The influences of monomer structure and solvent on the radical copolymerization of tertiary amine and PEGylated methacrylates
Literature Information
Priscila Quiñonez-Angulo, Robin A. Hutchinson, Ángel Licea-Claveríe, Enrique Saldívar-Guerra, Iván Zapata-González
Tertiary Amine Methacrylates (TAMAs), such as 2-(N,N-diethylamino)ethyl methacrylate (DEAEMA) and 2-(N,N-dimethylamino)ethyl methacrylate (DMAEMA), and PEGylated (macro)monomers, such as 2-ethoxyethyl methacrylate (EEMA1) and poly(ethylene glycol) methyl ether methacrylates with 9 and 23 units (PEGMA9 and PEGMA23, respectively), are two families of monomers frequently used in the synthesis of stimuli-responsive and biocompatible materials. They, along with methyl (MMA) and butyl (BMA) methacrylate, were used to synthesize a minilibrary of copolymers, namely poly(DEAEMA-co-EEMA1), poly(DEAEMA-co-PEGMA23), poly(DMAEMA-co-PEGMA9), poly(DMAEMA-co-PEGMA23), poly(DEAEMA-co-MMA), and poly(BMA-co-PEGMA9). The rate of copolymerization increased as the length of the PEG-side chain is decreased, and was higher for DEAEMA compared to DMAEMA systems. The estimated values of the reactivity ratios are: rDEAEMA = 0.61 ± 0.06 and rEEMA1 = 0.92 ± 0.09, rDEAEMA = 0.71 ± 0.15 and rPEGMA23 = 1.05 ± 0.21, rDMAEMA = 0.83 ± 0.01 and rPEGMA9 = 1.08 ± 0.02, rDMAEMA = 0.52 ± 0.09 and rPEGMA23 = 0.76 ± 0.14, and rBMA = 0.55 ± 0.13 and rPEGMA9 = 0.38 ± 0.09; p-dioxane at 70 °C: rDEAEMA = 0.91 ± 0.12 and rPEGMA9 = 0.75 ± 0.09; and tetrahydrofuran at 66 °C: rDEAEMA = 0.96 ± 0.13 and rPEGMA9 = 0.81 ± 0.11. While there was no difference in relative reactivity between the two amine-functional monomers when copolymerized with PEGylated methacrylates, the increased relative activity of the TAMAs compared to BMA is attributed to the formation of a cyclic intermediate. Additionally, as the PEG side-chain length is extended, the reactivity ratios for the amino monomers decreased. Finally, although a higher content of DEAEMA is incorporated in the copolymer for the poly(DEAEMA-co-MMA) when a more polar solvent is used, no differences were observed in the Mayo–Lewis plots for the poly(DEAEMA-co-PEGMA23) using p-dioxane, tetrahydrofuran and ethanol.
Related Literature
Two new quinoline-based regenerable fluorescent probes with AIE characteristics for selective recognition of Cu2+ in aqueous solution and test strips
Jingwen Xiong, Zongzhi Li, Jihua Tan, Shaomin Ji, Jianwei Sun, Xianwei Li, Yanping Huo
DOI: 10.1039/C8AN00940F
Determination of the illegal adulteration of natural healthcare products with chemical drugs using surface-enhanced Raman scattering
Jiawei Wu, Lixia Zhang, Xiangfeng Bu, Peng Li, Bing Zhao, Yuan Tian
DOI: 10.1039/C8AN01286E
Real time plasmonic qPCR: how fast is ultra-fast? 30 cycles in 54 seconds
Philip J. R. Roche, Mohamed Najih, Seung S. Lee, Lenore K. Beitel, Matthew L. Carnevale, Andrew G. Kirk
DOI: 10.1039/C7AN00304H
A reusable cyanide sensor via activation of C–H group: trifluoromethylcarbinol-directed meta-C–H cyanomethylation of naphthalimide
Yayun Chen, Xiaoxue Hu, Caihui Rao, Zheyao Li, Lu Chen, Chao Fu, Chuanxiang Liu
DOI: 10.1039/C8AN00718G
An efficient two-photon fluorescent probe for measuring γ-glutamyltranspeptidase activity during the oxidative stress process in tumor cells and tissues
Peng Wang, Jing Zhang, Hong-Wen Liu, Xiao-Xiao Hu, Xia Yin, Xiao-Bing Zhang
DOI: 10.1039/C7AN00229G
Nicotinamide adenine dinucleotide detection based on silver nanoclusters stabilized by a dumbbell-shaped probe
Hong-Ya Wang, Jin-Liang Ma, Bin-Cheng Yin
DOI: 10.1039/C7AN00293A
Can all bulk-phase reactions be accelerated in microdroplets?
Shibdas Banerjee, Elumalai Gnanamani, Xin Yan, Richard N. Zare
DOI: 10.1039/C6AN02225A
Efficient synthesis of riboflavin-imprinted magnetic nanoparticles by boronate affinity-based surface imprinting for the selective recognition of riboflavin
Daojin Li, Zijun Bie, Fangfang Wang, Enhui Guo
DOI: 10.1039/C8AN01044G
Effects and controls of capacitive hysteresis in ionic liquid electrochemical measurements
Anthony J. Lucio, Scott K. Shaw
DOI: 10.1039/C8AN01085D
You might also like
What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?
N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...
What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?
When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...
What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?
Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...
What is the market or research trend for oxocopper (CAS: 12053-18-8)?
The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...
What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?
The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...
What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?
2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...
What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?
2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...
How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?
(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...
What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?
3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...
How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?
Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...
Source Journal
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.











![1,10-bis(3,5-dimethylphenyl)-12-hydroxy-4,5,6,7-tetrahydroiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocine 12-oxide structure 1,10-bis(3,5-dimethylphenyl)-12-hydroxy-4,5,6,7-tetrahydroiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocine 12-oxide structure](https://static.chemtradehub.com/structs/141/1412439-82-7-b9a9.webp)


