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Volumn 16, Issue 46, 2010, Pages 13622-13628

Contrasting self-assembly and gelation properties among bis-urea- and bis-amide-functionalised dialkoxynaphthalene (DAN) π systems

Author keywords

dialkoxynaphthalene; gels; hydrogen bonds; organogels; self assembly

Indexed keywords

AGGREGATION PROPERTY; DIALKOXYNAPHTHALENE; GELATION PROPERTIES; GELATORS; ORGANOGELS; THERMAL STABILITY;

EID: 78649938460     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201002208     Document Type: Article
Times cited : (35)

References (64)
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    • For a recent review on nucleic acid-guided chromophore assembly, see
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    • Similar spectral variations have been reported in a recent paper related to J-aggregating PBI dyes, see
    • Similar spectral variations have been reported in a recent paper related to J-aggregating PBI dyes, see:, X-Q. Li, X. Zhang, S. Ghosh, F. Würthner, Chem. Eur. J. 2008, 14, 8074.
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    • The synthesis of DAN-A' is described in the Supporting Information
    • The synthesis of DAN-A' is described in the Supporting Information.
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    • 78649957808 scopus 로고    scopus 로고
    • See the Supporting Information for details
    • See the Supporting Information for details.
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    • For a recent review on various attempts to correlate molecular structure with gelation, see
    • For a recent review on various attempts to correlate molecular structure with gelation, see:, P. Dastidar, Chem. Soc. Rev. 2008, 37, 2699.
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    • Such extremely low CGC values in aromatic solvents could be attributed to the favourable π-π interactions among the π cloud of the solvent molecules with that of the DAN-U chromophore. Please note that this could be possible because in the J aggregate the chromophores stack with longitudinal displacement along the long axis and thus part of the π cloud remains exposed to interact with the solvent molecules
    • Such extremely low CGC values in aromatic solvents could be attributed to the favourable π-π interactions among the π cloud of the solvent molecules with that of the DAN-U chromophore. Please note that this could be possible because in the J aggregate the chromophores stack with longitudinal displacement along the long axis and thus part of the π cloud remains exposed to interact with the solvent molecules.
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    • For a recent report on a structure-property relationship study in the context of self-assembly and gelation, see
    • For a recent report on a structure-property relationship study in the context of self-assembly and gelation, see:, S. Yagai, S. Kubota, T. Iwashima, K. Kishikawa, T. Nakanishi, T. Karatsu, A. Kitamura, Chem. Eur. J. 2008, 14, 5246.
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    • For a comparative gelation study among tris-amide- and tris-urea-containing discotic systems, see
    • For a comparative gelation study among tris-amide- and tris-urea-containing discotic systems, see:, J. J. van Gorp, J. A. J. M. Vekemans, E. W. Meijer, J. Am. Chem. Soc. 2002, 124, 14759.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.