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41.
Subramanian S Devasahayam N McMillan A Matsumoto S Munasinghe JP Saito K Mitchell JB Chandramouli GV Krishna MC 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2012,214(1):244-251
Oxygen maps derived from electron paramagnetic resonance spectral-spatial imaging (EPRI) are based upon the relaxivity of molecular oxygen with paramagnetic spin probes. This technique can be combined with MRI to facilitate mapping of pO(2) values in specific anatomic locations with high precision. The co-registration procedure, which matches the physical and digital dimensions of EPR and MR images, may present the pO(2) map at the higher MRI resolution, exaggerating the spatial resolution of oxygen, making it difficult to precisely distinguish hypoxic regions from normoxic regions. The latter distinction is critical in monitoring the treatment of cancer by radiation and chemotherapy, since it is well-established that hypoxic regions are three or four times more resistant to treatment compared to normoxic regions. The aim of this article is to describe pO(2) maps based on the intrinsic resolution of EPRI. A spectral parameter that affects the intrinsic spatial resolution of EPRI is the full width at half maximum (FWHM) height of the gradient-free EPR absorption line in frequency-encoded imaging. In single point imaging too, the transverse relaxation times (T(2)(?)) limit the resolution since the signal decays by exp(-t(p)/T(2)(?)) where the delay time after excitation pulse, t(p), is related to the resolution. Although the spin densities of two point objects may be resolved at this separation, it is inadequate to evaluate quantitative changes of pO(2) levels since the linewidths are proportionately affected by pO(2). A spatial separation of at least twice this resolution is necessary to correctly identify a change in pO(2) level. In addition, the pO(2) values are blurred by uncertainties arising from spectral dimensions. Blurring due to noise and low resolution modulates the pO(2) levels at the boundaries of hypoxic and normoxic regions resulting in higher apparent pO(2) levels in hypoxic regions. Therefore, specification of intrinsic resolution and pO(2) uncertainties are necessary to interpret digitally processed pO(2) illustrations. 相似文献
42.
43.
Role of aspartic acid in collagen structure and stability: A molecular dynamics investigation 总被引:3,自引:0,他引:3
Raman SS Parthasarathi R Subramanian V Ramasami T 《The journal of physical chemistry. B》2006,110(41):20678-20685
A molecular dynamics (MD) simulation study has been carried out to understand the stability of the triple helical collagen models. The calculations show that the presence of the aspartic acid residue in different positions leads to the local variation in the structure. Analyses of root-mean-square deviation (RMSD), radial distribution function (RDF), puckering effect, dihedral angle variation, hydrogen bond (H-bond), and conformational changes during molecular dynamics simulation reveal that the local perturbation in the sequences, increase in chain flexibility due to removal of five membered rings in the collagen by aspartic acid, change of intermolecular H-bonding pattern, and differences in the association of water are mainly influencing the nature of stabilization of collagen by aspartic acid. 相似文献
44.
pi-Conjugated macrocycles consisting of thiophenes and benzenes exhibit benzenoid features for 4npi macrocycles, whereas (4n + 2)pi macrocycles are annulenoid due to rapid interconversion between quinoid and Kekule canonical forms in the benzene units. 相似文献
45.
Monolayers of alkanethiols with varied chain lengths, CH3(CH2)nSH where n = 3, 5, and 7, on gold substrates have been prepared by adsorption from (1) neat thiol, (2) millimolar thiol solution
in alcohol (conventional method), and (3) potential-controlled adsorption. Reflection absorption infrared spectroscopy (RAIRS)
and electrochemical quartz crystal microbalance (EQCM) have been used to characterize the integrity of the monolayers. Methylene
and methyl stretching modes along with C–S stretching modes have been used as benchmarks to follow the order–disorder transitions
in the monolayer structure, in the temperature range from 25 to 175 °C. Monolayers adsorbed from neat thiol show superior
quality in terms of stability and structural arrangement. Short chain thiols with n = 3, 5, and 7 do show substantial stability.
