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Volumn 25, Issue 2, 2009, Pages 1131-1137

Organic styryl dye nanoparticles: Synthesis and unique spectroscopic properties

Author keywords

[No Author keywords available]

Indexed keywords

FLUORESCENCE; IONS; MONOMERS; QUANTUM CHEMISTRY; WATER ABSORPTION;

EID: 61849129506     PISSN: 07437463     EISSN: None     Source Type: Journal    
DOI: 10.1021/la802879e     Document Type: Article
Times cited : (43)

References (56)
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    • 1H NMR spectra. See the Supporting Information for more detail.
    • 1H NMR spectra. See the Supporting Information for more detail.
  • 32
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    • Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Montgomery, J. A, Jr, Vreven, T, Kudin, K. N, Burant, J. C, Millam, J. M, Iyengar, S. S, Tomasi, J, Barone, V, Mennucci, B, Cossi, M, Scalmani, G, Rega, N, Petersson, G. A, Nakatsuji, H, Hada, M, Ehara, M, Toyota, K, Fukuda, R, Hasegawa, J, Ishida, M, Nakajima, T, Honda, Y, Kitao, O, Nakai, H, Klene, M, Li, X, Knox, J. E, Hratchian, H. P, Cross, J. B, Bakken, V, Adamo, C, Jaramillo, J, Gomperts, R, Stratmann, R. E, Yazyev, O, Austin, A. J, Cammi, R, Pomelli, C, Ochterski, J. W, Ayala, P. Y, Morokuma, K, Voth, G. A, Salvador, P, Dannenberg, J. J, Zakrzewski, V. G, Dapprich, S, Daniels, A. D, Strain, M. C, Farkas, O, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Ortiz, J. V, Cui, Q, Baboul, A. G, Clifford, S, Cioslowski, J, Stefanov, B. B, Liu, G, Liashenko, A, Piskorz, P, Komaromi, I, Martin, R. L, Fox, D. J, Keit
    • Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A., Jr.; Vreven, T.; Kudin, K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez, C.; Pople, J. A. Gaussian 03; Gaussian: Wallingford, CT, 2004.
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    • According to the Onsager's reaction field model, negative solvatochromism is expected for transitions from a state with a high dipole moment to a state with a smaller one. An enhanced stabilization of the ground state by polar solvents leads to an increased transition energy.
    • (c) According to the Onsager's reaction field model, negative solvatochromism is expected for transitions from a state with a high dipole moment to a state with a smaller one. An enhanced stabilization of the ground state by polar solvents leads to an increased transition energy.
  • 44
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    • The Royal Society of Chemistry: London
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    • (1997) Solvatochromism
    • Suppan, P.1    Ghoneim, N.2
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    • Internal Stark effect and the related screening of the positive charge on DASPE by the counteranions would also influence the fluorescence properties of the chromophore. However, since the φf value of DASPE-I was almost identical with that of DASPE-TPB in chloroform, the influence of screening and the consequent electrochromic modulation on φf would be very small
    • f would be very small.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.