全文获取类型
收费全文 | 672篇 |
免费 | 44篇 |
国内免费 | 59篇 |
专业分类
化学 | 759篇 |
晶体学 | 2篇 |
力学 | 1篇 |
综合类 | 1篇 |
物理学 | 12篇 |
出版年
2024年 | 2篇 |
2023年 | 3篇 |
2022年 | 9篇 |
2021年 | 3篇 |
2020年 | 15篇 |
2019年 | 14篇 |
2018年 | 17篇 |
2017年 | 30篇 |
2016年 | 27篇 |
2015年 | 28篇 |
2014年 | 14篇 |
2013年 | 59篇 |
2012年 | 53篇 |
2011年 | 46篇 |
2010年 | 49篇 |
2009年 | 49篇 |
2008年 | 54篇 |
2007年 | 53篇 |
2006年 | 44篇 |
2005年 | 42篇 |
2004年 | 49篇 |
2003年 | 36篇 |
2002年 | 25篇 |
2001年 | 17篇 |
2000年 | 13篇 |
1999年 | 5篇 |
1998年 | 5篇 |
1997年 | 8篇 |
1996年 | 2篇 |
1995年 | 3篇 |
1993年 | 1篇 |
排序方式: 共有775条查询结果,搜索用时 15 毫秒
21.
Edson G.R. Fernandes Valtencir Zucolotto Alvaro A.A. De Queiroz 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):1203-1207
Electrospun polyaniline nanofibers are one of the most promising materials for cardiac tissue engineering due to their tunable electroactive properties. Moreover, the biocompatibility of polyaniline nanofibes can be improved by grafting of adhesive peptides during the synthesis. In this paper, we describe the biocompatible properties and cardiomyocytes proliferation on polyaniline electrospun nanofibers modified by hyperbranched poly-L-lysine dendrimers (HPLys). The microstructure characterization of the HPLys/polyaniline nanofibers was carried out by scanning electron microscopy (SEM). It was observed that the application of electrical current stimulates the differentiation of cardiac cells cultured on the nanofiber scaffolds. Both electroactivity and biocompatibility of the HPLys based nanofibers suggest the use this material for culture of cardiac cells and opens the possibility of using this material as a biocompatible electroactive 3-D matrix in cardiac tissue engineering. 相似文献
22.
Accurate numerical methods for the propagation of light in large 3D samples with strong lateral variation of the director field require prohibitive amounts of time. We consider and compare a standard spectral method and the Finite Difference in Frequency Domain method, showing that the CPU time can be reduced by one or two orders of magnitude using a perturbation approach or a recently developed Reduced Order Method. The equations obtained are applied to liquid crystal cells with in-plane switching, illuminated by a large incoherent source. The developed formalism, based on numerically exact equations, is particularly suitable for treating magnetic or optically active media and for extending to such media the well known approximations based on the 4 × 4 (Berreman) or 2 × 2 (Jones) matrices. 相似文献
23.
Adrian M. Tomuta Xavier Fernández‐Francos Francesc Ferrando Xavier Ramis Àngels Serra 《先进技术聚合物》2013,24(11):962-970
A hyperbranched aromatic polyester (HBPOH) has been synthesized, and poly(ε‐caprolactone) arms have been grown on some of its end hydroxyl groups (HBPCL). These modifiers have been used in cationic diglycidyl ether of bisphenol A formulations cured with ytterbium triflate as cationic initiator. The effect of HBPOH and HBPCL on the curing kinetics has been studied using differential scanning calorimetry (DSC). The obtained materials have been characterized by dynamomechanical analysis, DSC, thermogravimetric analysis and mechanical tests. The modifiers are incorporated into the thermosetting network because of the participation of the end hydroxyl groups in the cationic curing of epoxides by the activated monomer mechanism. Homogeneous thermosets have been obtained with a remarkable increase in impact strength without sacrificing elastic modulus or hardness. A compromise between the rigid structure of the aromatic hyperbranched core and the flexibilizing effect of the poly(ε‐caprolactone) arms is believed to be responsible for the overall thermal and mechanical properties of the materials. The use of these polymeric modifiers increases the thermal stability of the resulting materials because of the low degradability of the aromatic ester groups in the hyperbranched core and the incorporation of the modifier into the network structure. However, the presence of such ester groups makes them reworkable by hydrolysis or alcoholysis in an alkaline medium, thus opening a way for recovery of valuable substrates. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
24.
