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Volumn 37, Issue 3, 2008, Pages 264-265

Photophysical and photocatalytic properties of β-sulfonatoporphycenes

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EID: 42049101277     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2008.264     Document Type: Article
Times cited : (21)

References (19)
  • 1
    • 0000303285 scopus 로고    scopus 로고
    • ed. by K. M. Kadish, K. M. Smith, R. Guilard, Academic Press, Chap. 43, pp
    • a) R. K. Pandey, G. Zheng, in The Porphyrin Handbook, ed. by K. M. Kadish, K. M. Smith, R. Guilard, Academic Press, 2000, Vol. 6, Chap. 43, pp. 157-230.
    • (2000) The Porphyrin Handbook , vol.6 , pp. 157-230
    • Pandey, R.K.1    Zheng, G.2
  • 13
    • 42049113991 scopus 로고    scopus 로고
    • 49 and 5 were obtained in 83% and 75% yields, respectively. The hydrolysis of the chlorosulfonated porphycenes quantitatively proceeded. 4: UV-vis (in CH2Cl2, λmax/nm, 386, 577, 632, 669: MALDI-TOF-MS (dithranol matrix, m/z, M, 576.65. 5: UV-vis (in CH2Cl 2, λmax/nm, 386, 594, 644, 683: MALDI-TOF-MS (dithranol matrix, m/z, M, 674.77. The ratio of isomers (cis-2 and trans-2) was determined by peak integration of the 1HNMR spectrum. Route A: cis-2: trans-2, 1.8:1 Route B: cis-2:trans- 2, 2.5:1 Sample 2 synthesized by the Route B method was used for these experiments
    • 1HNMR spectrum. Route A: cis-2: trans-2 = 1.8:1 Route B: cis-2:trans- 2 = 2.5:1 Sample 2 synthesized by the Route B method was used for these experiments.


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