Polymerizations ring opering

Sumitomo, H. and Okada, M. Ring-Opering Polymerization of Bicyclic Acetals, Oxalactone, and Oxalactam. Vol. 28, pp. 47—82. 

This scheme is remarkably close to the coordination insertion mechanism believed to operate in the metal alkoxide-catalyzed ring-opening polymerization of cyclic esters (see Section 2.3.6). It shares many features with the mechanism proposed above for the metal alkoxide-catalyzed direct polyesterification (Scheme 2.18), including the difficulty of defining reaction orders. 

Microspheres by solvent extraction method were obtained with rate of mixing equal 300 rev/s. Particles by spray drying were produced with spray dryer operated with an inlet temperature of 50°C and outlet temperature of 45°C. The air flow indicator was set at 700 and the aspirator at 5. The polymer solution (concentration 0.5% wt/v) was supplied at 10 mL/min. The concentrations of monomer, initiator, and surfactant in ring-opening dispersion polymerization leading to microspheres were as follows [Lc]o = 2.77 10 mol/L, [tin(II) 2-ethyUiexanoate]o = 4.9 10 mol/L, [poly(DA-CL)] = 1.6 g/L. 

The most common units found in borate structures are shown in Fig. 1. Many of the known borate structures can be rationalized by assigning appropriate charges, protons, or hydroxyl groups (which change the coordination of boron from trigonal to tetrahedral) to these basic units. Thus the B03 unit can become BOj -, B(OH)3, or B(0H)4, respectively. Polymerization by elimination of one water molecule between two hydrated units results in chain formation, and further water elimination gives sheets or networks. These operations are illustrated in Fig. 2 for the triborate ring unit. 

Another curing mechanism is operative in the curing reaction initiated by a polymerization catalyst for epoxy ring opening, where anionic catalysts such as tertiary amines 1S-l9) and imidazols 20 21> and cationic catalysts such as amine complexes of... 

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