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Volumn 130, Issue 44, 2008, Pages 14440-14441

Pt(II)- and Pt(IV)-bridged cofacial diporphyrins via carbon-transition metal σ-bonds

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; COFACIAL DIPORPHYRIN; HYDROGEN; PLATINUM DERIVATIVE; PORPHYRIN DERIVATIVE; TRANSITION ELEMENT; UNCLASSIFIED DRUG;

EID: 55549099285     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja8066385     Document Type: Article
Times cited : (65)

References (23)
  • 10
    • 0013214947 scopus 로고    scopus 로고
    • Arnold, D. P.; Sakata, Y.; Sugiura, K.; Worthington, E. I. Chem. Commun. 1998, n/a, 2331.
    • (b) Arnold, D. P.; Sakata, Y.; Sugiura, K.; Worthington, E. I. Chem. Commun. 1998, n/a, 2331.
  • 18
    • 55549111389 scopus 로고    scopus 로고
    • 4 and so on), which resulted in no reaction or decomposition of 4.
    • 4 and so on), which resulted in no reaction or decomposition of 4.
  • 20
    • 0034717131 scopus 로고    scopus 로고
    • and references therein. For other examples of helicity inversion by redox stimuli, see
    • For other examples of helicity inversion by redox stimuli, see: Zahn, S.; Canary, W. J. Science 2000, 288, 1404, and references therein.
    • (2000) Science , vol.288 , pp. 1404
    • Zahn, S.1    Canary, W.J.2
  • 21
    • 0033582668 scopus 로고    scopus 로고
    • ox1 of 2 was determined by differential pulse voltammetry because of existence of the reactive pyridyl group and free meso-position. For electrochemical reaction of pyridine derivatives with porphyrins, see: Ruhlmann, L.; Lobstein, S.; Gross, M.; Giraudeau, A. J. Org. Chem. 1999, 64, 1352.
    • ox1 of 2 was determined by differential pulse voltammetry because of existence of the reactive pyridyl group and free meso-position. For electrochemical reaction of pyridine derivatives with porphyrins, see: Ruhlmann, L.; Lobstein, S.; Gross, M.; Giraudeau, A. J. Org. Chem. 1999, 64, 1352.
  • 22
    • 55549106966 scopus 로고    scopus 로고
    • The DFT calculation indicates that 2 also takes a ruffled conformation (Figure S16). The structural difference in macrocycles between 2 and 4 only slightly influences the difference of the oxidation potentials.
    • The DFT calculation indicates that 2 also takes a ruffled conformation (Figure S16). The structural difference in macrocycles between 2 and 4 only slightly influences the difference of the oxidation potentials.
  • 23
    • 55549139328 scopus 로고    scopus 로고
    • The reason is not clear why 3 shows only two waves despite the close proximity of two porphyrins. The reduction waves for 4 have not been fully characterized due to their complicated features.
    • The reason is not clear why 3 shows only two waves despite the close proximity of two porphyrins. The reduction waves for 4 have not been fully characterized due to their complicated features.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.