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Volumn 3, Issue 4, 1997, Pages 601-608

Homoleptic cuprates(II) with multiply deprotonated α-cyclodextrin ligands

Author keywords

copper; cuprates; cyclodextrins; structure elucidation

Indexed keywords


EID: 0040254925     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.19970030416     Document Type: Article
Times cited : (39)

References (28)
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    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 884-887
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    • N. Habermann, M. Klaassen, P. Klüfers, Carbohydr. Res. 1993, 241, 9-23; N. Habermann, G. Jung, M. Klaassen, P. Klüfers, Chem. Ber. 1992, 125, 809-814; M. Klaassen, P. Klüfers, Z. Anorg. Allg. Chem. 1993, 619, 661-666; M. Klaassen, P. Klüfers, Acta Crystallogr. Sect. C 1994, 50, 686-688; M. Klaassen, P. Klüfers, Z. Anorg. Allg. Chem. 1994, 620, 1631-1634.
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    • Habermann, N.1    Klaassen, M.2    Klüfers, P.3
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    • N. Habermann, M. Klaassen, P. Klüfers, Carbohydr. Res. 1993, 241, 9-23; N. Habermann, G. Jung, M. Klaassen, P. Klüfers, Chem. Ber. 1992, 125, 809-814; M. Klaassen, P. Klüfers, Z. Anorg. Allg. Chem. 1993, 619, 661-666; M. Klaassen, P. Klüfers, Acta Crystallogr. Sect. C 1994, 50, 686-688; M. Klaassen, P. Klüfers, Z. Anorg. Allg. Chem. 1994, 620, 1631-1634.
    • (1992) Chem. Ber. , vol.125 , pp. 809-814
    • Habermann, N.1    Jung, G.2    Klaassen, M.3    Klüfers, P.4
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    • 84987245988 scopus 로고
    • N. Habermann, M. Klaassen, P. Klüfers, Carbohydr. Res. 1993, 241, 9-23; N. Habermann, G. Jung, M. Klaassen, P. Klüfers, Chem. Ber. 1992, 125, 809-814; M. Klaassen, P. Klüfers, Z. Anorg. Allg. Chem. 1993, 619, 661-666; M. Klaassen, P. Klüfers, Acta Crystallogr. Sect. C 1994, 50, 686-688; M. Klaassen, P. Klüfers, Z. Anorg. Allg. Chem. 1994, 620, 1631-1634.
    • (1993) Z. Anorg. Allg. Chem. , vol.619 , pp. 661-666
    • Klaassen, M.1    Klüfers, P.2
  • 6
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    • N. Habermann, M. Klaassen, P. Klüfers, Carbohydr. Res. 1993, 241, 9-23; N. Habermann, G. Jung, M. Klaassen, P. Klüfers, Chem. Ber. 1992, 125, 809-814; M. Klaassen, P. Klüfers, Z. Anorg. Allg. Chem. 1993, 619, 661-666; M. Klaassen, P. Klüfers, Acta Crystallogr. Sect. C 1994, 50, 686-688; M. Klaassen, P. Klüfers, Z. Anorg. Allg. Chem. 1994, 620, 1631-1634.
    • (1994) Acta Crystallogr. Sect. C , vol.50 , pp. 686-688
    • Klaassen, M.1    Klüfers, P.2
  • 7
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    • N. Habermann, M. Klaassen, P. Klüfers, Carbohydr. Res. 1993, 241, 9-23; N. Habermann, G. Jung, M. Klaassen, P. Klüfers, Chem. Ber. 1992, 125, 809-814; M. Klaassen, P. Klüfers, Z. Anorg. Allg. Chem. 1993, 619, 661-666; M. Klaassen, P. Klüfers, Acta Crystallogr. Sect. C 1994, 50, 686-688; M. Klaassen, P. Klüfers, Z. Anorg. Allg. Chem. 1994, 620, 1631-1634.
    • (1994) Z. Anorg. Allg. Chem. , vol.620 , pp. 1631-1634
    • Klaassen, M.1    Klüfers, P.2
  • 10
    • 0012850058 scopus 로고
    • Compare with the structures of the cuprates formed with the isomeric hexitols dulcitol (P. Klüfers, J. Schuhmacher, Angew. Chem. 1994, 106, 1839-1841; Angew. Chem. Int. Ed. Engl. 1994, 33, 1742-1744) and D-sorbitol (P. Klüfers. J. Schuhmacher. Angew. Chem. 1995, 107, 2290-2292; Angew. Chem. Int. Ed. Engl. 1995, 34, 2119-2121).
    • (1994) Angew. Chem. , vol.106 , pp. 1839-1841
    • Klüfers, P.1    Schuhmacher, J.2
  • 11
    • 33748243498 scopus 로고
