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161.
Yanfeng Chu Huan Yu Yunti Zhang Guangyan Zhang Yingying Ma Renxi Zhuo Xulin Jiang 《Journal of polymer science. Part A, Polymer chemistry》2014,52(23):3346-3355
Biodegradable amphiphilic ABC Y‐shaped triblock copolymer (MPBC) containing PEG, PBLA, and PCL segments was synthesized via the combination of enzymatic ring‐opening polymerization (ROP) of epsilon‐caprolactone, ROP of BLA‐N‐carboxyanhydride and click chemistry, where PEG, PBLA, and PCL are poly(ethylene glycol), poly(benzyl‐l ‐aspartate), and polycaprolactone, respectively. Propynylamine was employed as ROP initiator for the preparation of alkynyl‐terminated PBLA and methyloxy‐PEG with hydroxyl and azide groups at the chain‐end was used as enzymatic ROP initiator for synthesis of monoazido‐midfunctionalized block copolymer mPEG‐b‐PCL. The subsequent click reaction led to the formation of Y‐shaped asymmetric heteroarm terpolymer MPBC. The polymer structures were characterized by different analyses. The MPBC terpolymer self‐assembled into micelles and physically encapsulated drug doxorubicin (DOX) to form DOX‐loaded micelles, which showed good stability and slow drug release. In vitro cytotoxicity study indicated that the MPBC micelles were nontoxic and the DOX‐loaded micelles displayed obvious anticancer activity similar to free DOX against HeLa cells. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3346–3355 相似文献
162.
Andre Arnebold Oliver Schorsch Johannes Stelten Andreas Hartwig 《Journal of polymer science. Part A, Polymer chemistry》2014,52(12):1693-1699
The industrial applications of benzoxazines are limited due to their high curing temperatures. This drawback can be overcome by more reactive precursor compared to conventional benzoxazines or by application of efficient initiators. We report the synthesis of a new resorcinol‐based benzoxazine and its cationic polymerization with thermolatent super acids, namely organic sulfonium hexafluoroantimonates. This combination of a reactive precursor and an efficient initiator results in a curing temperature below 100 °C (differential scanning calorimetry onset) which is up to now one of the lowest polymerization temperatures for benzoxazine systems. Furthermore, the thermal stability of the formed polybenzoxazine has not been influenced by the applied initiators. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1693–1699 相似文献
163.
Dr. Lan Hu Prof. Dr. Yan Zhao 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(32):7702-7710
Outcomes of chemical reactions are generally dominated by the intrinsic reactivities of reaction partners, but enzymes frequently override such constraints to transform less reactive molecules in the presence of more reactive ones. Despite the attractiveness of such catalysis, it is difficult to build synthetic catalysts with these features. Micellar imprinting is a powerful method to create template-complementary binding sites inside protein-sized water-soluble nanoparticles. When a photocleavable functional monomer was used to bind two phosphonate/phosphate templates as transition-state analogues, active sites with predetermined size and shape were formed inside doubly cross-linked micelles through molecular imprinting. Postmodification replaced the binding group with a catalytic pyridyl group, forming highly selective artificial esterases. The catalysts displayed enzyme-like kinetics and turnover numbers that were in the hundreds. The selectivity of the catalysts, derived from the substrate-complementary imprinted active sites, enabled transformation of less reactive esters in the presence of more reactive ones. 相似文献
164.
Carbon black was modified using various liquid‐phase oxidation methods (modified carbon black = m‐CB, m = (1, 2, 3): 1, sulfuric acid/potassium permanganate method; 2, nitric acid method; 3, hydrogen peroxide method). With acetone–ethylene glycol as initiator, dimethyldiallylammonium chloride (DMDAAC) and acrylamide (AM) as monomer, cationic polyacrylamide (CPAM) was prepared by UV excitation of the monomer. The m‐CB/CPAM nanocomposites were synthesized using a hydrothermal method. The factors that affected the molecular weight of CPAM were investigated, including the total monomer concentration, the dosage of the complex initiator, the mass ratio of mAM:mDMDAAC and the UV irradiation time. The chemical structures and morphologies of the samples were characterized using Fourier transform infrared spectroscopy, thermogravimetric analysis, elemental composition, X‐ray diffraction and scanning electron microscopy. 1‐CB/CPAM was utilized to flocculate oil sludge suspension, and the effects of 1‐CB quality, 1‐CB/CPAM dosage, temperature and pH value on the flocculation performance of 1‐CB/CPAM were investigated. The flocculation mechanism of 1‐CB/CPAM was also analyzed. The results show that 1‐CB/CPAM has an outstanding flocculation effect, and it flocculates oil sludge particles by adsorption bridging and charge neutralization in acidic and alkaline conditions. 相似文献
165.
166.
