Metal-free polymerization: synthesis and properties of fused benzo[1,2-:4,5-′]bis[]benzothiophene (BBBT) polymers

We report the "green" synthesis and characterization of a series of fused benzo[1,2- b :4,5- b ′]bis[ b ]benzothiophene (BBBT) polymers containing a phenyl ring and naphthalene as comonomers, as well as BBBT homopolymers. These novel fused polymers have been obtained from simple acid and h...

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Published inPolymer chemistry Vol. 11; no. 22; pp. 3695 - 37
Main Authors Yao, Liping, Liao, Hailiang, Ravva, Mahesh Kumar, Guo, Yanjun, Duan, Jiayao, Wang, Yazhou, Yu, Yaping, Li, Zhengke, McCulloch, Iain, Yue, Wan
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 14.06.2020
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Abstract We report the "green" synthesis and characterization of a series of fused benzo[1,2- b :4,5- b ′]bis[ b ]benzothiophene (BBBT) polymers containing a phenyl ring and naphthalene as comonomers, as well as BBBT homopolymers. These novel fused polymers have been obtained from simple acid and hexaethyltriaminophosphine catalyzed polymerization without involving any metal catalyst. The effect of the different aromatic units on the optical and electronic properties of the resulting polymers has been studied. It was found that these polymers possess high electron affinities due to the presence of electron-deficient lactams on each repeat unit. BBBT-P and BBBT-N exhibit NIR absorption spectra with the tail extending to 1000 nm, while the BBBT homopolymer exhibits a large blue-shifted absorption. A family of fused semiconducting polymers containing the thienoacenes BBBT has been synthesized efficiently by non-metal and environmentally benign polymerization.
AbstractList We report the "green" synthesis and characterization of a series of fused benzo[1,2- b :4,5- b ′]bis[ b ]benzothiophene (BBBT) polymers containing a phenyl ring and naphthalene as comonomers, as well as BBBT homopolymers. These novel fused polymers have been obtained from simple acid and hexaethyltriaminophosphine catalyzed polymerization without involving any metal catalyst. The effect of the different aromatic units on the optical and electronic properties of the resulting polymers has been studied. It was found that these polymers possess high electron affinities due to the presence of electron-deficient lactams on each repeat unit. BBBT-P and BBBT-N exhibit NIR absorption spectra with the tail extending to 1000 nm, while the BBBT homopolymer exhibits a large blue-shifted absorption. A family of fused semiconducting polymers containing the thienoacenes BBBT has been synthesized efficiently by non-metal and environmentally benign polymerization.
We report the “green” synthesis and characterization of a series of fused benzo[1,2-b:4,5-b′]bis[b]benzothiophene (BBBT) polymers containing a phenyl ring and naphthalene as comonomers, as well as BBBT homopolymers. These novel fused polymers have been obtained from simple acid and hexaethyltriaminophosphine catalyzed polymerization without involving any metal catalyst. The effect of the different aromatic units on the optical and electronic properties of the resulting polymers has been studied. It was found that these polymers possess high electron affinities due to the presence of electron-deficient lactams on each repeat unit. BBBT-P and BBBT-N exhibit NIR absorption spectra with the tail extending to 1000 nm, while the BBBT homopolymer exhibits a large blue-shifted absorption.
We report the “green” synthesis and characterization of a series of fused benzo[1,2- b :4,5- b ′]bis[ b ]benzothiophene (BBBT) polymers containing a phenyl ring and naphthalene as comonomers, as well as BBBT homopolymers. These novel fused polymers have been obtained from simple acid and hexaethyltriaminophosphine catalyzed polymerization without involving any metal catalyst. The effect of the different aromatic units on the optical and electronic properties of the resulting polymers has been studied. It was found that these polymers possess high electron affinities due to the presence of electron-deficient lactams on each repeat unit. BBBT-P and BBBT-N exhibit NIR absorption spectra with the tail extending to 1000 nm, while the BBBT homopolymer exhibits a large blue-shifted absorption.
