Carbon dioxide copolymerization with

Copolymerization of carbon dioxide possibly also belongs to this class of polymerizations. Carbon dioxide copolymerizes with epoxides to polyanhydrides, with aziridines to polyurethanes, and with vinyl ethers to poly-ketoethers, i.e.. 

Some copolymerizations have been studied where one of the reactants is a compound not usually considered as a monomer. These include copolymerizations of epoxides and higher cyclic ethers with carbon dioxide, episulhdes with carbon dioxide and carbon disulhde, and epoxides with sulfur dioxide [Aida et al., 1986 Baran et al., 1984 Chisholm et al., 2002 Inoue and Aida, 1989 Soga et al., 1977]. The copolymers are reported to be either 1 1 alternating copolymers or contain 1 1 alternating sequences together with blocks of the cyclic monomer. 

Transformation of carbon dioxide, particularly, in synthesis of oxazolidi-nones and cyclic carbonates or copolymerization with oxiranes 07CRV2365. 

A novel catalytic system based on aluminum porphyrins has been developed. It is particularly effective for the living ring-opening polymerization of epoxides and lactones and for the copolymerization of epoxides with carbon dioxide and with cyclic anhydrides. HNMR has demonstrated that the growing species of this initiating system is that shown in (3). 

Azelaic, sebacic, dodecanedioic, and brassyhc acids may be used in copolyetheresteramides (111). Two patents describe additional apphcations for the C-9—C-40 diacids for the preparation of polyester carbonates (112), and the copolymerization of epoxides and carbon dioxide by reaction of either glutaric or adipic acids with zinc oxide (113). 

An alternative method for generating enriched 1,2-diols from meso-epoxides consists of asymmetric copolymerization with carbon dioxide. Nozaki demonstrated that a zinc complex formed in situ from diethylzinc and diphenylprolinol catalyzed the copolymerization with cyclohexene oxide in high yield. Alkaline hydrolysis of the isotactic polymer then liberated the trans diol in 94% yield and 70% ee (Scheme 7.20) [40]. Coates later found that other zinc complexes such as 12 are also effective in forming isotactic polymers [41-42]. 

Copolymers of carbon monoxide, carbon dioxide, sulfur dioxide or carbon disulfide are frequently formed in combination with oxiranes, thiiranes or aziridines. Copolymerization of carbon monoxide and ethylenimine was carried out under radiation and the formation of 3-nylon was observed238. ... 

In our previous work [8], we rqjorted the synthesis of (2-oxo-l,3-dioxolan-4-yl)methacrylate (DOMA) finrn carbon dioxide and glycidyl methacrylate (GMA) using quaternary salt catalysts. In the present work, we studied the catalytic pra rmance of alkyhnethyl imidazolium salt ionic liquid in the synthesis of polycarbonate from the copolyraerization of CO2 with GMA. The influences of copolymerization variable like catalyst structure and reaction tenperature on the conversion of GMA and the yield of the polycarbonate have been discussed. 

It has been shown by Barb and by Dainton and Ivin that a 1 1 complex formed from the unsaturated monomer (n-butene or styrene) and sulfur dioxide, and not the latter alone, figures as the comonomer reactant in vinyl monomer-sulfur dioxide polymerizations. Thus the copolymer composition may be interpreted by assuming that this complex copolymerizes with the olefin, or unsaturated monomer. The copolymerization of ethylene and carbon monoxide may similarly involve a 1 1 complex (Barb, 1953). 

Palladium(II) complexes possessing bidentate ligands are known to efficiently catalyze the copolymerization of olefins with carbon monoxide to form polyketones.594-596 Sulfur dioxide is an attractive monomer for catalytic copolymerizations with olefins since S02, like CO, is known to undergo facile insertion reactions into a variety of transition metal-alkyl bonds. Indeed, Drent has patented alternating copolymerization of ethylene with S02 using various palladium(II) complexes.597 In 1998, Sen and coworkers also reported that [(dppp)PdMe(NCMe)]BF4 was an effective catalyst for the copolymerization of S02 with ethylene, propylene, and cyclopentene.598 There is a report of the insertion reactions of S02 into PdII-methyl bonds and the attempted spectroscopic detection of the copolymerization of ethylene and S02.599... 