    • Compare with the structures of the cuprates formed with the isomeric hexitols dulcitol (P. Klüfers, J. Schuhmacher, Angew. Chem. 1994, 106, 1839-1841; Angew. Chem. Int. Ed. Engl. 1994, 33, 1742-1744) and D-sorbitol (P. Klüfers. J. Schuhmacher. Angew. Chem. 1995, 107, 2290-2292; Angew. Chem. Int. Ed. Engl. 1995, 34, 2119-2121).
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 1742-1744
  • 12
    • 0004963606 scopus 로고
    • Compare with the structures of the cuprates formed with the isomeric hexitols dulcitol (P. Klüfers, J. Schuhmacher, Angew. Chem. 1994, 106, 1839-1841; Angew. Chem. Int. Ed. Engl. 1994, 33, 1742-1744) and D-sorbitol (P. Klüfers. J. Schuhmacher. Angew. Chem. 1995, 107, 2290-2292; Angew. Chem. Int. Ed. Engl. 1995, 34, 2119-2121).
    • (1995) Angew. Chem. , vol.107 , pp. 2290-2292
    • Klüfers, P.1    Schuhmacher, J.2
  • 13
    • 33748245893 scopus 로고
    • Compare with the structures of the cuprates formed with the isomeric hexitols dulcitol (P. Klüfers, J. Schuhmacher, Angew. Chem. 1994, 106, 1839-1841; Angew. Chem. Int. Ed. Engl. 1994, 33, 1742-1744) and D-sorbitol (P. Klüfers. J. Schuhmacher. Angew. Chem. 1995, 107, 2290-2292; Angew. Chem. Int. Ed. Engl. 1995, 34, 2119-2121).
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 2119-2121
  • 16
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    • F. Hoelkeskamp, Papier (Darmstadt) 1962, 16, 102-105: ibid. 1964, 18, 201-204.
    • (1964) Papier (Darmstadt) , vol.18 , pp. 201-204
  • 19
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    • a) R. Fuchs, N. Habermann, P. Klüfers, Angew. Chem. 1993, 105, 895-897; Angew. Chem. Int. Ed. Engl. 1993, 32, 852-854;
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 852-854
  • 21
    • 33749279503 scopus 로고
    • b) for the structure of a lead(II) complex of γ-cyclodextrin see: P. Klüfers, J. Schuhmacher, ibid. 1994, 106, 1925-1927; 1994, 33, 1863-1865.
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 1863-1865
  • 22
    • 85036447220 scopus 로고    scopus 로고
    • note
    • Further details of the crystal structure investigation may be obtained from the Fachinformationszentrum Karlsruhe, D-76344 Eggenstein-Leopoldshafen (Germany), on quoting the depository numbers CSD-405771 (1), CSD-405770 (2), CSD-405769 (3a) and CSD-405768 (3b).
  • 24
    • 0008271897 scopus 로고
    • 2] establishing O2⋯O2 hydrogen bonds: R. Fuchs, N. Habermann, P. Klüfers, Angew. Chem. 1993, 105, 895-897; Angew. Chem. Int. Ed. Engl. 1993, 32, 852-854.
    • (1993) Angew. Chem. , vol.105 , pp. 895-897
    • Fuchs, R.1    Habermann, N.2    Klüfers, P.3
  • 25
    • 33748232757 scopus 로고
    • 2] establishing O2⋯O2 hydrogen bonds: R. Fuchs, N. Habermann, P. Klüfers, Angew. Chem. 1993, 105, 895-897; Angew. Chem. Int. Ed. Engl. 1993, 32, 852-854.
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 852-854
  • 26
    • 0003766353 scopus 로고
    • Springer, Berlin
    • G. A. Jeffrey, W. Saenger. Hydrogen Bonding in Biological Structures, Springer, Berlin, 1991, p. 312: the authors interpret structural changes of cyclodextrin hosts on forming inclusion compounds in terms of an induced-fit mechanism exhibited by enzymes.
    • (1991) Hydrogen Bonding in Biological Structures , pp. 312
    • Jeffrey, G.A.1    Saenger, W.2
  • 27
    • 0000604323 scopus 로고    scopus 로고
    • D. Philp, J. F. Stoddart, Angew. Chem. 1996, 108, 1243-1286; Angew. Chem. Int. Ed. Engl. 1996, 35, 1154-1196.
    • (1996) Angew. Chem. , vol.108 , pp. 1243-1286
    • Philp, D.1    Stoddart, J.F.2
  • 28
    • 0029811409 scopus 로고    scopus 로고
    • D. Philp, J. F. Stoddart, Angew. Chem. 1996, 108, 1243-1286; Angew. Chem. Int. Ed. Engl. 1996, 35, 1154-1196.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1154-1196


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.