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Volumn 9, Issue 5, 2007, Pages 345-349

Polypseudorotaxane architecture of poly-bis4-(N-benzyl- pyridinium)piperazine-hexa-thiocyanato-di-cadmium(ii) with 2-D honeycomb-like Cd(SCN)3nn- anionic polymeric framework

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EID: 34248212279     PISSN: 14668033     EISSN: 14668033     Source Type: Journal    
DOI: 10.1039/b701229b     Document Type: Article
Times cited : (27)

References (58)
  • 3
    • 34248144740 scopus 로고    scopus 로고
    • J. L. Atwood and J. W. Steed, Marcel Dekker, New York, 1453
    • D. V. Soldatov and J. A. Ripmeester, Supramolecular Stabilization, in Encyclopedia of Supramolecular Chemistry, ed., J. L. Atwood, and, J. W. Steed, Marcel Dekker, New York, 2004, 1453
    • (2004) Supramolecular Stabilization, in
    • Soldatov, D.V.1    Ripmeester, J.A.2
  • 8
    • 0004260153 scopus 로고
    • J. R. Norris and D. Meisel, Elsevier, New York
    • Photochemical Energy Conversion, ed., J. R. Norris, and, D. Meisel, Elsevier, New York, 1989
    • (1989) Photochemical Energy Conversion, Ed.
  • 18
    • 34248153569 scopus 로고    scopus 로고
    • Rotaxanes and Pseudorotaxanes
    • J. L. Atwood and J. W. Steed, Marcel Dekker, New York, 1194
    • P. Linnartz and C. A. Schalley, Rotaxanes and Pseudorotaxanes, in Encyclopedia of Supramolecular Chemistry, ed., J. L. Atwood, and, J. W. Steed, Marcel Dekker, New York, 2004, 1194
    • (2004) Encyclopedia of Supramolecular Chemistry, Ed.
    • Linnartz, P.1    Schalley, C.A.2
  • 20
    • 34248160831 scopus 로고    scopus 로고
    • In a true rotaxane the axle is restrained to remain inside the wheel due to bulky ending groups, while in a pseudorotaxane the restriction occurs due to noncovalent forces between the two molecules
    • In a true rotaxane the axle is restrained to remain inside the wheel due to bulky ending groups, while in a pseudorotaxane the restriction occurs due to noncovalent forces between the two molecules


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.