Controlled free-radical polymerization of methyl acrylate in the presence of a cyclic trithiocarbonate under γ-ray irradiation at low temperature

• Published in: European polymer journal Vol. 43; no. 3; pp. 847 - 854
• Main Authors: Hua, Daoben, Ge, Xueping, Tang, Jing, Zhu, Xiulin, Bai, Ruke
• Format: Journal Article
• Language: English
• Published: Oxford Elsevier Ltd 01.03.2007; Elsevier
• Subjects: Applied sciences; Cyclic trithiocarbonate; Exact sciences and technology; Irradiation; Living polymerization; Low temperature; MALDI-TOF MS; Physicochemistry of polymers; Polymerization; Polymers and radiations; Irradiation; MALDI-TOF MS; Cyclic trithiocarbonate; Living polymerization; Low temperature; Organic trithiocarbonate; Radiochemical polymerization; Bulk polymerization; Living polymer; Experimental study; Methyl acrylate polymer; Macrocycle; Sulfur heterocycle; Gamma radiation; Preparation; Reaction mechanism; Room temperature
• ISSN: 0014-3057; 1873-1945
• DOI: 10.1016/j.eurpolymj.2006.12.022

Controlled radical polymerization of MA has been achieved in the presence of a cyclic trithiocarbonate, 1,5-dihydro-2,4-benzodiehiepine-3-thione, under γ-ray irradiation (60 Gy/min) at low temperature. The narrow molecular weight distributions and the linear kinetics curve indicate that the polymerization is a controlled free-radical process at low temperature (especially at −76 °C). The structures of resultant polymers were characterized by matrix assisted laser desorption/ionization time-of-flight mass spectrometry, and the results show that cyclic polymers can be formed at −76 °C, which may result from the reduced diffusion rate and the suppressed chain-transfer reaction at the lower temperature. It is further evidenced that the good control of the polymerization at the lower temperature may be associated with the suppressed chain-transfer reaction, not like reversible addition-fragmentation transfer polymerization. The linear polymers probably result from the polymer chain radicals reacting with the radicals produced by the interaction of the irradiation and the monomer.