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Synthesis, Optical, Thermal and Structural Characteristics of Novel Thermocleavable Polymers Based on Phthalate Esters
In this work three novel phthalate-based thermocleavable copolymers, PBTP-11, PBTDTP-11 and PFDTP-11 have been designed and synthesized. PBTP-11 and PBTDTP-11 were prepared by copolymerizing distannylated bithiophene without or with flanked thienyl groups as the electron-donor units with dibrominate...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760361/ https://www.ncbi.nlm.nih.gov/pubmed/33255813 http://dx.doi.org/10.3390/polym12122791 |
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author | R. Murad, Ary Iraqi, A. Aziz, Shujahadeen B. N. Abdullah, Sozan Abdulwahid, Rebar T. |
author_facet | R. Murad, Ary Iraqi, A. Aziz, Shujahadeen B. N. Abdullah, Sozan Abdulwahid, Rebar T. |
author_sort | R. Murad, Ary |
collection | PubMed |
description | In this work three novel phthalate-based thermocleavable copolymers, PBTP-11, PBTDTP-11 and PFDTP-11 have been designed and synthesized. PBTP-11 and PBTDTP-11 were prepared by copolymerizing distannylated bithiophene without or with flanked thienyl groups as the electron-donor units with dibrominated secondary phthalate ester as the electron-acceptor units. PFDTP-11 was prepared by copolymerizing distannylated fluorene flanked by thienyl groups as the electron-donor moieties with dibrominated secondary phthalate ester as the electron-acceptor moieties. All polymers were prepared via the Stille polymerization. The impact of two different electron-donor units on the solubility, molecular weights, optical properties, thermal and structural properties of the resulting polymers were investigated. PFDTP-11 had the highest average molecular weight (M(n) = 16,400 g mol(−1)). The polymers had E(g) in the range of 2.11–2.58 eV. After thermal treatment, the E(g) of the polymers were reduced by around 0.3–0.4 eV. This significant control over bandgap is promising and opens a gate towards commercializing these copolymers in energy harvesting devices such as solar cells. TGA data showed weight loss at around 300 °C, corresponding to the elimination of the secondary ester groups. After annealing, the soluble precursor polymers were transformed into active phthalic anhydride polymers and the resulting films were completely insoluble in all solvents, which shows good stability. Powder XRD studies showed that all polymers have an amorphous nature in the solid state, and therefore can be employed as electrolytes in energy devices. |
format | Online Article Text |
id | pubmed-7760361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77603612020-12-26 Synthesis, Optical, Thermal and Structural Characteristics of Novel Thermocleavable Polymers Based on Phthalate Esters R. Murad, Ary Iraqi, A. Aziz, Shujahadeen B. N. Abdullah, Sozan Abdulwahid, Rebar T. Polymers (Basel) Article In this work three novel phthalate-based thermocleavable copolymers, PBTP-11, PBTDTP-11 and PFDTP-11 have been designed and synthesized. PBTP-11 and PBTDTP-11 were prepared by copolymerizing distannylated bithiophene without or with flanked thienyl groups as the electron-donor units with dibrominated secondary phthalate ester as the electron-acceptor units. PFDTP-11 was prepared by copolymerizing distannylated fluorene flanked by thienyl groups as the electron-donor moieties with dibrominated secondary phthalate ester as the electron-acceptor moieties. All polymers were prepared via the Stille polymerization. The impact of two different electron-donor units on the solubility, molecular weights, optical properties, thermal and structural properties of the resulting polymers were investigated. PFDTP-11 had the highest average molecular weight (M(n) = 16,400 g mol(−1)). The polymers had E(g) in the range of 2.11–2.58 eV. After thermal treatment, the E(g) of the polymers were reduced by around 0.3–0.4 eV. This significant control over bandgap is promising and opens a gate towards commercializing these copolymers in energy harvesting devices such as solar cells. TGA data showed weight loss at around 300 °C, corresponding to the elimination of the secondary ester groups. After annealing, the soluble precursor polymers were transformed into active phthalic anhydride polymers and the resulting films were completely insoluble in all solvents, which shows good stability. Powder XRD studies showed that all polymers have an amorphous nature in the solid state, and therefore can be employed as electrolytes in energy devices. MDPI 2020-11-25 /pmc/articles/PMC7760361/ /pubmed/33255813 http://dx.doi.org/10.3390/polym12122791 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article R. Murad, Ary Iraqi, A. Aziz, Shujahadeen B. N. Abdullah, Sozan Abdulwahid, Rebar T. Synthesis, Optical, Thermal and Structural Characteristics of Novel Thermocleavable Polymers Based on Phthalate Esters |
title | Synthesis, Optical, Thermal and Structural Characteristics of Novel Thermocleavable Polymers Based on Phthalate Esters |
title_full | Synthesis, Optical, Thermal and Structural Characteristics of Novel Thermocleavable Polymers Based on Phthalate Esters |
title_fullStr | Synthesis, Optical, Thermal and Structural Characteristics of Novel Thermocleavable Polymers Based on Phthalate Esters |
title_full_unstemmed | Synthesis, Optical, Thermal and Structural Characteristics of Novel Thermocleavable Polymers Based on Phthalate Esters |
title_short | Synthesis, Optical, Thermal and Structural Characteristics of Novel Thermocleavable Polymers Based on Phthalate Esters |
title_sort | synthesis, optical, thermal and structural characteristics of novel thermocleavable polymers based on phthalate esters |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760361/ https://www.ncbi.nlm.nih.gov/pubmed/33255813 http://dx.doi.org/10.3390/polym12122791 |
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