메뉴 건너뛰기




Volumn 77, Issue 7, 2012, Pages 3038-3048

Meso-tetrakis(pentafluorophenyl)porphyrin-derived chromene-annulated chlorins

Author keywords

[No Author keywords available]

Indexed keywords

CHLORINS; DIAGNOSTIC TOOLS; DIHYDROXYLATION REACTION; FREE BASE; NMR SPECTRUM; NUCLEOPHILIC AROMATIC SUBSTITUTION REACTION; OPTICAL SPECTRA; PENTAFLUOROPHENYL; PORPHYRINOIDS; PT COMPLEXES; REACTION SEQUENCES; RED-SHIFTED; REFERENCE POINTS; UV-VIS AND FLUORESCENCE SPECTRA;

EID: 84859611359     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3001436     Document Type: Article
Times cited : (48)

References (89)
  • 2
    • 0001938751 scopus 로고    scopus 로고
    • Kadish, K. M. Smith, K. M. Guilard, R. Academic Press: San Diego
    • Lindsey, J. S. In The Porphyrin Handbook; Kadish, K. M.; Smith, K. M.; Guilard, R., Eds.; Academic Press: San Diego, 2000; Vol. 1, pp 45-118.
    • (2000) The Porphyrin Handbook , vol.1 , pp. 45-118
    • Lindsey, J.S.1
  • 3
    • 0035106285 scopus 로고    scopus 로고
    • Resonance effects that other substituents might be able to show are nearly always entirely eliminated by virtue of the orthogonal arrangement of the aryl group and the porphyrin ring. For exceptions, see, e.g.: Vitasovic, M.; Gouterman, M.; Linschitz, H. J. Porphyrins Phthalocyanines 2001, 5, 191-197
    • (2001) J. Porphyrins Phthalocyanines , vol.5 , pp. 191-197
    • Vitasovic, M.1    Gouterman, M.2    Linschitz, H.3
  • 52
    • 0002136604 scopus 로고
    • Dolphin, D. Academic Press: New York
    • Scheer, H.; Inhoffen, H. H. In The Porphyrins; Dolphin, D., Ed.; Academic Press: New York, 1978; Vol. 2, pp 45-90.
    • (1978) The Porphyrins , vol.2 , pp. 45-90
    • Scheer, H.1    Inhoffen, H.H.2
  • 72
    • 84859592728 scopus 로고    scopus 로고
    • Private communication, Freie Universität, Berlin, Germany
    • Stark, C. B. W.; Aicher, D.; Wiehe, A. Private communication, Freie Universität, Berlin, Germany.
    • Stark, C.B.W.1    Aicher, D.2    Wiehe, A.3
  • 79
    • 70450206724 scopus 로고    scopus 로고
    • Revision A.02, Wallingford, CT
    • Gaussian 09, Revision A.02, Wallingford, CT.
    • Gaussian 09
  • 81
    • 84855945126 scopus 로고    scopus 로고
    • Interestingly, it has been pointed out that nearly all of the methods for the synthesis of chromenes involve the closure of the pyran ring on a substrate containing a preformed phenol unit, while we observe here a deviation from this pattern: Majumdar, N.; Korthals, K. A.; Wulff, W. D. J. Am. Chem. Soc. 2012, 134, 1357-1362
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 1357-1362
    • Majumdar, N.1    Korthals, K.A.2    Wulff, W.D.3
  • 84
    • 84859564064 scopus 로고    scopus 로고
    • Radii as per Cambridge Crystallographic Data Centre: (accessed 12/)
    • Radii as per Cambridge Crystallographic Data Centre: http://www.ccdc.cam. ac.uk/products/csd/radii/table.php4 (accessed 12/ 2011)
    • (2011)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.