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Volumn 73, Issue 23, 2008, Pages 9417-9425

Synthesis and reactivity of N-methyl and N-phenyl meso-unsubstituted N-confused porphyrins

Author keywords

[No Author keywords available]

Indexed keywords

ACETONITRILE; AROMATIC COMPOUNDS; ATOMS; CHEMICAL OXYGEN DEMAND; CHEMICAL REACTIONS; CHEMICAL REACTIVITY; COMPLEXATION; DERIVATIVES; DICHLOROMETHANE; ELECTRIC POWER PLANTS; GOLD COMPOUNDS; NICKEL; NICKEL ALLOYS; NICKEL COMPOUNDS; NUCLEAR MAGNETIC RESONANCE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ORGANIC POLYMERS; OXIDATION; PALLADIUM; PALLADIUM COMPOUNDS; PORPHYRINS; POSITIVE IONS; PROTONATION; PROTONS; SILVER; SILVER COMPOUNDS; SYNTHESIS (CHEMICAL);

EID: 57449095360     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo802040q     Document Type: Article
Times cited : (43)

References (72)
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    • Latos-Grazynski, L. Core-Modified Heteroanalogues of Porphyrins and Metalloporphyrins. In The Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic Press: San Diego, 2000; 2, pp 361-416.
    • (a) Latos-Grazynski, L. Core-Modified Heteroanalogues of Porphyrins and Metalloporphyrins. In The Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic Press: San Diego, 2000; Vol. 2, pp 361-416.
  • 17
    • 0030916482 scopus 로고    scopus 로고
    • Benzocarbaporphyrins: (a) Lash, T. D.; Hayes, M. J. Angew. Chem., Int. Ed. Engl. 1997, 36, 840-842.
    • Benzocarbaporphyrins: (a) Lash, T. D.; Hayes, M. J. Angew. Chem., Int. Ed. Engl. 1997, 36, 840-842.
  • 21
    • 0030905554 scopus 로고    scopus 로고
    • Azuliporphyrins: (a) Lash, T. D.; Chaney, S. T. Angew. Chem., Int. Ed. 1997, 36, 839-840.
    • Azuliporphyrins: (a) Lash, T. D.; Chaney, S. T. Angew. Chem., Int. Ed. 1997, 36, 839-840.
  • 27
    • 0030566857 scopus 로고    scopus 로고
    • Tropiporphyrins: (a) Lash, T. D.; Chaney, S. T. Tetrahedron Lett. 1996, 37, 8825-8828.
    • Tropiporphyrins: (a) Lash, T. D.; Chaney, S. T. Tetrahedron Lett. 1996, 37, 8825-8828.
  • 50
    • 0001004194 scopus 로고    scopus 로고
    • Synthesis of Novel Porphyrinoid Chromophores
    • Kadish, K. M, Smith, K. M, Guilard, R, Eds, Academic Press: San Diego
    • Lash, T. D. Synthesis of Novel Porphyrinoid Chromophores, In The Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic Press: San Diego, 2000; Vol. 2, pp 125-199.
    • (2000) The Porphyrin Handbook , vol.2 , pp. 125-199
    • Lash, T.D.1
  • 55
    • 57449092470 scopus 로고    scopus 로고
    • These results were presented, in part, at the following meeting: 233rd National American Chemical Society Meeting, Chicago, IL, March 2007 (Von Ruden, A. L.; Lash, T. D. Book of Abstracts, ORGN 192).
    • These results were presented, in part, at the following meeting: 233rd National American Chemical Society Meeting, Chicago, IL, March 2007 (Von Ruden, A. L.; Lash, T. D. Book of Abstracts, ORGN 192).
  • 58
    • 49249090956 scopus 로고    scopus 로고
    • Halide anion binding has recently been demonstrated for a protonated meso-unsubstituted 3-oxoNCP. See: Furuta, H, Nanami, H, Morimoto, T, Ogawa, T, Krai, V, Sessler, J. L, Lynch, V. Chem. Asian J. 2008, 3, 592-599. We thank a referee for bringing this paper to our attention
    • Halide anion binding has recently been demonstrated for a protonated meso-unsubstituted 3-oxoNCP. See: Furuta, H.; Nanami, H.; Morimoto, T.; Ogawa, T.; Krai, V.; Sessler, J. L.; Lynch, V. Chem. Asian J. 2008, 3, 592-599. We thank a referee for bringing this paper to our attention.
  • 64
    • 57449087779 scopus 로고    scopus 로고
    • The validity of this type of interpretation for these types of macrocyclic systems is generally supported in the literature34,36 and while it is considered to be a naïve model, theoretical studies also support these interpretations.37
    • 37


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