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Volumn , Issue 3, 1998, Pages 299-303

Dinuclear molybdenum(III) and tungsten(III) Calix[4]arene complexes - Metal-metal triple bonds supported by bridging Calix[4]arene Ligands

Author keywords

Calix 4 arene complexes; Calix 4 arenes; Metal metal bonding; Molybdenum; Tungsten

Indexed keywords

CHEMICAL BONDS; LIGANDS; MOLYBDENUM COMPOUNDS; SPECTROSCOPIC ANALYSIS; TRANSITION METALS; TUNGSTEN COMPOUNDS; X RAY DIFFRACTION;

EID: 0001812278     PISSN: 14341948     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-0682(199803)1998:3<299::AID-EJIC299>3.0.CO;2-Q     Document Type: Article
Times cited : (11)

References (33)
  • 1
    • 0004146786 scopus 로고
    • The Royal Society of Chemistry, Cambridge
    • For reviews on calixarenes see for example: - [1a] C. D. Gutsche, Calixarenes, The Royal Society of Chemistry, Cambridge 1989. [1b] J. Vincens, V. Böhmer (ed.), Calixarenes: A versatile Class of Macrocyclic Compounds, Kluwer, Dordrecht 1991. [1c] C. D. Gutsche, Prog. Macrocycl. Chem. 1987, 3, 93-165. [1d] V. Böhmer, Angew. Chem. 1995, 107, 785-818; Angew. Chem. Int. Ed. Engl. 1995, 34, 713-745. [1e] D. M. Roundhill, Prog. Inorg. Chem. 1995, 43, 533-565.
    • (1989) Calixarenes
    • Gutsche, C.D.1
  • 2
    • 0003433022 scopus 로고
    • Kluwer, Dordrecht
    • For reviews on calixarenes see for example: - [1a] C. D. Gutsche, Calixarenes, The Royal Society of Chemistry, Cambridge 1989. [1b] J. Vincens, V. Böhmer (ed.), Calixarenes: A versatile Class of Macrocyclic Compounds, Kluwer, Dordrecht 1991. [1c] C. D. Gutsche, Prog. Macrocycl. Chem. 1987, 3, 93-165. [1d] V. Böhmer, Angew. Chem. 1995, 107, 785-818; Angew. Chem. Int. Ed. Engl. 1995, 34, 713-745. [1e] D. M. Roundhill, Prog. Inorg. Chem. 1995, 43, 533-565.
    • (1991) Calixarenes: A Versatile Class of Macrocyclic Compounds
    • Vincens, J.1    Böhmer, V.2
  • 3
    • 0002137126 scopus 로고
    • For reviews on calixarenes see for example: - [1a] C. D. Gutsche, Calixarenes, The Royal Society of Chemistry, Cambridge 1989. [1b] J. Vincens, V. Böhmer (ed.), Calixarenes: A versatile Class of Macrocyclic Compounds, Kluwer, Dordrecht 1991. [1c] C. D. Gutsche, Prog. Macrocycl. Chem. 1987, 3, 93-165. [1d] V. Böhmer, Angew. Chem. 1995, 107, 785-818; Angew. Chem. Int. Ed. Engl. 1995, 34, 713-745. [1e] D. M. Roundhill, Prog. Inorg. Chem. 1995, 43, 533-565.
    • (1987) Prog. Macrocycl. Chem. , vol.3 , pp. 93-165
    • Gutsche, C.D.1
  • 4
    • 0000948055 scopus 로고
    • For reviews on calixarenes see for example: - [1a] C. D. Gutsche, Calixarenes, The Royal Society of Chemistry, Cambridge 1989. [1b] J. Vincens, V. Böhmer (ed.), Calixarenes: A versatile Class of Macrocyclic Compounds, Kluwer, Dordrecht 1991. [1c] C. D. Gutsche, Prog. Macrocycl. Chem. 1987, 3, 93-165. [1d] V. Böhmer, Angew. Chem. 1995, 107, 785-818; Angew. Chem. Int. Ed. Engl. 1995, 34, 713-745. [1e] D. M. Roundhill, Prog. Inorg. Chem. 1995, 43, 533-565.
    • (1995) Angew. Chem. , vol.107 , pp. 785-818
    • Böhmer, V.1
  • 5
    • 33748539998 scopus 로고
    • For reviews on calixarenes see for example: - [1a] C. D. Gutsche, Calixarenes, The Royal Society of Chemistry, Cambridge 1989. [1b] J. Vincens, V. Böhmer (ed.), Calixarenes: A versatile Class of Macrocyclic Compounds, Kluwer, Dordrecht 1991. [1c] C. D. Gutsche, Prog. Macrocycl. Chem. 1987, 3, 93-165. [1d] V. Böhmer, Angew. Chem. 1995, 107, 785-818; Angew. Chem. Int. Ed. Engl. 1995, 34, 713-745. [1e] D. M. Roundhill, Prog. Inorg. Chem. 1995, 43, 533-565.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 713-745
  • 6
    • 85050553296 scopus 로고
    • For reviews on calixarenes see for example: - [1a] C. D. Gutsche, Calixarenes, The Royal Society of Chemistry, Cambridge 1989. [1b] J. Vincens, V. Böhmer (ed.), Calixarenes: A versatile Class of Macrocyclic Compounds, Kluwer, Dordrecht 1991. [1c] C. D. Gutsche, Prog. Macrocycl. Chem. 1987, 3, 93-165. [1d] V. Böhmer, Angew. Chem. 1995, 107, 785-818; Angew. Chem. Int. Ed. Engl. 1995, 34, 713-745. [1e] D. M. Roundhill, Prog. Inorg. Chem. 1995, 43, 533-565.
    • (1995) Prog. Inorg. Chem. , vol.43 , pp. 533-565
    • Roundhill, D.M.1
  • 12
    • 0030499686 scopus 로고    scopus 로고
    • [2e] L. Giannini, E. Solari, A. Zanotti-Gerosa, C. Floriani, A. Chiesi-Villa, C. Rizzoli, Angew. Chem. 1996, 108, 3051-3053; Angew. Chem. Int. Ed. Engl. 1996, 35, 2825-2827.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 2825-2827
  • 15
    • 0000226773 scopus 로고    scopus 로고
    • [2g] L. Giannini, E. Solari, A. Zanotti-Gerosa, C. Floriani, A. Chiesi-Villa, C. Rizzoli, Angew. Chem. 1997, 109, 763-765; Angew. Chem Int. Ed. Engl. 1997, 36, 763-765.
    • (1997) Angew. Chem Int. Ed. Engl. , vol.36 , pp. 763-765
  • 23
    • 85163240242 scopus 로고    scopus 로고
    • manuscript in preparation
    • U. Radius, J. Attner, manuscript in preparation.
    • Radius, U.1    Attner, J.2
  • 25
    • 0003393086 scopus 로고
    • deGruyter, Berlin
    • The hydrogen oxygen distances in water are assumed to be 0.99 Å for the O-H bond and 1.76 Å for the hydrogen bridge to the next water molecule, see: A. F. Hollemann, E. Wiberg, Lehrbuch der Anorganischen Chemie, 33rd edition, deGruyter, Berlin 1985, p. 285.
    • (1985) Lehrbuch der Anorganischen Chemie, 33rd Edition , pp. 285
    • Hollemann, A.F.1    Wiberg, E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.