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Synthesis of Polycarbonates and Poly(ether carbonate)s Directly from Carbon Dioxide and Diols Promoted by a
Shi Bian1, Cale Pagan1, Anastasia A Andrianova Artemyeva1
1Department of Chemistry, University of North Dakota, 151 Cornell Street Stop 9024, Grand Forks, North Dakota 58202, United States.
Abstract:
Recently, polycarbonates have attracted considerable research interest because of their potential biodegradability and sustainability. Here, we present a direct route for the synthesis of polycarbonates and poly(ether carbonate)s from carbon dioxide (CO2) and diols, promoted by Cs2CO3 and CH2Cl2 under 1 atm of CO2. Quantitative conversion of diols and polymers with up to 11 kg/mol molecular weight could be obtained. While benzylic diols lead to predominantly carbonate linkage, aliphatic diols result in the incorporation of the methylene unit of CH2Cl2 that produces poly(ether carbonate)s. Both primary and secondary diols have been successfully incorporated into the polymer chain.
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Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.