Journal of Inorganic and Organometallic Polymers and Materials
·
2013
·Vol. 23
·期 6
·1492-1500
·
IF 1.174
Zhang Nan,Fan Yu-Hua,Bi Cai-Feng,Zhang Xia,Zhang Peng-Fei,Zhang Zhong-Yu,Li Xin
Three novel transition metal coordination polymers, [Ni(C 18 H 16 N 3 O 2 ) 2 ·2CH 3 OH]
n
( 1 ), [Zn(C 18 H 16 N 3 O 2 ) 2 ·4CH 3 OH]
n
( 2 ) and [Cd(C 18 H 16 N 3 O 2 ) 2 ·2CH 3 OH]
n
( 3 ) (C 18 H 16 N 3 O 2 =2-acetylpyridine- d -tryptophan) were synthesized and characterized by elemental analysis, IR, UV, 1 H NMR and X-ray diffraction single crystal analysis. The analyses of the structures indicate that all three materials crystallize in the tetragonal crystal system, space group P 4 1 2 1 2. They have similar structures; i.e., the Schiff base coordinates in its deprotonated form and behaves as a hexadentate (4N+2O) coordinated ligand to form a distorted octahedron geometry. On the other hand, as a result of the alternate arrangement of chains through N–H···O intermolecular hydrogen bonds interactions, 2-D layers are formed for the three complexes. Furthermore, the luminescent properties and thermal stabilities of the three complexes were investigated.
研究领域:
无机化学
·
配位化学
·
材料化学
·
晶体工程
·
光物理化学
✓ 已验证
DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2013
·
IF 2.672
Yinfeng Li,Lina Zou,Ge Song,Kunjing Li,Baoxian Ye
The electro-polymerization of l -Theanine was investigated for the first time on glassy carbon electrode and the polymeric conditions and mechanism were discussed in detail. Hereafter, a simple and sensitive electrochemical sensor based on the poly( l -Theanine) film was established for sophoridine sensing. The electrode process of sophoridine was then studied by cyclic voltammetry and its determination was achieved by amperometry . The results revealed that the poly( l -Theanine) membrane effectively decreased the oxidation potential of sophoridine and greatly increased its response current. And this sensor, fabricated easily and simply as well as very easy surface update, showed good response for sophoridine with a wide linear range from 1.0 × 10 −6 to 1.4 × 10 −4 mol L −1 and a low detection limit of 5 × 10 −7 mol L −1 . The application of proposed method in analysis of real sample was also evaluated with good performance. This work promoted the potential applications of amino acid materials in electrochemical sensors.
研究领域:
分析化学
·
电化学
·
药物分析
·
生物传感
·
分子诊断
·
药物代谢
✓ 已验证
DOI
高影响因子
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
·
2014
·Vol. 52
·期 17
·2442-2453
·
IF 3.245
Bingyan Jiang,Lei Zhang,Jie Yan,Qingquan Huang,Bing Liao,Hao Pang
A series of well-defined thermoresponsive graft polymers with different lengths and graft densities, poly(glycidyl methacrylate)- graft -poly( N -isopropylacrylate) (PGMA- g -PNIPAM), were successfully prepared by combination of controlled/living free radical polymerization and click chemistry. Effects of grafting length and density on the thermoresponsive behavior, aggregating mean diameter, and self-assembly morphology are systematically investigated. The thermosensitive characteristics of graft polymers in aqueous solution prove that the length and graft density had positive co-relationship with the lower critical solution temperature value and mean diameter of micelles as well as the size distribution, while the effect of graft length of polymers is more significant than that of density. Transmission electron microscopy analysis shows that the conformations of PGMA 45 - g -PNIPAM 20 and PGMA 45 - g -PNIPAM 46 with longer length and bigger grafting density in aqueous solutions are spherical nanoparticles with the increasing trend of the diameters, while that of PGMA 45 - g -PNIPAM (73, 50%) shows a spherical-like morphology, which indicates that the graft length and density have a significant effect on the mean diameter of micelle but not on the self-assembly morphology. These results reveal that to obtain desired thermoresponsive behavior and self-assembly morphology of functional polymers, it is essential to design and fabricate the structure of graft polymers with proper length and graft density. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52 , 2442–2453
