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Syntheses acrylate

The only report on chemoenzymatic synthesis of branched polymers is from Peelers et al. [58], Heterotelechelic PCL macroinimer was synthesized in a one-pot enzymatic procedure by using 2-hydroxyethyl a-bromoisobutyrate as a bifunctional initiator. A polymerizable endgroup was introduced by subsequent in sim enzymatic acrylation with vinyl acrylate. Synthesis of branched polymers by self-condensing ATRP of the macroinimers was successfully conducted with and without the addition of MMA as a comonomer. [Pg.95]

Probably the nickel carbonyl-catalyzed synthesis of acrylates from CO, acetylene, and hydroxylic solvent (78) involves an acetylene-hydride insertion reaction, followed by a CO insertion, and hydrolysis or acyl halide elimination. The actual catalyst in the acrylate synthesis is probably a hydride formed by the reversible addition of an acid to nickel carbonyl. [Pg.193]

It has been very difficult to obtain direct evidence on the mechanism of the acrylate synthesis because the intermediate compounds are extremely reactive. [Pg.194]

At a considerably later date. Frankland prepared ethyl methacrylate and methacrylic acid from ethyl a-hydroxyisobutyrate and phosphorus trichloride. Tollen prepared aciylate esters from 2,3-dibromopropionate esters and zinc. Otto Rohm, in 1901. described the structures of the liquid condensation products (including dimers and timers) obtained from the action of sodium alkoxides on methyl and ethyl acrylate. Shortly after World War 1, Rohm introduced a new acrylate synthesis, noting that an acrylate is formed in good yield from heating ethylene cyanohydrin and sulfuric acid and alcohol. A major incentive for the development of a clear, tough plastic acrylate was for use in the manufacture of safety glass. [Pg.19]

Although today, more is understood about C02 coordination, knowledge of the coordination site requirements in various C02 reactions remains poor, as does that of cooperative interactions with co-ligands. Consequently, systematic studies of this important mechanistic aspect are required, using physico-chemical techniques and computer modeling. It is important to elucidate reaction mechanisms at the molecular level, and topics such as acrylic synthesis from ethylene and C02... [Pg.84]

In conclusion, the parallel formation of succinates is in agreement with tlie C9dstence of the o organometallic species proposed as an intermediate in the acrylate synthesis. [Pg.165]

Natural heterocyclic -acyl acrylates, synthesis of 86YGK819. [Pg.285]

Amine Acrylate Synthesis. During this study a number of amine acrylates and model compounds were synthesised. The syntheses were based on the Michael type addition of a secondary amine to an activated acrylate double bond. Our procedure is as follows. [Pg.348]

Knoop CA, Studer A (2003) Hydroxy- and silyloxy-substituted TEMPO derivatives for the living free-radical polymerization of styrene and n-butyl acrylate synthesis, kinetics, and mechanistic studies. J Am Chem Soc 125 16327-16333... [Pg.48]

Crestey, R, Collot, V, Stiebing, S. and Rault, S. (2006) Synthesis of new dehydro 2-azahyptophans and derivatives via Heck cross-coupling reactions of 3-iodoindazoles with methyl 2-(acetylamino)acrylate. Synthesis, 3506-14. [Pg.120]

R. A. Dickie, M. F. Cheung, and S. Newman, Heterogeneous Polymer-Polymer Composites. II. Preparation and Properties of Model Systems, J. Appl. Polym. Sci. 17, 65 (1973). Latex Semi-IPNs. Poly(methyl methacrylate)/poly(n-butyl acrylate). Synthesis, morphology, mechanical behavior. [Pg.246]

A variation of the conventional acrylate synthesis was developed by Rohm and Haas in the USA [578, 579] and Montecatini in Italy [580]. This process tries to combine the advantages of both the pressureless stoichiometric procedure and the low Ni(CO)4 catalyst concentration of the catalytic procedure. [Pg.120]

Recently the economic aspects of the acrylate synthesis from acetylene, carbon monoxide and alcohols were reviewed in European Chemical News [583]. The technology of the acrylate synthesis was reviewed in detail by M. Sittig [584]. [Pg.121]

Lodge, T.P., Bang, J.A., Li, Z.B. et al. (2005) Strategies for controlling intra- and intermicellar packing in block copolymer solutions Illustrating the flexibility of the self-assembly toolbox. Faraday Discussions, 128,1-12. Lu, Z.H., Liu, G.J., and Duncan, S. (2004) Polysulfone-graft-poly(tert-butyl acrylate) Synthesis, nanophase separation, poly(tert-butyl acrylate) hydrolysis, and pH-dependent iridescence. Macromolecules, 37,174—180. [Pg.760]

Zheng, R.H., Liu, G.J., and Jao, T.C. (2007) Poly[(2-ethylhexyl acrylate)-ron-(butyl acrylate)]-h/ock-poly (2-cinnamoyloxyethyl acrylate) synthesis and properties. Polymer, 48,7049-7057. [Pg.761]


See other pages where Syntheses acrylate is mentioned: [Pg.84]    [Pg.16]    [Pg.566]    [Pg.91]    [Pg.107]   
See also in sourсe #XX -- [ Pg.162 ]




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