1985
DOI: 10.1016/0014-3057(85)90224-1
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Poly(alkyl itaconate)s. Formation of mixed esters and the properties of the resulting polymers

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Cited by 27 publications
(7 citation statements)
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“…It is well reported that the increase of the side-chain length leads to a decrease in T g values for both poly­(methacrylate)­s and poly­(itaconate)­s. However, the values obtained in the present work are quite close to those observed for PMMA and poly­(dimethyl itaconate) , polymers with considerable shorter side chains. Following this idea, poly­( n -propyl methacrylate) ( T g ≈ 35 °C), poly­( n -butyl methacrylate) ( T g ≈ 19 °C), poly­( n -propyl methyl itaconate) ( T g ≈ 63 °C), and poly­( n -butyl methyl itaconate) ( T g ≈ 42 °C) , can be considered as analogue polymers for PCNMA, PSO 2 MA, PCNMeiT, and PSO 2 MeiT, respectively, and present considerably lower transition temperatures. Higher T g values are observed for polymers containing functional groups with higher dipole moment, demonstrating that dipole interactions could play an important role.…”
Section: Resultsmentioning
confidence: 99%
“…It is well reported that the increase of the side-chain length leads to a decrease in T g values for both poly­(methacrylate)­s and poly­(itaconate)­s. However, the values obtained in the present work are quite close to those observed for PMMA and poly­(dimethyl itaconate) , polymers with considerable shorter side chains. Following this idea, poly­( n -propyl methacrylate) ( T g ≈ 35 °C), poly­( n -butyl methacrylate) ( T g ≈ 19 °C), poly­( n -propyl methyl itaconate) ( T g ≈ 63 °C), and poly­( n -butyl methyl itaconate) ( T g ≈ 42 °C) , can be considered as analogue polymers for PCNMA, PSO 2 MA, PCNMeiT, and PSO 2 MeiT, respectively, and present considerably lower transition temperatures. Higher T g values are observed for polymers containing functional groups with higher dipole moment, demonstrating that dipole interactions could play an important role.…”
Section: Resultsmentioning
confidence: 99%
“…20 Due to the structural similarity to acrylic acid (2) and methacrylic acid (3), itaconic acid and the corresponding esters, such as dimethylitaconate (4) and dibutylitaconate (5), have been intensively studied as an alternative monomer or comonomer to poly(meth)acrylates over the last few decades (Scheme 1a). 3,[21][22][23][24][25][26][27][28][29][30][31] Applications for this kind of polymer are widespread and range from corrosion inhibition 32 to dental materials, 33,34 elastomers, 35 and drug-delivery. [36][37][38][39][40][41] However, so far there have only been few studies in the field of polyesters based on itaconic acid (Scheme 1b).…”
Section: Stefan Friebelmentioning
confidence: 99%
“…The mono-esterification of the itaconic acid by using an alcohol such as methanol is a simple strategy for solving this issue because the effect of electron withdrawing from the vinyl group will be suppressed [7]. In spite of a number of monoesters, diesters and mixed-esters of itaconic acid have been synthesized and polymerized by radical polymerization [8]. The simplest and most inexpensive polymer based on itaconic acid derivative is poly(monomethyl itaconate).…”
Section: Introductionmentioning
confidence: 99%