研究领域:
高分子化学
·
材料科学
·
纳米医学
·
药物递送
·
生物材料
·
智能响应材料
✓ 已验证
DOI
高影响因子
MACROMOLECULAR CHEMISTRY AND PHYSICS
·
2016
·Vol. 217
·期 24
·2726-2735
·
IF 2.495
Huiliang Sun,Shuren Zhang,Yike Yang,Xiao Li,Hongmei Zhan,Yanxiang Cheng
Six aryl Pd(II) bromide complexes based on perylene diimide derivative (Ar) and phosphine mixed-ligands are successfully synthesized by directly oxidative addition of Ar–Br to the Pd(0) precursor. These complexes with the general formulas ArPdBr(PCy 3 ) 2 (PCy 3 = tricyclohexylphosphine; Pd1–Pd3 ) and [ArPdBr(TXP-2,4)] 2 (TXP-2,4 = tri-2,4-xylylphosphine; Pd4–Pd6 ) are stable and can be handled in air at room temperature. By employing the Pd(II) complexes as initiators, Suzuki catalyst transfer polymerization (SCTP) of AB-type fluorene monomer is investigated for preparing polyfluorenes (PFs) with the defined end group. Complexes Pd4–Pd6 with auxiliary TXP-2,4 ligand can initiate polymerization of AB-type fluorene monomer at room temperature, while higher polymerization temperature is required for Pd1–Pd3 with alkyl phosphine PCy 3 . The obtained polymers are analyzed by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry, which confirms that the Ar group is appended to the terminus of the polymer chain. Moreover, PFs prepared by Pd4–Pd6 -catalyzed SCTP bear precisely the Ar group on one chain end and 4- tert -butylphenyl end-capping group on the opposite end, which indicates that Pd4–Pd6 with the bulky TXP-2,4 exhibit better catalytic performance in SCTP. Photoluminescence spectra of the obtained polymers show a dual or a blue emission resulting from the difference of the molecular weight.
研究领域:
高分子化学
·
有机合成
·
功能材料
·
聚合反应机理
·
光电子材料
✓ 已验证
DOI
高影响因子
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
·
2018
·
IF 2.831
Xiaoping Liang,Ping Hu,Hongyang Zhang,Wen Tan
In this work, hypercrosslinked strong anion-exchange polymer resins (HXLPP-SAX) were synthesized and evaluated as solid-phase extraction (SPE) sorbents for extracting fluoroquinolones (FQs) in milk samples. These particles were prepared using a protocol that was facile and cost-effective by combining hypercrosslinking reactions and quaternisation reactions in one step. After the synthesis, the morphological properties and anion-exchange, adsorption, and selectivity performances of the HXLPP-SAX resins were characterized and evaluated. It was shown that the polymers were monodisperse microspheres, with the mean diameters of 2–4 μm, ion-exchange capacity (IEC) of 0.311 meq/g, and specific surface area more than 1000 m 2 /g. The resins applied as SPE sorbents possessed high selectivity in the extraction of amphoteric compounds (enoxacin and enrofloxacin as the representatives) followed by HPLC-UV analysis, as compared to commercially available strong anion-exchange sorbents (Oasis MAX). The SPE-HPLC-UV method was fully validated and exhibited good linearity (10–2000 ng/g, R 2 ≥ 0.997), low limits of detection (2.8–5.1 ng/g), good recoveries (85.8%–117.9%, RSDs ≤ 7.1%) and precisions (intra-day RSDs ≤ 7.7% and inter-day RSDs ≤ 9.4%). Then the method was performed the selective enrichment of six FQs (enoxacin, norfloxacin, ciprofloxacin, lomefloxacin, enrofloxacin, and sparfloxacin) in milk samples. The present results demonstrated that the proposed resins exhibited a promising potential for the enrichment and determination of FQ residues in milk samples as well as in other samples with complex matrices.
