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EUROPEAN POLYMER JOURNAL · 2020 · IF 3.862

Synthesis of amphiphilic star-shaped block copolymers through photo-induced metal free atom transfer radical polymerization

Xiuzhe Yin,Linan Wang,Xiaomeng Zhang,Haitao Zhao,Zhe Cui,Peng Fu,Minying Liu,Xinchang Pang,Xiaoguang Qiao

Photo-induced metal free ATRP method was employed for the synthesis of star-shaped polymers. By using 21-Br-β-CD as the macroinitiator, 10-phenylphenothiazine as the photoredox catalyst, star-shaped PtBA homopolymers were synthesized. The photo-induced ATRP displayed all the characteristics of controlled/living polymerization systems and the good light control over the polymerization process. The successful chain extension with MMA demonstrated the high livingness of PtBA “arms” and good controllability of the Photo-induced metal free ATRP. Finally, the achieved PtBA-b-PMMA star-shaped copolymers were used as templates for the preparation of precisely size-tunable CdSe quantum dots after a simple hydrolyzing process.

研究领域: 高分子化学 · 纳米医学 · 药物递送 · 生物材料 · 胶体与界面科学
✓ 已验证 DOI 高影响因子
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RSC Advances · 2022 ·Vol. 12 ·期 19 ·11715-11721 · IF 4.036

Synthesis of ultrahigh-molecular-weight ethylene/1-octene copolymers with salalen titanium(IV) complexes activated by methyaluminoxane

Baokang Zou,Yipeng Zhan,Xiuli Xie,TongTong Zhang,Runkai Qiu,Fangming Zhu

Two salalen titanium(IV) complexes ((H-salalen)TiCl2 and (F-salalen)TiCl2) containing hydrogen and fluorine respectively on the phenolate ring close to the imine were synthesized for the copolymerization of ethylene with 1-octene to prepare poly(ethylene-co-1-octene) in the presence of methylaluminoxane (MAO). The (F-salalen)TiCl2/MAO showed higher catalytic activity and better copolymer characteristics such as a higher molecular weight, narrower molecular weight distribution, and higher 1-octene incorporation than (H-salalen)TiCl2/MAO, which revealed that the electron-withdrawing conjugated effect introduced by fluorine substituents led to improvements on catalytic performance and thermal stability. The influences of copolymerization conditions including temperature, Al/Ti molar ratios and comonomer feed ratios on the copolymerization behavior of (F-salalen)TiCl2/MAO and the copolymer microstructure were investigated in detail. Under the activation of MAO, the (F-salalen)TiCl2 could produce ultrahigh molecular weight poly(ethylene-co-1-octene) with 1-octene incorporation ratios in the range of 0.9–3.1 mol% and exhibit relatively high activity. It could be inferred that long ethylene sequences in the copolymer were segregated by the isolated 1-octene units based on the 13C NMR characterization of the copolymer. Moreover, the thermal properties and crystallization of copolymers were determined by DSC and XRD and correlated to the ethylene sequence length distribution. The reactivity ratios calculated by the triad distribution in 13C NMR revealed the random comonomer distribution in the copolymer chain.

研究领域: 高分子化学 · 配位聚合 · 催化化学 · 材料科学 · 高分子物理
✓ 已验证 DOI 高影响因子
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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2015 ·Vol. 54 ·期 3 ·368-380 · IF 3.113

Hyperbranched block copolymer from AB2 macromonomer: Synthesis and its reaction-induced microphase separation in epoxy thermosets

Jingang Li,Yixin Xiang,Sixun Zheng

In this contribution, we reported the synthesis of a hyperbranched block copolymer composed of poly(ε-caprolactone) (PCL) and polystyrene (PS) subchains. Toward this end, we first synthesized an α-alkynyl- and ω,ω′-diazido-terminated PCL- b -(PS) 2 macromonomer via the combination of ring-opening polymerization and atom transfer radical polymerization. By the use of this AB 2 macromonomer, the hyperbranched block copolymer ( h -[PCL- b -(PS) 2 ]) was synthesized via a copper-catalyzed Huisgen 1,3-dipolar cycloaddition (i.e., click reaction) polymerization. The hyperbranched block copolymer was characterized by means of 1 H nuclear magnetic resonance spectroscopy and gel permeation chromatography. Both differential scanning calorimetry and atomic force microscopy showed that the hyperbranched block copolymer was microphase-separated in bulk. While this hyperbranched block copolymer was incorporated into epoxy, the nanostructured thermosets were successfully obtained; the formation of the nanophases in epoxy followed reaction-induced microphase separation mechanism as evidenced by atomic force microscopy, small angle X-ray scattering, and dynamic mechanical thermal analysis. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54 , 368–380