Equations 1 to 3 show some of fixation reactions of carbon dioxide. Equations la and lb present coupling reactions of CO2 with diene, triene, and alkyne affording lactone and similar molecules [2], in a process catalyzed by low valent transition metal compounds such as nickel(O) and palladium(O) complexes. Another interesting CO2 fixation reaction is copolymerization of CO2 and epoxide yielding polycarbonate (equation 2). This reaction is catalyzed by aluminum porphyrin and zinc diphenoxide [3],... 

Lu and coworkers have synthesized a related bifunctional cobalt(lll) salen catalyst similar to that seen in Fig. 11 that contains an attached quaternary ammonium salt (Fig. 13) [36]. This catalyst was found to be very effective at copolymerizing propylene oxide and CO2. For example, in a reaction carried out at 90°C and 2.5 MPa pressure, a high molecular weight poly(propylene carbonate) = 59,000 and PDI = 1.22) was obtained with only 6% propylene carbonate byproduct. For a polymerization process performed under these reaction conditions for 0.5 h, a TOF (turnover frequency) of 5,160 h was reported. For comparative purposes, the best TOF observed for a binary catalyst system of (salen)CoX (where X is 2,4-dinitrophenolate) onium salt or base for the copolymerization of propylene oxide and CO2 at 25°C was 400-500 h for a process performed at 1.5 MPa pressure [21, 37]. On the other hand, employing catalysts of the type shown in Fig. 12, TOFs as high as 13,000 h with >99% selectivity for copolymers withMn 170,000 were obtained at 75°C and 2.0 MPa pressure [35]. The cobalt catalyst in Fig. 13 has also been shown to be effective for selective copolymer formation from styrene oxide and carbon dioxide [38]. 

We have utilized somewhat less-effective optional approaches to copolymer purification with attendant catalyst recovery. One of these methods involved the replacement of the f-butyl substituents on the 5-position of the phenolate ligands with poly(isobutylene) (PIB) groups, as illustrated in Fig. 14 [39]. Importantly, this chromium(III) catalyst exhibited nearly identical activity as its 3,5-di-t-butyl analog for the copolymerization of cyclohexene oxide and carbon dioxide. The PIB substituents on the (salen)CrCl catalysts provide high solubility in heptanes once the copolymer is separated from the metal center by a weak acid. 

Wang JT, Zhu Q, Lu XL, Meng YZ (1995) ZnGA-MMT catalyzed the copolymerization of carbon dioxide with propylene oxide. Eur Polym J 41 1108-1114... 

Shi L, Lu X-B, Zhang R, Peng X-J, Zhang C-Q, Li J-E, Peng X-M (2006) Asymmetric alternating copolymerization and terpolymerization of epoxides with carbon dioxide at mild conditions. Macromolecules 39 5679-5685... 

Hsu T, Tan C (2002) Block copolymerization of carbon dioxide with cyclohexene oxide and 4-vinyl-1-cyclohexene-1,2-epoxide in based poly(propylene carbonate) by yttrium-metal... 

Kim G, Ree M, Kim H, Kim IJ, Kim JR, I-ee JI (2008) Biological affinity and biodegradability of poly(propylene carbonate) prepared from copolymerization of carbon dioxide with propylene oxide. Macromol Res 16 473-480... 

The living anionic ends can be functionalized by adding such agents as ethylene oxide, carbon dioxide, and methacryloyl chloride [33]. The resulting new polymer is capable of being copolymerized with additional monomers. This process can lead to the formation of various graft copolymers [29-32]. 

Oxetanes can be copolymerized very successfully with a wide range of other monomers and even carbon dioxide, to give plastic compositions with a wide variety of properties. Naturally, this area has been the subject of a great deal of research, and many patents have appeared which are beyond the scope of this survey. 

In 1978, Inoue reported the first example of a single-site catalyst, a tetraphenyl-porphyrin aluminium chloride complex (Fig. 18a), which was used with EtPh3PBr as a co-catalyst [109, 110]. The complex was used to copolymerize PO and carbon dioxide it was very slow (taking up to 23 days) but did produce PPC of low molecular weight and narrow PDI. Later, in 2003, the manganese(III) acetate analogue of this complex was the first example of a catalyst capable of copolymerizing CHO and C02 under 1 atm pressure. 

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