研究领域:
分析化学
·
食品科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED SURFACE SCIENCE
·
2018
·
IF 4.439
Shuai Zhou,Xiang Zhou,Gazi Hao,Wei Jiang,Tianhe Wang
Modulation of the density (from 3.5 to 64 mg cm −3 ), hydrophobicity and oil-uptake capability of graphene aerogels in extensive ranges were achieved by reacting (3-Mercaptopropyl)trimethoxysilane (MPS) with graphene oxide solutions under heating. The reaction allowed a characteristic silicone substructure to be formed on graphene and joint the graphene layers firmly together. With the increase of MPS concentrations (≤ca. 0.2 vol%), the nano silicone polymer grown on graphene functioned as a “linker” and “spacer”, leading to a substantial decrease of the aerogel density. Because of the formation of silicone polymer and the characteristic nano-micro substructures on the backbones of graphene aerogels, the graphene aerogels exhibited a high hydrophobicity with the water contact angle consistently exceeding 142 degrees. Functionalized graphene aerogels with a density of 3.5 mg cm −3 were conveniently fabricated that displayed an extraordinary oil absorption capacity, 182 times for lubricating oil and 143 times for n-hexane of its own weight. Furthermore, the aerogels maintained their ultra-high absorption capability even after 20 absorption-distillation cycles, due to structural integrity held by the strong interfacial adhesion between graphene sheets and polymer chains of aerogels. This study offers a promising graphene aerogels and also provides a strategy for fabricating extra low dense functional materials.
研究领域:
材料科学
·
纳米科技
·
高分子化学
·
环境功能材料
·
表面与界面工程
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2018
·Vol. 44
·期 9
·10420-10425
·
IF 3.057
Yurun Feng,Xue Guo,Hongyu Gong,Yujun Zhang,Yu Liu,Xiao Lin,Junjie Mao
PDCs-SiCN(Fe) ceramics were successfully fabricated with different content of ferric acetylacetonate (FA) by polymer-derived method. The effects of FA on the phase composition, microstructure, resistivity, dielectric properties , magnetic properties and microwave absorption properties of PDCs-SiCN(Fe) ceramics in the range of 2–18 GHz were investigated. The samples presented amorphous structure with a few crystalline phases of α-Fe and free carbon in the gaps, which were expected to be good soft magnetic materials . The average real permittivity and imaginary permittivity of PDCs-SiCN(Fe) ceramics with 50 wt% FA was about 14.1 and 5.3 respectively. Furthermore, the PDCs-SiCN(Fe) ceramics with 50 wt% FA addition content showed the broad absorption bandwidth in the 5.1–8.4 GHz with RL ≤ −10 dB (> 90% absorption) at 4 mm.
研究领域:
材料科学
·
功能陶瓷
·
电磁特性
·
吸波材料
·
复合材料
✓ 已验证
DOI
高影响因子
RSC Advances
·
2014
·Vol. 4
·期 90
·49153-49160
·
IF 3.708
Dan Liu,Nan Song,Ye-Chun Cheng,Dai-Xiong Chen,Qiong Jia,Ying-Wei Yang
Poly(glycidyl methacrylate-co-ethylene dimethacrylate) modified with a new supramolecular macrocycle, carboxylatopillar[5]arene, was successfully prepared inside a capillary. The functionalized polymer monolith material was characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, thermogravimetric analysis, and Fourier-transformed infrared spectra. The experimental results showed that this type of polymer possess a good network skeleton structure and excellent extraction properties for the enrichment of parabens by polymer monolith solid-phase microextraction coupled with high performance liquid chromatography. Compared with other pre-treatment methods, the simple operation and inexpensive instrumentation characteristics of the developed polymer monolith SPME method make it more suitable for the extraction of parabens in red wine samples with great potential for further broadening its applications in the enrichment of other real samples.
研究领域:
分析化学
·
环境科学
·
食品安全
·
材料科学
·
色谱学
✓ 已验证
DOI
高影响因子
Small
·
2024
·Vol. 20
·期 40
·2400578
·
IF 13
Yike Du,Aotian Li,Fan Zhang,Han Gao,Xuan Zhou,Jiliang Zhu,Zhicheng Ye
Passive radiative cooling (PRC) can spontaneously dissipate heat to outer space through atmospheric transparent windows, providing a promising path to meet sustainable development goals. However, achieving simultaneously high transparency, color-customizable, and thermal management of PRC anti ultraviolet (anti-UV) films remains a challenge. Herein, a simple strategy is proposed to utilize liquid crystalline polymer, with high mid-infrared emissive, forming customizable structural color film by molecular self-assembly and polymerization-induced pitch gradient, which guarantees the balance of transparency in visible spectrum and sunlight reflection, rendering anti-UV colored window for thermal management. By performing tests, temperature fall of 5.4 and 7.9 °C are demonstrated at noon with solar intensity of 717 W m −2 and night, respectively. Vivid red-, green-, blue-structured colors, and colorless films are designed and implemented to suppress the solar input and control the effective visible light transmissivity considering the efficiency function of human vision. In addition, temperature rise of 11.1 °C is achieved by applying an alternating current field on the PRC film. This study provides a new perspective on the thermal management and aesthetic functionalities of smart windows and wearables.
