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71.
72.
Ali Jinnah MM Sasirekha V Ramakrishnan V 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,62(4-5):840-844
Infrared and Raman spectra of L-citrullinium perchlorate crystals have been recorded at room temperature. The vibrational assignments of the observed wavenumbers are proposed on the basis of group theoretical analysis. The presence of carbonyl group indicates that the molecule exists in the ionic form. The shifting of stretching and bending wavenumbers indicates the presence of extensive hydrogen bonding in the crystal. The anion fundamentals however continue to be degenerated. This suggests that its symmetry is not affected in the crystal. 相似文献
73.
74.
Ramakrishnan V Ranbhor R Kumar A Durani S 《The journal of physical chemistry. B》2006,110(18):9314-9323
In search of the link between sequence and conformation in protein structures, we perform molecular dynamics analysis of the effect of stereochemical mutation in end-protected octa-alanine Ac-Ala8-NHMe from poly-L to an alternating-L,D structure. The mutation has a dramatic effect, transforming the peptide from a condition of extreme sensitivity to one of extreme insensitivity to solvent. Examining the molecular folds of poly-L and alternating-L,D structure in atomistic detail, we find them to differ in the relationship between peptide dipolar interactions at the local and nonlocal levels, either conflicting or harmonious depending upon the chain stereochemistry. The stereochemical transformation of interpeptide electrostatics from a condition of conflict to one of harmony explains the long-standing puzzle of why poly-L and alternating-L,D peptides strongly differ in properties such as "stiffness" and solvent sensitivity. Furthermore, it is possible that poly-L stereochemistry is also the fulcrum of protein sensitivity to the effects of amino acid side-chain structures via dielectric arbitrations in interpeptide electrostatics. Indeed the evidence is accumulating that the amino acid side chains differing in alpha-helix and beta-sheet propensities also differ in their desolvating effects in the adjacent and nearest-neighbor peptides and thus possibly in the solvent screening of peptide dipolar interactions. 相似文献
75.
High aspect ratio (>500), neat poly(ethyl 2-cyanoacrylate) nanofibers were synthesized catalytically by vapour phase polymerization under high relative humidity and ambient conditions. 相似文献
76.
V. Ramakrishnan A. Sarua M. Kuball A. Fathima Abdullah 《Journal of Raman spectroscopy : JRS》2010,41(3):320-324
The molecular interaction in the binary mixture of 3‐phenoxybenzaldhyde (3Phbz) and 4‐ethoxybenzaldehyde (4Etob) was analysed in four different solvents. The concentration dependence of vibrational relaxation of the CO stretching band of 3Phbz in different solvents was investigated by varying the concentration of the solute molecule in the solvents by performing Raman spectroscopic measurements. The self‐associated nature and the formation of hydrogen‐bonded complexes in the solute molecule, 4Etob, were considered to analyse the wavenumber separation between the peaks of hydrogen‐bonded and free carbonyl groups. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
77.
Janak Ramakrishnan 《Mathematical Logic Quarterly》2010,56(4):406-408
We prove that a function definable with parameters in an o‐minimal structure is bounded away from ∞ as its argument goes to ∞ by a function definable without parameters, and that this new function can be chosen independently of the parameters in the original function. This generalizes a result in [1]. Moreover, this remains true if the argument is taken to approach any element of the structure (or ±∞), and the function has limit any element of the structure (or ±∞) (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
78.
Seebauer EG Dev K Jung MY Vaidyanathan R Kwok CT Ager JW Haller EE Braatz RD 《Physical review letters》2006,97(5):055503
The technologically useful properties of a crystalline solid depend upon the concentration of defects it contains. Here we show that defect concentrations as deep as 0.5 microm within a semiconductor can be profoundly influenced by gas adsorption. Self-diffusion rates within silicon show that nitrogen atoms adsorbed at less than 1% of a monolayer lead to defect concentrations that vary controllably over several orders of magnitude. The results show that previous measurements of diffusion and defect thermodynamics in semiconductors may have suffered from neglect of adsorption effects. 相似文献
79.
M. Giffhorn B. Becker A. A. Menovsky J. A. Mydosh G. J. Nieuwenhuys S. Ramakrishnan 《高压研究》2013,33(1-6):159-163
Abstract An uniaxial pressure cell for low temperature use is described in detail. Then we present data of the electrical resistance of single crystals of Lu5Ir4Si10, which is known to show a charge-density-wave transition around 83 K and to become superconducting near 3.8 K, both phenomena being anticorrelated under pressure. Since the CDW in Lu5Ir4Si10 is a quasi one-dimensional phenomenon because of a chain-like structure, it responds to uniaxial pressure in a specific way. 相似文献
80.
Umadevi M Vanelle P Terme T Rajkumar BJ Ramakrishnan V 《Journal of fluorescence》2008,18(6):1139-1149
Solvatochromic and preferential solvation of 1,4-dihydroxy-2,3-dimethyl-9,10-anthraquinone (DHDMAQ) have been investigated
using optical absorption and fluorescence emission techniques. Optical absorption spectra of DHDMAQ in different solvents
show the intra molecular charge transfer band in the region 400–550nm. The observed blue shift with solvent polarity indicates
the delocalisation of the excited state, owing to reduction in quasiaromaticity of the chelate rings formed by intra molecular
hydrogen bonds, due to electrostatic or hydrogen bonding interaction. This is also confirmed by the observed low oscillator
strength and the transition dipole moment. The observed quantum yield of DHDMAQ in different solvents is due to the inter
molecular hydrogen bond in the excited state in addition to the intra molecular hydrogen bond. It also reveals from the low
oscillator strength, which indicates that the radiative decay is low. Excited state dipole moment of DHDMAQ is calculated
by solvatochromic data
and it shows a lower value than ground state dipole moment. The preferential solvation parameter shows that in dimethyl formamide
(DMF) + ethanol mixture, the DHDMAQ is preferentially solvated by ethanol in DMF rich region and by DMF in ethanol rich region.
In the case of DMF + dichloromethane mixture DHDMAQ is preferentially solvated by DMF. 相似文献