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101.
Elisabeth Holder Veronica Marin Alexander Alexeev Ulrich S. Schubert 《Journal of polymer science. Part A, Polymer chemistry》2005,43(13):2765-2776
A set of novel greenish‐yellow‐, yellow‐, and orange‐light‐emitting polymeric iridium(III) complexes were synthesized with the bridge‐splitting method. The respective dimeric precursor complexes, [Ir(ppy)2‐μ‐Cl]2 (ppy = 2‐phenylpyridine) and [Ir(ppy? CHO)2‐μ‐Cl]2 [ppy? CHO = 4‐(2‐pyridyl)benzaldehyde], were coordinated to 2,2′‐bipyridine carrying poly(ε‐caprolactone) tails. The resulting emissive polymers were characterized with one‐dimensional (1H) and two‐dimensional (1H? 1H correlation spectroscopy) nuclear magnetic resonance and infrared spectroscopy, gel permeation chromatography, and matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry, and the successful coordination of the iridium(III) centers to the 2,2′‐bipyridine macroligand was revealed. The thermal behavior was studied with differential scanning calorimetry and correlated with atomic force microscopy. Furthermore, the quantitative coordination was verified by both the photophysical and electrochemical properties of the mononuclear iridium(III) compounds. The photoluminescence spectra showed strong emissions at 535 and 570 nm. The color shifts depended on the substituents of the cyclometallating ligands. Cyclic voltammetry gave oxidation potentials of 1.23 V and 1.46 V. Upon the excitation of the films at 365 nm, yellow light was observed, and this could allow potential applications in light‐emitting devices. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2765–2776, 2005 相似文献
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104.
The novel tridentate chiral ligand 2,6-bis{[(1R,2S,4R)-2-hydroxy-1,3,3-trimethyl-bicyclo[2.2.1]hept-2-yl]}pyridine (1) was readily prepared by reaction of 2,6-dilithiopyridine with (R)-(−)-fenchone. Reaction of 1 with [MoO2(acac)2] resulted in the formation of the new metal-oxo five-coordinated complex [MoO2(ONO)] (2) [ONO = (1 – 2H)]. The reactivity of 2 has been studied and the derivatives [MoS2(ONO)] (3) and [MoO(O2)(ONO)] (4) were prepared. The compounds 1–4 have been characterised by 1H and 13C{1H} NMR, microanalysis and IR spectroscopy. Furthermore, the molecular structures of 1 and 2 have been determined by single-crystal X-ray diffraction. The behaviour of 2 as catalyst in oxotransfer and in nucleophilic substitution of propargylic alcohols reactions has been tested. 相似文献
105.
Mata S Cortijo V Caminati W Alonso JL Sanz ME López JC Blanco S 《The journal of physical chemistry. A》2010,114(43):11393-11398
The Fourier transform microwave spectra of the hydrated forms of the tautomeric pair 2-pyridinone/2-hydroxypyridine (2PO/2HP) have been investigated in a supersonic expansion. Three hydrated species, 2PO-H?O, 2HP-H?O, and 2PO-(H?O)?, have been observed in the rotational spectrum. Each molecular complex was confidently identified by the features of the 1?N quadrupole hyperfine structure of the rotational transitions. The presence of water affects the tautomeric equilibrium -N═C(OH)- ? -NH-C(═O)-, which is shifted to the enol form for the bare molecules 2PO/2HP but to the keto tautomer for the hydrated forms. 相似文献
106.
An efficient synthesis of 3-halo-7-oxygen-functionalized benzo[b]thiophenes bearing different substituents at C-2 has been developed from N,N-diethyl O-3-halophenylcarbamates. The key steps are an ortho-lithiation reaction, which gives rise to 3-halo-2-sulfanylphenol derivatives, and a electrophilic cyclization. The subsequent functionalization of the prepared halobenzothiophenes allows the access of a wide variety of 2,3,7-regioselectively functionalized benzo[b]thiophenes in good overall yields. 相似文献
107.
Jung A. Jung Young Baek Kim Young A. Kim Seung Bum Ryu Veronica Kim 《Journal of nanoparticle research》2011,13(6):2361-2374
Functional spherical solid and hollow particles of polysilsesquioxanes (PSQs) containing amine, thiol, and vinyl groups were
prepared by polymerizing organotrialkoxysilanes (OTASs) containing corresponding chemical groups. Fluorescent PSQ particles
were prepared by physically entrapping Rhodamine 6G, Coumarin 7, and Fluoresceine sodium salts. The intensity of fluorescent
light increased initially with increasing amount of entrapped fluorophores and then leveled off or decreased slightly after
reaching a maximum value. PSQ particles containing gold nanoparticles (GNPs), both inside and on the surface, were prepared
by the in situ reduction of gold ions by the PSQ particles. When the reduction reaction was carried out for extended periods
of time, the GNP that had formed inside the poly(3-mercaptopropyl)silsesquioxane (PMPSQ) and polyvinylsilsesequioxane (PVSQ)
particles underwent interesting morphological changes. PSQ particles containing amine and thiol groups fixed the GNPs on the
surface, which could be utilized further in binding amine-modified oligo-DNA strands. The aggregation of PSQ/GNP particles
combined with complementary oligo-DNA strands was examined to demonstrate that these particles could be applied to DNA assays
and isolation. The particles were characterized by scanning electron microscopy, transmission electron microscopy, solid state
nuclear magnetic resonance spectroscopy, ultraviolet/visible spectroscopy, and fluorescence microscopy. 相似文献
108.
Cyclic voltammetry, galvanostatic charge?Cdischarge technique, potentiostatic intermittent titration technique (PITT), and electrochemical impedance spectroscopy (EIS) were used to study the behavior of a LiMn1.95Cr0.05O4 (substituted lithium?Cmanganese spinel) electrode in nonaqueous electrolytes at 25 °C. Quantitative and qualitative changes of the electrode transport parameters as functions of lithium concentration were analyzed. Several equivalent circuits are discussed; the results obtained by different methods are compared. The PITT and EIS results are in good agreement; the chemical diffusion coefficient D varies within 10?14?C10?9 cm2 s?1 depending on the lithium content in the LixMn1.95Cr0.05O4 electrode. 相似文献
109.
J. M. Sanz Báñez J. A. Sastre López M. R. Molina Patiño T. Gómez Santacana C. Romero-Ávila García 《Journal of carbohydrate chemistry》2013,32(4):403-417
ABSTRACT The synthesis of several 3-aryl-5-glycosylisoxazole derivatives has been achieved. By condensation of the protected aldehydo-sugars 2,3-O-isopropylidene-D-glyceraldehyde (1), 2,3:4,5-di-O-isopropylidene-aldehydo-D-arabinose (2) and D-xylose (3), and 2,5-anhydro-3,4,5-tri-O-benzoyl-D-mannose (4) with benzoylmethylenetriphenylphosphorane, enulose derivatives were formed, which were later converted into a,ß-unsaturated ketoximes. These ketoximes were oxidatively cyclized with iodine and, after removal of the hydroxyl protecting groups, 3-phenyl-5-glycosylisoxazoles were formed. 相似文献
110.
Andrés Reyes José Luis Sanz‐Vicario 《International journal of quantum chemistry》2010,110(13):2331-2331