Modification of chitosan with polystyrene and poly(n-butyl acrylate) via nitroxide-mediated polymerization and grafting from approach in homogeneous media

2015 ◽  
Vol 6 (15) ◽  
pp. 2827-2836 ◽  
Author(s):  
O. García-Valdez ◽  
R. Champagne-Hartley ◽  
E. Saldívar-Guerra ◽  
P. Champagne ◽  
M. F. Cunningham

Nitroxide-mediated polymerization was used to graft modify solubilized chitosan, allowing the reaction to be performed homogeneously.

2021 ◽  
pp. 096739112110245
Author(s):  
Amrita Sharma ◽  
PP Pande

It has been observed that acrylate monomers are very difficult to polymerize with the low cost nitroxide catalyst 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO). Therefore, costly acyclic nitroxides such as N-tert-butyl-N-(1-diethylphosphono-2,2-dimethyl)-N-oxyl, (SG1), 2,2,5-Trimethyl-4-phenyl-3-azahexane-3-nitroxide (TIPNO) and TIPNO derivatives have to be used for the polymerization of the acrylic acid derivatives. There are very few reports on the use of TEMPO-derivatives toward the polymerization of n-butyl acrylate. Generally different reducing agents viz. glucose, ascorbic acid, hydroxyacetone etc. have been used to destroy excess TEMPO during the polymerization reaction. The acrylate polymerizations fail in the presence of TEMPO due to the strong C–O bond formed between the acrylate chain end and nitroxide. To the best of our knowledge, no literature report is available on the use of TEMPO without reducing agent or high temperature initiators, toward the polymerization of n-butyl acrylate. The present study has been carried out with a view to re-examine the application of low cost nitroxide TEMPO, so that it can be utilized towards the polymerization of acrylate monomers (e.g. n-butyl acrylate). We have been able to polymerize n-butyl acrylate using the nitroxide TEMPO as initiator (via a macroinitiator). In this synthesis, a polystyrene macroinitiator was synthesized in the first step from TEMPO, after this TEMPO end-capped styrene macroinitiator (PSt-TEMPO) is used to polymerize n-butyl acrylate monomer. The amount of macroinitiator taken was varied from 0.05% to 50% by weight of n-butyl acrylate monomer. The polymerization was carried out at 120°C by bulk polymerization method. The experimental findings showed a gradual increase in molecular weight of the polymer formed and decrease in the polydispersity index (PDI) with increase in amount of PSt-TEMPO macroinitiator taken. In all experiments conversion was more than 80%. These results indicate that the polymerization takes place through controlled polymerization process. Effect of different solvents on polymerization has also been investigated. In the following experiments TEMPO capped styrene has been used as macroinitiator leading to the successful synthesis of poly n-Butyl acrylate. It has been found that styrene macroinitiator is highly efficient for the nitroxide mediated polymerization, even in very small concentration for the synthesis of poly n-butyl acrylate. High concentration of macroinitiator results in the formation of block copolymers of polystyrene and poly ( n-butyl acrylate) viz. polystyrene-block-poly-( n-butyl acrylate). The use of TEMPO toward controlled polymerization is of much importance, because it is the nitroxide commercially available at the lowest cost.


2019 ◽  
Vol 40 (10) ◽  
pp. 1800834 ◽  
Author(s):  
Jaime C. Cazotti ◽  
Alexander T. Fritz ◽  
Omar Garcia‐Valdez ◽  
Niels M. B. Smeets ◽  
Marc A. Dubé ◽  
...  

2010 ◽  
Vol 63 (8) ◽  
pp. 1237 ◽  
Author(s):  
Jessica Marchand ◽  
Laurent Autissier ◽  
Yohann Guillaneuf ◽  
Jean-Luc Couturier ◽  
Didier Gigmes ◽  
...  

Due to a specific balance between steric, polar, and stabilization effects, SG1 nitroxide and its corresponding alkoxyamine BlocBuilder MA are now well recognized as two of the most potent compounds in nitroxide-mediated polymerization (NMP). In this work, alternatives to SG1, based on various aldehydes, were targeted using structure–reactivity relationships already developed by our group. Compared with SG1, we show that the substitution of the tert-butyl group on the carbon α to the aminoxyl function by a 2-ethylhexyl group led to a new nitroxide (ETHEXNO), which exhibited an half-life time at 120°C similar to SG1 and a slightly slower kd for the alkoxyamine (2–3 times lower than the SG1). The styrene polymerization mediated by the ETHEXNO nitroxide has a similar behaviour to the one mediated by the SG1 in terms of livingness and control but the kinetics is affected (2–3 times lower). Concerning the n-butyl acrylate polymerization, an unexpected overheating occurred at 120°C, which led us to perform the polymerization in toluene at 100°C. The slow kinetics impedes the use of this nitroxide as a good alternative to SG1 and shows that the structure of the SG1 nitroxide is already delicately optimized and finding good alternatives is not straightforward.


Synthesis ◽  
2012 ◽  
Vol 44 (16) ◽  
pp. 2555-2559 ◽  
Author(s):  
Ilhyong Ryu ◽  
Armido Studer ◽  
Takahide Fukuyama ◽  
Yoshito Kajihara

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