Low cost bifunctional initiators for bidirectional living cationic polymerization of olefins. I. isobutylene 下载免费PDF全文
Turgut Nugay Balazs L. Keszler Tejal Deodhar Nihan Nugay Joseph P. Kennedy 《Journal of polymer science. Part A, Polymer chemistry》2017,55(22):3716-3724
We describe the discovery of novel low cost bifunctional initiators 2,4,7,9‐tetramethyl‐tricyclo[6.2.0.036]deca‐1(8),2,6‐triene‐4,9‐diol (bBCB‐diOH) and 4,9‐dichloro,2,4,7,9‐tetramethyl‐tricyclo[6.2.0.036]deca‐1(8),2,6‐triene (bBCB‐diCl), for living cationic bidirectional polymerization of olefins, for example, isobutylene. bBCB‐diOH was quantitatively synthesized in one step by UV radiation of commercially available diacetyl durene (DAD) and bBCB‐diCl by hydrochlorination of bBCB‐diOH. These molecules, in conjunction with TiCl4 coinitiator, initiate the living polymerization of isobutylene. Livingness was demonstrated by linear conversion versus molecular weight (MW) plots and narrow MW distributions. Polymerizations are slower than those initiated by the universally used “hindered” bifunctional initiator 5‐tert‐butyl‐1,3‐bis(1‐chloro‐1‐methyl)benzene and are suitable for rate studies. Herein, we report the synthesis, by the use of bBCB‐diCl, of relatively low MW (M n < 3000 g mol?1) allyl‐telechelic polyisobutylene (PIB) used for the synthesis of PIB‐based polyurethanes and that of relatively high MW (M n > 30,000) living PIB telechelics for the synthesis of thermoplastic elastomers. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55 , 3716–3724 相似文献
167.
168.
Nikos Karanikolopoulos Ioannis Choinopoulos Marinos Pitsikalis 《Journal of polymer science. Part A, Polymer chemistry》2020,58(11):1582-1600
A series of well-defined poly{dl -lactide-b-[oligo(ethylene glycol) methyl ether (meth)acrylate)]} (PDLLA-b-POEG[M]A) functional amphiphilic diblock copolymers was synthesized by employing a multistep procedure involving: (a) ring-opening polymerization of dl -lactide using n-decanol and stannous octoate as the initiating system, (b) esterification reaction of the PDLLA hydroxyl end groups with 2-bromoisobutyryl bromide, (c) atom transfer radical polymerization of OEG(M)A with the newly created bromoisobutyryl initiating site, and (d) incorporation of biotin or folic acid at the POEGA chain ends using click chemistry. The products were characterized by NMR spectroscopy and SEC analysis. The aggregation behavior of the synthesized block copolymers was investigated by dynamic light scattering at 25°C in aqueous solutions. The hydrophobic model compounds Nile red and pyrene were efficiently incorporated into the copolymer aggregates in aqueous solutions. High partition coefficient values were determined by fluorescence spectroscopy. 相似文献
169.
Thermo‐ and pH‐sensitive triblock copolymers with tunable hydrophilic/hydrophobic properties 下载免费PDF全文
Christophe Pottier Gaëlle Morandi Virginie Dulong Zied Souguir Luc Picton Didier Le Cerf 《Journal of polymer science. Part A, Polymer chemistry》2015,53(22):2606-2616
Polymers consisting of poly(acrylic acid) (PAA) and statistical poly[(acrylic acid)‐co‐(tert‐butylacrylate)] (P(AA‐co‐tBA)), attached to both extremities of Jeffamine® (D series based on a poly(propylene oxide) (PPO) with one amine function at each end) using atom transfer radical polymerization (ATRP) are presented in this article. An original bifunctional amide‐based macroinitiator was first elaborated from Jeffamine®. tBA polymerization was subsequently initiated from this macroinitiator. This polymerization occurs in a well‐controlled manner leading to narrow molecular weights distribution. Amphiphilic copolymers were finally obtained after complete or partial hydrolysis of the PtBA blocks into PAA. The control of the partial hydrolysis of tBA units, conducted in a concentrated HCl/tetrahydrofuran mixture, is demonstrated. The properties of the triblock copolymers were preliminary investigated in aqueous solution by absorbance, DLS measurements and SEC/MALS/DV/DRI analysis as a function of temperature and pH modifications, providing evidences of thermo‐ and pH‐sensitive self‐assembly of the copolymers. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 2606–2616 相似文献
170.
Shixiong Chen Xiaotian Zhao Ming Jin Wanqiu Huang Guodong Ye Haiyan Pan Decheng Wan 《Journal of polymer science. Part A, Polymer chemistry》2021,59(17):1899-1911
Four 1,5-diphenyl-3-aromatic heterocyclyl-2-pyrazoline-based sulfonium salt photoacid generators (PAGs) with different aromatic heterocycles substituted on C3 atom and dimethyl sulfonium group on C5 atom were synthesized. These PAGs were highly photosensitive in the 365–425 nm light-emitting diode region, and the intramolecular charge transfer from the pyrazoline ring to sulfonium salts induced efficient photolysis and high ΦH+. The heterocycles as well as their substituted positions significantly influenced the energy of the S2 orbital, which was determined by the electrochemical and absorption properties of the PAGs. The raising of the S2 orbital energy enlarged the energy gap of S0–S2 and S1–S2, resulting in blue shift of the absorption spectra and increase in the quantum yield of photoacid generation (ΦH+), respectively. When the energy of excited electrons was higher than that of the S2 orbital, the transition from S0 to S2 (π–π*) occurred before the C-S cleavage on S1 and the PAGs showed high ΦH+ values (0.52–0.72). The transition from S0 to S1 (π–σ*) occurred when the energy of electrons is lower than that of the S2 orbital, and the PAGs showed low ΦH+ value. The photopolymerization kinetics demonstrated that these PAGs were highly efficient cationic photoinitiators. 相似文献