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Volumn 129, Issue 28, 2007, Pages 8801-8810

Monocopper center embedded in a biomimetic cavity: From supramolecular control of copper coordination to redox regulation

Author keywords

[No Author keywords available]

Indexed keywords

BIOMIMETIC CAVITY; STERIC EFFECTS; SUPRAMOLECULAR CONTROL;

EID: 34548455036     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja071219h     Document Type: Article
Times cited : (74)

References (71)
  • 26
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    • 3v geometry have also been reported (see refs 3, 5, and 8).
    • 3v geometry have also been reported (see refs 3, 5, and 8).
  • 52
    • 34848861786 scopus 로고    scopus 로고
    • Thesis, Universit'e Paris XI
    • (f) Rondelez, Y. Ph. D. Thesis, Universit'e Paris XI, 2002.
    • (2002)
    • Rondelez, Y.P.D.1
  • 53
    • 34848846830 scopus 로고    scopus 로고
    • Le Clainche, L. Ph. D. Thesis, Université Paris VI, 2000.
    • (g) Le Clainche, L. Ph. D. Thesis, Université Paris VI, 2000.
  • 55
    • 18744397224 scopus 로고    scopus 로고
    • Two other generations of calix[6]arene ligands have been synthesized since. For the most recent, the calix-aza-cryptand ligands display covalently bound functional groups, and the metal is totally entrapped leading to an almost blocked trigonal geometry for Cu. See: (a) Izzet, G.; Douziech, B.; Prangé, T.; Thomas, A.; Jabin, I.; Le Mest, Y.; Reinaud, O. Proc. Natl. Acad. Sci. U.S.A. 2005, 102, 6831-6836.
    • Two other generations of calix[6]arene ligands have been synthesized since. For the most recent, the calix-aza-cryptand ligands display covalently bound functional groups, and the metal is totally entrapped leading to an almost blocked trigonal geometry for Cu. See: (a) Izzet, G.; Douziech, B.; Prangé, T.; Thomas, A.; Jabin, I.; Le Mest, Y.; Reinaud, O. Proc. Natl. Acad. Sci. U.S.A. 2005, 102, 6831-6836.
  • 57
    • 34848918457 scopus 로고    scopus 로고
    • Harrowfield J, Vicens, J, Eds, Springer: Dordrecht, The Netherlands, Chapter 13
    • Reinaud, O.; Le Mest, Y.; Jabin, I. In Calixarenes in the Nanoworld; Harrowfield J., Vicens, J., Eds.; Springer: Dordrecht, The Netherlands, 2006; Chapter 13.
    • (2006) Calixarenes in the Nanoworld
    • Reinaud, O.1    Le Mest, Y.2    Jabin, I.3
  • 58
    • 0001286011 scopus 로고    scopus 로고
    • A similar behavior has been reported in the rare cases of Cu complexes in a hydrophobic environment. See: (a) Carrier, S. M, Ruggiero, C. E, Houser, R. P, Tolman, W. B. Inorg. Chem. 1993, 32, 4889-4899
    • A similar behavior has been reported in the rare cases of Cu complexes in a hydrophobic environment. See: (a) Carrier, S. M.; Ruggiero, C. E.; Houser, R. P.; Tolman, W. B. Inorg. Chem. 1993, 32, 4889-4899.
  • 61
    • 34848899483 scopus 로고    scopus 로고
    • In some cases, especially for the Cu(I) compound, a second system can be observed at a higher potential of ca, 0.8 V, but this system is irreproducible in intensity. It is attributed to partial decomplexation which has been emphasized by NMR studies. See ref 19e
    • In some cases, especially for the Cu(I) compound, a second system can be observed at a higher potential of ca. +0.8 V, but this system is irreproducible in intensity. It is attributed to partial decomplexation which has been emphasized by NMR studies. See ref 19e.
  • 62
    • 34848913112 scopus 로고    scopus 로고
    • The impact of the nature of the -OR1 and -NR2 substituents on the conformation and flexibility of the calixarene structure for the different complexes has been the subject of detailed NMR and modeling studies on Cu1CO complexes. See ref 19d
    • 1CO complexes. See ref 19d.
  • 63
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    • 2 at a very low partial pressure.
    • 2 at a very low partial pressure.
  • 64
    • 34848908638 scopus 로고    scopus 로고
    • a's of pyrrolidine and tris(methyl)amine are, respectively, 11.27 and 9.10.
    • a's of pyrrolidine and tris(methyl)amine are, respectively, 11.27 and 9.10.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.