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991.
Guan‐E Wang Gang Xu Ning‐Ning Zhang Ming‐Shui Yao Ming‐Sheng Wang Guo‐Cong Guo 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(9):2718-2721
Superlattice materials offer new opportunities to modify optical and electrical properties of recently emerging 2D materials. The insertion of tetraethylbenzidine (EtDAB) into interlamination of the established 2D PbI2 semiconductor through a mild solution method yielded the first lead iodide superlattice, EtDAB?4PbI2 (EtDAB=tetraethylbenzidine), with radical and non‐radical forms. The non‐radical form has a non‐ionic structure that differs from the common ionic structures for inorganic–organic hybrid lead halides. The radical form shows five orders of magnitude greater conductance and broader photoconductive response range (UV/Vis → UV/Vis‐IR), than pure PbI2 and the non‐radical form of the superlattice. 相似文献
992.
Dioxomolybdenum(VI) complex covalently attached to amino‐modified graphene oxide: heterogeneous catalyst for the epoxidation of alkenes 下载免费PDF全文
Zhifang Li Shujie Wu Dafang Zheng Jiayin Liu Heng Liu Haiming Lu Qisheng Huo Jingqi Guan Qiubin Kan 《应用有机金属化学》2014,28(5):317-323
Transition metal salen complex MoO2–salen was successfully tethered onto amino‐functionalized graphene oxide (designated as MoO2–salen–GO), which was tested in the epoxidation of various alkenes using tert‐butylhydroperoxide or H2O2 as oxidant. Characterization results showed that dioxomolybdenum(VI) complex was successfully grafted onto the amino‐functionalized graphene oxide and the structure of the graphene oxide was well preserved after several stepwise synthesis procedures. Catalytic tests showed that heterogeneous catalyst MoO2–salen–GO was more active than its homogeneous analogue MoO2–salen in the epoxidation of cyclooctene due to site isolation. In addition, the MoO2–salen–GO catalyst could be reused three times without significant loss of activity. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
993.
Dr. Lubna Ghani Dr. Seonghoon Kim Dr. Haoqing Wang Hyun Sung Lee Dr. Jonas S. Mortensen Dr. Satoshi Katsube Dr. Yang Du Dr. Aiman Sadaf Dr. Waqar Ahmed Prof. Bernadette Byrne Prof. Lan Guan Prof. Claus J. Loland Prof. Brian K. Kobilka Prof. Wonpil Im Prof. Pil Seok Chae 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(21):e202200116
Membrane proteins are of biological and pharmaceutical significance. However, their structural study is extremely challenging mainly due to the fact that only a small number of chemical tools are suitable for stabilizing membrane proteins in solution. Detergents are widely used in membrane protein study, but conventional detergents are generally poor at stabilizing challenging membrane proteins such as G protein-coupled receptors and protein complexes. In the current study, we prepared tandem triazine-based maltosides (TZMs) with two amphiphilic triazine units connected by different diamine linkers, hydrazine (TZM−Hs) and 1,2-ethylenediamine (TZM−Es). These TZMs were consistently superior to a gold standard detergent (DDM) in terms of stabilizing a few membrane proteins. In addition, the TZM−Es containing a long linker showed more general protein stabilization efficacy with multiple membrane proteins than the TZM−Hs containing a short linker. This result indicates that introduction of the flexible1,2-ethylenediamine linker between two rigid triazine rings enables the TZM−Es to fold into favourable conformations in order to promote membrane protein stability. The novel concept of detergent foldability introduced in the current study has potential in rational detergent design and membrane protein applications. 相似文献
994.
