Chain transfer polymerization of methyl methacrylate initiated by organolanthanide complexes

• Published in: Macromolecular chemistry and physics Vol. 201; no. 17; pp. 2282 - 2288
• Main Authors: Nodono, Mitsufumi, Tokimitsu, Toru, Tone, Seiji, Makino, Takayuki, Yanagase, Akira
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY-VCH Verlag GmbH 01.11.2000; WILEY‐VCH Verlag GmbH; Wiley
• Subjects: Applied sciences; Exact sciences and technology; Organic polymers; Physical Sciences; Physicochemistry of polymers; Polymer Science; Polymerization; Preparation, kinetics, thermodynamics, mechanism and catalysts; Science & Technology; THERMAL-DEGRADATION; CATALYSIS; POLYMERS; POLY(METHYL METHACRYLATE); ETHYLENE; LINKAGES; ZIEGLER-NATTA POLYMERIZATION; Polymerization modifier; Thiol; Rare earth metal complex; Living polymer; Methyl methacrylate polymer; Samarium Organic compounds; Complex catalyst polymerization; Experimental study; Syndiotactic polymer; Ketone; Metallocene; Samarium complex; Thermal stability; Chain transfer; Optical properties; Reaction mechanism; Stereospecific polymerization; Chemical reactivity
• ISSN: 1022-1352; 1521-3935
• DOI: 10.1002/1521-3935(20001101)201:17<2282::AID-MACP2282>3.0.CO;2-K

A novel chain transfer polymerization mediated by Cp*2 Sm(III) species and organic acids is described. The chain transfer polymerization involves the reaction of organic acids such as thiols or ketones with an active bond between samarium(III) and the enolate at a living chain end of poly(methyl methacrylate) (PMMA). This chain transfer reaction resulted in termination of the living chain end and the regeneration of the active initiator which would consist of (C5Me5)2Sm(III) and deprotonated organic acids. The chain transfer polymerization were confirmed by turnover numbers (TON). tert‐Butyl thiol exhibited the chain transfer reactivity effectively to control the molecular weight of PMMA without decreasing of the polymer yield and the stereoregularity. As a result of this chain transfer polymerization, thermal and optical properties of the PMMA obtained were improved by the control of chain end groups or by reducing a large amount of the samarium initiator.