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排序方式: 共有388条查询结果,搜索用时 31 毫秒
81.
Oscillations of the aggregate sizes of SiO2 particles covered by an adsorbed layer of poly(vinylpyridine) (PVP) at pH 3 with a periodicity of about 15 h were observed using a particle counting technique. The same oscillation was found for the contact angle values of water on the surface of Si wafers (with top silica layer) covered by adsorbed PVP as a function of exposure time in a PVP water solution. 相似文献
82.
Anton I. Manilov Aleksey V. Kozinetz Sergiy V. Litvinenko Valeriy A. Skryshevsky Mohammed Al Araimi Alex Rozhin 《Current Applied Physics》2019,19(3):308-313
We identified different nano-carbon species such as graphene nanoplatelets, graphite flakes and carbon nanotubes dispersed in N-methyl-2-pyrrolidone using a novel sensor structure based on a “deep” silicon barrier working as a photoelectrical transducer. Each nano-carbon particle has specific signature in both 2D photocurrent distribution and photocurrent dependencies on bias changing surface band-bending. Additionally, all nano-carbon particles have characteristic features in the time-dependent evolution of photocurrent. The obtained results can be explained by the influence of nano-carbon molecules' local electric field on the recombination parameters of defect centers on the silicon surface. 相似文献
83.
Kedziera D Stanke M Bubin S Barysz M Adamowicz L 《The Journal of chemical physics》2006,125(8):084303
The Pauli approach to account for the mass-velocity and Darwin relativistic corrections has been applied to the formalism for quantum mechanical molecular calculations that does not assume the Born-Oppenheimer (BO) approximation regarding separability of the electronic and nuclear motions in molecular systems. The corrections are determined using the first order perturbation theory and are derived for the non-BO wave function of a diatomic system expressed in terms of explicitly correlated Gaussian functions with premultipliers in the form of even powers of the internuclear distance. As a numerical example we used calculations of the transition energies for pure vibrational states of the HD(+) ion. 相似文献
84.
A two-step preparation of 2,3-trans disubstituted tetrahydrofuran derivatives is reported from S-alkyl dithiocarbonates. The study of the group transfer reaction from xanthates and alkenes afforded intermediate S-alkyl dithiocarbonates. From 2,3-dihydrofuran derivatives, the displacement of the resulting anomeric xanthates with various nucleophiles in the presence of Lewis acid allowed the formation of new carbon-carbon and carbon-heteroatom bonds. This strategy was illustrated by a two-step synthesis of a precursor of modified 2'-beta-C-branched nucleoside analogues. 相似文献
85.
Arene cation-radicals and anion-radicals result directly from the one-electron oxidation and reduction of many aromatic hydrocarbons, yet virtually nothing is known of their intrinsic (thermodynamic) stability and hence "aromatic character". Since such paramagnetic ion radicals lie intermediate between aromatic (Hückel) hydrocarbons with 4n + 2-electrons and antiaromatic analogues with 4n-electrons, we can now address the question of pi-delocalization in these odd-electron counterparts. Application of the structure-based "harmonic oscillator model of aromaticity" or the HOMA method leads to the surprising conclusion that the aromaticity of these rather reactive, kinetically unstable arene cation and anion radicals (as measured by the HOMA index) is actually higher than that of their (diamagnetic) parent-contrary to conventional expectations. 相似文献
86.
Permanent binary phase masks with planar surfaces and high tolerance to laser radiation are recorded in the volume of photo-thermo-refractive glass using the contact copying technique and binary amplitude master masks. Conversion of a Gaussian beam to higher order modes is shown. 相似文献
87.
We consider a system of ordinary differential equations used to describe the dynamics of two coupled single-mode semiconductor
lasers. In particular, we study solutions corresponding to the amplitude synchronization. It is shown that the set of these
solutions forms a three-dimensional invariant manifold in the phase space. We study the stability of trajectories on this
manifold both in the tangential direction and in the transverse direction. We establish conditions for the existence of globally
asymptotically stable solutions of equations on the manifold synchronized with respect to the amplitude.
__________
Translated from Ukrains’kyi Matematychnyi Zhurnal, Vol. 60, No. 3, pp. 426–435, March, 2008. 相似文献
88.
