Synthesis of 1-(vinylbenzyl)thymine, a novel, versatile multi-functional monomer

1995 ◽  
Vol 33 (14) ◽  
pp. 2515-2519 ◽  
Author(s):  
C. M. Cheng ◽  
M. I. Egbe ◽  
J. M. Grasshoff ◽  
D. J. Guarrera ◽  
R. P. Pai ◽  
...  
2021 ◽  
Author(s):  
Yifei Guo ◽  
Jingjing Du ◽  
Jianjun Li ◽  
Ran Yang ◽  
Peter B. de Harrington ◽  
...  

In this work, cysteamine-coated CdTe quantum dots (CA-CdTe QDs) were synthesized by a simple hydrothermal method employing cadmium chloride as the cadmium source and cysteamine hydrochloride as the functional monomer....


2006 ◽  
Vol 11-12 ◽  
pp. 757-760
Author(s):  
Jun Ying Zhang ◽  
Peng Dou

Environmentally benign adhesive was synthesized by dispersion copolymerization of styrene(St) and butyl acrylate (BA) in an ethanol medium with benzoyl peroxide (BPO) as the initiator and poly(vinylpyrrolidone) as the stabilizer in the presence of acrylic acid(AA) as the functional monomer. The effect of the concentration of stabilizer, initiator and functional monomer on the conversions, molecular weights and molecular weight distributions was investigated. The results show that the conversions almost keep invariable with the increasing of stabilizer concentration, but the molecular weights increase and molecular weight distributions decrease. Conversions increase with the increasing of initiator concentration, but the molecular weights and molecular weight distributions decrease. However with the increasing of functional monomer concentration, conversions and molecular weight distributions increase but the molecular weights decrease.


RSC Advances ◽  
2016 ◽  
Vol 6 (45) ◽  
pp. 39522-39529 ◽  
Author(s):  
Wanfen Pu ◽  
Daijun Du ◽  
Rui Liu ◽  
Jiongyi Gu ◽  
Kewei Li ◽  
...  

HDPAM was synthesized by water free-radical copolymerization based on functional hyperbranched polyamide-modified ultrafine silica as functional monomer.


2015 ◽  
Vol 124 (1) ◽  
pp. 96-102 ◽  
Author(s):  
Kenji Tsuchiya ◽  
Toshiki Takamizawa ◽  
Wayne W. Barkmeier ◽  
Keishi Tsubota ◽  
Akimasa Tsujimoto ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (18) ◽  
pp. 14496-14504 ◽  
Author(s):  
Sofyane Andjouh ◽  
Christine Bressy ◽  
Yves Blache

A series of bromotyramine-based 4-acryloyl-1,2,3-triazole monomers and polymers using click chemistry and RAFT polymerization.


2018 ◽  
Vol 16 (1) ◽  
pp. 12 ◽  
Author(s):  
Saeful Amin ◽  
Sophi Damayanti ◽  
Slamet Ibrahim

The research related to the interaction study, synthesis and characterization of molecular imprinted polymer using dimethylamylamine (DMAA) as the template molecule and the functional monomer methacrylate acid has been conducted. Molecular Imprinted Polymer (MIP) is a separation method made by the molecule template in the polymer matrix followed by removing the template molecule by washing for giving the permanent framework groove. The MIP was made by mixing the DMAA as the template molecule, with the methacrylate acid as the functional monomer, and the ethylene glycol dimethacrylate (EGDMA) as the crosslinker with the ratio 1:6:20. Porogen solvents used were the chloroform and the initiator azobisisobutyronitrile (AIBN). The crystal MIP and the NIP without the DMAA were characterized using Infrared Spectrophotometer (FTIR), and the result showed that there have been differences among the MIP, the NIP and the MIP after being extracted. The characterization using Scanning Electron Microscope (SEM) showed that the NIP as the comparison having flat morphology, while the MIP having irregular morphology and less pores. Then the MIP after being extracted has irregular, rough morphology and a lot of pores. The result reveals the interaction between the DMAA and the methacrylate acid that is the hydrogen bonded with the Gibbs free energy obtained is -5.434 j/mol. The imprinting factor of 2,353 is obtained. The highest desorption descending capacity is chloroform with the MIP 738% better. For the MIP and NIP methanol, it is found that the MIP is 123% better. Then the MIP which is desorbed by the chloroform is better 602% than the MIP resorbed by the methanol, and the ethyl acetate cannot desorb the DMAA.


Author(s):  
Marlene Prinsloo
Keyword(s):  

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