메뉴 건너뛰기




Volumn , Issue 4, 2004, Pages 770-775

A [2]catenane containing 1,1′-binaphthyl units and 1,10-phenanthroline fragments: Synthesis and intermolecular energy transfer processes

Author keywords

Catenanes; Chirality; Copper; Luminescence; Template synthesis

Indexed keywords

1,1' BINAPHTHYL DERIVATIVE; 1,10 PHENANTHROLINE; 2,9 DIPHENYL 1,10 PHENANTHROLINE; CATENANE; COPPER COMPLEX; PHENYL GROUP; TRANSITION ELEMENT; UNCLASSIFIED DRUG;

EID: 4644273571     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200300572     Document Type: Article
Times cited : (20)

References (39)
  • 2
    • 0001063693 scopus 로고
    • [2a] D. M. Walba, Tetrahedron 1985, 41, 3161-3212.
    • (1985) Tetrahedron , vol.41 , pp. 3161-3212
    • Walba, D.M.1
  • 4
    • 84990165706 scopus 로고
    • [2b] C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. 1989, 101, 192-194; Angew. Chem. Int. Ed. Engl. 1989, 28, 189-192.
    • (1989) Angew. Chem. Int. Ed. Engl. , vol.28 , pp. 189-192
  • 7
    • 0035796728 scopus 로고    scopus 로고
    • [2d] F. Vögtle, A. Hünten, E. Vogel, S. Buschbeck, O. Safarowsky, J. Recker, A.-H. Parham, M. Knott, W. M. Müller, U. Müller, Y. Okamoto, T. Kudota, W. Lindner, E. Francotte, S. Grimme, Angew. Chem. 2001, 113, 2534-2537; Angew. Chem. Int. Ed. 2001, 40, 2468-2471.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 2468-2471
  • 13
    • 0000493601 scopus 로고
    • Topologically chiral catenanes and rotaxanes: [3f] D. K. Mitchell, J.-P. Sauvage, Angew. Chem. 1988, 700, 985-987; Angew. Chem. Int. Ed. Engl. 1988, 27, 930-931.
    • (1988) Angew. Chem. , vol.700 , pp. 985-987
    • Mitchell, D.K.1    Sauvage, J.-P.2
  • 14
    • 84990149537 scopus 로고
    • Topologically chiral catenanes and rotaxanes: [3f] D. K. Mitchell, J.-P. Sauvage, Angew. Chem. 1988, 700, 985-987; Angew. Chem. Int. Ed. Engl. 1988, 27, 930-931.
    • (1988) Angew. Chem. Int. Ed. Engl. , vol.27 , pp. 930-931
  • 20
    • 0000718373 scopus 로고    scopus 로고
    • Pertinent review: L. Pu, Chem. Rev. 1998, 98, 2405-2494.
    • (1998) Chem. Rev. , vol.98 , pp. 2405-2494
    • Pu, L.1
  • 22
    • 0003445429 scopus 로고    scopus 로고
    • (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin
    • [6b] Comprehensive Asymmetric Catalysis, vols. 1-3 (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999.
    • (1999) Comprehensive Asymmetric Catalysis , vol.1-3
  • 25
    • 0002670124 scopus 로고    scopus 로고
    • (Eds.: J. L. Atwood, J. E. D. Davies, D. D. MacNicol, F. Vögtle, J.-M. Lehn, J.-P. Sauvage, M. W. Hosseini), Pergamon, Oxford
    • J.-C. Chambron, C. Dietrich-Buchecker, J.-P. Sauvage, in Comprehensive Supramolecular Chemistry, vol. 9 (Eds.: J. L. Atwood, J. E. D. Davies, D. D. MacNicol, F. Vögtle, J.-M. Lehn, J.-P. Sauvage, M. W. Hosseini), Pergamon, Oxford, 1996, pp. 43-83.
    • (1996) Comprehensive Supramolecular Chemistry , vol.9 , pp. 43-83
    • Chambron, J.-C.1    Dietrich-Buchecker, C.2    Sauvage, J.-P.3
  • 26
    • 4644354851 scopus 로고    scopus 로고
    • note
    • Preparation of 2-[2-(iodoethoxy)ethoxy]ethanol: A solution of 2-[2-(chloroethoxy)ethoxy]ethanol (1.68 g, 10.0 mmol) and NaI (3.2 g, 16.0 mmol) in acetone (50 mL) was heated under reflux for 4 h. The solvent was then evaporated and diethyl ether (30 mL) was added to the residue. The suspension was filtered to remove the excess of NaI and NaCl. The solution was concentrated to dryness to afford 2-[2-(iodoethoxy)ethoxy]ethanol in quantitative yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.