Sergiy O. Nikitin Rostyslav D. Lampeka Yulian M. Volovenko Gennady V. Palamarchuk Oleg V. Shishkin 《Polyhedron》2010
A series of new 3d-metal complexes have been prepared by the reaction of M(CH3COO)2 (M = Zn(II), Co(II), Ni(II)) and 1,2-diamino-3-(2-benzothiazolyl)-4(5H)-ketopyrrole (HL) in a methanol (3) or a methanol/dmf (1, 2) medium. All the complexes have been studied by elemental analyses, electronic and IR spectroscopies. The zinc(II) complex 1 and the ligand HL have been investigated using the method of 1H NMR-spectroscopy at various temperatures. The disappearance of the signal from one proton of the amino group H(5) in the spectrum of complex 1 confirmed the existence of the ligand in the deprotonated form. According to the data of the 1H NMR-spectroscopy, the ligand HL is coordinated to zinc(II) through the nitrogen atom of the deprotonated amino group and the nitrogen atom of the benzothiazole substituent. These data are in agreement with X-ray structural studies for the ligand HL and the zinc(II) complex 1. 相似文献
89.
Joseph Wontcheu Wolfgang Bensch Sergiy Mankovsky Svitlana Polesya Hubert Ebert 《Progress in Solid State Chemistry》2009,37(2-3):226-242
We investigated experimentally and theoretically the effect of the substitution of Te by Se onto the structural, magnetic and electronic properties of ferromagnetic Cr5±xTe8 as parent material. Whereas Cr5Te8 is dimorphic crystallizing in a monoclinic and trigonal modification, Se substituted samples crystallize in two different trigonal modifications depending on the synthesis conditions. One of the modifications can be viewed as self-intercalated dichalcogenides Cr1+xQ2 (Q = Te, Se) and the other is a superstructure which is isostructural to one of the Cr5±xTe8 modifications. For the Se richest samples (Te:Se = 1:7) a new modification is identified which was formerly reported for Cr3+xSe4. For a distinct Cr content the replacement of Se by Te induces a reduction of the unit cell volumes, of the Cr-Cr and Cr-Te/Se distances. Increasing the Cr content for a constant Te:Se ratio has the opposite effect. The results also suggest that the homogeneity range extends to more Cr rich compounds with decreasing Te content. For a given Cr content the substitution of Te by Se weakens the ferromagnetic exchange interactions and strengthens the antiferromagnetic exchange. With increasing Cr content and a fixed Te:Se ratio ferromagnetic properties become more pronounced. The low temperature magnetic behavior is characterized by spin-glass, spin-glass like or cluster-glass properties depending on the Cr content and the Te:Se ratio. Electronic structure calculations done within the framework of LSDA (local spin density approximation) gave a detailed insight into the electronic and magnetic properties of the investigated systems supporting the interpretation of the achieved experimental results. This applies in particular for the calculated exchange coupling constants that provided the necessary input for Monte Carlo simulations used for theoretical investigations on the magnetic properties at finite temperatures. 相似文献
90.
Kovalska VB Volkova KD Losytskyy MY Tolmachev OI Balanda AO Yarmoluk SM 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2006,65(2):271-277
The influence of methyl-, 2-hydroxyethyl-, dimethyl-, diethyl- and benzoyl-amino substituents in the 6,6'-positions of benzothiazole heterocycle of trimethine cyanines on their spectral-luminescent properties and behavior in presence of DNA, RNA and BSA was studied. It was shown that incorporation of 6,6'-substituents generally leads to the increase in dyes tendency to aggregation, resulting in the considerable decrease in the emission intensity of the disubstituted dyes as compared to the unsubstituted ones. Emission of the studied 6,6'-disubstited dyes in DNA presence is considerably more intensive than in presence of RNA, that points on the existing of DNA binding preference for the mentioned dyes. Insertion of benzoyl-amino groups into the 6,6'-positions permitted us to design the DNA-sensitive dyes on the basis of symmetric trimethine cyanines with unsubstituted polymethine chain, while typically such dyes slightly respond on the presence of biopolymers. 6,6'-Benzoyl-amino-disubstituted trimethine cyanines are proposed as efficient dyes for DNA detection. 相似文献