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Volumn 17, Issue 18, 2011, Pages 5011-5018

N-2-Aryl-1,2,3-triazoles: A novel class of UV/blue-light-emitting fluorophores with tunable optical properties

Author keywords

charge transfer; fluorescent probes; quantum yield; Stokes shift; triazoles

Indexed keywords

ARYL GROUP; COMPUTATIONAL STUDIES; DERIVATIZATIONS; FLUORESCENCE EMISSION; FLUORESCENT PROBES; HIGH EFFICIENCY; INTRA-MOLECULAR CHARGE TRANSFER; MATERIAL SCIENCE; PHOTOABSORPTIONS; SOLVENT EFFECTS; STOKES SHIFT; SUBSTITUTED GROUPS; TRIAZOLE DERIVATIVES; TRIAZOLE RING; TRIAZOLES; X RAY CRYSTAL STRUCTURES;

EID: 79954618319     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201002937     Document Type: Article
Times cited : (86)

References (55)
  • 1
    • 79954574214 scopus 로고    scopus 로고
    • For selected recent reviews, see
    • For selected recent reviews, see
  • 8
    • 79954569916 scopus 로고    scopus 로고
    • For selected recent examples, see
    • For selected recent examples, see
  • 15
    • 79954625647 scopus 로고    scopus 로고
    • For selected recent examples, see
    • For selected recent examples, see
  • 49
    • 79954604554 scopus 로고    scopus 로고
    • See the detailed excitation/emission data in the Supporting Information
    • See the detailed excitation/emission data in the Supporting Information.
  • 50
    • 79954621975 scopus 로고    scopus 로고
    • note
    • Gaussian03 (RevisionA.1), M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, J. A. Montgomery, Jr., T. Vreven, K. N. Kudin, J. C. Burant, J. M. Millam, S. S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G. A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J. E. Knox, H. P. Hratchian, J. B. Cross, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, P. Y. Ayala, K. Morokuma, G. A. Voth, P. Salvador, J. J. Dannenberg, V. G. Zakrzewski, S. Dapprich, A. D. Daniels, M. C. Strain, O. Farkas, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. V. Ortiz, Q. Cui, A. G. Baboul, S. Clifford, J. Cioslowski, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. L. Martin, D. J. Fox, T. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, M. Challacombe, P. M. W. Gill, B. Johnson, W. Chen, M. W. Wong, C. Gonzalez, J. A. Pople, Gaussian, Inc., Pittsburgh, PA, 2003.
  • 54
    • 79954622597 scopus 로고    scopus 로고
    • note
    • Solvatotochromism studies of compound 1e, 2a, 2d, 2e have been carried out in various solvents. Detailed experimental results are shown in the Supporting Information, where little changes were observed in different solvent systems, strongly supported the proposed PICT mechanism. For example, for compound 2a, the quantum yield in different solvents are observed as following: in MeOH Φ=0.31; in dichloromethane Φ=0.37; in acetonitrile Φ=0.34; in ethyl acetate Φ=0.37; in THF Φ=0.34.
  • 55
    • 79954573910 scopus 로고    scopus 로고
    • See detailed computational results of all compounds 1e - 3o in the Supporting Information
    • See detailed computational results of all compounds 1e-3o in the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.