vinyl polymers
Recently Published Documents


TOTAL DOCUMENTS

519
(FIVE YEARS 33)

H-INDEX

42
(FIVE YEARS 4)

2022 ◽  
Author(s):  
Nathaniel Bingham ◽  
Qamar Nisa ◽  
Priyanka Gupta ◽  
Neil Young ◽  
Eirini Velliou ◽  
...  

Being non-degradable, vinyl polymers have limited biomedical applicability. Unfortunately, backbone esters incorporated through conventional radical ring-opening methods do not undergo appreciable abiotic hydrolysis under physiologically relevant conditions. Here, PEG acrylate and di(ethylene glycol) acrylamide-based copolymers containing backbone thioesters were prepared through the radical ring-opening copolymerization of the thionolactone dibenzo[c,e]oxepin-5(7H)-thione. The thioesters degraded fully in the presence of 10 mM cysteine at pH 7.4, with the mechanism presumed to involve an irreversible S–N switch. Degradations with N-acetylcysteine and glutathione were reversible through the thiol–thioester exchange polycondensation of R–SC(=O)–polymer–SH fragments with full degradation relying on an increased thiolate:thioester ratio. Treatment with 10 mM glutathione at pH 7.2 (mimicking intracellular conditions) triggered an insoluble–soluble switch of a temperature-responsive copolymer at 37 °C and the release of encapsulated Nile Red (as a drug model) from core-degradable diblock copolymer micelles. Copolymers and their cysteinolytic degradation products were found to be non-cytotoxic, making thioester backbone-functional polymers promising for drug delivery applications.


Author(s):  
Kouki Oka ◽  
Miho Kataoka ◽  
Yusuke Kaiwa ◽  
Kenichi Oyaizu
Keyword(s):  

2021 ◽  
Author(s):  
Wenqi Wang ◽  
Zefeng Zhou ◽  
Xuanting Tang ◽  
Stephanie Moran ◽  
Jing Jin ◽  
...  

Degradable vinyl polymers by radical ring-opening polymerization have become a promising solution to the challenges caused by the widespread use of non-degradable vinyl plastics. However, achieving even distribution of labile functional groups in the backbone of degradable vinyl polymers remains challenging. Herein, we report a photocatalytic approach to truly random degradable vinyl copolymers with tunable main-chain composition via radical ring-opening cascade copolymerization (rROCCP). The rROCCP of the macrocyclic allylic sulfone and acrylates or acrylamides mediated by visible light at ambient temperature achieved near-unity reactivity ratios of both comonomers over the entire range of the comonomer compositions and afforded truly random vinyl copolymers with degradable units evenly distributed in the polymer backbone. Experimental and computational evidence revealed an unusual reversible inhibition of chain propagation by in situ generated sulfur dioxide, which was successfully overcome by reducing the solubility of sulfur dioxide in the reaction mixture. This study provided a powerful approach to truly random degradable vinyl copolymers with tunable main-chain labile functionalities and comparable thermal and mechanical properties to traditional non-degradable vinyl polymers.


Polymers ◽  
2021 ◽  
Vol 13 (17) ◽  
pp. 3005
Author(s):  
Elsayed Elbayoumy ◽  
Nasser A. El-Ghamaz ◽  
Farid Sh. Mohamed ◽  
Mostafa A. Diab ◽  
Tamaki Nakano

Semiconductor materials based on metal high crosslinked-vinyl polymer composites were prepared through loading of Pd(OAc)2 on both Poly(ethylene-1,2-diyl dimethacrylate) (poly(EDMA)) and poly(ethylene-1,2-diyl dimethacrylate-co-methyl methacrylate) (Poly(EDMA-co-MMA)). The thermochemical properties for both poly(EDMA) and poly(EDMA-co-MMA) were investigated by thermal gravimetric analysis TGA technique. The dielectric permittivity, AC electrical conductivity and conduction mechanism for all the prepared polymers and their Pd(OAc)2 composites were studied. The results showed that the loading of polymers with Pd(OAc)2 led to an increase in the magnitudes of both the dielectric permittivity and AC electrical conductivity (σac). The value of σac increased from 1.38 × 10−5 to 5.84 × 10−5 S m−1 and from 6.40 × 10−6 to 2.48 × 10−5 S m−1 for poly(EDMA) and poly(EDMA-co-MMA), respectively, at 1 MHz and 340 K after loading with Pd(OAc)2. Additionally, all the prepared polymers and composites were considered as semiconductors at all the test frequencies and in the temperature range of 300–340 K. Furthermore, it seems that a conduction mechanism for all the samples could be Quantum Mechanical Tunneling (QMT).


Author(s):  
Cristian Castro ◽  
Ligia Gargallo ◽  
Deodato Radić

: This mini-review deals with the miscibility behavior of two biopolymers, chitosan, and alginate. It is well known that the miscibility in multifunctional polymers blends is favored due to specific interactions, which origin a negative heat of mixing. Particular interest is focused on functionalized polymers because they are the most suitable way to obtain interacting polymers, producing a single-phase material. Due to the polyfunctionality of chitosan (CS) and other biopolymers, they can be taken into account as a basis of a strongly interacting polymer. They would allow obtaining compatible polymeric materials. For this reason, blends containing CS with different vinyl polymers have been studied. The most significant polymeric blends with these natural polymers will be analyzed in this review. Chitosan is obtained from the biopolymer chitin through sequential processes of demineralization, deproteinization, and deacetylation. The native chitin is obtained by direct separation from the marine crustaceans shell, abundant on the sea coasts. Some classic results that relate to the polymeric blends containing amphiphilic polymers will be discussed. Another biopolymer of the coast is Sodium Alginate (SA). Alginate also allows the formation of compatible polymer blends. Results in this regard will also be analyzed in this review.


Sign in / Sign up

Export Citation Format

Share Document