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2,4,5-Trichlorophenyl acrylate

Theato et al. [19] studied the polymerization of activated esters such as 2,4,5-trichlorophenyl acrylate and endo-N-hydroxy-5-norbornene-2,3-dicarboxyimide acrylate (NORB, Fig. 1) using ATRP. They showed that the polymer side chains were reactive by performing a couphng reaction with ammonia. [Pg.22]

Table 5. C-13 chemical shifts of 2,4,5-trichlorophenyl acrylate (AOTcp), polyAOTcp and equimolar copoly(AOTcp-styrene)... Table 5. C-13 chemical shifts of 2,4,5-trichlorophenyl acrylate (AOTcp), polyAOTcp and equimolar copoly(AOTcp-styrene)...
Table b. Examples of activated resin intermediates (8) produced by suspension copolymerization of styrene with 2,4,5-trichlorophenyl acrylate and a crosslinking monomer [46]... [Pg.13]

Reddy, B. S. R., Arshady, R., and George, M. H., 1985, Copolymerization of N-vinyl-2-pyrrolidone with 2,4,5-trichlorophenyl acrylate and with 2-hydroxyethyl methacrylate. Reactivity ratios and molecular weights. Eur. Polym. J. 21 (6) 511-515. [Pg.222]

A reactive methylene may be joined to a ring-nitrogen by heating with one of several malonic acid derivatives methyl 2-cyano-3,3-di(methyIthio)acrylate [207IJ, a 2,4,6-trichlorophenyl malonate (1(M.I0) [2382, 3258] or diethyl ethoxymethylenemalonate [3S. The last named reagent was successful where several others failed. [Pg.678]

See other pages where 2,4,5-Trichlorophenyl acrylate is mentioned: [Pg.8]    [Pg.10]    [Pg.60]    [Pg.8]    [Pg.10]    [Pg.60]    [Pg.191]    [Pg.191]    [Pg.648]    [Pg.219]    [Pg.219]    [Pg.281]   
See also in sourсe #XX -- [ Pg.22 ]



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3.4.5- Trichlorophenyl

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