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Volumn 59, Issue 14, 2003, Pages 2409-2415

Calixarene-based metalloporphyrins: Molecular tweezers for complexation of DABCO

Author keywords

Calixarenes; DABCO; Porphyrins

Indexed keywords

1,4 DIAZABICYCLO[2.2.2]OCTANE; AMIDE; CALIXARENE; CALIX[4]ARENE; MACROCYCLIC COMPOUND; METALLOPORPHYRIN; NITROGEN; PORPHYRIN DERIVATIVE; THIACALIX[4]ARENE; UNCLASSIFIED DRUG; ZINC DERIVATIVE;

EID: 0037474629     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)00290-4     Document Type: Article
Times cited : (58)

References (40)
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    • Sanders, J.K.M.1
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    • Kluwer Academic: Dordrecht
    • For books on calixarenes see: (a) In Calixarenes; Asfari, Z., Böhmer V., Harrowfield J., Vicens J., Eds.; Kluwer Academic: Dordrecht, 2001. (b) Gutsche, C. D. In Calixarenes rivisited. Monographs in Supramolecular Chemistry. Stoddart, J. F., Ed,; The Royal Society of Chemistry: Cambridge, 1998; Vol. 6. (c) Calixarenes 50th Aniversary: Commemorative Issue; Vicens, J., Asfari, Z., Harrowfield, J. M., Eds.; Kluwer Academic: Dordrecht, 1994. (d) In Calixarenes: A Versatile Class of Macrocyclic Compounds; Vicens J., Böhmer V. Kluwer Academic: Dordrecht, 1991.
    • (2001) Calixarenes
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    • The Royal Society of Chemistry: Cambridge
    • For books on calixarenes see: (a) In Calixarenes; Asfari, Z., Böhmer V., Harrowfield J., Vicens J., Eds.; Kluwer Academic: Dordrecht, 2001. (b) Gutsche, C. D. In Calixarenes rivisited. Monographs in Supramolecular Chemistry. Stoddart, J. F., Ed,; The Royal Society of Chemistry: Cambridge, 1998; Vol. 6. (c) Calixarenes 50th Aniversary: Commemorative Issue; Vicens, J., Asfari, Z., Harrowfield, J. M., Eds.; Kluwer Academic: Dordrecht, 1994. (d) In Calixarenes: A Versatile Class of Macrocyclic Compounds; Vicens J., Böhmer V. Kluwer Academic: Dordrecht, 1991.
    • (1998) Monographs in Supramolecular Chemistry , vol.6
    • Gutsche, C.D.1
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    • Kluwer Academic: Dordrecht
    • For books on calixarenes see: (a) In Calixarenes; Asfari, Z., Böhmer V., Harrowfield J., Vicens J., Eds.; Kluwer Academic: Dordrecht, 2001. (b) Gutsche, C. D. In Calixarenes rivisited. Monographs in Supramolecular Chemistry. Stoddart, J. F., Ed,; The Royal Society of Chemistry: Cambridge, 1998; Vol. 6. (c) Calixarenes 50th Aniversary: Commemorative Issue; Vicens, J., Asfari, Z., Harrowfield, J. M., Eds.; Kluwer Academic: Dordrecht, 1994. (d) In Calixarenes: A Versatile Class of Macrocyclic Compounds; Vicens J., Böhmer V. Kluwer Academic: Dordrecht, 1991.
    • (1994) Calixarenes 50th Aniversary: Commemorative Issue
    • Vicens, J.1    Asfari, Z.2    Harrowfield, J.M.3
  • 9
    • 0003433022 scopus 로고
    • Kluwer Academic: Dordrecht
    • For books on calixarenes see: (a) In Calixarenes; Asfari, Z., Böhmer V., Harrowfield J., Vicens J., Eds.; Kluwer Academic: Dordrecht, 2001. (b) Gutsche, C. D. In Calixarenes rivisited. Monographs in Supramolecular Chemistry. Stoddart, J. F., Ed,; The Royal Society of Chemistry: Cambridge, 1998; Vol. 6. (c) Calixarenes 50th Aniversary: Commemorative Issue; Vicens, J., Asfari, Z., Harrowfield, J. M., Eds.; Kluwer Academic: Dordrecht, 1994. (d) In Calixarenes: A Versatile Class of Macrocyclic Compounds; Vicens J., Böhmer V. Kluwer Academic: Dordrecht, 1991.
    • (1991) Calixarenes: A Versatile Class of Macrocyclic Compounds
    • Vicens, J.1    Böhmer, V.2
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    • range=3.19-67.90°). Hydrogen atoms linked to carbon atoms were located from expected geometry and were not refined. Hydroxyl hydrogen atoms were located from Fourier difference electron density map
    • range=3.19-67.90°). Hydrogen atoms linked to carbon atoms were located from expected geometry and were not refined. Hydroxyl hydrogen atoms were located from Fourier difference electron density map.
  • 30
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    • range=2.85-59.91°). Hydrogen atoms linked to carbon atoms were located from expected geometry and were not refined. Hydroxyl hydrogen atoms were located from Fourier difference electron density map. Ψ-scan was used for absorption correction
    • range=2.85-59.91°). Hydrogen atoms linked to carbon atoms were located from expected geometry and were not refined. Hydroxyl hydrogen atoms were located from Fourier difference electron density map. Ψ-scan was used for absorption correction.
  • 31
    • 85031206804 scopus 로고    scopus 로고
    • range=2.75-67.93°). Hydrogen atoms linked to carbon atoms were located from expected geometry and were not refined. Hydroxyl hydrogen atoms were located from Fourier difference electron density map. Ψ-scan was used for absorption correction
    • range=2.75-67.93°). Hydrogen atoms linked to carbon atoms were located from expected geometry and were not refined. Hydroxyl hydrogen atoms were located from Fourier difference electron density map. Ψ-scan was used for absorption correction.


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