Author Yue, Wan
Liao, Hailiang
Li, Zhengke
Yao, Liping
Ravva, Mahesh Kumar
McCulloch, Iain
Wang, Yazhou
Guo, Yanjun
Yu, Yaping
Duan, Jiayao
AuthorAffiliation State Key Laboratory of Optoelectronic Materials and Technologies
Guangxi University for Nationalities
King Abdullah University of Science and Technology (KAUST) KAUST Solar Centre
Imperial College London
Sun Yet-Sen University
Guangxi Key Laboratory of Chemistry and Engineering of Forest Products
Guangxi Collaborative Innovation Center for Chemistry and Engineering of Forest Products
Department of Chemistry
Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education
School of Materials and Engineering
Department of Chemistry and Centre for Plastic Electronics
College of Chemistry and Chemical Engineering
SRM University - AP
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– name: Guangxi Key Laboratory of Chemistry and Engineering of Forest Products
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Cites_doi 10.1021/ma0625915
10.1039/C4CS00250D
10.1021/ol701815j
10.1021/cr100320w
10.1021/cm402219v
10.1021/jacs.5b10175
10.1002/adma.201201795
10.1039/b717608b
10.1021/ma00046a046
10.1007/s11426-019-9645-1
10.1016/j.progpolymsci.2013.05.001
10.1002/(SICI)1521-4095(199810)10:14<1119::AID-ADMA1119>3.0.CO;2-K
10.1038/s41467-018-02852-6
10.1039/b914956m
10.1080/00397911.2011.558232
10.1039/C7SC00154A
10.1038/s41557-018-0200-y
10.1002/adma.201704843
10.1038/s41570-019-0152-9
10.1021/acs.accounts.9b00022
10.1039/C5TA07511D
10.1002/marc.201100037
10.1039/C8CC05608K
10.1002/adma.201501841
10.1002/adfm.201807623
10.1021/acs.macromol.9b01233
10.1021/mz500590d
10.1021/jacs.9b09374
10.1021/acs.accounts.7b00624
10.1021/acsmacrolett.9b00368
10.1021/acsami.9b23064
10.1055/s-0030-1258219
10.1039/C9QO00645A
10.1039/C7PY00484B
10.1002/adma.201102007
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References Stalder (D0PY00623H-(cit11)/*[position()=1]) 2014; 26
Zhu (D0PY00623H-(cit25)/*[position()=1]) 2019; 52
Randell (D0PY00623H-(cit35)/*[position()=1]) 2016; 4
Heeger (D0PY00623H-(cit9)/*[position()=1]) 2010; 39
Bronstein (D0PY00623H-(cit2)/*[position()=1]) 2020; 4
Yokozawa (D0PY00623H-(cit19)/*[position()=1]) 2011; 32
Hertel (D0PY00623H-(cit24)/*[position()=1]) 1998; 10
Maximilian (D0PY00623H-(cit6)/*[position()=1]) 2018
Ni (D0PY00623H-(cit14)/*[position()=1]) 2018
Nielsen (D0PY00623H-(cit10)/*[position()=1]) 2013; 25
Andrew (D0PY00623H-(cit15)/*[position()=1]) 2020; 142
Lee (D0PY00623H-(cit23)/*[position()=1]) 2017; 8
Scharber (D0PY00623H-(cit3)/*[position()=1]) 2013; 38
Ada (D0PY00623H-(cit26)/*[position()=1]) 2018; 9
Yang (D0PY00623H-(cit17)/*[position()=1]) 2019; 8
Carsten (D0PY00623H-(cit20)/*[position()=1]) 2011; 111
Özlem (D0PY00623H-(cit22)/*[position()=1]) 2014; 3
Ebata (D0PY00623H-(cit32)/*[position()=1]) 2007; 9
Tang (D0PY00623H-(cit18)/*[position()=1]) 2019; 52
Zampetti (D0PY00623H-(cit4)/*[position()=1]) 2019; 29
Gao (D0PY00623H-(cit33)/*[position()=1]) 2008
Bogdanov (D0PY00623H-(cit36)/*[position()=1]) 2012; 42
Geng (D0PY00623H-(cit7)/*[position()=1]) 2016; 1
Wu (D0PY00623H-(cit8)/*[position()=1]) 2015; 44
Takimiya (D0PY00623H-(cit30)/*[position()=1]) 2011; 23
Yang (D0PY00623H-(cit16)/*[position()=1]) 2019; 62
Yue (D0PY00623H-(cit12)/*[position()=1]) 2015; 27
Sessions (D0PY00623H-(cit21)/*[position()=1]) 2007; 40
Ni (D0PY00623H-(cit1)/*[position()=1]) 2019; 11
Zheng (D0PY00623H-(cit31)/*[position()=1]) 2016; 138
Ganguly (D0PY00623H-(cit27)/*[position()=1]) 2020; 12
Hong (D0PY00623H-(cit29)/*[position()=1]) 1991; 25
Wang (D0PY00623H-(cit13)/*[position()=1]) 2019; 6
Zhang (D0PY00623H-(cit28)/*[position()=1]) 2017; 8
Bogdanov (D0PY00623H-(cit37)/*[position()=1]) 2010; 19
Liao (D0PY00623H-(cit34)/*[position()=1]) 2018; 54
Sahika (D0PY00623H-(cit5)/*[position()=1]) 2018; 51
References_xml – volume: 40
  start-page: 1926
  year: 2007
  ident: D0PY00623H-(cit21)/*[position()=1]
  publication-title: Macromolecules
  doi: 10.1021/ma0625915
  contributor:
    fullname: Sessions
– volume: 44
  start-page: 1113
  year: 2015
  ident: D0PY00623H-(cit8)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C4CS00250D
  contributor:
    fullname: Wu
– volume: 9
  start-page: 4499
  year: 2007
  ident: D0PY00623H-(cit32)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/ol701815j
  contributor:
    fullname: Ebata
– volume: 111
  start-page: 1493
  year: 2011
  ident: D0PY00623H-(cit20)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/cr100320w
  contributor:
    fullname: Carsten
– volume: 26
  start-page: 664
  year: 2014
  ident: D0PY00623H-(cit11)/*[position()=1]
  publication-title: Chem. Mater.