The possibility of multilayer formation is ruled out by EQCM studies comparing the frequency and mass change associated with
the monolayer desorption. Self-assembled monolayers (SAMs) adsorbed under potential control behave very similarly to the monolayers
adsorbed from neat thiol as far as stability and structural orientation are concerned, irrespective of the chain length. The
adsorption from neat thiol gets rid of the solvent-induced defects and arrests the propagation of defects under temperature
constraints. 相似文献
46.
V. Kavan Kumar R. Mahendiran P. Subramanian S. Karthikeyan A. Surendrakumar 《印度化学会志》2022,99(3):100384
One of the most significant issues of the last few decades has been tracing for renewable energy sources. Animal fleshing (ANFL) is the most common proteinaceous solid waste accured during the production of leather and it must be disposed of in an environmentally responsible manner. This paper is attempts to assess the biogas production from solid waste originating from the chrome based tannery. Anaerobic digestion of these wastes will be a viable option for waste stabilization and energy production in the form of biogas to be utilized in the industry. The bio-methane potential of the wastes were examined by mixing these wastes with various sources of inoculum and different inoculum to substrate (I/S) ratio considered. The batch experiments were carried out in 2.5 l glass reactors with a various source of inoculumviz., Cow Dung (CD), Elephant Dung (ED) and Bio-Digested Slurry (BDS) with varied inoculum to substrate (LFs) ratios for a retention time of 50 days with replications. The results obtained from the experiments showed that BDS:LF (25:75) had the highest gas production of 14505 ml (651.85 ml CH4g?1 VS) followed by CD:LF (50:50) produced 12072.5 ml (789.36 ml CH4g?1 VS) and ED:LF (75:25) produced 11252.5 ml (1492.08 ml CH4g?1 VS)with a methane content of 63.77, 61.92 and 62.72%, respectively. 相似文献
47.
48.
Ghorai PK Yashonath S Demontis P Suffritti GB 《Journal of the American Chemical Society》2003,125(23):7116-7123
Previous work on monatomic spherical sorbates has shown the existence of an anomalous peak in self-diffusivity (D) when plotted as a function of size of the diffusant. Molecular dynamics studies on linear molecules of different lengths l in zeolite NaY at 140 and 200 K are reported. It is seen that there is a peak in D as a function of l, suggesting that the levitation effect exists for linear molecules, the simplest member of polyatomics. This is confirmed by the lowering of the activation energy for the molecule whose length l exhibits highest D. Related quantities of interest such as the guest-host interaction energy and preexponential factor are discussed. 相似文献
49.
Rajendran Arunachalam Eswaran Chinnaraja Arto Valkonen Kari Rissanen Palani S. Subramanian 《应用有机金属化学》2019,33(11)
The multidentate ligand H2 L upon complexation with Zn (II) and Cd (II) provide a one‐dimensional polymeric networks. These coordination polymers (CPs) CP‐1 and CP‐2 containing Zn (II) and Cd (II) metals respectively are well characterized. The single crystal structural analysis confirms the formation of one‐dimensional coordination polymer with zigzag fashion in CP‐1 and ladder chain CP‐2 . Both the CPs are applied as catalysts to synthesize various cyclic carbonates from epoxides and carbon dioxide. The catalysts are giving better conversion under solvent‐free and additive‐free condition using 10 bar CO2 and 100 °C as optimized pressure and temperature. The detailed kinetic experiments suggesting the first order kinetics, the energy of activation (Ea) is calculated for this catalytic conversion. 相似文献
50.
Kótai László Gács István Kazinczy Béla Sajó István E. Sreedhar B. 《Transition Metal Chemistry》2003,28(3):292-295
The theoretical investigation on the distribution of chemical species obtainable as a function of the temperature of the aqueous solutions of metal complexes containing a basic ligand, altogether with the solubility relationship of the compounds to be formed, offers a simple means of planning the preparation of various types of complexes, double and single salts of the central metal cation and onium type compounds of protonated ligand of the central ion and the anion. 相似文献