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891.
F. B. Xiong W. Z. Zhu H. F. Lin X. G. Meng 《Applied physics. B, Lasers and optics》2014,115(1):129-135
The feasibility of sapphire fiber-optic sensors based on evanescent wave absorption spectroscopy in the infrared range for quantitative determination of water content in polar organic solvents has been investigated. Evanescent wave absorption spectra of sapphire fiber-optic sensors in glycerol, ethanol, and glycol with different water concentrations obtained and analyzed, respectively. Evanescent absorbance of the sensors in those organic solvents has been utilized to implement for in situ monitoring water concentration in organic solvents. The evanescent absorbance of sensors in glycerol and glycol has been found to vary linearly with water content in the range 0–30 % and in ethanol in the range 0–10 %, respectively. The fiber-optic sensors based on evanescent absorbance for monitoring water concentrations in those organic solvents are acceptably accurate, cost-effective, and reliable. Some methods to improve the accuracy of predicated water content in those organic solvents are also suggested. Overall, the results demonstrate that the sapphire fiber-optic sensor based on evanescent absorption spectroscopy is a promising candidate for prediction of water content in polar organic solvents in on-line and remote situation. 相似文献
892.
长期观测显示,耀变体S5 0716+714具有复杂的光变行为.本文运用混沌理论,研究了S5 0716+714四个较大爆发阶段的射电、光学和X波段的光变曲线.分别计算了它们的关联维和Lyapunov指数.结果表明:1)光变曲线的关联维和Lyapunov指数都介于纯混沌系统与随机噪声之间;2)相轨迹是一个与Rossler吸引子相似的混沌系统,由于受到各种内在或外在因素的影响产生噪声,导致关联维和Lyapunov指数均比Rossler吸引子大,相轨迹出现紊乱.从这两个混沌判据上看,三个波段均表现出很强的混沌特性,因此推断S50714+716的光变是一个混沌现象. 相似文献
893.
采用水热法制备了ZnO和不同掺杂浓度的ZnO:Cd纳米棒,通过SEM,XRD、拉曼光谱等的分析,研究了ZnO和ZnO:Cd的微结构并测试分析了其光致发光特性.结果表明,ZnO和ZnO:Cd纳米棒呈六角纤锌矿结构,Cd掺杂使得纳米棒体积更小.由于内部张应力的影响,Cd掺杂使得材料光学带隙减少.当掺杂浓度为2%时,合成的材料光致发光谱中出现了位于2.67 eV处,由导带底和Zn空位(VZn)缺陷能级跃迁造成的蓝光发射峰,并且Cd的掺入使得位于2.90 eV附近的紫光发射峰强度增强,对于研究ZnO蓝紫发光器件具有重要的意义. 相似文献
894.
Zhou XJ Shi J Yoshida T Cuk T Yang WL Brouet V Nakamura J Mannella N Komiya S Ando Y Zhou F Ti WX Xiong JW Zhao ZX Sasagawa T Kakeshita T Eisaki H Uchida S Fujimori A Zhang Z Plummer EW Laughlin RB Hussain Z Shen ZX 《Physical review letters》2005,95(11):117001
High resolution angle-resolved photoemission spectroscopy data along the (0,0)-(pi,pi) nodal direction with significantly improved statistics reveal fine structure in the electron self-energy of the underdoped (La2-xSrx)CuO4 samples in the normal state. Fine structure at energies of (40-46) meV and (58-63) meV, and possible fine structure at energies of (23-29) meV and (75-85) meV, have been identified. These observations indicate that, in (La2-xSrx)CuO4, more than one bosonic modes are involved in the coupling with electrons. 相似文献
895.
896.
Huan Huan Zhang Ya Ting Liu Rong Wang Xiao Yan Yu Xiong Wei Qu Qing Xin Zhang 《中国化学快报》2011,22(4):485-488
A novel nanodiamond-epoxy derivative(ND-EP) was synthesized by grafting epoxy monomers onto the surface of nanodiamond(ND),and characterized by FTIR and TGA.The ratio of grafted epoxy groups was determined to be 32.5 wt% by TGA.The developed methodology provides an efficient method for the functionalization of nanodiamond material,which enables a variety of advanced engineering and biomedical applications of ND. 相似文献
897.
