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901.
Nojin Park Myungeun Seo Sang Youl Kim 《Journal of polymer science. Part A, Polymer chemistry》2012,50(21):4408-4414
Novel triblock copolymers having self‐complementary hydrogen‐bonding units were synthesized by using reversible addition–fragmentation transfer polymerization. As characterized by dynamic light scattering and atomic force microscopy, these polymers formed noncovalently crosslinked polymer particles and showed an aggregation behavior by intermolecular and intramolecular interactions. At low concentration, polymers formed nanoparticles, and the particle diameter increased with increasing polymer concentration. Well‐ordered hexagonal microstructures were prepared by “Breath Figure” technique with the triblock copolymers. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
902.
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
903.
904.
Ji Hye Park Byung Kyu Kim 《Journal of polymer science. Part A, Polymer chemistry》2013,51(5):1255-1261
A minute amount (0.01–0.3 wt %) of ally isocyanate functionalized hyperbranched 2,2‐bis (hydroxymethyl) propionic acid (bis‐MPA) polyester‐16‐hydroxyl (HBP) was incorporated covalently into polyurethane acrylate‐based holographic polymer dispersed liquid crystals (HPDLCs), and its effects on the compound viscosity, grating kinetics, morphology, diffraction efficiency (DE), and electro‐optical properties of the HPDLC films were examined. HBP at low concentrations (0.01–0.05%) reduced the compound viscosity and domain size of liquid crystal (LC) significantly and augmented the cure rate and saturation DE by up to threefold compared to the HBP‐free compound. At high concentrations (0.10 and 0.30%), HBP increased the compound viscosity and decreased the rate of grating formation, giving rise to distorted LC‐polymer interfaces, which caused a significant decrease in the threshold and operating voltages. The rise and decay time showed a minimum and maximum, respectively, when the compound viscosity was a minimum at 0.03% HBP. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
905.
R. Chandrasekaran Struther Arnott R.-G. He R. P. Millane H.-S. Park L. C. Puigjaner 《Journal of Macromolecular Science: Physics》2013,52(1-4):1-20
Fibrous polynucleotide duplexes are very polymorphic. Detailed x-ray analysis of the D forms of poly d(AT) ·poly d(AT) and poly d(IC) ·poly d(IC) and of the B form of poly d(GC) ·poly d(GC) show that 5′RpY3′ dinucleoside monophosphates in these molecules have either t,t or t,g conformations at C3′–03′, 03′-P which lead to similar orientations of phosphate groups. On the other hand, 5′YpR3′ fragments commonly have g,t conformations and hence a markedly different orientation of the phosphate group. Studies of the more complex structures of the C form of poly d(ACC) ·poly d(GGT) and of a pleiomeric D form of poly d(AT) ·poly d(AT) where the repeated structural motifs are hexanucleotides reveal further details of the surface “wrinkles” on DNA. In the case of the H form of poly d(A) ·poly d(T), the sugar rings in each strand are puckered differently-C2′-endo in poly d(T) and C3′-endo in poly d(A). Such heteromerous duplexes have unusually pronounced directional properties. Similar structure ma be present in some DNA-RNA hybrids. These surface feature might enable regulatory proteins and enzymes to recognize their host DNA sequences more easily in the blinding process. 相似文献
906.
Min Ju Cho U Ra Lee Youn Sun Kim Jicheol Shin Young Min Kim Young Wook Park Byeong‐Kwon Ju Jung‐Il Jin Dong Hoon Choi 《Journal of polymer science. Part A, Polymer chemistry》2010,48(9):1913-1918
A functionalized deoxyribonucleic acid (Cz‐DNA) was prepared with carbazolyl ammonium lipid as a triplet host material for phosphorescent material system. It is soluble in organic solvents, which facilitates the sample preparation for the absorption and luminescent properties in solid states. A highly soluble iridium complex, Ir(Cz‐ppy)3 with carbazolyl‐substituted 2‐phenylpyridine ligands was employed for studying the phosphorescence in Cz‐DNA. There is a good overlap between the photoluminescence spectrum of Cz‐DNA and the metal‐to‐ligand charge transfer (MLCT) absorption bands of the iridium complex. This overlap enables efficient energy transfer from the excited state in the host to the MLCT band of Ir(Cz‐ppy)3. In addition, photoluminescence quantum yield of Cz‐DNA was found to be relatively larger than the copolymer (PCzSt) with vinylcarbazole and styrene. Thus, Cz‐DNA was employed as a triplet host material for fabricating multilayered electrophosphorescence devices via modification of its property by doping 5,4‐tert‐butylhexyl‐1,3,4‐oxadiazole (PBD). After doping 30 wt % PBD and 10 wt % Ir(Cz‐ppy)3 into Cz‐DNA, we achieved much improvement in electron injection/transport from an adjacent carrier transport layer, resulting in much improved device performances. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1913–1918, 2010 相似文献
907.
Facile,Template‐Free Synthesis of Stimuli‐Responsive Polymer Nanocapsules for Targeted Drug Delivery
908.
Min‐Jung Lee Moon Seong Kang Min‐Ki Shin Jong‐Won Park Dae Sung Chung Chan Eun Park Soon‐Ki Kwon Yun‐Hi Kim 《Journal of polymer science. Part A, Polymer chemistry》2010,48(18):3942-3949
New amorphous semiconducting copolymers, poly(9,9‐dialkylfluorene)‐alt‐(3‐dodecylthienyl‐divinylbenzene‐3‐dodecylthienyl) derivatives (PEFTVB and POFTVB), were designed, synthesized, and characterized. The structure of copolymers was confirmed by H NMR, IR, and elemental analysis. The copolymers showed very good solubility in organic solvents and high thermal stability with high Tg of 178–185 °C. The weight average molecular weight was found to be 107,900 with polydispersity of 3.14 for PEFTVB and 76,700 with that of 3.31 for POFTVB. UV–vis absorption studies showed the maximum absorption at 428 nm (in solution) and 435 nm (in film) for PEFTVB and at 430 nm (in solution) and 436 nm (in film) for POFTVB. Photoluminescence studies showed the emission at 498 nm (in solution) and 557 nm (in film) for PEFTVB and at 498 nm (in solution) and 536 nm (in film) for POFTVB. The solution‐processed thin‐film transistors showed the carrier mobility of 2 × 10?4 cm2 V?1 s?1 for PEFTVB‐based devices and 2 × 10?5 cm2 V?1 s?1 for POFTVB‐based devices. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3942–3949, 2010 相似文献
909.
In this paper, we study the Ruelle zeta function and the Selberg zeta functions attached to the fundamental representations
for real hyperbolic manifolds with cusps. In particular, we show that they have meromorphic extensions to
\mathbbC{\mathbb{C}} and satisfy functional equations. We also derive the order of the singularity of the Ruelle zeta function at the origin.
To prove these results, we completely analyze the weighted unipotent orbital integrals on the geometric side of the Selberg
trace formula when test functions are defined for the fundamental representations. 相似文献
910.