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Han Peng,1,2 Demin Jia,1 and Ben Zhong Tang2
1 Institute of Material Science and Engineering, South China University of Technology,Guangzhou 510641, China
2 Department of Chemistry, The Hong Kong University of Science & Technology,Clear Water Bay, Kowloon, Hong Kong, China
Poly(aryleneethynylene)s (PAEs) are conjugated polymers consisting of aromatic rings and alkyne rods. The high fluorescence quantum yields and excellent stability of PAEs make the polymers a class of prospective materials for photoluminescence (PL) applications.1 Linear unsubstituted PAE is, however, infusible and insoluble.1 Different strategies have been developed to improve its processability and the most common approach is to attach linear alkyl or alkoxy side chains to the rigid-rod polymer backbone. The solubility of the polymers is, however, still a problem limiting the scope of their potential applications. We have recently designed and synthesized a series of hyperbranched polyarylenes by simple one-pot polycyclotrimerizations of aromatic diynes with monoynes.2,3 The resultant polymers show excellent PL and optical limiting properties as well as outstanding thermal stability. In this work, a series of new hyperbranched PAEs were synthesized by the polycyclotrimerizations of polyynes (I and II) with monoynes (A, B and C) catalyzed by tantalum-, niobium- and cobalt-based catalysts (Scheme 1).
The copolymerizations of I and II with 1-octyne, 1-decyne, and 1-dodecyne are effected by tantalum-, niobium-, and cobalt-based catalysts, producing hyperbranched polyarylenes 1−4 with high molecular weights (Mw up to 2.8 × 104 Da) in high isolation yields (up to 97%). The polymerization results are summarized in Table 1. The