1973
DOI: 10.1016/0032-3861(73)90003-7
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Copolymers of methyl methacrylate with cinnamic acid

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Cited by 8 publications
(4 citation statements)
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“…Recently, they have been applied as antibacterial agents for suppression of bacterial growth [1][2][3] or as a monomer unit to modify the properties of polymer materials. 4,5 Trans-cinnamic acid undergoes a [2+2] cycloaddition reaction under photoirradiation, and therefore it has a potential application in memory storage materials. 6,7 In connection with these various applications, 13 C-labelled derivatives of cinnamic acid can serve as valuable mechanistic probes.…”
Section: Introductionmentioning
confidence: 99%
“…Recently, they have been applied as antibacterial agents for suppression of bacterial growth [1][2][3] or as a monomer unit to modify the properties of polymer materials. 4,5 Trans-cinnamic acid undergoes a [2+2] cycloaddition reaction under photoirradiation, and therefore it has a potential application in memory storage materials. 6,7 In connection with these various applications, 13 C-labelled derivatives of cinnamic acid can serve as valuable mechanistic probes.…”
Section: Introductionmentioning
confidence: 99%
“…[62][63][64] Methacrylic acid and acrylic acid both possess lower volatility 65 than styrene and can be modified to further reduce volatility, impart higher strength, or promote adhesion. [66][67][68] Beyond the present work, there is a wide slate of olefinic monomers that can be obtained from lignin deconstruction. 69 These monomers resemble substituted methylstyrenes and eugenols and might require further reaction development or modification.…”
Section: Discussionmentioning
confidence: 89%
“…[ 456 ] However, these harsh conditions hamper the large‐scale use of this methodology. Due to the difficulty of homopolymerizing cinnamates, several research groups have focused on their radical copolymerization with various comonomers, including MMA, [ 459,460 ] maleic anhydride, [ 461 ] fumarates, [ 462 ] methyl acrylate, [ 460 ] acrylonitrile, [ 460 ] or electron‐donating styrene. [ 460,463–468 ] M n of the order of 10 000 g mol −1 could be obtained but the incorporation of cinnamates was generally low.…”
Section: Polymerization Of (Meth)acrylic Monomers and Analogsmentioning
confidence: 99%