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61.
New Spiro Compounds from Cyclophosphazenes and Cyclodi[phosphadiazanes] Chlorocyclophosphazenes (Cl2P = N)3 and (Cl2p = N)4 react with dihydrazidophosphoric acid derivatives in THF in the presence of triethylamine to give the spirocyclic compounds Cl4N3P3(NHN(CH3))2P(S)OC6H5, Cl6N4P4(NHNH)2P(S)OC6H5. Constitutions have been confirmed by MS, NMR, IR and elemental analysis. 相似文献
62.
In the core of the seminal Graph Minor Theory of Robertson and Seymour lies a powerful theorem capturing the ``rough' structure
of graphs excluding a fixed minor. This result was used to prove Wagner's Conjecture that finite graphs are well-quasi-ordered
under the graph minor relation. Recently, a number of beautiful results that use this structural result have appeared. Some
of these along with some other recent advances on graph minors are surveyed.
Research partly supported by Japan Society for the Promotion of Science, Grant-in-Aid for Scientific Research, Grant number
16740044, by Sumitomo Foundation, by C & C Foundation and by Inoue Research Award for Young Scientists
Supported in part by the Research Grant P1–0297 and by the CRC program
On leave from: IMFM & FMF, Department of Mathematics, University of Ljubljana, Ljubljana, Slovenia 相似文献
63.
Yu. S. Dedkov 《The European Physical Journal B - Condensed Matter and Complex Systems》2007,57(1):15-19
The spin-resolved electronic structure of thin Cr overlayers on top of the Fe(110) surface was investigated by means of spin-
and angle-resolved photoelectron spectroscopy. The initial fast drop of photoelectron spin-polarization at the Fermi level,
followed by weak oscillatory behavior with the period of about 2 ML, can give an evidence for the first time spectroscopic
observation of the short period oscillations in (110)-oriented thin Cr films. 相似文献
64.
氯代5-氟脲嘧啶卟啉的红外光谱特性的研究 总被引:6,自引:0,他引:6
本文对新合成的对位及间位两类氯代苯基 5 氟脲嘧啶卟啉的红外光谱吸收峰进行了归属和总结 ,讨论了其红外吸收频率随取代基位置变化的规律。指出了苯环上的取代基为电负性强的基团时 ,由于场效应的存在 ,使被测化合物的羰基伸缩振动吸收峰的相对强度发生改变。同时 ,表明了嘧啶环上N原子发生了取代 ,形成单、双取代 5 氟脲嘧啶卟啉化合物的红外光谱特性。 相似文献
65.
For the NO molecule, modelled as a Morse oscillator, time-dependent (TD) nuclear Schr?dinger equation has been numerically
solved for the multiphoton vibrational dynamics of the molecule under a far-infrared laser of wavelength 10503 nm, and four
different intensities,I = 1 × 108, 1 × 1013, 5 × 1016, and 5 × 1018 W cm−2 respectively. Starting from the vibrational ground state at zero time, various TD quantities such as the norm, dissociation
probability, potential energy curve and dipole moment are examined. Rich high-harmonics generation (HHG) spectra and above-threshold
dissociation (ATD) spectra, due to the multiphoton interaction of vibrational motions with the laser field, and consequent
elevation to the vibrational continuum, have been obtained and analysed.
Dedicated to Professor C N R Rao on his 70th birthday
An erratum to this article is available at . 相似文献
66.
采用溶胶-凝胶法在Pt/Ti/SiO2/Si衬底上制备了不同La掺杂浓度PLZT(x/40/60)薄膜- x射线衍射分析表明制备的PLZT(x/40/60)薄膜是具有单一钙钛矿结构的多晶薄膜- 通过红外椭圆偏振光谱仪测量了波长为2-5—12-6μm范围内PLZT薄膜的椭偏光谱,采用经典色 散模型拟合获得PLZT薄膜的红外光学常数,同时也拟合获得PLZT薄膜的厚度- 随着La掺杂浓 度的增大,折射率逐渐减小- 而消光系数除PLZT(4/40/60)薄膜外,呈现逐渐增大的趋势- 分析表明这些差异主要与PLZ
关键词:
PLZT薄膜
红外光学性质
红外椭圆偏振光谱 相似文献
67.
V. B. Sokolov A. N. Chekhlov T. A. Epishina I. V. Martynov 《Russian Chemical Bulletin》1992,41(2):236-240
The O-(arylcarbamoyl)butyrhydroximoyl chlorides were synthesized, and the x-ray structural analysis (XSA) of one of them — O-(o-tolylcarbamoyl)butyrhydroximoyl chloride — was performed. It was established from the data of the XSA and the PMR spectra that all synthesized compounds are the Z isomers.Institute of Physiologically Active Substances, Russian Academy of Sciences, 142432 Chernogolovka. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 2, pp. 315–319, February, 1992. 相似文献
68.
This paper overviews the electro-optical and thermal performances of different types of infrared detectors manufactured by
Sofradir. The detector’s fabrication processes and detector’s performance are shortly described. New staring arrays are more
compact and offer system solutions required by infrared market. Special attention is directed to some reliability advantages
of new dewar design. Finally, the development trends for highest resolution infrared detector are discussed.
The paper presented there appears in Infrared Photoelectronics, edited by Antoni Rogalski, Eustace L. Dereniak, Fiodor F. Sizov, Proc. SPIE Vol. 5957, 59570U (2005). 相似文献
69.
Summary The modifications induced by a magnetic field of arbitrary direction and intermediate strength (i.e not larger than 2.35·105 tesla, the ?atomic tesla?) on the lowest singlet and triplet energy states of the hydrogen molecule are studied. Using a
linear combination of products of field-modified atomic orbitals, it is found that increasing the field strength the depth
of the singlet energy well increases and the equilibrium internuclear distance decreases, yielding more rigid and localized
nuclear vibrations. For sufficiently strong fields perpendicular to the internuclear axis, the triplet state exhibits a bonding
behaviour. An explanation of the above results is given in terms of the field-modified electronic-charge distributions in
the internuclear region.
Based on the thesis submitted by S. Basile to the University of Palermo for graduation in Physics. 相似文献
70.
Orotic acid (vitamin B13) is a key intermediate in biosynthesis of the pyrimidine nucleotides in living organisms, moreover, it may serve as the biological carrier for some metal ions. cis-Diammine(orotato)platinum(II), cis-[Pt(C5H2N2O4)(NH3)2] can be considered as a new potential cisplatin analogue. The FT-Raman and FT-IR spectra of the title complex are reported, for the first time. The molecular structure, vibrational frequencies, and the theoretical infrared and Raman intensities have been calculated by the density functional mPW1PW91 method. The detailed vibrational assignment has been made on the basis of the calculated potential energy distribution. The theoretically predicted IR and Raman spectra show very good agreement with experiment. Natural bond orbital (NBO) analyses were performed for cisplatin, carboplatin and the title complex. The results provided new data on the nature of platinum–ligand bonding in these compounds. Strong intramolecular hydrogen bond between the orotate ligand and the coordinated ammonia group stabilizes the structure of the platinum(II) complex. Thus, it is suggested that the orotate ligand in the title complex is more inert to the substitution reactions than the chloride ligands in cisplatin. 相似文献