Journal ArticleDOI
Physical properties of aliphatic polycarbonates made from CO2 and epoxides
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TLDR
In this paper, a homologous series of aliphatic polycar-bonates with different side-chain lengths was synthesized by ring-opening polymerization of terminal epoxides with CO2 using zinc adipionate as catalyst.Abstract:
A homologous series of aliphatic polycar- bonates with different side-chain lengths was synthesized by ring-opening polymerization of terminal epoxides with CO2 using zinc adipionate as catalyst (patented process of Empower Materials (formerly PAC Polymers Inc.)). Addi- tionally, a polycarbonate was made having a cyclohexane unit in its backbone, together with a terpolymer having both cyclohexane and propylene units. After characterization of thermal properties the aliphatic polycarbonates were found to be completely amorphous. Polycarbonates derived from long-chain epoxides showed a glass-transition temperature (Tg) below room temperature, whereas polycarbonates de- rived from cyclohexene oxide showed a Tg of 105°C, the highest yet reported for this class of polymers. The initial decomposition temperature of the polymers in air and ni- trogen atmospheres was found to be less than 300°C. The mechanical properties and the dynamic mechanical relax- ation behavior of the polymers were also reported. The effect of the chemical structure on the physical properties of ali- phatic polycarbonates was discussed. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1163-1176, 2003read more
Citations
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Journal ArticleDOI
Making plastics from carbon dioxide: salen metal complexes as catalysts for the production of polycarbonates from epoxides and CO2.
Journal ArticleDOI
Discrete Metal-Based Catalysts for the Copolymerization of CO2 and Epoxides: Discovery, Reactivity, Optimization, and Mechanism
TL;DR: Well-defined catalysts for epoxide-CO(2) copolymerization and related reactions are reviewed here.
Journal ArticleDOI
Transition-metal-catalyzed C–C bond formation through the fixation of carbon dioxide
TL;DR: This critical review summarizes the recent advances on transition-metal-catalyzed C-C bond formation through the fixation of carbon dioxide and their synthetic applications.
Journal ArticleDOI
Catalysts for CO2/epoxide copolymerisation
TL;DR: The article reviews recent developments (mostly since 2004 until June 2010) in catalysts for CO(2)/epoxide copolymerisation and in the properties of the polycarbonates.
Journal ArticleDOI
CO2-fixation into cyclic and polymeric carbonates: Principles and applications
TL;DR: In this paper, a review of the advancements made within this field is critically discussed with special attention to the potential of these two classes of compounds as green chemical products: cyclic and polymeric carbonates.
References
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Book
Anelastic and Dielectric Effects in Polymeric Solids
TL;DR: Menard et al. as mentioned in this paper discuss the use of dynamic mechanical analysis (DMA) as a tool for thermal analysis, rheology, and materials science in the analytical laboratory.
Journal ArticleDOI
Copolymerization of carbon dioxide and epoxide
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Copolymerization of carbon dioxide and epoxide with organometallic compounds
TL;DR: In this paper, the first success in using carbon dioxide as a direct starting material for synthesizing high polymers was reported, which was confirmed with the aid of IR, NMR and elemental analysis.
Journal ArticleDOI
Catalytic Reactions Involving C1 Feedstocks: New High-Activity Zn(II)-Based Catalysts for the Alternating Copolymerization of Carbon Dioxide and Epoxides
Journal ArticleDOI
Phenyl-perfluorophenyl stacking interactions : topochemical 2+2 photodimerization and photopolymerization of olefinic compounds
Geoffrey W. Coates,Alexander R. Dunn,Lawrence M. Henling,Joseph W. Ziller,and Emil B. Lobkovsky,Robert H. Grubbs +5 more
TL;DR: The face-to-face stacking interaction between phenyl and perfluorophenyl groups is emerging as a common non-covalent interaction as mentioned in this paper, and the generality of this supramolecular synthon, the solid-state packing structure and reactivity of several monoole fins and diolefins substituted with phenyl groups was investigated.