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Volumn , Issue 1, 2000, Pages 60-61

Calix[n]arenes provided with thiols for modified electrode applications; ring-size dependent voltammetric behavior toward ferrocene derivatives

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Indexed keywords


EID: 0034340848     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2000.60     Document Type: Article
Times cited : (8)

References (11)
  • 4
    • 33847497915 scopus 로고
    • In this paper calixarene derivatives used in the present study were further modified with L-cysteine and inclusion complex formation of the corresponding compounds was studied in an aqueous, homogeneous system. These authors reported that complex formation occurred with 8-anilino-1-naphthalenesulfonate (ANS) and pyrene. However, hole-size selectivity between the guest molecular size and the calixarene cavity size was somewhat unclear
    • T. Nagasaki, Y. Tajiri, and S. Shinkai, Recl. Trav. Chim. Pays-Bas, 112, 407 (1993). In this paper calixarene derivatives used in the present study were further modified with L-cysteine and inclusion complex formation of the corresponding compounds was studied in an aqueous, homogeneous system. These authors reported that complex formation occurred with 8-anilino-1-naphthalenesulfonate (ANS) and pyrene. However, hole-size selectivity between the guest molecular size and the calixarene cavity size was somewhat unclear.
    • (1993) Recl. Trav. Chim. Pays-Bas , vol.112 , pp. 407
    • Nagasaki, T.1    Tajiri, Y.2    Shinkai, S.3
  • 6
    • 0002134582 scopus 로고
    • ed by The Chemical Society of Japan, Maruzen, Tokyo
    • "Kagakubinran," 3rd ed (in Japanese), ed by The Chemical Society of Japan, Maruzen, Tokyo (1984), p. 11-68, p. 11-486.
    • (1984) "Kagakubinran," 3rd Ed (In Japanese) , pp. 11-68


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.