  doi: 10.1021/cm402219v
  contributor:
    fullname: Stalder
– volume: 138
  start-page: 868
  year: 2016
  ident: D0PY00623H-(cit31)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.5b10175
  contributor:
    fullname: Zheng
– volume: 25
  start-page: 1859
  year: 2013
  ident: D0PY00623H-(cit10)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.201201795
  contributor:
    fullname: Nielsen
– start-page: 1548
  year: 2008
  ident: D0PY00623H-(cit33)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/b717608b
  contributor:
    fullname: Gao
– volume: 25
  start-page: 5424
  year: 1991
  ident: D0PY00623H-(cit29)/*[position()=1]
  publication-title: Macromolecules
  doi: 10.1021/ma00046a046
  contributor:
    fullname: Hong
– volume: 62
  start-page: 1649
  year: 2019
  ident: D0PY00623H-(cit16)/*[position()=1]
  publication-title: Sci. China: Chem.
  doi: 10.1007/s11426-019-9645-1
  contributor:
    fullname: Yang
– volume: 1
  start-page: 128
  year: 2016
  ident: D0PY00623H-(cit7)/*[position()=1]
  publication-title: J. Sci: Adv. Mater. Devices
  contributor:
    fullname: Geng
– volume: 38
  start-page: 1929
  year: 2013
  ident: D0PY00623H-(cit3)/*[position()=1]
  publication-title: Prog. Polym. Sci.
  doi: 10.1016/j.progpolymsci.2013.05.001
  contributor:
    fullname: Scharber
– start-page: 1807033
  year: 2018
  ident: D0PY00623H-(cit6)/*[position()=1]
  publication-title: Adv. Funct. Mater.
  contributor:
    fullname: Maximilian
– volume: 10
  start-page: 1119
  year: 1998
  ident: D0PY00623H-(cit24)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/(SICI)1521-4095(199810)10:14<1119::AID-ADMA1119>3.0.CO;2-K
  contributor:
    fullname: Hertel
– volume: 9
  start-page: 416
  year: 2018
  ident: D0PY00623H-(cit26)/*[position()=1]
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-018-02852-6
  contributor:
    fullname: Ada
– volume: 39
  start-page: 2534
  year: 2010
  ident: D0PY00623H-(cit9)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/b914956m
  contributor:
    fullname: Heeger
– volume: 42
  start-page: 2388
  year: 2012
  ident: D0PY00623H-(cit36)/*[position()=1]
  publication-title: Synth. Commun.
  doi: 10.1080/00397911.2011.558232
  contributor:
    fullname: Bogdanov
– volume: 8
  start-page: 2503
  year: 2017
  ident: D0PY00623H-(cit23)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C7SC00154A
  contributor:
    fullname: Lee
– volume: 11
  start-page: 271
  year: 2019
  ident: D0PY00623H-(cit1)/*[position()=1]
  publication-title: Nat. Chem.
  doi: 10.1038/s41557-018-0200-y
  contributor:
    fullname: Ni
– start-page: 1704843
  year: 2018
  ident: D0PY00623H-(cit14)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.201704843
  contributor:
    fullname: Ni
– volume: 4
  start-page: 66
  year: 2020
  ident: D0PY00623H-(cit2)/*[position()=1]
  publication-title: Nat. Rev. Chem.