A novel Selectfluor-mediated copper-catalyzed highly selective benzylic C-O cyclization for the synthesis 4H-3,1-benzoxazines is reported. The predominant selectivity for a benzylic C(sp(3))-H over an aromatic C(sp(2))-H bond in N-o-tolylbenzamides is achieved. 相似文献
898.
Xiong DB Okamoto NL Waki T Zhao Y Kishida K Inui H 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(9):2536-2542
Heusler phases, including the full- and half-Heusler families, represent an outstanding class of multifunctional materials on account of their great tunability in compositions, valence electron counts (VEC), and properties. Here we demonstrate a systematic design of a series of new compounds with a 2×2×2 superstructure of the half-Heusler unit cell in X-Y-Z (X=Fe, Ru, Co, Rh, Ir; Y=Zn, Mn; Z=Sn, Sb) systems. Their structures were solved by using both powder and single-crystal X-ray diffraction, and also directly observed by using high-angle annular dark-field imaging in a scanning transmission electron microscope (HAADF-STEM). The VEC values of these new compounds span a wide and continuous range comparable to those for the full- and half-Heusler families, thereby implying tunability in compositions and physical properties in the superstructure. In fact, we observed abnormal electrical properties and a ferromagnetic semiconductor-like behavior with a high and tunable Curie temperature in these superstructures. 相似文献
899.
Huaping Tan Qixin Zhou Haifeng Qi Dan Zhu Xiaoxue Ma Dangsheng Xiong 《Macromolecular bioscience》2012,12(5):621-627
A new methodology is developed to conjugate hyaluronic acid (HA) hydrogel with novel nano‐fibrous architectures via non‐covalent assembly that specifically allows for targeted adipose‐derived stem cells (ASCs) differentiation and soft tissue engineering. The assembly of non‐covalently associated hydrogel network produced via the interaction of a low molecular weight heparin (LMWH) modified HA derivative and heparin interacting protein (HIP). The multifunctional star poly(ethylene glycol) (PEG) and HIP copolymer has the capability to mediate the non‐covalent assembly of nano‐fibrous HA hydrogel networks via affinity interactions with LMWH. The effect of the HIP mediation on in vitro gelation, rheological characteristics, degradation, equilibrium swelling, adipose‐derived stem cells (ASCs) proliferation and differentiation of nano‐fibrous hydrogel is examined. The results suggest the potential utility of this unique design of the bioactive nano‐fibrous HA hydrogel in directing the differentiation of ASCs and adipogenesis in ECM‐mimetic scaffolds in vitro. These studies demonstrate that this nano‐fibrous HA hydrogel can render the formulation of a therapeutically effective platform for in vitro adipogenesis applications.
900.
Modifying the β‐diketimine ligand LH 1 (LH=[ArN?C(Me)? CH?C(Me)? NHAr], Ar=2,6‐iPr2C6H3) through replacement of the proton in 3‐position by a benzyl group (Bz) leads to the new BzLH ligand 2, which could be isolated in 77 % yield. According to 1H NMR spectroscopy, 2 is a mixture of the bis(imino) form [(ArN?C(Me)]2CH(Bz) 2a and its tautomer [ArN?C(Me)? C(Bz)?C(Me)NHAr] 2b. Nevertheless, lithiation of the mixture of 2a and 2b affords solely the N‐lithiated β‐diketiminate [ArN?C(Me)? C(Bz)?C(Me)? NLiAr], BzLLi 3. The latter reacts readily with GeCl2?dioxane to form the chlorogermylene BzLGeCl 4, which serves as a precursor for a new zwitterionic germylene by dehydrochlorination with LiN(SiMe3)2. This reaction leads to the zwitterionic germylene BzL′Ge: 5 (BzL′=ArNC(?CH2)C(Bz)?C(Me)NAr) which could be isolated in 83 % yield. The benzyl group has a distinct influence on the reactivity of zwitterionic 5 in comparison to its benzyl‐free analogue, as shown by the reaction of 5 with phenylacetylene, which yields solely the 1,4‐addition product 6, that is, the alkynyl germylene BzLGeCCPh. Compounds 2–8 have been fully characterized by multinuclear NMR spectroscopy, mass spectrometry, elemental analyses, and single‐crystal X‐ray diffraction analyses. 相似文献