研究领域: 高分子化学 · 材料科学 · 纳米结构功能材料 · 聚合物自组装 · 热固性树脂改性
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2012 ·Vol. 125 ·期 4 ·2867-2873 · IF 1.289

Synthesis of fluorescent poly(1-vinylimidazole-co-(1-pyrene) methyl 2-methyl-2-propenote) and determination of monomer reactivity ratios

Yehai Yan,Na Lu,Jian Cui,Jinfang Zhang

A new fluorescent copolymer, poly(1-vinylimidazole- co -(1-pyrene) methyl 2-methyl-2-propenote) (VI- co -PyMMP), has been designed and synthesized by a free-radical copolymerization of VI and PyMMP as well as characterized using ultraviolet (UV), Fourier transform infrared spectroscopy (FTIR), 1 H NMR, and fluorescence spectroscopies. The monomer reactivity ratios are determined by two methods of Fineman-Ross ( r 1 = 0.28 ± 0.04 for VI, r 2 = 1.32 ± 0.11 for PyMMP) and Kelen-Tüdös ( r 1 = 0.23 ± 0.05, r 2 = 1.22 ± 0.12). Based on the reactivity ratios, the monomer sequence lengths and Q and e for PyMMP monomer are further calculated. The results suggest that the copolymerization of VI and PyMMP is a nonideal copolymerization without an azeotropic point (i.e., r 1 < 1, r 2 > 1 and r 1 r 2 < 1) and has a low alternation tendency. The conclusions drawn in this work may not only direct the later synthesis of the copolymers but also enrich the database of free-radical copolymerization. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012

研究领域: 高分子化学 · 功能高分子 · 荧光材料 · 聚合物合成 · 材料化学
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF POLYMER SCIENCE · 2014 ·Vol. 32 ·期 11 ·1564-1574 · IF 1.42

Photo-induced living cationic copolymerization of isobutyl vinyl ether and vinyl ether with carbazolyl groups

Li Ming,Zhang Li-fen,Tao Mei-xia,Cheng Zhen-ping,Zhu Xiu-lin

In this work, a fluorescent monomer 2-(9-carbazolyl) ethyl vinyl ether (CEVE) was synthesized in our lab, and its photo-induced living cationic copolymerization behavior with isobutyl vinyl ether (IBVE) was investigated in detail using diphenyliodonium chloride (DPICl)/2,2-dimethoxy-2-phenylacetophenone (DMPA) and zinc bromide (ZnBr 2 ) initiating system in dichloromethane solution at 5 °C, −5 °C, and −15 °C, respectively. The living nature of this copolymerization system was confirmed by adding fresh comonomer method after the copolymerization almost finished. In addition, the obtained fluorescent copolymer poly(IBVE- co -CEVE) has a low glass transition temperature ( T g ), below −10 °C.

研究领域: 高分子化学 · 功能高分子 · 光响应材料 · 聚合反应机理 · 荧光材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF MATERIALS SCIENCE · 2019 ·Vol. 54 ·期 7 ·5961-5970 · IF 3.442

Excellent self-healing and antifogging coatings based on polyvinyl alcohol/hydrolyzed poly(styrene-co-maleic anhydride)

Luo Shuai,Qiao Xuan,Wang Qiu-Yu,Zhang Yun-Fei,Fu Ping,Lin Zhi-Dong,Du Fei-Peng,Cheng Chun

To develop low-cost and high-performance self-healing antifogging coatings, polyvinyl alcohol/hydrolyzed poly(styrene-co-maleic anhydride) (PVA/H-PSMA) coatings were prepared from a mixed solution of polyvinyl alcohol (PVA) and hydrolyzed poly(styrene-co-maleic anhydride) (H-PSMA) via spin coating and annealing. The microstructure, antifogging behavior, and self-healing ability were investigated. High transparency and low surface roughness were observed when the PVA/H-PSMA film was coated on glass slides. The PVA/H-PSMA coatings showed excellent antifogging performance in a warm, humid environment. The coatings also performed well when transferred from a refrigerator to room temperature. The antifogging coatings showed desirable water resistance due to strong chemical bonding between PVA and H-PSMA, as well as excellent self-healing ability due to hydrogen bonding self-assembly in the PVA/H-PSMA structure. The coatings still exhibited excellent antifogging effects after 20 scratching-repairing cycles, illustrating their potential use in practical applications.