  doi: 10.1038/s41570-019-0152-9
  contributor:
    fullname: Bronstein
– volume: 52
  start-page: 1089
  year: 2019
  ident: D0PY00623H-(cit25)/*[position()=1]
  publication-title: Acc. Chem. Res.
  doi: 10.1021/acs.accounts.9b00022
  contributor:
    fullname: Zhu
– volume: 4
  start-page: 6940
  year: 2016
  ident: D0PY00623H-(cit35)/*[position()=1]
  publication-title: J. Mater. Chem. A
  doi: 10.1039/C5TA07511D
  contributor:
    fullname: Randell
– volume: 32
  start-page: 801
  year: 2011
  ident: D0PY00623H-(cit19)/*[position()=1]
  publication-title: Macromol. Rapid Commun.
  doi: 10.1002/marc.201100037
  contributor:
    fullname: Yokozawa
– volume: 54
  start-page: 11152
  year: 2018
  ident: D0PY00623H-(cit34)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC05608K
  contributor:
    fullname: Liao
– volume: 27
  start-page: 4702
  year: 2015
  ident: D0PY00623H-(cit12)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.201501841
  contributor:
    fullname: Yue
– volume: 29
  start-page: 1807623
  year: 2019
  ident: D0PY00623H-(cit4)/*[position()=1]
  publication-title: Adv. Funct. Mater.
  doi: 10.1002/adfm.201807623
  contributor:
    fullname: Zampetti
– volume: 52
  start-page: 6227
  year: 2019
  ident: D0PY00623H-(cit18)/*[position()=1]
  publication-title: Macromolecules
  doi: 10.1021/acs.macromol.9b01233
  contributor:
    fullname: Tang
– volume: 3
  start-page: 1134
  year: 2014
  ident: D0PY00623H-(cit22)/*[position()=1]
  publication-title: ACS Macro Lett.
  doi: 10.1021/mz500590d
  contributor:
    fullname: Özlem
– volume: 142
  start-page: 652
  year: 2020
  ident: D0PY00623H-(cit15)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b09374
  contributor:
    fullname: Andrew
– volume: 51
  start-page: 1368
  year: 2018
  ident: D0PY00623H-(cit5)/*[position()=1]
  publication-title: Acc. Chem. Res.
  doi: 10.1021/acs.accounts.7b00624
  contributor:
    fullname: Sahika
– volume: 8
  start-page: 743
  year: 2019
  ident: D0PY00623H-(cit17)/*[position()=1]
  publication-title: ACS Macro Lett.
  doi: 10.1021/acsmacrolett.9b00368
  contributor:
    fullname: Yang
– volume: 12
  start-page: 14265
  year: 2020
  ident: D0PY00623H-(cit27)/*[position()=1]
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.9b23064
  contributor:
    fullname: Ganguly
– volume: 19
  start-page: 3268
  year: 2010
  ident: D0PY00623H-(cit37)/*[position()=1]
  publication-title: Synthesis
  doi: 10.1055/s-0030-1258219
  contributor:
    fullname: Bogdanov
– volume: 6
  start-page: 2974
  year: 2019
  ident: D0PY00623H-(cit13)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C9QO00645A
  contributor:
    fullname: Wang
– volume: 8
  start-page: 3448
  year: 2017
  ident: D0PY00623H-(cit28)/*[position()=1]
  publication-title: Polym. Chem.
  doi: 10.1039/C7PY00484B
  contributor:
    fullname: Zhang
– volume: 23
  start-page: 4347
  year: 2011
  ident: D0PY00623H-(cit30)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.201102007
  contributor:
    fullname: Takimiya
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Snippet We report the "green" synthesis and characterization of a series of fused benzo[1,2- b :4,5- b ′]bis[ b ]benzothiophene (BBBT) polymers containing a phenyl...
We report the “green” synthesis and characterization of a series of fused benzo[1,2- b :4,5- b ′]bis[ b ]benzothiophene (BBBT) polymers containing a phenyl...
We report the “green” synthesis and characterization of a series of fused benzo[1,2-b:4,5-b′]bis[b]benzothiophene (BBBT) polymers containing a phenyl ring and...
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SubjectTerms Absorption spectra
Benzothiophene
Blue shift
Chemical synthesis
Naphthalene
Optical properties
Polymer chemistry
Polymerization
Polymers
Title Metal-free polymerization: synthesis and properties of fused benzo[1,2-:4,5-′]bis[]benzothiophene (BBBT) polymers
URI https://www.proquest.com/docview/2410738409/abstract/
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link.rule.ids 315,786,790,27957,27958
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