全文获取类型
收费全文 | 2402篇 |
免费 | 159篇 |
国内免费 | 513篇 |
专业分类
化学 | 2829篇 |
晶体学 | 8篇 |
力学 | 11篇 |
综合类 | 11篇 |
数学 | 3篇 |
物理学 | 212篇 |
出版年
2024年 | 1篇 |
2023年 | 16篇 |
2022年 | 21篇 |
2021年 | 43篇 |
2020年 | 68篇 |
2019年 | 59篇 |
2018年 | 53篇 |
2017年 | 87篇 |
2016年 | 92篇 |
2015年 | 73篇 |
2014年 | 99篇 |
2013年 | 270篇 |
2012年 | 109篇 |
2011年 | 137篇 |
2010年 | 124篇 |
2009年 | 146篇 |
2008年 | 164篇 |
2007年 | 174篇 |
2006年 | 176篇 |
2005年 | 168篇 |
2004年 | 162篇 |
2003年 | 139篇 |
2002年 | 115篇 |
2001年 | 78篇 |
2000年 | 48篇 |
1999年 | 42篇 |
1998年 | 36篇 |
1997年 | 32篇 |
1996年 | 34篇 |
1995年 | 66篇 |
1994年 | 58篇 |
1993年 | 49篇 |
1992年 | 47篇 |
1991年 | 19篇 |
1990年 | 16篇 |
1989年 | 9篇 |
1988年 | 4篇 |
1987年 | 8篇 |
1986年 | 2篇 |
1985年 | 5篇 |
1984年 | 7篇 |
1983年 | 4篇 |
1982年 | 2篇 |
1980年 | 2篇 |
1979年 | 2篇 |
1978年 | 5篇 |
1976年 | 1篇 |
1975年 | 1篇 |
1974年 | 1篇 |
排序方式: 共有3074条查询结果,搜索用时 31 毫秒
71.
72.
73.
Young-Woon Cho Kyung-Seok Kang Chanhyuk Jee Ji-Hyun Kim Dongju Jang 《Molecular Crystals and Liquid Crystals》2016,634(1):73-81
Polyamic acid (PAA) made from 3,3, 4,4-biphenyltetracarboxylic dianhydride and 4,4-diaminodiphenyl ether was synthesized and used as the backbone of nanoporous polyimide. Thermally labile polyethylene glycol (PEG) at 10, 20 or 30 wt% was introduced to the end group of PAA. Self-assembled PAA-b-PEG micelle-like nanoparticles could be formed as a result of amphiphilic characteristics of hydrophobic PAA and hydrophilic PEG. Thermal imidization and degradation of spin-coated amphiphilic PAA-b-PEG film were performed sequentially through one-step heat treatment to obtain polyimide film with nanopores. Pore sizes decreased with increasing amount of PEG block and their dielectric constants decreased from 2.71 ± 0.13 to 2.38 ± 0.11. 相似文献
74.
Episodic release of bioactive compounds is often necessary for appropriate biological effects under specific physiological conditions. Here, we aimed to develop an injectable, biocompatible, and thermosensitive hydrogel system for ultrasound (US)-triggered drug release. An mPEG-PLGA-BOX block copolymer hydrogel was synthesized. The viscosity of 15 wt% hydrogel is 0.03 Pa*s at 25 °C (liquid form) and 34.37 Pa*s at 37 °C (gel form). Baseline and US-responsive in vitro release profile of a small molecule (doxorubicin) and that of a large molecule (FITC-dextran), from the hydrogel, was tested. A constant baseline release was observed in vitro for 7 d. When triggered by US (1 MHz, continuous, 0.4 W/cm2), the release rate increased by approximately 70 times. Without US, the release rate returned to baseline. Baseline and US-responsive in vivo release profile of doxorubicin was tested by subcutaneous injection in the back of mice and rats. Following injection into the subcutaneous layer, in vivo results also suggested that the hydrogels remained in situ and provided a steady release for at least 7 d; in the presence of the US-trigger, in vivo release from the hydrogel increased by approximately 10 times. Therefore, the mPEG-PLGA-BOX block copolymer hydrogel may serve as an injectable, biocompatible, and thermosensitive hydrogel system that is applicable for US-triggered drug release. 相似文献
75.
J. Nassar J. Goldbach 《International journal of environmental analytical chemistry》2013,93(2):145-159
Abstract The problem of determining the concentration changes of reactive hydrocarbon immissions as a function of time was solved by means of an automatic gas chromatograph which, without enrichment, could record ethylene and acetylene in ppb concentrations. At the same time various other pollutants were covered, so that by a mutual allocation of the individual components it was possible to identify certain emitter groups. The results clearly show that ethylene and acetylene primarily originate from the combustion processes of the automobiles, while the handling and storage of petroleum products and their processing do not exert any influence on the immission of the two components. By way of time series measurements during a summer week in 1976 with very intensive solar radiation it was possible to show indirect secondary photochemical reactions. 相似文献
76.
