Evaluating the Effect of Termination by Chain - Chain Coupling in Living Free-Radical Polymerizations

2003 ◽  
Vol 56 (8) ◽  
pp. 775 ◽  
Author(s):  
Jeffrey Pyun ◽  
Ian Rees ◽  
Jean M. J. Fréchet ◽  
Craig J. Hawker

A novel approach based on the reaction of multifunctional star polymers with chromophore-labelled linear polymers is presented for evaluating the extent of termination by chain–chain coupling during living free-radical polymerizations. A mixed initiating system consisting of an unlabelled, multifunctional initiator and an excess of a monofunctional alkoxyamine initiator containing a chromophore, such as pyrene, is used to initiate the living polymerization of vinyl monomers leading to a mixture of star and linear polymers. The occurrence of chain–chain coupling is readily identified and quantified by isolating the star polymer that is obtained and elucidating the level of incorporation of pyrene units by UV/vis spectroscopy. This allows the level of chain–chain coupling to be determined since the inclusion of pyrene into the star structure is a direct result of termination by radical coupling.

2010 ◽  
Vol 48 (22) ◽  
pp. 5206-5214 ◽  
Author(s):  
Yuefang Yan ◽  
Wei Zhang ◽  
Yansheng Qiu ◽  
Zhengbiao Zhang ◽  
Jian Zhu ◽  
...  

2012 ◽  
Vol 1403 ◽  
Author(s):  
Danish Iqbal ◽  
C. Melchert ◽  
M. Behl ◽  
A. Lendlein ◽  
S. Beuermann

ABSTRACTModeling of free radical polymerizations of the liquid-crystalline monomer 6-[4-(4-heptyloxyphenylazo)phenoxy]hexylacrylate using the PREDICI software package is reported. The model accounts for all elemental reactions that were identified to be important for radical polymerizations of acrylate-type monomers. On the basis of butyl acrylate kinetic data a remarkable agreement between number average molar masses from modelling (Mn,sim) and from experiments (Mn,exp) is observed: Mn,sim = 17800 g·mol−1 and Mn,exp = 17400 g·mol−1. Similarly, dispersity values of 1.8 and 1.6 were determined via modelling and experiments, respectively. It is shown that the assumption of butyl acrylate kinetics provides a reasonable approximation even for acrylate-based monomers having mesogenic substituents.


2021 ◽  
Vol 2 (3) ◽  
Author(s):  
Patihul Husni ◽  
Muhammad Alvien Ghifari ◽  
Norisca Aliza Putriana

Application of stimuli-responsive star polymers in cancer targeting and drug delivery has been extensively researched because of their several advantages in comparison with their linear counterparts. Functionalization and recombination of various arm architectures of the star polymer are very possible to be conducted to suit various needs. The star polymers could not only load more therapeutic drug due to more arms than linear polymers but also be functionalized with targeted moieties for more targeted delivery. Furthermore, the chains in star polymers could be regulated to produce stimuli-responsive star polymer for cancer targeting. The review article aimed to describe the benefits of star polymers and the types of stimuli-responsive delivery system for cancer targeting. Over the last decade, stimuli-responsive star polymers for cancer targeting using either internal stimuli (e.g., pH, redox, enzyme, hypoxia) or external stimuli (e.g., thermal, ultrasound, light, magnetic) has garnered immense interest for researchers. Possibility to mimic a complex natural phenomenon  could be achieved by incorporating various stimuli-responsive functionalities in the star polymer.


2012 ◽  
Vol 65 (8) ◽  
pp. 1117 ◽  
Author(s):  
Jianfu Ding ◽  
Steven Holdcroft

Star polymers of sodium styrenesulfonate with controlled arm length were prepared in a one-pot polymerization. Sodium styrenesulfonate was first polymerized with controlled molecular weight and narrow polydispersity by stable free radical polymerization. Poly(sodium styrenesulfonate) was terminated with divinyl benzene and star polymers prepared via stable free radical coupling of vinylic terminal groups. Star polymers based on arms of 20 and 32 repeat units possessed ~33 and ~41 arms per star respectively. Formation of star polymers with much longer arms was limited by poor coupling kinetics.


Author(s):  
Kyle J. Rodriguez ◽  
Michela M. Pellizzoni ◽  
Robert J. Chadwick ◽  
Chao Guo ◽  
Nico Bruns

2008 ◽  
Vol 110 (1) ◽  
pp. 468-474 ◽  
Author(s):  
Zi Wang ◽  
Ya Jun Yang ◽  
Qing Zhi Dong ◽  
Chun Pu Hu

2015 ◽  
Vol 98 (4) ◽  
pp. 866-870 ◽  
Author(s):  
Violetta Kozik ◽  
Krystyna Jarzembek ◽  
Agnieszka Jędrzejowska ◽  
Andrzej Bąk ◽  
Justyna Polak ◽  
...  

Abstract Pomegranate fruit (Punica granatum L.) is a source of numerous phenolic compounds, and it contains flavonoids such as anthocyanins, anthocyanidins, cyanidins, catechins and other complexes of flavonoids, ellagitannins, and hydrolyzed tannins. Pomegranate juice shows antioxidant, antiproliferative, and anti-atherosclerotic properties. The antioxidant capacity (TEAC) of the pomegranate juices was measured using electron paramagnetic resonance (EPR) spectroscopy and 1,1-diphenyl-2-picrylhydrazyl (DPPH•) as a source of free radicals, and the total phenolic (TP) content was measured using UV-Vis spectroscopy. All the examined pomegranate juices exhibited relatively high antioxidant properties. The TEAC values determined by means of EPR spectroscopy using Trolox (TE) as a free radical scavenger were in the range of 463.12 to 1911.91 μmol TE/100 mL juice. The TP content measured by the Folin-Ciocalteu method, using gallic acid (GA) as a free radical scavenger, widely varied in the investigated pomegranate juice samples and ranged from 1673.62 to 5263.87 mg GA/1 L juice. The strongest antioxidant properties were observed with the fresh pomegranate juices obtained from the fruits originating from Israel, Lebanon, and Azerbaijan. Correlation analysis of numerical data obtained by means of EPR spectroscopy (TEAC) and UV-Vis spectroscopy (TP) gave correlation coefficient (r) = 0.90 and determination coefficient (r2) = 0.81 (P <0.05).


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