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Volumn 129, Issue 40, 2007, Pages 12148-12158

On the mechanism of intramolecular sensitization of photocleavage of the 2-(2-nitrophenyl)propoxycarbonyl (NPPOC) protecting group

Author keywords

[No Author keywords available]

Indexed keywords

ELECTRONIC ENERGY TRANSFER; SENSITIZATION; SENSITIZERS; TIME-RESOLVED LASER SPECTROSCOPY;

EID: 35048851485     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja072355p     Document Type: Article
Times cited : (61)

References (54)
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    • An overview of photoremovable protecting groups used in DNA chip synthesis has been given by Pirrung, M. C, Rana, V. S, Photoremovable Protecting Groups in DNA Synthesis and Microarray Fabrication. In Dynamic Studies in Biology: Phototriggers, Photoswitches, and Caged Compounds; Givens, R. S, Goeldner, M, Eds, J. Wiley & Sons: New York, 2005; p 341
    • An overview of photoremovable protecting groups used in DNA chip synthesis has been given by Pirrung, M. C.; Rana, V. S., Photoremovable Protecting Groups in DNA Synthesis and Microarray Fabrication. In Dynamic Studies in Biology: Phototriggers, Photoswitches, and Caged Compounds; Givens, R. S., Goeldner, M., Eds.; J. Wiley & Sons: New York, 2005; p 341.
  • 6
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    • Other sensitizers investigated, such as acridone or xanthone, showed considerable photochemical side reactions with the solvent
    • Other sensitizers investigated, such as acridone or xanthone, showed considerable photochemical side reactions with the solvent.
  • 7
    • 35048847704 scopus 로고    scopus 로고
    • Efficient photolithographic synthesis of DNA-chips by photosensitization
    • DE 10315772A1, WO 2004089529, 2004 [Chem. Abstr. 2004, 141, 366034
    • Steiner, U.; Wöll, D. Efficient photolithographic synthesis of DNA-chips by photosensitization. DE 10315772(A1), WO 2004089529, 2004 [Chem. Abstr. 2004, 141, 366034].
    • Steiner, U.1    Wöll, D.2
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    • 3943082506 scopus 로고    scopus 로고
    • Speiser, S. Chem. Rev. 1996, 96, 1953-1976.
    • (1996) Chem. Rev , vol.96 , pp. 1953-1976
    • Speiser, S.1
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    • 0001104368 scopus 로고    scopus 로고
    • A similar observation with linked benzyol/styryl energy donor acceptor systems was made by Cowan, D. O.; Baum, A. A. J. Am. Chem. Soc. 1971, 93, 1153-1162.
    • A similar observation with linked benzyol/styryl energy donor acceptor systems was made by Cowan, D. O.; Baum, A. A. J. Am. Chem. Soc. 1971, 93, 1153-1162.
  • 36
    • 85050068560 scopus 로고
    • Spin-Statistical Factors in Diffusion-Controlled Reactions
    • Gollnick, K, Volman, D. H, Hammond, G. S, Eds, John Wiley & Sons
    • Saltiel, J.; Atwater, B. W. Spin-Statistical Factors in Diffusion-Controlled Reactions. In Advances in Photochemistry; Gollnick, K., Volman, D. H., Hammond, G. S., Eds.; John Wiley & Sons: 1988; pp 1-90.
    • (1988) Advances in Photochemistry , pp. 1-90
    • Saltiel, J.1    Atwater, B.W.2
  • 46
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    • Chain Effect and Magnetic Field Effect on the Photoinduced Electron Transfer Reactions of Polymethylene-Linked Donor Acceptor Systems
    • Balzani, V, Ed, D. Reidel Publishing Company: Dordrecht, The Netherlands
    • Weller, A. Chain Effect and Magnetic Field Effect on the Photoinduced Electron Transfer Reactions of Polymethylene-Linked Donor Acceptor Systems. In Supramolecular Photochemistry; Balzani, V., Ed.; D. Reidel Publishing Company: Dordrecht, The Netherlands, 1987; pp 343-354.
    • (1987) Supramolecular Photochemistry , pp. 343-354
    • Weller, A.1
  • 47
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    • Recently, using intramolecular triplet - triplet energy transfer between the xanthone triplet and naphthalene, it has been confirmed that time constants of about 20 ns do indeed represent the slowest temporal components of the folding kinetics which otherwise extend to the 50-500 ps regime. Cf. Fierz, B.; Satzger, H.; Root, C.; Gilch, P.; Zinth, W.; Kiefhaber, T. Proc. Natl. Acad. Sci. U.S.A. 2007, 104, 2163-2168.
    • Recently, using intramolecular triplet - triplet energy transfer between the xanthone triplet and naphthalene, it has been confirmed that time constants of about 20 ns do indeed represent the slowest temporal components of the folding kinetics which otherwise extend to the 50-500 ps regime. Cf. Fierz, B.; Satzger, H.; Root, C.; Gilch, P.; Zinth, W.; Kiefhaber, T. Proc. Natl. Acad. Sci. U.S.A. 2007, 104, 2163-2168.
  • 49
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    • These singlet energies were estimated from the onsets of the first absorption bands in MeOH yielding 420 nm for thioxanthone and 380 nm for NPPOC
    • These singlet energies were estimated from the onsets of the first absorption bands in MeOH yielding 420 nm for thioxanthone and 380 nm for NPPOC.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.