Mitsutoshi Jikei Daisuke Uchida Yuuki Haruta Yuuki Takahashi Kazuya Matsumoto 《Journal of polymer science. Part A, Polymer chemistry》2012,50(18):3830-3839
Hyperbranched poly(ether sulfone)s were prepared by the self‐polycondensation of the novel AB2 monomer, 4‐(3,5‐hydroxyphenoxy)‐4′‐fluorodiphenylsulfone. The high‐molecular‐weight polymers were isolated in good yields. The degree of branching (DB) of the resulting polymers was investigated by the preparation of dendritic and linear model compounds. The DB determined by gated decoupling 13C NMR measurements was in the range 0.17–0.41 and was dependent on the base used for the self‐polycondensation. It was found that cesium fluoride was an effective base to form the polymer having the DB of 0.41. The resulting hyperbranched poly(ether sulfone)s showed good solubility in organic solvents. The solubility and the glass transition temperature of the polymers were influenced by the terminal functional groups. The unique thermal crosslinking phenomenon was observed during the DSC measurements of the hydroxyl‐terminated hyperbranched poly(ether sulfone) under air condition. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
25.
Yuichi Mori Kosei Nakaya Xianqing Piao Kazuhiro Yamamoto Akira Otomo Shiyoshi Yokoyama 《Journal of polymer science. Part A, Polymer chemistry》2012,50(7):1254-1260
A methacrylate‐based crosslinking hyperbranced polymers have been synthesized through initiator‐fragment incorporation radical polymerization and used for the temperature stable electro‐optic (EO) polymer application. This polymer consists of methyl methacrylate, 2‐metacryloxyethyl isocyanate, and ethylene glycol dimethacrylate (EGDMA) monomers. The use of EGDMA as a bifunctional unit resulted in the solvent‐soluble crosslinking hyperbranched chain, so that the EO polymer enhanced glass transition temperatures. A phenyl vinylene thiophene vinylene bridge nonlinear optical chromophore was attached to the polymer backbone as the side‐chain by a post‐functionalization reaction. The loading concentration of the chromophore was varied between 30 and 50 wt % by simply changing the mixing ratio of the precursor polymer to the chromophore. The synthesized EO polymers produced optical quality films with a light propagation loss of 0.61 dB/cm in a slab waveguide at 1.31 μm. The electrically poled film had an EO coefficient (r33) of 139 pm/V at 1.31 μm. The EO crosslinking hyperbranced polymer had a high‐glass transition temperature of 170 °C, and exhibited excellent temporal stability of the EO activity at 85 °C for 500 h. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
26.
Muhammad Imran ul‐haq Rajesh A. Shenoi Donald E. Brooks Jayachandran N. Kizhakkedathu 《Journal of polymer science. Part A, Polymer chemistry》2013,51(12):2614-2621
Hyperbranched polyglycerols (HPGs) are globular structures with a large number of functionalizable hydroxyl groups and have excellent in vitro and in vivo biocompatibility profiles comparable to polyethylene glycol. This work introduces a facile method for the synthesis of medium molecular weights (Mws) (50–300 kDa) HPGs, which has been difficult to synthesize with low polydispersity, with the assistance of solvents by ring opening polymerization. The influence of different solvents (1,4‐dioxane, tetrahydropyran (THP), ethylene glycol diethyl ether (EGDE) and decane), solvent to glycidol ratio, concentration of glycidol and the time of polymerization on Mw and polydispersity of HPGs has been studied. The Mw and polydispersity of HPGs are significantly affected by the nature of the polymerization phase (homogeneous or heterogeneous) and chemical structure of the solvent. The differences in the solvation of the potassium cations and change in the nucleophilicity of the alkoxide anion in various solvents may be responsible for the changes in Mw and PDI of the HPG. The Mw of the HPG decreases in the order 1,4‐dioxane > THP > EGDE >decane. The microstructure, solution and thermal properties of the HPG do not depend on the nature of solvent. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 2614–2621 相似文献
27.