Yan Wen Fang Lian Yan Ren Hong‐Yan Guan 《Journal of Polymer Science.Polymer Physics》2014,52(8):572-577
Polyvinyl formal (PVFM)‐based dense polymer membranes with nano‐Al2O3 doping are prepared via phase inversion method. The membranes and also their performances as gel polymer electrolytes (GPEs) for lithium ion battery are studied by field emission scanning electron microscope, X‐ray diffraction, differential scanning calorimetry, mechanical strength test, electrolyte uptake test, electrochemical impedance spectroscopy, cyclic voltammetry, and charge–discharge test. The polymer membrane with 3 wt % nano‐Al2O3 doping shows the improved mechanical strength of 12.16 MPa and electrolyte uptake of 431.25% compared with 10.47 MPa and 310.59% of the undoped sample, respectively. The membrane absorbs and swells liquid electrolyte to form stable GPE with ionic conductivity of 4.92 × 10?4 S cm?1 at room temperature, which is higher than 1.77 × 10?4 S cm?1 of GPE from the undoped membrane. Moreover, the Al2O3‐modified membrane supporting GPE exhibits wide electrochemical stability window of 1.2–4.8 V (vs. Li/Li+) and good compatibility with LiFePO4 electrode, which implies Al2O3‐modified PVFM‐based GPE to be a promising candidate for lithium ion batteries. © 2014 Wiley Periodicals, Inc. J. Polym. Sci. Part B: Polym. Phys. 2014 , 52, 572–577 相似文献
995.
996.
Experimental modal analysis of a tire was carried out. Mode shapes in the radial, tangential and lateral directions of the
tire under radial and tangential excitation, respectively, were obtained for the first time. The consistency of tire experimental
modal frequencies in three directions was observed after careful design and adjustment of the test method. This indicates
the accuracy of the experiments. The phenomena discovered in this experimental study, such as the mode shapes of the rim and
the complex modes of the tire, are discussed in detail. The modal parameters acquired from experimental modal analysis of
the tire can be used for the modeling of tire dynamics. 相似文献
997.
Hongyan Yao Yunhe Zhang Yu Liu Kaiyuan You Shanyou Liu Baijun Liu Shaowei Guan 《Journal of polymer science. Part A, Polymer chemistry》2014,52(3):349-359
A series of novel high molecular weight fluorinated co‐polyimides (Co‐PIs) containing styryl side chain based on 1,3‐bis(2‐trifluoromethyl‐4‐aminophenoxy)‐5‐(2,3,4,5‐tetrafluorophenoxy)benzene (6FTFPB) were successfully synthesized. The weight‐average molecular weights (Mws) and polydispersities of the co‐polyimides were in the range 8.93–10.81 × 104 and 1.33–1.82, respectively. The co‐polyimide film showed excellent solubility in organic solvents, high tensile properties (tensile strength exceeded 91 MPa), excellent optical transparency (cutoff wavelength at 332–339 nm and light transparencies above 89% at a wavelength of 550 nm), and high thermal stability (5% thermal weight‐loss temperature up to 510 °C). The casting and spinning films could be cross‐linked by thermal curing. The cured films show better combination property (including excellent resistance to solvents) than that of co‐polyimides. For instance, the glass transition temperature of Co‐PI‐1 (the molar weight ratio of 6FTFPB was 30%) increased from 217 to 271 °C, the tensile strength enhanced from 94 to 96 MPa, the 5% thermal weight‐loss temperature improved from 514 to 525 °C. Moreover, after cured, Co‐PI‐1 film also has a coefficient of thermal expansion (CTE) value of 60.3 ppm °C?1, low root mean square surface roughness (Rq) at 4.130 nm and low dielectric constant of 2.60. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 349–359 相似文献
998.
999.
Xin-Meng Fan Xian-Tao Yang Yu-Jia Guo Ren-Min Wu De-Lin Pan Zhu Guan Xiao-Mei Ling Li-He Zhang Zhen-Jun Yang 《中国化学快报》2016,27(12):1759-1762
Deamination is a crucial step in the transformation of 6-cyclopropylamino guanosine prodrug to its active form. A convenient method using capillary electrophoresis (CE) without sample labeling was developed to analyze the deamination of a series of D-/L-6-cyclopropylamino guanosine analogs by mouse liver homogenate, mouse liver microsome, and adenosine deaminase (ADA). A two-step process involving a 6-amino guanosine intermediate formed by oxidative N-dealkylation was demonstrated in the metabolism of 6-cyclopropylamino guanosine to 6-hydroxy guanosine. The results indicated that the transformation rates of different prodrugs to the active form varied greatly, which were closely correlated with the configuration of nucleosides and the structure of glycosyl groups. Most importantly, D-form analogs were metabolized much faster than their L-counterparts, thus clearly pointed out that compared to guanine, modification of glycosyl part might be a better choice for the development of L-guanosine analogs for the treatment of HIV. 相似文献
1000.