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Volumn 47, Issue 18, 2008, Pages 3367-3371

Transformation from H- to J-aggregated perylene bisimide dyes by complexation with cyanurates

Author keywords

Hydrogen bonding; Perylene dyes; Self assembly; Supramolecular chemistry

Indexed keywords

AGGREGATES; COLOR FILMS; ELECTRON TRANSITIONS; HEAT TREATMENT; HYDROGEN; MELAMINE FORMALDEHYDE RESINS; STOICHIOMETRY;

EID: 49149109419     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200705385     Document Type: Article
Times cited : (284)

References (52)
  • 8
    • 24944516927 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 5592-5629;
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 5592-5629
  • 21
    • 34547462512 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 5541-5544.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 5541-5544
  • 23
    • 0001128996 scopus 로고    scopus 로고
    • Mizuguchi reported the irreversible transformation from H-to J-type solid-state packing of a core-unsubstituted PBI (N,N′-bis(2- phenylethyl) derivative) by thermal treatment or exposure to acetone vapor. The J-type crystalline state shows red-shifted absorption at around 610 nm: J. Mizuguchi, J. Appl. Phys. 1998, 84, 4479-4486
    • Mizuguchi reported the irreversible transformation from H-to J-type solid-state packing of a core-unsubstituted PBI (N,N′-bis(2- phenylethyl) derivative) by thermal treatment or exposure to acetone vapor. The J-type crystalline state shows red-shifted absorption at around 610 nm: J. Mizuguchi, J. Appl. Phys. 1998, 84, 4479-4486.
  • 24
    • 4043080491 scopus 로고    scopus 로고
    • J-aggregates of core-unsubstituted PBIs have been reported, but they showed relatively small red shifts of the absorption band, see ref. [1b] and also: J. van Herrikhuyzen, A. Syamakumari, A. P. H. J. Schenning, E. W. Meijer, J. Am. Chem. Soc. 2004, 126, 10021-10027.
    • J-aggregates of core-unsubstituted PBIs have been reported, but they showed relatively small red shifts of the absorption band, see ref. [1b] and also: J. van Herrikhuyzen, A. Syamakumari, A. P. H. J. Schenning, E. W. Meijer, J. Am. Chem. Soc. 2004, 126, 10021-10027.
  • 26
    • 0001578695 scopus 로고    scopus 로고
    • For examples of multiple hydrogen-bond-directed PBI assemblies, see: a F. Würthner, C. Thalacker, A. Sautter, Adv. Mater. 1999, 11, 754-758;
    • For examples of multiple hydrogen-bond-directed PBI assemblies, see: a) F. Würthner, C. Thalacker, A. Sautter, Adv. Mater. 1999, 11, 754-758;
  • 30
    • 33847394581 scopus 로고    scopus 로고
    • For a recent review focusing on hydrogen-bonded supramolecular assemblies of functional dyes, see
    • For a recent review focusing on hydrogen-bonded supramolecular assemblies of functional dyes, see: S. Yagai, J. Photochem. Photobiol. C 2006, 7, 164-182.
    • (2006) J. Photochem. Photobiol. C , vol.7 , pp. 164-182
    • Yagai, S.1
  • 35
    • 53549103166 scopus 로고    scopus 로고
    • For details, see the Supporting Information
    • For details, see the Supporting Information.
  • 36
    • 53549092369 scopus 로고    scopus 로고
    • For the molecular modeled structure, see the Supporting Information
    • For the molecular modeled structure, see the Supporting Information.
  • 37
    • 0037008603 scopus 로고    scopus 로고
    • For an example of PBI dimer formed by π-stacking and hydrogen-bonding interactions, see
    • For an example of PBI dimer formed by π-stacking and hydrogen-bonding interactions, see: A. Syamakumari, A. P. H. J. Schenning, E. W. Meijer, Chem. Eur. J. 2002, 8, 3353-3361.
    • (2002) Chem. Eur. J , vol.8 , pp. 3353-3361
    • Syamakumari, A.1    Schenning, A.P.H.J.2    Meijer, E.W.3
  • 42
    • 53549118142 scopus 로고    scopus 로고
    • For characterization of the green precipitates, see the Supporting Information
    • For characterization of the green precipitates, see the Supporting Information.
  • 45
  • 46
    • 37049089746 scopus 로고
    • For supramolecular polymers obtained from ditopic melamines and barbiturates that are structurally related to cyanurates, see: a
    • For supramolecular polymers obtained from ditopic melamines and barbiturates that are structurally related to cyanurates, see: a) J. M. Lehn, M. Mascal, A. DeCian, J. Fischer, J. Chem. Soc. Chem. Commun. 1990, 479-481;
    • (1990) J. Chem. Soc. Chem. Commun , pp. 479-481
    • Lehn, J.M.1    Mascal, M.2    DeCian, A.3    Fischer, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.