Chen He Ban‐Kun Jin Wei‐Dong He Xue‐Song Ge Jing Tao Jing Yang Sheng‐Qi Chen 《Journal of polymer science. Part A, Polymer chemistry》2013,51(10):2142-2149
Long‐subchain hyperbranched polystyrene (lsc‐hp PSt) with uniform subchain length was obtained through copper‐catalyzed azide‐alkyne cycloaddition click chemistry from seesaw macromonomer of PSt having one alkynyl group anchored at the chain centre and two azido group attached to both chain ends [alkynyl‐(PSt‐N3)2]. After precipitation fraction, different portions of lsc‐hp PSt having narrow overall molecular weight distribution were obtained for further grafting with alkynyl‐capped poly(N‐isopropylacrylamide) (alkynyl‐PNIPAM), which was obtained via single‐electron transfer living radical polymerization of NIPAM with propargyl 2‐bromoisobutyrate as the initiator and grafted onto the peripheral azido groups of lsc‐hp PSt via click chemistry. Thus, amphiphilic lsc‐hp PSt grafted with PNIPAM chains (lsc‐hp PSt‐g‐PNIPAM) was obtained and would have star‐like conformation in tetrahydrofuran (THF). By replacing THF with water, lsc‐hp PSt‐g‐PNIPAM was dissolved at molecular level in aqueous solution due to the hydrophilicity of PNIPAM and exhibited thermal induced shrinkage of PNIPAM arms. The water‐insoluble lsc‐hp PSt would collapse densely and could be served as a reservoir to absorb hydrophobic chemicals in aqueous solution. The influence of overall molecular weight of lsc‐hp PSt on the absorption of pyrene was studied. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
28.
Lianwei Li Xu Wang Chen He Weidong He 《Journal of polymer science. Part A, Polymer chemistry》2014,52(1):128-138
Amphiphilic hyperbranched copolymer chains made of large hyperbranched poly(acrylic acid) cores grafted with short polystyrene stickers (HB‐PAAn‐g‐PSn + 1) with different n values (n = 1, 10, 47) were well prepared and confirmed by size exclusion chromatography, Fourier transform infrared spectroscopy and 1H nuclear magnetic resonance. The study on the interchain association behavior of these amphiphilic chains indicates that larger HB‐(PAA)n‐g‐(PS)n + 1 copolymer chains have a less tendency to undergo interchain association. Moreover, the simple vial‐inversion and rheological experiments show that the apparent critical gel concentration (Cg) decreases with n, but no sol–gel transition was observed for triblock PS‐PAA‐PS even when the concentration is up to 200 g L?1. Further transmission electron microscopy study of the latex particles prepared with HB‐(PAA)n‐g‐(PS)n + 1 as surfactant reveals that the latex particles are spherical and narrowly dispersed; while the measured latex particle number (Np) indicates the surfactant efficiency of HB‐(PAA)47‐g‐(PS)48 is poorer than that of triblock PS‐PAA‐PS (n = 1). Finally, pyrene solubilization measurement shows the solubilization efficiency of HB‐(PAA)n‐g‐(PS)n + 1 copolymers decreases with n, consistent with the previous observed interchain association result. The present study demonstrates that both the chain topology and the styrene weight fraction dominates the final solution properties of amphiphilic HB‐(PAA)n‐g‐(PS)n + 1 chains in aqueous solution. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 128–138 相似文献
29.
《Mendeleev Communications》2022,32(4):561-563
Hyperbranched Kaustamin as a commercially available cationic flocculant adsorbs on a glass surface with formation of the polymer film. Kaustamin has antimicrobial effect on Gram-negative and Gram-positive bacteria, its film on glass keeps integrity and shape after absorption of water from air, which make the polymer appropriate as an antibacterial cover. 相似文献
30.
Muhammad Waqas Ali Siyuan Cheng Jianhao Si Muhammad Siddiq Xiaodong Ye 《Journal of polymer science. Part A, Polymer chemistry》2019,57(19):2030-2037
Hyperbranched poly(2‐ethyl‐2‐oxazoline) was synthesized by a combination of cationic ring‐opening polymerization and the oxidation of thiol to disulfide groups. A three‐arm star poly(2‐ethyl‐2‐oxazoline) (PEtOx) was first synthesized using 1,3,5‐tris(bromomethyl) benzene as an initiator. The star PEtOx was end‐capped with potassium ethyl xanthate. Similarly, a linear PEtOx was synthesized and end‐capped with potassium ethyl xanthate using benzyl bromide as an initiator. Hyperbranched PEtOx was then obtained by in situ cleaving and subsequent oxidation of the star PEtOx and linear PEtOx mixture with n‐butylamine as both a cleaving agent and a base in tetrahydrofuran. The linear PEtOx was used to prevent the formation of gel. The hyperbranched PEtOx can be cleaved with dithiothreitol to trithiol and monothiol polymer. The hyperbranched PEtOx shows no remaining thiols using Ellman's assay. The resulting hyperbranched PEtOx was hydrolyzed to a novel hyperbranched polyethyleneimine with degradable disulfide linkages. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 2030–2037 相似文献