Microwave-Assisted Reversible Addition-Fragmentation Chain Transfer Polymerization of Cationic Monomers in Mixed Aqueous Solvents

被引:2
作者
Tran, Jonathan D. [1 ]
Mikulec, Sydney N. [1 ]
Calzada, Oscar M. [1 ]
Prossnitz, Alexander N. [2 ]
Ennis, Amanda F. [1 ]
Sherwin, William J. [1 ]
Magsumbol, Alisson S. [1 ]
Jameson, Alexandra [1 ]
Schellinger, Joan G. [1 ]
机构
[1] Univ San Diego, Dept Chem & Biochem, 5998 Alcala Pk, San Diego, CA 92110 USA
[2] Univ Washington, Dept Bioengn, 3720 15th Ave NE, Seattle, WA 98105 USA
基金
美国国家科学基金会;
关键词
cationic monomers; microwave-assisted; N-(3-aminopropyl)methacrylamide hydrochloride; N-(3-dimethylaminopropyl)methacrylamide; reversible addition-fragmentation chain transfer; RAFT POLYMERIZATION; FACILE SYNTHESIS; TRANSFER AGENTS; POLYMERS; METHACRYLAMIDE; COPOLYMERS; ACRYLAMIDE; MEDIA; ATRP;
D O I
10.1002/macp.201900397
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Cationic polymers are an interesting class of macromolecules due to their versatility and emerging properties that can be used for various industrial and biomedical purposes. This report is focused on investigating the use of microwave heating in the reversible addition-fragmentation chain transfer polymerization of functional cationic monomers, N-(3-aminopropyl)methacrylamide hydrochloride (APMA) and N-[3-(dimethylamino)propyl]methacrylamide (DMAPMA). Under comparable polymerization reaction conditions, the microwave-assisted reaction achieves up to 270% (APMA) and 375% (DMAPMA) rate enhancement over conventional oil-bath mediated set-up. Linear relationships are observed between number average molecular weight and monomer conversion for different target degrees of polymerization to give low- to high-molecular-weight cationic polymers. Chain extension experiments show increase in molecular weight of the cationic polymers with narrow dispersities (<SIC> < 1.2) indicating retention of the chain transfer agent with no observable aminolysis or hydrolysis during polymerization.
引用
收藏
页数:7
相关论文
共 39 条
[1]   Progress of RAFT based polymers in gene delivery [J].
Ahmed, Marya ;
Narain, Ravin .
PROGRESS IN POLYMER SCIENCE, 2013, 38 (05) :767-790
[2]  
Alasino R.V., 2016, FRONT BIOMATER, V2, P3
[3]   Micrcowave-assisted controlled ring-closing cyclopolymerization of diallyldimethylammonium chloride via the RAFT process [J].
Assem, Yasser ;
Greiner, Andreas ;
Agarwal, Seema .
MACROMOLECULAR RAPID COMMUNICATIONS, 2007, 28 (18-19) :1923-1928
[4]   Shale inhibition by low-molecular-weight cationic polymer in water-based mud [J].
Beg, Mukarram ;
Singh, Priyanka ;
Sharma, Shivanjali ;
Ojha, Umaprasana .
JOURNAL OF PETROLEUM EXPLORATION AND PRODUCTION TECHNOLOGY, 2019, 9 (03) :1995-2007
[5]   Microwave-Assisted RAFT Polymerization [J].
Brooks, William L. A. ;
Sumerlin, Brent S. .
ISRAEL JOURNAL OF CHEMISTRY, 2012, 52 (3-4) :256-263
[6]   Ultra-fast microwave enhanced reversible addition-fragmentation chain transfer (RAFT) polymerization: monomers to polymers in minutes [J].
Brown, Steven L. ;
Rayner, Christopher M. ;
Graham, Susan ;
Cooper, Andrew ;
Rannard, Steven ;
Perrier, Sebastien .
CHEMICAL COMMUNICATIONS, 2007, (21) :2145-2147
[7]   Microwave-accelerated RAFT polymerization of polar monomers [J].
Brown, Steven L. ;
Rayner, Christopher M. ;
Perrier, Sebastien .
MACROMOLECULAR RAPID COMMUNICATIONS, 2007, 28 (04) :478-483
[8]   Cationic Antimicrobial Polymers and Their Assemblies [J].
Carmona-Ribeiro, Ana Maria ;
de Melo Carrasco, Leticia Dias .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (05) :9906-9946
[9]   Facile synthesis of controlled-structure primary amine-based methacrylamide polymers via the reversible addition-fragmentation chain transfer process [J].
Deng, Zhicheng ;
Bouchekif, Hassen ;
Babooram, Keshwaree ;
Housni, Adelghani ;
Choytun, Nankishoresing ;
Narain, Ravin .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2008, 46 (15) :4984-4996
[10]   Correspondence on Microwave Effects in Organic Synthesis [J].
Dudley, Gregory B. ;
Stiegman, Albert E. ;
Rosana, Michael R. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (31) :7918-7923