研究领域:
材料科学
·
高分子化学
·
光学工程
·
能源材料
·
纳米科技
✓ 已验证
DOI
高影响因子
MACROMOLECULAR RAPID COMMUNICATIONS
·
2015
·Vol. 36
·期 15
·1437-1443
·
IF 4.941
Linge Wang,Paul D. Topham,Oleksandr O. Mykhaylyk,Hao Yu,Anthony J. Ryan,J. Patrick A. Fairclough,Wim Bras
Polymer beads have attracted considerable interest for use in catalysis, drug delivery, and photonics due to their particular shape and surface morphology. Electrospinning, typically used for producing nanofibers, can also be used to fabricate polymer beads if the solution has a sufficiently low concentration. In this work, a novel approach for producing more uniform, intact beads is presented by electrospinning self-assembled block copolymer (BCP) solutions. This approach allows a relatively high polymer concentration to be used, yet with a low degree of entanglement between polymer chains due to microphase separation of the BCP in a selective solvent system. Herein, to demonstrate the technology, a well-studied polystyrene-poly(ethylene butylene)–polystyrene triblock copolymer is dissolved in a co-solvent system. The effect of solvent composition on the characteristics of the fibers and beads is intensively studied, and the mechanism of this fiber-to-bead is found to be dependent on microphase separation of the BCP.
研究领域:
高分子科学
·
纳米材料
·
生物医学工程
·
药物递送
·
组织工程
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS CHEMISTRY
·
2011
·Vol. 21
·期 18
·6569-6575
·
IF 5.101
Xintao Luo,Jishu Han,Yang Ning,Zhe Lin,Hao Zhang,Bai Yang
1-Thioglycerol (TG)-stabilized quantum dots (QDs) are good candidate for performing a stepwise polymerization reaction with polyurethane (PU) prepolymers, but their use is limited by their worse photoluminescence (PL) in comparison to QDs stabilized by other mercapto-ligands. To overcome this problem, TG-stabilized CdTe QDs with enhanced PL were synthesized in water through a N2H4-promoted growth approach. The current synthesis significantly shortened the duration of the size evolution of QDs, particularly for obtaining samples with orange and red emissions. It also permitted QD growth at low temperatures, such as room temperature, which avoided the decomposition of TG and subsequent embedment of sulfur into the QDs as occurs in the conventional synthesis. Most importantly, the TG ligand endowed the QDs with hydroxyl coverage, making the QDs miscible with PU prepolymers in dimethyl sulfoxide, and therefore overcoming the main problem in fabricating PU-based nanocomposites of eliminating water. The hydroxyl coverage further allowed for the linkage of PU on the surface of the QDs through the reaction between –OH and –NCO, producing CdTe QD–PU bulk nanocomposites. Systematic characterization indicated that the QDs were well dispersed in the PU medium, and the size-dependent PL of QDs was also maintained.
研究领域:
材料科学
·
纳米科技
·
高分子化学
·
光电子学
·
胶体与界面化学
✓ 已验证
DOI
高影响因子
Desalination and Water Treatment
·
2024
·
IF 1
Dapeng Zhang,Zicheng Yao,Han Zhang,Guiru Zhu,Lu Liu,Congjie Gao
A novel strategy to fabricate thin film nanocomposite (TFN) membrane was reported by dispersing nanofillers in the aqueous and organic phase simultaneously via interfacial polymerization of m-phenylenediamine and trimesoyl chloride. Two different nanofillers (hydrophilic MCM-48 and hydrophobic ZIF-8) were used to investigate the new strategy. Both hydrophilic MCM-48 and hydrophobic ZIF-8 can effectively improve the separation performance of the TFN membrane with higher water flux value maintaining high salt rejection via the novel strategy than conventional TFN membrane prepared with same total amount nanoparticles in singly organic phase or aqueous phase. It indicates that the new strategy is feasible to obtain the TFN membrane with excellence separation performance compared with the conventional method by dispersing nanofillers in singly phase. The new strategy is realized by dispersing less amount nanofillers in both phases simultaneously, which is possible to avoid the aggregation of nanoparticles and maximize the effect of nanoparticles.
研究领域:
材料科学
·
膜分离技术
·
纳米复合材料
·
环境工程
·
化学工程
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）