Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator

Poly(3-hexyl thiophene)-b-poly(styrene-co-chloromethylstyrene) copolymers, to be used as a prepolymer for preparing donor-acceptor block copolymers for organic solar cells, have been synthesised by reacting P3HT macroinitiators with styrene and chloromethylstyrene via three types of atom transfer ra...

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Main Authors: Nattawoot Rattanathamwat, Jatuphorn Wootthikanokkhan, Nonsee Nimitsiriwat, Chanchana Thanachayanont, Udom Asawapirom
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Advances in Materials Science and Engineering
Online Access:http://dx.doi.org/10.1155/2015/973632
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author Nattawoot Rattanathamwat
Jatuphorn Wootthikanokkhan
Nonsee Nimitsiriwat
Chanchana Thanachayanont
Udom Asawapirom
author_facet Nattawoot Rattanathamwat
Jatuphorn Wootthikanokkhan
Nonsee Nimitsiriwat
Chanchana Thanachayanont
Udom Asawapirom
author_sort Nattawoot Rattanathamwat
collection DOAJ
description Poly(3-hexyl thiophene)-b-poly(styrene-co-chloromethylstyrene) copolymers, to be used as a prepolymer for preparing donor-acceptor block copolymers for organic solar cells, have been synthesised by reacting P3HT macroinitiators with styrene and chloromethylstyrene via three types of atom transfer radical polymerisation (ATRP) systems, which are (1) a normal ATRP, (2) activators generated by electron transfer (AGET), and (3) a simultaneous reverse and normal initiation (SR&NI). The kinetics of these ATRP systems were studied as a function of monomers to the macroinitiator molar ratio. It was found that all of the three types of ATRP systems led to first order kinetics with respect to monomers. The highest rate constant (k) of 3.4 × 10−3 s−1 was obtained from the SR&NI ATRP system. The molecular weights of the product determined by the GPC were lower than were the theoretical values. The result was discussed in light of the chain transfer reaction to the poly(chloromethylstyrene) repeating units. Morphology of the synthesized block copolymers, examined by an atomic force microscopy (AFM), were also compared and discussed.
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institution Kabale University
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publishDate 2015-01-01
publisher Wiley
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series Advances in Materials Science and Engineering
spelling doaj-art-7639b8d7467b4513ad9c558bede0876b2025-02-03T06:13:52ZengWileyAdvances in Materials Science and Engineering1687-84341687-84422015-01-01201510.1155/2015/973632973632Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) MacroinitiatorNattawoot Rattanathamwat0Jatuphorn Wootthikanokkhan1Nonsee Nimitsiriwat2Chanchana Thanachayanont3Udom Asawapirom4Division of Materials Technology, School of Energy, Environment and Materials, King Mongkut’s University of Technology Thonburi (KMUTT), Bangkok 10140, ThailandDivision of Materials Technology, School of Energy, Environment and Materials, King Mongkut’s University of Technology Thonburi (KMUTT), Bangkok 10140, ThailandNanotec-KMUTT Center of Excellence on Hybrid Nanomaterials for Alternative Energy (HyNAE), Bangkok 10140, ThailandNational Metal and Materials Technology Center (MTEC), Pathumthani 12120, ThailandNational Nanotechnology Center (NANOTEC), Pathumthani 12120, ThailandPoly(3-hexyl thiophene)-b-poly(styrene-co-chloromethylstyrene) copolymers, to be used as a prepolymer for preparing donor-acceptor block copolymers for organic solar cells, have been synthesised by reacting P3HT macroinitiators with styrene and chloromethylstyrene via three types of atom transfer radical polymerisation (ATRP) systems, which are (1) a normal ATRP, (2) activators generated by electron transfer (AGET), and (3) a simultaneous reverse and normal initiation (SR&NI). The kinetics of these ATRP systems were studied as a function of monomers to the macroinitiator molar ratio. It was found that all of the three types of ATRP systems led to first order kinetics with respect to monomers. The highest rate constant (k) of 3.4 × 10−3 s−1 was obtained from the SR&NI ATRP system. The molecular weights of the product determined by the GPC were lower than were the theoretical values. The result was discussed in light of the chain transfer reaction to the poly(chloromethylstyrene) repeating units. Morphology of the synthesized block copolymers, examined by an atomic force microscopy (AFM), were also compared and discussed.http://dx.doi.org/10.1155/2015/973632
spellingShingle Nattawoot Rattanathamwat
Jatuphorn Wootthikanokkhan
Nonsee Nimitsiriwat
Chanchana Thanachayanont
Udom Asawapirom
Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator
Advances in Materials Science and Engineering
title Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator
title_full Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator
title_fullStr Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator
title_full_unstemmed Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator
title_short Kinetic Studies of Atom Transfer Radical Polymerisations of Styrene and Chloromethylstyrene with Poly(3-hexyl thiophene) Macroinitiator
title_sort kinetic studies of atom transfer radical polymerisations of styrene and chloromethylstyrene with poly 3 hexyl thiophene macroinitiator
url http://dx.doi.org/10.1155/2015/973632
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