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21.
Kazem Jeddi Nader Taheri Qazvini Daniele Cangialosi P. Chen 《Journal of Macromolecular Science: Physics》2013,52(4):590-603
A solid-state membrane of a polymer/ionic liquid miscible mixture, poly(methyl methacrylate) (PMMA) and 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF6) doped with lithium perchlorate (LiClO4), was prepared and characterized. Miscibility, segmental dynamics, glass transition and ionic conductivity were investigated. Based on the results from differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA), the system is fully miscible and of single phase. Broadening of the glass transition was observed when increasing the amount of ionic liquid, which can be attributed to mobility and flexibility differences between the polymer and ionic liquid. A large dynamical asymmetry and intrinsic mobility difference allow segmental and structural motion/relaxation over a wider temperature range by increasing the amount of ionic liquid. Saturation recovery spin–lattice relaxation time (T1) versus temperature obtained from 7Li nuclear magnetic resonance (NMR) showed high mobility of lithium ions, which was almost temperature independent. Lithium ion conductivity significantly increases with increasing ionic liquid amount. It is concluded that lithium ion mobility and its conduction is positively correlated to segmental dynamics of ion carriers in this model system, which is more noticeable in mixtures with higher amounts of the ionic liquid. 相似文献
22.
Maria das Graças Andrade Korn Elane Santos da Boa Morte Daniele Cristina Muniz Batista dos Santos Jacira Teixeira Castro José Tiago Pereira Barbosa Alete Paixão Teixeira 《应用光谱学评论》2013,48(2):67-92
Abstract The present article gives an overview of recent publications and modern techniques of sample preparation for food analysis employing atomic and inorganic mass spectrometric techniques, such as flame atomic absorption spectrometry, chemical vapor generation atomic absorption and atomic fluorescence spectrometry, graphite furnace atomic absorption spectrometry, inductively coupled plasma optical emission spectrometry, and inductively coupled plasma mass spectrometry. Among the most frequently applied sample preparation techniques for food analysis are dry ashing, usually with the addition of an ashing aid, and acid digestion, preferably with the assistance of microwave energy. Slurry preparation, particularly with the assistance of ultrasound, is increasingly used to reduce acid consumption and sample preparation time. Direct analysis of solid samples is gaining importance in the field of food analysis as it offers the highest sensitivity, avoids the use of acids and other aggressive reagents, makes possible the analysis of micro‐samples, and can be applied for fast screening analysis, e.g., of fresh meat. 相似文献
23.
Let A1,…,AN be complex self-adjoint matrices and let ρ be a density matrix. The Robertson uncertainty principle
24.
In this paper we consider the derivation of a finite element model for fully–coupled magneto–mechanical boundary value problems based on a vector–valued magnetic potential. The formulation allows for the incorporation of nonlinear, anisotropic and hysteretic constitutive response. A piezomagnetic inclusion problem is computed to test the implementation. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
25.
Daniele Di Gioacchino Augusto Marcelli Antonio Bianconi 《Journal of Physics and Chemistry of Solids》2010,71(8):1046-1052
In this contribution we present the analysis of the third harmonic susceptibility data of the new superconductor NdFeAs1−0.14F0.14. ‘Cole-Cole’ polar plots respect to the magnetic frequency of the exciting field are presented and discussed. Data show that NdFeAs1−0.14F0.14 exhibit a ‘bulk pinning’ with a 3D flux dynamic character. A comparison of the responses of high Tc materials and an evaluation of theoretical critical states is also presented. 相似文献
26.
Daniele Pergolesi Emiliana Fabbri Enrico Traversa 《Electrochemistry communications》2010,12(7):977-980
Anode-supported solid oxide fuel cells (SOFCs) based on thin BaZr0.8Y0.2O3 ? δ (BZY) electrolyte films were fabricated by pulsed laser deposition (PLD) on sintered NiO–BZY composite anodes. After in situ reduction of NiO to Ni, the anode substrates became porous, while retaining good adhesion with the electrolyte. A slurry-coated composite cathode made of La0.6Sr0.4Co0.2Fe0.8O3 ? δ (LSCF) and BaCe0.9Yb0.1O3 ? δ (BCYb), specifically developed for proton conducting electrolytes, was used to assemble fuel cell prototypes. Depositing by PLD 100 nm thick LSCF porous films onto the BZY thin films was essential to improve the cathode/electrolyte adhesion. A power density output of 110 mW/cm2 at 600 °C, the largest reported value for an anode-supported fuel cell based on BZY at this temperature, was achieved. Electrochemical impedance spectroscopy (EIS) measurements were used to investigate the different contributions to the total polarization losses. 相似文献
27.
