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Volumn 27, Issue 24, 2008, Pages 6396-6399

Diferrocenylbispyrylium salts and electron-rich diferrocenylbispyran from oxidative coupling of ferrocenylpyran. induced electron transfer C-C bond making/breaking involving a metallocenyl radical intermediate

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EID: 61849145259     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om800638q     Document Type: Article
Times cited : (20)

References (81)
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  • 2
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    • For a recent review see
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    • (2005) Tetrahedron , vol.61 , pp. 3889
    • Sarhan, A.O.1
  • 9
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    • For selected articles related to pyrans, bispyrans, and extended bispyrans see
    • (a) For selected articles related to pyrans, bispyrans, and extended bispyrans see: Detty, M. R.; Hassett, J. W.; Murray, B. J.; Reynolds, G. A. Tetrahedron 1985, 41, 4853.
    • (1985) Tetrahedron , vol.41 , pp. 4853
    • Detty, M.R.1    Hassett, J.W.2    Murray, B.J.3    Reynolds, G.A.4
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    • Suzuki, T.; Higuchi, H.; Tsuji, T.; Nishida, J.; Yamashita, Y.; Miyashi, T. In Chemistry of Nanomolecular Systems; Nakamura, T., Matsumoto, T., Tada, T., Sugiura, K., Eds.; Springer: Heidelberg, 2003; Chapter 1: Dynamic Redox Systems, p 3.
    • (a) Suzuki, T.; Higuchi, H.; Tsuji, T.; Nishida, J.; Yamashita, Y.; Miyashi, T. In Chemistry of Nanomolecular Systems; Nakamura, T., Matsumoto, T., Tada, T., Sugiura, K., Eds.; Springer: Heidelberg, 2003; Chapter 1: Dynamic Redox Systems, p 3.
  • 50
    • 61849107092 scopus 로고    scopus 로고
    • For examples of bispyrylium salts see: Balaban, A. T, Dinculescu, A, Dorofeenko, G. N, Mezheritskii, V. V, Kobik, A. V, Fischer, G. W. In Pyrylium Salts: Syntheses, Reactions and Physical Properties. Advances in Heterocyclic Chemistry; Katrisky, A. R, Ed, Academic: New York, 1982; Suppl. 2
    • (a) For examples of bispyrylium salts see: Balaban, A. T.; Dinculescu, A.; Dorofeenko, G. N.; Mezheritskii, V. V.; Kobik, A. V.; Fischer, G. W. In Pyrylium Salts: Syntheses, Reactions and Physical Properties. Advances in Heterocyclic Chemistry; Katrisky, A. R., Ed.; Academic: New York, 1982; Suppl. 2.
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    • 61849108224 scopus 로고    scopus 로고
    • For the formation of (2,6-diphenyl-4H-pyran-4-yl)triphenylphosphonium tetrafluoroborate used to obtain 1, see: Abaev, V. T.; Kisarova, L. I.; Emanuilidi, S. E.; Bumber, A. A.; Mikhailov, I. E.; Blank, I. B.; Yanovskii, A. I.; Struchkov, Y. T.; Okhlobystin, O. Y. Zh. Obshch Khim. 1989, 59, 1337.
    • For the formation of (2,6-diphenyl-4H-pyran-4-yl)triphenylphosphonium tetrafluoroborate used to obtain 1, see: Abaev, V. T.; Kisarova, L. I.; Emanuilidi, S. E.; Bumber, A. A.; Mikhailov, I. E.; Blank, I. B.; Yanovskii, A. I.; Struchkov, Y. T.; Okhlobystin, O. Y. Zh. Obshch Khim. 1989, 59, 1337.
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  • 61
    • 61849138399 scopus 로고    scopus 로고
    • o' = - 0.32 V vs Fc, corresponding to the one-electron oxidation/reduction of the pyran moiety. Ba, F
    • unpublished results
    • o' = - 0.32 V vs Fc, corresponding to the one-electron oxidation/reduction of the pyran moiety. Ba, F., unpublished results,
  • 62
    • 0345349425 scopus 로고    scopus 로고
    • The sharp-like shape of the oxidation one-electron peak at E = - 0.15 V vs Fc may be due to a weak adsorption of compound 1 onto the Pt working electrode. Wopschall, R.-H.; Shain, I. Anal. Chem. 1967, 39, 1514.
    • (b) The sharp-like shape of the oxidation one-electron peak at E = - 0.15 V vs Fc may be due to a weak adsorption of compound 1 onto the Pt working electrode. Wopschall, R.-H.; Shain, I. Anal. Chem. 1967, 39, 1514.
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    • 2 (all data) 0.1709.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.