메뉴 건너뛰기




Volumn 1, Issue 33, 2013, Pages 5093-5100

2-Bromo perylene diimide: Synthesis using C-H activation and use in the synthesis of bis(perylene diimide)-donor electron-transport materials

Author keywords

[No Author keywords available]

Indexed keywords

BITHIOPHENES; C-H ACTIVATION; ELECTRON-TRANSPORT MATERIALS; FIELD-EFFECT MOBILITIES; LOWER ENERGIES; PERYLENEDIIMIDES; REVERSIBLE REDUCTION; STILLE COUPLING;

EID: 84881411208     PISSN: 20507534     EISSN: 20507526     Source Type: Journal    
DOI: 10.1039/c3tc30918e     Document Type: Article
Times cited : (38)

References (44)
  • 36
    • 84879336735 scopus 로고    scopus 로고
    • During the review process for the present paper, a very similar procedure for the monoborylation of a PDI in the 2-position has been published elsewhere
    • During the review process for the present paper, a very similar procedure for the monoborylation of a PDI in the 2-position has been published elsewhere: S. Ito, S. Hiroto and H. Shinokubo, Org. Lett., 2013, 15, 3110 3113
    • (2013) Org. Lett. , vol.15 , pp. 3110-3113
    • Ito, S.1    Hiroto, S.2    Shinokubo, H.3
  • 38
    • 79952657415 scopus 로고    scopus 로고
    • The triads are not measurably fluorescent in solution, at least in the range 550-850 nm
    • B. Carsten F. He H. J. Son T. Xu L. Yu Chem. Rev. 2011 111 1493 1528
    • (2011) Chem. Rev. , vol.111 , pp. 1493-1528
    • Carsten, B.1    He, F.2    Son, H.J.3    Xu, T.4    Yu, L.5
  • 41
    • 0035906799 scopus 로고    scopus 로고
    • Although electronic coupling between redox centers can contribute to such splittings, electrostatic interactions mediated by the solvent are also important
    • F. Würthner C. Thalacker S. Diele C. Tschierske Chem.-Eur. J. 2001 7 2245 2253
    • (2001) Chem.-Eur. J. , vol.7 , pp. 2245-2253
    • Würthner, F.1    Thalacker, C.2    Diele, S.3    Tschierske, C.4
  • 42
    • 33845555815 scopus 로고
    • and so the differences may reflect different conformational preferences and/or the influence of the bridge on solvation
    • J. E. Sutton H. Taube Inorg. Chem. 1981 20 3125 3134
    • (1981) Inorg. Chem. , vol.20 , pp. 3125-3134
    • Sutton, J.E.1    Taube, H.2
  • 43
    • 0003938641 scopus 로고    scopus 로고
    • Blending with insulating polymers has long been used to enable formation of relatively thick films for time-of-flight measurements (for example, Marcel Dekker, New York
    • Blending with insulating polymers has long been used to enable formation of relatively thick films for time-of-flight measurements (for example, P. M. Borsenberger and D. S. Weiss, Organic Photoreceptors for Xerography, Marcel Dekker, New York, 1998
    • (1998) Organic Photoreceptors for Xerography
    • Borsenberger, P.M.1    Weiss, D.S.2
  • 44
    • 0037465419 scopus 로고    scopus 로고
    • More recently, blends of organics semiconductors with insulators such as polystyrene have also been used in OFETs; notably in the case of TIPS-pentacene (for example, M.-B. Madec, D. Crouch, G. Rincon Llorente, T. J. Whittle, M. Geoghegan and S. G. Yeates, J. Mater. Chem., 2008, 18, 3230-3236) and related compounds (W. H. Lee, D. Kwak, J. E. Anthony, H. S. Lee, H. H. Choi, D. H. Kim, S. G. Lee and K. Cho, Adv. Funct. Mater., 2013, 22, 267-281), where the polymer is thought to affect the alignment and size of acene crystallites in the OFET channel
    • J. L. Maldonado M. Bishop C. Fuentes-Hernandez P. Caron B. Domercq Y.-D. Zhang S. Barlow S. Thayumanavan M. Malagoli J.-L. Brédas S. R. Marder B. Kippelen Chem. Mater. 2003 15 994 999
    • (2003) Chem. Mater. , vol.15 , pp. 994-999
    • Maldonado, J.L.1    Bishop, M.2    Fuentes-Hernandez, C.3    Caron, P.4    Domercq, B.5    Zhang, Y.-D.6    Barlow, S.7    Thayumanavan, S.8    Malagoli, M.9    Brédas, J.-L.10    Marder, S.R.11    Kippelen, B.12


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.