CAS / MDL: 9002-89-5
研究领域: 材料科学 · 表面化学
✓ 已验证 产品关联 DOI 高影响因子
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JOURNAL OF MOLECULAR LIQUIDS · 2019 · IF 4.561

Removal of toluene and Pb(II) using a novel adsorbent modified by titanium dioxide and chitosan

Guoli Chen,Kun Song,Xiaoming Huang,Wenbo Wang

Titanium dioxide (TiO 2 ) colloid was synthesized by using tetrabutyl titanate . TiO 2 (KH-570) intermediate was prepared by etherification reaction of TiO 2 colloid and KH-570. The CS-GMA intermediate was prepared by ring-opening reaction of chitosan (CS) and glycidyl methacrylate (GMA). Finally, copolymerization two intermediates obtain a new adsorbent, TiO 2 (KH-570)-g-(CS-GMA). The results manifest that the maximum adsorption amounts of toluene and Pb(II) are 56.62 mg/g and 623.56 mg/g, respectively. The adsorption of TiO 2 (KH-570)-g-(CS-GMA) adsorbent for toluene and Pb(II) accord with the pseudo-second-order kinetics mechanism and Langmuir equation, indicate that the TiO 2 (KH-570)-g-(CS-GMA) adsorbent has better adsorption effect on toluene and Pb(II).

研究领域: 环境科学 · 材料科学 · 化学工程 · 污染控制 · 吸附技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2016 ·Vol. 134 ·期 10 · IF 1.866

Enhanced emission from Alq3 in amphiphilic block copolymers PEG-b-PVK-co-Alq3 synthesized via RAFT polymerization

Fei Fang,Fan Kong,Xueqin Zhang,Mengqi Lin,Yichi Zhang,Shounian Ding

A series of amphiphilic poly(N-vinyl carbazole) (PVK) block copolymers containing tris(8-hydroxyquinoline) aluminum (Alq 3 ) have been synthesized via reversible addition-fragmentation chain transfer (RAFT) radical polymerization with trithiocarbonate terminated polyethylene glycol (PEG) as a RAFT agent. The chemical structures of the block copolymers have been identified by 1 H nuclear magnetic resonance and Fourier transform infrared spectrometer. The analysis of gel permeation chromatography indicates that the polydispersity indices of the block copolymers are lower than 1.30. The results of thermogravimetric analysis show that the decomposition temperatures of the copolymers are higher than 330 ° C . The optical properties of the copolymers have been investigated and the obviously enhanced emission from Alq 3 has been found due to resonance energy transfer from PVK to Alq 3 . © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44573.

研究领域: 高分子化学 · 材料科学 · 光电子学 · 纳米功能材料 · 聚合物合成 · 荧光材料 · 能量转移
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2022 ·Vol. 139 ·期 24 ·52368 · IF 3.057

Study on the compounding of a new type of trimer epoxy resin curing agent

Xiongfei Zhang,Tianhui Zhao,Ting Cao,Peiyu Liu,Chuang Ma,Pengyun Li,Dang Huang

In this paper, bisphenol A (BPA), epichlorohydrin (ECH), and isocyanate trimer (TDI-T) are used as raw materials to synthesize a high toughness/trimer epoxy resin by graft copolymerization. It was cured at room temperature with low molecular weight polyamide 650 (PA650)/isophorone diamine (IPDA) and low molecular weight polyamide 650/triethylene tetramine (TETA) composite curing system respectively. The cured products of the two compound systems were studied by Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), thermogravimetry (TG), and mechanical property testing. The results show that with the increase of TETA and IPDA curing agents, the heat released during the curing process of the two systems also greatly increases, and the temperature rises from the initial 33.9–69.7°C and 52.8°C. The curing time is shortened from a few days to a few hours, and the controllability of the curing time is effectively realized. When the ratio of triethylene tetramine to low molecular weight polyamide 650 is 2.86:100, the compressive strength is the best, reaching 112.7 MPa, 12% higher than pure polyamide as curing agent, and the specimen can be completely restored to its original shape in a few minutes. When the ratio of TETA to PA650 is 2.86:100, the elongation at break reaches 21.4%.

