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Volumn 10, Issue 6, 2004, Pages 1445-1455

Diaroyl(methanato)boron Difluoride Compounds as Medium-Sensitive Two-Photon Fluorescent Probes

Author keywords

Boron; Fluorescent probes; Structure activity relationships; Two photon absorption

Indexed keywords

ABSORPTION; DERIVATIVES; FLUORESCENCE; SYNTHESIS (CHEMICAL);

EID: 1842510545     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200305321     Document Type: Article
Times cited : (192)

References (90)
  • 2
    • 0037034404 scopus 로고    scopus 로고
    • For a recent review see, for example: W. E. Moerner, J. Phys. Chem. B 2002, 106, 910-927.
    • (2002) J. Phys. Chem. B , vol.106 , pp. 910-927
    • Moerner, W.E.1
  • 10
    • 1842562449 scopus 로고    scopus 로고
    • Chemically Reactive Dipyrromethene-boron Difluoride Dyes, US 4774339, 1988
    • R. P. Haugland, H. C. Kang, Chemically Reactive Dipyrromethene-boron Difluoride Dyes, US 4774339, 1988.
    • Haugland, R.P.1    Kang, H.C.2
  • 11
    • 1842614443 scopus 로고    scopus 로고
    • Ethenyl-Substituted Dipyrrometheneboron Difluoride Dyes and Their Synthesis, US 5187288, 1993
    • H. C. Kang, R. P. Haugland, Ethenyl-Substituted Dipyrrometheneboron Difluoride Dyes and Their Synthesis, US 5187288, 1993.
    • Kang, H.C.1    Haugland, R.P.2
  • 29
    • 0004273681 scopus 로고
    • (Ed.: R. R. C. New), Oxford University Press, Oxford, New York, Tokyo
    • Liposomes a Practical Approach (Ed.: R. R. C. New), Oxford University Press, Oxford, New York, Tokyo, 1990.
    • (1990) Liposomes a Practical Approach
  • 32
    • 0004152586 scopus 로고    scopus 로고
    • Butterworth Heinemann, Oxford, Auckland, Boston, Johannesburg, Melbourne, New Delhi
    • N. N. Greenwood, A. Earnshaw, Chemistry of the Elements, 2nd ed., Butterworth Heinemann, Oxford, Auckland, Boston, Johannesburg, Melbourne, New Delhi, 1997.
    • (1997) Chemistry of the Elements, 2nd Ed.
    • Greenwood, N.N.1    Earnshaw, A.2
  • 35
    • 0000651795 scopus 로고
    • We note that the large amplitude of the fluorescence solvatochomism might be related to a charge-transfer phenomenon coupled to a molecular change of geometry in the excited state in the polar environment. Such behavior would be reminiscent of the Twisted Intramolecular Charge Transfer occurring in some donor-acceptor derivatives. See, for example: W. Rettig, Angew. Chem. 1986, 98, 969-986; Angew. Chem. Int. Ed. Engl. 1986, 25, 971-988.
    • (1986) Angew. Chem. , vol.98 , pp. 969-986
    • Rettig, W.1
  • 36
    • 84985609328 scopus 로고
    • We note that the large amplitude of the fluorescence solvatochomism might be related to a charge-transfer phenomenon coupled to a molecular change of geometry in the excited state in the polar environment. Such behavior would be reminiscent of the Twisted Intramolecular Charge Transfer occurring in some donor-acceptor derivatives. See, for example: W. Rettig, Angew. Chem. 1986, 98, 969-986; Angew. Chem. Int. Ed. Engl. 1986, 25, 971-988.
    • (1986) Angew. Chem. Int. Ed. Engl. , vol.25 , pp. 971-988
  • 64
    • 0001188113 scopus 로고    scopus 로고
    • c) L. Ventelon, S. Charier, L. Moreaux, J. Mertz, M. Blanchard-Desce, Angew. Chem. 2001, 113, 2156-2159; Angew. Chem. Int. Ed. 2001, 40, 2098-2101;
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 2098-2101


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.