The phase transformation from the tetragonal to the hexagonal crystal modification in highly oriented lamellae of poly-butene-1 has been followed by transmission electron microscopy (TEM). It is found that the reaction-controlling step is the nucleation process. No lattice orientation relationship (besides the [001]-direction, which is parallel in both crystal modifications) exists between non-transformed and transformed crystals. The nucleation is strongly enhanced by thermal or external stresses. Crystal growth, nucleated by external stresses, was observed at temperatures as low as — 150°C. The molecular mechanisms of the transformation are discussed. 相似文献
77.
Synthesis of ethylene/vinyl ester copolymers with pendent linear branches via ring‐opening metathesis polymerization of fatty acid‐derived cyclooctenes 下载免费PDF全文
Yuchen Feng Suyun Jie Bo‐Geng Li 《Journal of polymer science. Part A, Polymer chemistry》2017,55(13):2211-2220
Fatty acid‐derived cyclooctenes, including n‐hexanoic acid ( M1 ), n‐octanoic acid ( M2 ), lauric acid ( M3 ), and palmitic acid ( M4 ), were prepared as monomers and polymerized by ring‐opening metathesis polymerization (ROMP) using Grubbs second‐generation catalyst ( G2 ). In all the cases, the regio‐irregular unsaturated polymers with pendent linear branches were obtained, which could be saturated by chemical hydrogenation with TSH/TPA in high conversion, yielding ethylene/vinyl ester copolymers with pendent linear branches on precisely every eighth backbone carbon. Both unsaturated and saturated polymers were amorphous, and their structures were characterized by FTIR, 1H and 13C NMR spectra, and elemental analysis. Differential scanning calorimetry (DSC) and thermo‐gravimetric analysis (TGA) were used to study their thermal properties. The chain length of branches greatly affected the thermal properties of polymers. After hydrogenation, the thermal degradation stability of polymers was relatively improved. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2211–2220 相似文献
78.
Crystallization in ultrathin Poly(Ethylene Oxide)/Poly(Methyl Methacrylate) (PEO/PMMA) blend films with thickness of ca. 10 nm was investigated by means of microscopic and in situ spectroscopic methods. It was revealed that the blend films undergo a phase ordering in a humid atmosphere before or during crystallization, with PEO de-mixing with PMMA and segregating to the free film interface on the PMMA layer. The de-mixed PEO chains crystallize into a fractal-like morphology by a diffusion-limited process, and the crystal growth is 1-dimensional with Avrami exponent n ≈ 1, resulting in flat-on crystal lamellae with the PEO chains oriented normal to the film plane. 相似文献
79.
《Journal of Macromolecular Science: Physics》2013,52(5-6):701-710
Permanganic etching was performed on high-speed spun (HSS) and regular fibers of poly(ethylene terephthalate) (PET), and their surface morphologies were investigated via the two-stage carbon replica method using a transmission electron microscope (TEM). The HSS PET fibers, with disordered amorphous regions, showed peculiar surface morphology; many small warts corresponding to the pits of etched disordered amorphous regions were observed. Such unevenness, however, was hardly observed on the surface of the permanganic-etched regular PET fibers, with well-oriented amorphous regions, or on the surface of alkali-etched HSS PET fibers. The permanganic etchant removed the disordered amorphous regions more preferentially compared with the alkali etchant. 相似文献
80.
Floraine Collette Régis Delatouche Christophe Blanquart Fabien Gueugnon Marc Grégoire Philippe Bertrand Valérie Héroguez 《Journal of polymer science. Part A, Polymer chemistry》2013,51(1):176-189
In this contribution, a versatile approach for the synthesis of functionalized particles for drug delivery is presented, using two nonaggressive standardized procedures. The first procedure considered is the functionalization of an azido‐terminated α‐norbornenyl poly(ethylene oxide) (PEO) macromonomer with an alkyne‐containing active molecule via the copper catalyzed azide alkyne cycloaddition, click type reaction. The functionalized macromonomer is then polymerized by Ring‐Opening Metathesis Polymerization (ROMP) in dispersion to form functionalized particles. The second procedure consists in synthesizing particles by ROMP in dispersed media of norbornene with azido‐terminated α‐norbornenyl PEO macromonomer. The ROMP was initiated by the first generation Grubbs catalyst. Such functionalized core‐shell particles have stealthy properties due to their PEO shell and can be viewed as universal nanocarriers on which any alkyne‐modified active molecule can be grafted by click chemistry. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献