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Volumn 3, Issue 3, 2005, Pages 414-422

Hydrogen bond directed self-assembly of core-substituted naphthalene bisimides with melamines in solution and at the graphite interface

Author keywords

[No Author keywords available]

Indexed keywords

DYES; ELECTRON MICROSCOPY; FLUORESCENCE; GRAPHITE; MELAMINE; NAPHTHALENE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SCANNING TUNNELING MICROSCOPY; SELF ASSEMBLY; SOLUTIONS; SUPRAMOLECULAR CHEMISTRY; SYNTHESIS (CHEMICAL); TEMPERATURE DISTRIBUTION; ULTRAVIOLET RADIATION;

EID: 14244250417     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b414443k     Document Type: Article
Times cited : (73)

References (62)
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    • F. Würthner, S. Ahmed, C. Thalacker and T. Debaerdemaeker, Chem. Eur. J., 2002, 8, 4742-4750; for earlier work on amino-substituted naphthaline bisimides where the color but not the fluorescence properties have been described see: (a) E. Bonnet, P. Gangneux and E. Maréchal, Bull. Soc. Chim. Fr., 1976, 504-507; (b) E. F. Bondarenko, V. A. Shigalevskii and G. A. Yugai, Zh. Org. Khim., 1982, 18, 610-615.
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    • note
    • In MCH the absorption maximum is shifted by about 12 nm to lower wavelengths with respect to chloroaliphatic solvents, indicating a higher dependence of the optical properties of core-substituted naphthalene bisimides on solvent effects than for perylene bisimides.
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    • note
    • Two more possibilities arise if we consider the position of the NH-alkyl chains in space. However, as these could not be resolved by STM they are not discussed here. Nevertheless, they constitute another reason for the observed disorder.


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