Li-qin Xie a, Jun-xiao Yang a, Fang-hua Zhu b, et al. SYNTHESIS AND CHARACTERIZATION OF BENZOCYCLOBUTEN-4-YL ACRYLATE MONOMER AND ITS RADICAL POLYMERIZATION[J]. 2010, 28(6): 877-885.
DOI:
Li-qin Xie a, Jun-xiao Yang a, Fang-hua Zhu b, et al. SYNTHESIS AND CHARACTERIZATION OF BENZOCYCLOBUTEN-4-YL ACRYLATE MONOMER AND ITS RADICAL POLYMERIZATION[J]. 2010, 28(6): 877-885.DOI: 10.1007/s10118-010-9160-4.
SYNTHESIS AND CHARACTERIZATION OF BENZOCYCLOBUTEN-4-YL ACRYLATE MONOMER AND ITS RADICAL POLYMERIZATION
A benzocyclobuten-4-yl acrylate (1) monomer was prepared by esterification of 4-hydroxybenzocyclobutene with acryloyl chloride. The radical homopolymerization of 1 and copolymerization of 1 with styrene or n-butyl acrylate were carried out to produce linear polymers 2a
2b and 2c. Heating of these linear polymers under thermal initiation gave corresponding cross-linked polymers 3a
3b and 3c. The ring-opening reaction in the cross-linking process was confirmed by on-line infrared spectra. Differential scanning calorimetry showed that the glass transition temperatures of linear polymers 2a and 2b were 83.2°C and 68.1°C
respectively. Thermogravimetric analysis of the cross-linked polymers showed that they all exhibited good thermal stability.
Abstract
A benzocyclobuten-4-yl acrylate (1) monomer was prepared by esterification of 4-hydroxybenzocyclobutene with acryloyl chloride. The radical homopolymerization of 1 and copolymerization of 1 with styrene or n-butyl acrylate were carried out to produce linear polymers 2a
2b and 2c. Heating of these linear polymers under thermal initiation gave corresponding cross-linked polymers 3a
3b and 3c. The ring-opening reaction in the cross-linking process was confirmed by on-line infrared spectra. Differential scanning calorimetry showed that the glass transition temperatures of linear polymers 2a and 2b were 83.2°C and 68.1°C
respectively. Thermogravimetric analysis of the cross-linked polymers showed that they all exhibited good thermal stability.
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