Propylene oxide with cyclic acid anhydrides

Finally, the catalytic activity of DMCs in esterification reactions can be readily combined with their catalytic activity in epoxide ring-opening polymerizations, as was reported by Suh et al. [35]. This study showed that the copolymerization of propylene oxide with cyclic acid anhydrides such as succinic, maleic, or phthalic anhydride, catalyzed by a Zn-Co-DMC, afforded polyester polyols characterized by a moderate molecular weight and narrow polydispersity index. 

The tendency towards alternation in the oxirane/cyclic acid anhydride system with the zinc-based coordination catalyst is connected, according to literature data [193], with the stronger nucleophilic properties of the oxygen atom of the zinc alcoholate species and the weaker electrophilic properties of the zinc atom in such species compared with the respective properties of zinc carboxylate species. Studies of the copolymerisation of propylene oxide and maleic anhydride in the presence of catalysts such as diethylzinc-monoprotic compound (1 1) showed an increasing tendency towards alternation in systems with catalysts of decreasing electrophilicity of the zinc atom [186], which may corroborate the coordination mechanism proposed scheme (24). 

Among such oxidations, note that liquid-phase oxidations of solid paraffins in the presence of heterogeneous and colloidal forms of manganese are accompanied by a substantial increase (compared with homogeneous catalysis) in acid yield [3]. The effectiveness of n-paraffin oxidations by Co(III) macrocomplexes is high, but the selectivity is low the ratio between fatty acids, esters, ketones and alcohols is 3 3 3 1. Liquid-phase oxidations of paraffins proceed in the presence of Cu(II) and Mn(II) complexes boimd with copolymers of vinyl ether, P-pinene and maleic anhydride (Amberlite IRS-50) [130]. Oxidations of both linear and cyclic olefins have been studied more intensively. Oxidations of linear olefins proceed by a free-radical mechanism the accumulation of epoxides, ROOH, RCHO, ketones and RCOOH in the course of the reaction testifies to the chain character of these reactions. The main requirement for these processes is selectivity non-catalytic oxidation of propylene (at 423 K) results in the formation of more than 20 products. Acrylic acid is obtained by oxidation of propylene (in water at 338 K) in the presence of catalyst by two steps at first to acrolein, then to the acid with a selectivity up to 91%. Oxidation of ethylene by oxygen at 383 K in acetic acid in... 

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