Propargyl calix[4]arenes and their complexes with silver(I) and gold(I)

Wei Xu, Jagadese J. Vittal, Richard J. Puddephatt*

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    39 Scopus citations


    A calix[4]arene 1b has been substituted at the lower rim by reaction with propargyl bromide to give either the 1,3- bis(propargyl) derivative 26, which is formed regioselectively, or the tetrakis(O-propargyl)calix[4]arene 3 under different reaction conditions. The molecular structure of 2b has been characterized by X-ray analysis (monoclinic, space group P21/c, Z = 4, a = 10.960(1), b = 24.302(3), c = 10.673(1) Å, β = 112.99(8)°, R = 0.0516). The molecules of 2b in the crystal are arranged in a "head-to-head, tail-to-tail" manner with a phenyl substituent of one molecule partly enclosed in the bowlic cavity of another. Since the two OCH2C≡CH groups are accessible, 2b can be polymerized by heating to 250°C and the polymerized propargyl calix[4]arene derivatives are stable up to 460°C. Compound 3 exists as a mixture of conformers, the ratio of partial cone to 1,3-alternate conformations being 4:1 or 2:1, dependent on the preparative conditions. These propargyl calix[4]arene derivatives can be further derivatized to form silver(I) or gold(I) alkynyl units by reaction with AgNO3 or [AuCl(SMe2)], respectively, and base. Further reaction of these transition metal complexes with phosphines yields calixarene derivatives with two metalphosphine units at the lower rim of the calix[4]arene bowl.

    Original languageEnglish (US)
    Pages (from-to)766-774
    Number of pages9
    JournalCanadian Journal of Chemistry
    Issue number5
    StatePublished - Jan 1 1996


    • Calix[4]arene
    • Gold
    • Polymer
    • Propargyl
    • Silver

    ASJC Scopus subject areas

    • Catalysis
    • Chemistry(all)
    • Organic Chemistry


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