Ioannou TA Koutentis PA Krassos H Loizou G Re DL 《Organic & biomolecular chemistry》2012,10(7):1339-1348
Regioselective nucleophilic addition of bisnucleophiles 1,2-benzenediamine, 2-amino-benzenethiol, and N-phenyl-1,2-benzenediamine to 1,3-diphenylbenzo[e][1,2,4]triazin-7(1H)-one (1) at C6 followed by intramolecular cyclocondensation at the C7 carbonyl afforded highly coloured tetracenes 1,3-diphenyl-1,6-dihydro-[1,2,4]triazino[5,6-b]phenazin-4-ium 4-methylbenzenesulfonate (12), 1,3-diphenyl-1H-[1,2,4]triazino[6,5-b]phenothiazine (14) and 1,3,11-triphenyl-1,6-dihydro-[1,2,4]triazino[5,6-b]phenazin-11-ium 4-methylbenzenesulfonate (15), respectively. Neutralization of the latter with alkali gave the free base 1,3,11-triphenyl-1H-[1,2,4]triazino[5,6-b]phenazin-11-ium-6-ide (16). Furthermore, the benzotriazinone 1 reacts with dimethyl malonate to give 6-(methoxycarbonyl)-7-oxo-1,3-diphenyl-7H-benzofuro[5,6-e][1,2,4]triazin-1-ium-4-ide (17) in 74% yield, while with S(4)N(4) [5,6-c]-thiadiazolo-7-oxo-1,3-diphenyl-1,2,4-benzotriazine (22) was formed in 15% yield. The free bases 16 and 17 display negative solvatochromism, which supports charge separated ground states similar to those of zwitterionic biscyanines, and DFT calculations at the UB3LYP/6-31G(d) level afford ΔE(ST) values of -13.6 and -18.7 kcal mol(-1), respectively that strongly favour the singlet ground state. All ring systems described are new and fully characterized. 相似文献
28.
Andrea Guerrini Greta Varchi Rizzo Daniele Cristian Samorì Arturo Battaglia 《Tetrahedron》2007,63(33):7949-7969
Reactions of chiral (2S)-enolates of dioxolan-4-ones, derived from lactic, mandelic, and phenyllactic acids, with aliphatic (SS)- and (SR)-tert-butylsulfinyl aldimines afforded conformationally restrained C2-disubstituted N,O-orthogonally protected 3-amino-2-hydroxyalkanoates in the form of N-sulfinyl protected 1′-aminodioxolan-4-ones. The product distribution showed that there is significant kinetic selectivity, due to the presence of ‘matched’ and ‘mismatched’ components, between the (S)- or (R)-tert-butylsulfinyl aldimines and the (2S)-enolates of the 1,3-dioxolan-4-ones. Selective methoxide-induced removal of the acetal group of the N-sulfinyl-1′-aminodioxolanones yielded the corresponding N-sulfinyl protected methyl alkanoates. In addition, the selective acid-induced removal of the sulfinyl group of the N-sulfinyl-1′-aminodioxolanones provided the corresponding N-unprotected 1′-aminodioxolanones, whose base-induced cyclization afforded the corresponding β-lactams. 相似文献
29.
The formation and stability of Li+, Na+ and K+ complexes with oxalate, malonate, succinate, maleate, DL-malate and phthalate were studied potentiometrically at various ionic strengths. From the data thus obtained, as well as from several literature data on the protonation of the above-mentioned ligands in various ionic media and at various temperatures, the dependence of Na+ and K+ complex formation on temperature was determined. The dependence on ionic strength, both for the protonation and the complex formation, is also discussed. 相似文献
30.
Dotsevi Y. Sogah Daniele Perle-Treves N. Voyer W. F. Degrado 《Macromolecular Symposia》1994,88(1):149-163
A linear neutral repetitive peptide, (Leu-Gln-Pro)n (n = 1-100), an analog of the Ca2+ ion-binding domain of the matrix protein, amelogenin, has been synthesized. The polypeptide is mostly unordered in trifluoroethanol (TFE) at 25°C and its circular dichroism (CD) spectrum resembles that of the protein itself. In TFE the CD spectrum of (Leu-Gln-Pro)n reveals that the polypeptide interacts strongly with divalent cations Mg2+, Ca2+, Sr2+, and Ba2+ accompanied by conformational rearrangement from a random to a more-ordered one. In the presence of Li+, Na+ and K+ ions no such conformational change has been observed. The CD curves of the complexes suggest the presence of type I β-turns and reinforce the hypothesis that the region Gln112-Leu138 in amelogenin is the Ca2+-binding domain. In the solid state, powder X-ray diffraction suggests that the polymeric (LQP)n may exist as isolated “rigid rods”. 相似文献