研究领域: 高分子化学 · 材料科学 · 复合材料 · 热固性树脂 · 功能材料
✓ 已验证 DOI 高影响因子
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Materials Science & Engineering C-Materials for Biological Applications · 2012 ·Vol. 32 ·期 6 ·1699-1703 · IF 2.686

Use of Yb-based catalyst for AGET ATRP of acrylonitrile to simultaneously control molecular mass distribution and tacticity

Jing Ma,Hou Chen,Min Zhang,Chunhua Wang,Ying Zhang,Rongjun Qu

Yb-based catalyst was used for the first time for atom transfer radical polymerization using activators generated by electron transfer (AGET ATRP) of acrylonitrile (AN) with 2-bromopropionitrile (BPN) as initiator, 2, 2′-bipyridine (bipy) as ligand, and tisn(II) bis(2-ethylhexanoate) (Sn(EH) 2 ) as reducing agent in the presence of air. With respect to AGET ATRP of AN catalyzed by CuBr 2 , an evident increase of polymer tacticity was observed for AGET ATRP of AN. The increase of syndiotacticity became more and more pronounced than the increase of isotacticity of polyacrylonitrile (PAN) along with YbBr 3 content. The block copolymer PAN-b-PMMA with molecular weight at 60,000 and polydispersity at 1.36 was successfully prepared.

研究领域: 高分子化学 · 材料科学 · 催化化学 · 聚合物合成 · 功能材料
✓ 已验证 DOI 高影响因子
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PHYSICAL CHEMISTRY CHEMICAL PHYSICS · 2015 ·Vol. 17 ·期 29 ·19457-19464 · IF 4.493

Preparation of superhydrophobic films based on the diblock copolymer P(TFEMA-r-Sty)-b-PCEMA

Ganwei Zhang,Jiwen Hu,Yuanyuan Tu,Guping He,Fei Li,Hailiang Zou,Shudong Lin,Gonghua Yang

The diblock copolymer poly[2,2,2-trifluoroethyl methacrylate-r-styrene]-block-poly[(2-cinnamoyloxyethyl methacrylate)] [P(TFEMA-r-Sty)-b-PCEMA] was synthesized via atom transfer radical polymerization. The copolymer underwent self-assembly in TFEMA/CH2Cl2 to form spherical micelles. Photo-cross-linking of the PCEMA domains of these micelles yielded cross-linked nanoparticles. The cross-linked nanoparticles were subsequently cast from CH2Cl2/methanol solvent mixtures at methanol volume fractions of more than 30% to yield rough surfaces bearing small nanobumps on micron-sized aggregations that were connected together to form cross-linked nanoparticles. These surfaces were superhydrophobic with a water contact angle of 161 ± 1° and a sliding angle of 6 ± 1°. Spraying these nanoparticles onto substrates exhibiting microscale roughness, such as filter paper, by a traditional coating technique also created superhydrophobic surfaces. A thin layer of nanoscale spherical protrusions was observed on the microscale fibers of filter paper by scanning electron microscopy. The coated filter paper samples exhibited a water contact angle and a sliding angle of 153 ± 1° and 9 ± 1°, respectively.

研究领域: 高分子化学 · 材料科学 · 表面科学 · 纳米技术 · 功能材料
✓ 已验证 DOI 高影响因子
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CARBOHYDRATE POLYMERS · 2018 · IF 5.158

Effect of a functional polymer on the rheology and microstructure of sodium alginate

Lei Du,Amin GhavamiNejad,Zhi-Chao Yan,Chandra Sekhar Biswas,Florian J. Stadler

Here, we report on the effect of functional copolymer poly(N-isopropylacrylamide-co-4-vinyl-phenylboronic acid) (NIBA) on the rheology and network structure formed by sodium alginate (SA) through linear and nonlinear viscoelasticity measurements. The hydrogel moduli at pH 3 increased with increasing NIBA addition, while the yield point decreased. Furthermore, these hydrogels showed strain-softening behavior, weak G″-overshoot marking the onset of nonlinearity, and good self-healing properties after large deformation. The zero-strain nonlinearity parameter (Q 0 ) was found to be more sensitive to NIBA-addition than the linear viscoelastic properties. The blends showed a clear peak in the startup test except for SA alone and the peak intensity increased with increasing NIBA-concentration. Finally, based on all data, gelation mechanism and interaction of SA and NIBA will be clarified.

研究领域: 高分子材料科学 · 生物医学工程 · 软物质物理 · 药剂学 · 组织工程
✓ 已验证 DOI 高影响因子
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