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Volumn 43, Issue 21, 2010, Pages 8709-8710

Syntheses of gradient π-conjugated copolymers of thiophene

Author keywords

[No Author keywords available]

Indexed keywords

BATCH POLYMERIZATIONS; CONJUGATED COPOLYMERS; GRIGNARD REAGENT; GROWTH MECHANISMS; HALOGEN EXCHANGE; IN-SITU; METATHESIS REACTIONS; MOLAR RATIO; MONOMER DECOMPOSITION; NUMBER-AVERAGE;

EID: 78149277188     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma102218y     Document Type: Article
Times cited : (58)

References (32)
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    • For recent reviews, see: Li, C.; Liu, M.; Pschirer, N. G.; Baumgarten, M.; Müllen, K. Chem. Rev. DOI: 10.1021/cr100052z.; published online June 29, 2010.
    • Chem. Rev.
    • Li, C.1    Liu, M.2    Pschirer, N.G.3    Baumgarten, M.4    Müllen, K.5
  • 4
    • 77953904913 scopus 로고    scopus 로고
    • For recent reviews, see
    • For recent reviews, see: Heeger, A. J. Chem. Soc. Rev. 2010, 39, 2354-2371
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    • Heeger, A.J.1
  • 6
    • 77953899130 scopus 로고    scopus 로고
    • For recent reviews, see
    • For recent reviews, see: Tsao, H. N.; Müllen, K. Chem. Soc. Rev. 2010, 39, 2372-2386
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 2372-2386
    • Tsao, H.N.1    Müllen, K.2
  • 9
    • 77956652829 scopus 로고    scopus 로고
    • For a recent review, see
    • For a recent review, see: Slota, J. E.; He, X.; Huck, W. T. S. Nano Today 2010, 5, 231-242
    • (2010) Nano Today , vol.5 , pp. 231-242
    • Slota, J.E.1    He, X.2    Huck, W.T.S.3
  • 19
    • 67650497918 scopus 로고    scopus 로고
    • Attempts at copolymerizing phenylene and fluorene were largely unsuccessful because we could not identify catalysts with chain-growth behavior under semibatch conditions. For other examples of challenging copolymerizations, see
    • Attempts at copolymerizing phenylene and fluorene were largely unsuccessful because we could not identify catalysts with chain-growth behavior under semibatch conditions. For other examples of challenging copolymerizations, see: Miyakoshi, R.; Yokoyama, A.; Yokozawa, T. Chem. Lett. 2008, 37, 1022-1023
    • (2008) Chem. Lett. , vol.37 , pp. 1022-1023
    • Miyakoshi, R.1    Yokoyama, A.2    Yokozawa, T.3
  • 24
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    • 2 with several equivalents of monomer. For reference, see
    • 2 with several equivalents of monomer. For reference, see: Lanni, E. L.; McNeil, A. J. J. Am. Chem. Soc. 2009, 131, 16573-16579
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 16573-16579
    • Lanni, E.L.1    McNeil, A.J.2
  • 28
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    • Chain Copolymerization
    • In, 4 th ed.; John Wiley & Sons: Hoboken, NJ,;
    • Odian, G. Chain Copolymerization. In Principles of Polymerization, 4 th ed.; John Wiley & Sons: Hoboken, NJ, 2004; pp 466 - 469.
    • (2004) Principles of Polymerization , pp. 466-469
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  • 30
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    • Note that for these studies it was necessary to generate 1 from the dibromo precursor to avoid monomer decomposition at rt (Supporting Information). Although an approximately 80:20 mixture of regioisomers is generated via this method, the minor regioisomer is unreactive during polymerization. See ref 14
    • Note that for these studies it was necessary to generate 1 from the dibromo precursor to avoid monomer decomposition at rt (Supporting Information). Although an approximately 80:20 mixture of regioisomers is generated via this method, the minor regioisomer is unreactive during polymerization. See ref 14.
  • 32
    • 78149242425 scopus 로고    scopus 로고
    • Although all gradient copolymer compositions were intended to have a final composition of 1:1 (1: 2), as the monomer 1 addition rate decreased, the incorporation of monomer 1 into the copolymer also decreased, possibly due to increased amounts of quenched monomer
    • Although all gradient copolymer compositions were intended to have a final composition of 1:1 (1: 2), as the monomer 1 addition rate decreased, the incorporation of monomer 1 into the copolymer also decreased, possibly due to increased amounts of quenched monomer.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.