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991.
Ying‐Hui Wang Li‐Jing Gong Wen‐Yue Dong Ping Lu Zhi‐Hui Kang Tian‐Hao Huang Yu‐Guang Ma Han‐Zhuang Zhang 《Journal of Polymer Science.Polymer Physics》2013,51(12):992-997
The photoexcitation processes of two donor–acceptor‐type copolymers PCFBT with different ratios between the donor and the acceptor ( PCFBT0.5 and PCFBT0.1 ) in the solution system are systematically studied. If the number of the donor is equal to that of the acceptor in one repeat unit (such as PCFBT0.5 ), intrachain charge transfer (ICT) can occur and participate in the relaxation of the excited state after photoexcitation. When the number of donors is much larger than that of acceptors (such as PCFBT0.1 ) in one repeat unit, the ICT character can disappear, and the localized exciton decay process is dominant in the relaxation of the copolymer, which also involves an excitation intensity‐independent vibrational thermal relaxation process at the initial time. The results further the understanding of the basic structure‐property relationship. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013 , 51, 992–996 相似文献
992.
Prabhakar Rai Yun-Su Kim Sang-Ki Kang Yeon-Tae Yu 《Plasma Chemistry and Plasma Processing》2012,32(2):211-218
A thermal plasma system was used for the preparation of nanosized SiC powder. First SiC was synthesized by solid-state reaction
using waste silicon and activated carbon powders and then plasma processing was carried out to form nanosized SiC. Phase and
structural analysis was carried out by X-ray diffraction which confirmed the formation of SiC in both cases. Plasma treatment
did not show any kind of change in structure and phase of SiC; except little free silicon. Morphological investigation showed
the formation of 20–30 nm spherical SiC particles after plasma treatment which was initially 1–5 μm. It was found that DC
current played an important role in the reduction of particle size. It was proposed that nanosized SiC was formed due to the
dissociation of grains from their grain boundary due to strong plasma gas stream. 相似文献
993.
本届会议于2009年9月6日至10口在奥地利Tyrol州首府--Inshruck市召开,由欧洲化学与分子科学协会分析化学部主办、奥地利分析化学会协办.大会报告有:(1) H Fuchs( Emich奖章获得者),纳级分析-物质在原子级的探测;(2) P K Dasgupta,离子学-在溶液中检测离子的新典范;(3) B Mizaikoff(Robert Kellner奖获得者),用于提高红外光区鉴别的先进波导;(4)C KBonn,应用于"组学"领域的浓集与分离技术的新固定相-分析分离科学中的挑战. 相似文献
994.
995.
Fen Ran Yong‐tao Tan Ji Liu Lei zhao Ling‐bin Kong Yong‐chun Luo Long Kang 《先进技术聚合物》2012,23(9):1297-1301
This article reports the preparation and self‐assembly of polyaniline (PANI) nanotubes, which were chemically synthesized by using in situ doping polymerization in the presence of ammonium persulfate (APS; (NH4)S2O8) as the oxidant without the use of an external template. The synthesized hierarchically nanotubes with a shape of a single nanotube with a length of 0.6 to 0.8 µm and an average with of 100 nm assembled from nanoparticles. The effects of the [salicylic acid]/[aniline] ratio on the size and capacitance of PANI nanotubes were studied. The specific capacitance behavior of the PANI nanotubes was also investigated by using cyclic voltammogram and galvanostatic charge–discharge tests. A maximum discharge‐specific capacitance of 422.5 F/g could be achieved, suggesting its potential application in electrode material for electrochemical capacitors. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
996.
997.
Seon‐Kyoung Son Yoon‐Suk Choi Woo‐Hyung Lee Yongtaek Hong Jae‐Ryoung Kim Won‐Suk Shin Sang‐Jin Moon Do‐Hoon Hwang In‐Nam Kang 《Journal of polymer science. Part A, Polymer chemistry》2010,48(3):635-646
A series of new phenothiazylene vinylene‐based semiconducting polymers, poly[3,7‐(4′‐dodecyloxyphenyl)phenothiazylene vinylene] ( P1 ), poly[3,7‐(4′‐dodecyloxyphenyl)phenothiazylene vinylene‐alt‐1,4‐phenylene vinylene] ( P2 ), and poly[3,7‐(4′‐dodecyloxyphenyl)phenothiazylene vinylene‐alt‐2,5‐thienylene vinylene] ( P3 ), have been synthesized via a Horner‐Emmons reaction. FTIR and 1H NMR spectroscopies confirmed that the configurations of the vinylene groups in the polymers were all‐trans (E). The weight‐averaged molecular weights (Mw) of P1 , P2 , and P3 were found to be 27,000, 22,000, and 29,000, with polydispersity indices of 1.91, 2.05, and 2.25, respectively. The thermograms for P1 , P2 , and P3 each contained only a broad glass transition, at 129, 167, and 155 °C, respectively, without the observation of melting features. UV–visible absorption spectra of the polymers showed two strong absorption bands in the ranges 315–370 nm and 450–500 nm, which arose from absorptions of the phenothiazine segments and the conjugated main chains. Solution‐processed field‐effect transistors fabricated from these polymers showed p‐type organic thin‐film transistor characteristics. The field‐effect mobilities of P1 , P2 , and P3 were measured to be 1.0 × 10?4, 3.6 × 10?5, and 1.0 × 10?3 cm2 V?1 s?1, respectively, and the on/off ratios were in the order of 102 for P1 and P2 , and 103 for P3 . Atomic force microscopy and X‐ray diffraction analysis of thin films of the polymers show that they have amorphous structures. A photovoltaic device in which a P3 /PC71BM (1/5) blend film was used as the active layer exhibited an open‐circuit voltage (VOC) of 0.42 V, a short circuit current (JSC) of 5.17 mA cm?2, a fill factor of 0.35, and a power conversion efficiency of 0.76% under AM 1.5 G (100 mW cm?2) illumination. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 635–646, 2010 相似文献
998.
