2015
DOI: 10.1016/j.jfluchem.2015.07.002
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Functional styrenic copolymer based on 2-(dimethylamino)ethyl methacrylate: Reactivity ratios, biological activity thermal properties and semi-conducting properties

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Cited by 17 publications
(12 citation statements)
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References 40 publications
(29 reference statements)
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“…The reactivity ratio of DMD ( r DMD ) increased from 0.42 for CPDA to 0.93 for TPDA, whereas the reactivity ratio of AM ( r AM ) decreased from 5.62 for CPDA to 3.84 for TPDA. These changes implied that the homopolymerization ability of DMD increased and that of AM declined . When two monomer reactivity ratios are both greater than 1 in the binary polymerization, the reaction can be considered to be block copolymerization, which generates a block structure in the polymer molecular chain .…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The reactivity ratio of DMD ( r DMD ) increased from 0.42 for CPDA to 0.93 for TPDA, whereas the reactivity ratio of AM ( r AM ) decreased from 5.62 for CPDA to 3.84 for TPDA. These changes implied that the homopolymerization ability of DMD increased and that of AM declined . When two monomer reactivity ratios are both greater than 1 in the binary polymerization, the reaction can be considered to be block copolymerization, which generates a block structure in the polymer molecular chain .…”
Section: Resultsmentioning
confidence: 99%
“…These changes implied that the homopolymerization ability of DMD increased and that of AM declined. 26 When two monomer reactivity ratios are both greater than 1 in the binary polymerization, the reaction can be considered to be block copolymerization, which generates a block structure in the polymer molecular chain. 27 In this study, r DMD and r AM were respectively 0.93 and 3.84 after template addition, which nearly met the requirement of block polymerization.…”
Section: Resultsmentioning
confidence: 99%
“…One of the ways to estimate the monomer distribution of a copolymer chain is to determine monomer reactivity ratios (MRRs) via diverse linear least-squares methods including the Finemann-Ross (FR), inverted FR and Kelen-Tudos (KT) methods. [39][40][41][42][43][44][45] In this study, MRRs of poly(SS-co-AMPS), and poly(SPA-co-AMPS) were determined (see Figure 2). The data fit best for the FR method (R 2 ≥ 0.92) although the reactivity ratios determined using the inverted FR and KT methods still predicted the same type of monomer distribution (data not shown).…”
Section: Monomer Reactivity Ratiosmentioning
confidence: 99%
“…In PAD copolymerization, r AM and r DMC were both lower than 1, which indicated the monomer copolymerization ability was stronger than that of homopolymerization [26]. Therefore, monomers inclined to copolymerize disorderly, forming shorter chain segments of same units in polymer molecule.…”
Section: Resultsmentioning
confidence: 99%
“…The reactivity ratios of AM and cationic monomers calculated according to three methods are shown in Table 3 and the results were close to those of the previous study. In PAD copolymerization, r AM and r DMC were both lower than 1, which indicated the monomer copolymerization ability was stronger than that of homopolymerization [ 26 ]. Therefore, monomers inclined to copolymerize disorderly, forming shorter chain segments of same units in polymer molecule.…”
Section: Resultsmentioning
confidence: 99%