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Volumn 47, Issue 9, 2008, Pages 3841-3850

Relative axial ligand orientation in bis(imidazole)iron(II) porphyrinates: Are "picket fence" derivatives different?

Author keywords

[No Author keywords available]

Indexed keywords

FERROUS ION; HEME; IMIDAZOLE DERIVATIVE; LIGAND; METALLOPORPHYRIN;

EID: 44149102661     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic702498c     Document Type: Article
Times cited : (38)

References (71)
  • 2
    • 44149124147 scopus 로고    scopus 로고
    • The following abbreviations are used in this paper: Porph, a generalized porphyrin dianion; TMP, dianion of meso-tetramesitylporphyrin; TPP, dianion of meso-tetraphenylporphyrin; TTP, dianion of meso-tetratolylporphyrin, TpivPP, dianion of α,α,α,α-tetrakis(o-pivalamidophenyl) porphyrin; TF5PPBr8, dianion of 2,3,7,8,12,13,17,18- octabromo-5,10,15,20-tetrakis(pentafluorophenyl)porphyrin; HIm, imidazole; 1-MeIm, 1-methylimidazole; 2-MeHIm, 2-methylimidazole; 4-MeHIm, 4-methylimidazole; 1,2-Me2Im, 1,2-dimethylimidazole; 1-AcIm, 1-acetyl-imidazole; 1-SiMe3Im, 1-(trimethylsilyl)imidazole; 1-VinylIm, 1-vinylimidazole; 1-BzylIm, 1-benzylimidazole; RIm, generalized imidazole;Py, pyridine; 3-ClPy, 3-chloropyridine; 4-CNPy, 4-cyanopyridine; 3-CNPy, 3-cyanopyridine; 4-MePy, 4-methylpyridine; 4-NMe2Py, 4-(dimethylamino)pyridine; Pip, piperidine; Pyz, pyrazine; Im, imidazolate; 2-MeIm, 2-methylimidazolate; N
    • im, nitrogen of imidazole ligands; EPR, electron paramagnetic resonance.
  • 18
    • 0001215319 scopus 로고
    • Dolphin, D, Ed, Academic Press: New York
    • Mathews, F. S.; Czerwinski, E. W.; Argos, P. In The Porphyrins; Dolphin, D., Ed.; Academic Press: New York, 1979; Vol. VII, pp 107-147.
    • (1979) The Porphyrins , vol.7 , pp. 107-147
    • Mathews, F.S.1    Czerwinski, E.W.2    Argos, P.3
  • 38
    • 44149112641 scopus 로고    scopus 로고
    • 2) are statistically about twice as large as those based on F, and R-factors based on ALL data will be even larger.
    • 2) are statistically about twice as large as those based on F, and R-factors based on ALL data will be even larger.
  • 47
    • 44149087672 scopus 로고    scopus 로고
    • CrystalMaker Version 7.2.3; CrystalMaker Software: Bicester, Oxfordshire OX26 3TA, England, 2007
    • CrystalMaker Version 7.2.3; CrystalMaker Software: Bicester, Oxfordshire OX26 3TA, England, 2007.
  • 48
    • 44149105980 scopus 로고    scopus 로고
    • Steffen, W. L.; Chun, H. K.; Hoard, J. L.; Reed, C. A. Abstracts of Papers, 175th National Meeting of the American Chemical Society, Anaheim, CA, March 13, 1978; American Chemical Society: Washington, DC, 1978; INOR 15.
    • Steffen, W. L.; Chun, H. K.; Hoard, J. L.; Reed, C. A. Abstracts of Papers, 175th National Meeting of the American Chemical Society, Anaheim, CA, March 13, 1978; American Chemical Society: Washington, DC, 1978; INOR 15.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.