTh) by chemical and microwave-assisted polymerization techniques. The synthesized oligomers were investigated for their spectral, morphological and thermal properties via FTIR, UV-visible, scanning electron microscopy (SEM) and thermogravimetric (TGA) analyses. Theoretical calculations were performed by using Gaussian 09 software via the DFT/B3LYP method with the 6-311G basis set. FTIR confirmed the formation of hydroquinone modified PTh when the polymerization was carried out by magnetic stirring and ultrasonication, while the formation of BQ modified PTh was obtained by microwave irradiation. The electronic transitions obtained via experimental UV-visible studies were also found to be in close agreement with the theoretical spectra. SEM revealed a well-formed morphology comprising needle shaped rods for the oligomer synthesized under microwave irradiation. The TGA-DTA studies revealed low char content for the above oligomer, while the florescence studies revealed intense emission around 450 nm. The highest quantum yield was found to be 0.024, which also showed high singlet oxygen generation tendency as well as a high single oxygen quantum yield of 0.30 and could be utilized to design imaging probes applicable in photodynamic therapy. The Royal Society of Chemistry 2020-10-09 /pmc/articles/PMC9057122/ /pubmed/35521288 http://dx.doi.org/10.1039/d0ra07714c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Singh, Neetika
Singh, Sumit
Kumar, Prabhat
Riaz, Ufana
A comparison of experimental and theoretical studies of benzoquinone modified poly(thiophene): effect of polymerization techniques on the structure and properties
title A comparison of experimental and theoretical studies of benzoquinone modified poly(thiophene): effect of polymerization techniques on the structure and properties
title_full A comparison of experimental and theoretical studies of benzoquinone modified poly(thiophene): effect of polymerization techniques on the structure and properties
title_fullStr A comparison of experimental and theoretical studies of benzoquinone modified poly(thiophene): effect of polymerization techniques on the structure and properties
title_full_unstemmed A comparison of experimental and theoretical studies of benzoquinone modified poly(thiophene): effect of polymerization techniques on the structure and properties
title_short A comparison of experimental and theoretical studies of benzoquinone modified poly(thiophene): effect of polymerization techniques on the structure and properties
title_sort comparison of experimental and theoretical studies of benzoquinone modified poly(thiophene): effect of polymerization techniques on the structure and properties
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057122/
https://www.ncbi.nlm.nih.gov/pubmed/35521288
http://dx.doi.org/10.1039/d0ra07714c
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