HoSeok Park Prof. Dr. Young Mee Jung Prof. Dr. Seong Ho Yang Dr. Weonho Shin Jung Ku Kang Prof. Dr. Hoon Sik Kim Prof. Dr. Hyun Joo Lee Dr. Won Hi Hong Prof. Dr. 《Chemphyschem》2010,11(8):1711-1717
Geometric and conformational changes of zwitter‐type ionic liquids (ZILs) due to hydrogen‐bonding interactions with water molecules are investigated by density functional theory (DFT), two‐dimensional IR correlation spectroscopy (2D IR COS), and pulsed‐gradient spin‐echo NMR (PGSE NMR). Simulation results indicate that molecular structures in the optimized states are strongly influenced by hydrogen bonding of water molecules with the sulfonate group or imidazolium and pyrrolidinium rings of 3‐(1‐methyl‐3‐imidazolio)propanesulfonate ( 1 ) and 3‐(1‐methyl‐1‐pyrrolidinio)propanesulfonate ( 2 ), respectively. Concentration‐dependent 2D IR COS reveals kinetic conformational changes of the two ZIL–H2O systems attributable to intermolecular interactions, as well as the interactions of sulfonate groups and imidazolium or pyrrolidinium rings with water molecules. The dramatic changes in the 1H self‐diffusion coefficients elucidate the formation of proton‐conduction pathways consisting of ZIL networks. In ZIL domains, protons are transferred by a Grotthuss‐type mechanism through formation, breaking, and restructuring of bonds between ZILs and H2O, leading to an energetically favorable state. The simulation and experimental investigations delineated herein provide a perspective to understanding the interactions with water from an academic point of view as well as to designing ILs with desired properties from the viewpoint of applications. 相似文献
999.
Ching Hsuan Lin Yu Ren Feng Kang Hong Dai Hou Chien Chang Tzong Yuan Juang 《Journal of polymer science. Part A, Polymer chemistry》2013,51(12):2686-2694
A phenolic OH‐containing benzoxazine ( F‐ap ), which cannot be directly synthesized from the condensation of bisphenol F, aminophenol, and formaldehyde by traditional procedures, has been successfully prepared in our alternative synthetic approach. F‐ap was prepared by three steps including (a) condensation of 4‐aminophenol and 5,5'‐methylenebis(2‐hydroxybenzaldehyde) (1) , (b) reduction of the resulting imine linkage by sodium borohydride, and (c) ring closure condensation by formaldehyde. The key starting material, (1) , was prepared from 2‐hydroxybenzaldehyde and s‐trioxane in the presence of sulfuric acid. F‐ap is structurally similar to bis(3,4‐dihydro‐2H‐3‐phenyl‐1,3‐benzoxazinyl)methane ( F‐a, a commercial benzoxazine based on bisphenol F/aniline/formaldehyde) except for two phenolic OHs. The phenolic OHs can provide reaction sites with epoxy and 1,1'‐(methylenedi‐p‐phenylene)bismaleimide (BMI). The structure–property relationships between the thermosets of F‐ap /epoxy, F‐a /epoxy, F‐ap /BMI, and F‐a /BMI were discussed. Experimental data showed that thermosets based on F‐ap /epoxy and F‐ap /BMI provided much better thermal properties than those based on F‐a /epoxy and F‐a /BMI. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 2686–2694 相似文献
1000.
In the paper,an experiment investigation was conducted for one-and two-degree of freedom vortex-induced vibration(VIV) of a horizontally-oriented cylinder with diameter of 11 cm and length of 120 cm.In the experiment,the spring constants in the cross-flow and in-line flow directions were regulated to change the natural vibration frequency of the model system.It was found that,in the one-degree of freedom VIV experiment,a "double peak" phenomenon was observed in its amplitude within the range of the reduced velocities tested,moreover,a "2T" wake appeared in the vicinity of the second peak.In the two-degree of freedom VIV experiment,the trajectory of cylinder exhibited a reverse "C" shape,i.e.,a "new moon" shape.Through analysis of these data,it appears that,besides the non-dimensional in-line and cross-flow natural vibration frequency ratios,the absolute value of the natural vibration frequency of cylinder is also one of the important parameters affecting its VIV behavior. 相似文献