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Volumn 48, Issue 9, 2009, Pages 4067-4074

Synthesis, Structure, and optical properties of the platinum(II) complexes of indaphyrin and thiaindaphyrin

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EID: 66149137307     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic802041z     Document Type: Article
Times cited : (18)

References (45)
  • 34
    • 66149113223 scopus 로고    scopus 로고
    • Bruker Advanced X-ray Solutions SAINT, version 6.45; Bruker AXS Inc, Madison, WI, 1997-2003
    • (a) Bruker Advanced X-ray Solutions SAINT, version 6.45; Bruker AXS Inc.: Madison, WI, 1997-2003.
  • 35
    • 66149094177 scopus 로고    scopus 로고
    • Bruker Advanced X-ray Solutions SMART for WNT/2000, version 5.628; Bruker AXS Inc, Madison, WI, 1997- 2002
    • (b) Bruker Advanced X-ray Solutions SMART for WNT/2000, version 5.628; Bruker AXS Inc.: Madison, WI, 1997- 2002.
  • 36
    • 66149093790 scopus 로고    scopus 로고
    • Bruker Advanced X-ray Solutions SHELXTL, version 6.10; Bruker AXS Inc, Madison, WI, 2000
    • (c) Bruker Advanced X-ray Solutions SHELXTL, version 6.10; Bruker AXS Inc., Madison, WI, 2000.
  • 37
    • 0000196392 scopus 로고
    • Dolphin, D, Ed, Academic Press: New York
    • Buchler, J. W. In The Porphyrins; Dolphin, D., Ed.; Academic Press: New York, 1978; Vol. 1, p 389-483.
    • (1978) The Porphyrins , vol.1 , pp. 389-483
    • Buchler, J.W.1
  • 39
    • 84868937485 scopus 로고    scopus 로고
    • The contribution of the various non-planar conformational modes to the overall conformation of a porphyrin can be computed using a normal coordinate structural analysis, see: Shelnutt, J. A. In The Porphyrin Handbook; Kadish, K. M, Smith, K. M, Guilard, R, Eds, Academic Press: San Diego, CA, 2000; 7,pp 167 -224. The different macrocycle connectivity of indaphyrins, however, does not allow their analysis along any porphyrin lowest-energy frequency mode using the NSD Engine, accessed Mar 2009
    • The contribution of the various non-planar conformational modes to the overall conformation of a porphyrin can be computed using a normal coordinate structural analysis, see: Shelnutt, J. A. In The Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic Press: San Diego, CA, 2000; Vol. 7,pp 167 -224. The different macrocycle connectivity of indaphyrins, however, does not allow their analysis along any porphyrin lowest-energy frequency mode using the NSD Engine (http://jasheln.unm.edu/jasheln/content/nsd/ NSDengine/start.htm, accessed Mar 2009).
  • 43
    • 66149093408 scopus 로고    scopus 로고
    • Hazell, A Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 1984, 40, 751. CSD code: CEZKEX.
    • Hazell, A Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 1984, 40, 751. CSD code: CEZKEX.
  • 44
    • 84981870281 scopus 로고    scopus 로고
    • The formal name for the resulting moiety is cyclopenta[b]thiophen- 4-one, also referred to as thiaindanone: Aparajithan, K.; Thompson, A. C.; Sam, J. J. Heterocycl. Chem. 1966, 3, 466-469.
    • The formal name for the resulting moiety is cyclopenta[b]thiophen- 4-one, also referred to as thiaindanone: Aparajithan, K.; Thompson, A. C.; Sam, J. J. Heterocycl. Chem. 1966, 3, 466-469.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.