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171.
R. N. Singh S. Sujatha G. K. Mishra 《Journal of Radioanalytical and Nuclear Chemistry》1990,146(6):427-436
The distribution ratios for the extraction of Zr(IV) by TBP and its binary mixtures with DMSO or Py in n-dodecane in the presence of HNO3, and HClO4 have been determined. Based on stoichiometric and slope analysis methods a possible mechanism for the extraction has been proposed. 相似文献
172.
The removal of Ce(III) from aqueous solutions by hydrous manganese oxide (HMO) and hydrous stannic oxide (HSO) was studied
as a function of concentrations (10−2−10−7 mol·dm−3) and pH (1.2–10.0) by using the radiotracer technique. The effects of co-ions and irradiation of HMO and HSO were also studied.
The uptake of Ce(III) fitted well with the Freundlich adsorption isotherm. No significant desorption of pre-adsorbed Ce(III)
in the studied temperature range (303–333 K) indicates that both the solids may be good adsorbents for the removal of Ce(III). 相似文献
173.
Devdutt Chaturvedi Nisha Mishra Virendra Mishra 《Monatshefte für Chemie / Chemical Monthly》2007,70(6):57-60
A novel Mitsunobu-based protocol was developed for the synthesis of carbamates from the corresponding alcohols using carbon dioxide and amines
in good to excellent yields. This protocol is mild, chemoselective, and efficient compared to other reported methods. 相似文献
174.
Summary A new chelating adsorbent, zinc silicate-bonded diethyldithiocarbamate (DTC) has been prepared for the separation and preconcentration of some transition metal ions. The distribution coefficients (Kd values) of 15 metal ions have been estimated in solution at various pH's and some quantitative separations have been achieved. The high selectivity for Pd(II) has been utilized for its preconcentration from dilute aqueous solutions; quantitative elution is effected with acidic 4% thiourea solution. 相似文献
175.
A. Ghosh K. S. Patel R. K. Mishra 《Journal of Radioanalytical and Nuclear Chemistry》1991,152(1):243-249
A new and simple method for selective spectrophotometric determination of uranium(VI) with 4-(2-pyridylazo)resorcinol (PAR) and N-octylacetamide into benzene over pH 7.0–9.0 is described. The molar absorptivity of the complex with 9 different amides is in the range of (0.40–3.2)·104 1·mol–1·cm–1 at the absorption maximum. Out of these, the most sensitive compound N-octylacetamide (OAA) was chosen for detailed studies in the present investigation. The detection limit of the method is 0.008 g U·ml–1. The system obeys Beer's law in the range of 0–5 g U·ml–1. The method is free from interferences of most of the common metal ions except vanadium(V) and copper(II), which are masked by proper masking agents. The composition of the complex is determined by curve-fitting method. The method has been applied for the recovery of the metal from rock samples and synthetic mixtures. 相似文献
176.
In the present work, single-walled carbon nanotubes (SWCNTs) were dispersed in a room temperature nematic liquid crystal 4-pentyl-4′-cyanobiphenyl at the concentration of 0.02 and 0.05 wt%. Differential scanning calorimetry and temperature-dependent dielectric studies suggest decrease in clearing temperature of the composite materials as compared to the pure material. Ionic conductivity increases by two orders of magnitude due to the dispersion of such a low concentration (0.05 wt%) of SWCNTs. Dielectric studies also show that the presence of the SWCNTs decreases the effective longitudinal as well as transverse components of the dielectric permittivity. For homeotropic aligned samples, a relaxation mechanism has been detected in the lower MHz region both for the pure as well as dispersed samples. Presence of SWCNTs increases the relaxation frequency corresponding to flip-flop motion of molecules around their short axes. From frequency-dependent dielectric studies, important dielectric parameters such as relaxation frequency, dielectric strength and distribution parameters have been determined. Electro-optical experiments show that the threshold voltage decreases and the steepness of the transmission voltage curve improves due to the dispersion of SWCNTs. 相似文献
177.
Arjun K. Mishra Nidhi Singh Pragati Agnihotri Shikha Mishra Saurabh P. Singh Bala K. Kolli Kwang Poo Chang Amogh A. Sahasrabuddhe M. I. Siddiqi J. Venkatesh Pratap 《Journal of computer-aided molecular design》2017,31(6):547-562
Nucleoside diphosphate kinases (NDKs) are ubiquitous enzymes that catalyze the transfer of the γ-phosphate moiety from an NTP donor to an NDP acceptor, crucial for maintaining the cellular level of nucleoside triphosphates (NTPs). The inability of trypanosomatids to synthesize purines de novo and their dependence on the salvage pathway makes NDK an attractive target to develop drugs for the diseases they cause. Here we report the discovery of novel inhibitors for Leishmania NDK based on the structural and functional characterization of purified recombinant NDK from Leishmania amazonensis. Recombinant LaNDK possesses auto-phosphorylation, phosphotransferase and kinase activities with Histidine 117 playing an essential role. LaNDK crystals were grown by hanging drop vapour diffusion method in a solution containing 18% PEG-MME 500, 100 mM Bis-Tris propane pH 6.0 and 50 mM MgCl2. It belongs to the hexagonal space group P6322 with unit cell parameters a?=?b?=?115.18, c?=?62.18 Å and α?=?β?=?90°, γ?=?120°. The structure solved by molecular replacement methods was refined to crystallographic R-factor and Rfree values of 22.54 and 26.52%, respectively. Molecular docking and dynamics simulation-based virtual screening identified putative binding compounds. Protein inhibition studies of selected hits identified five inhibitors effective at micromolar concentrations. One of the compounds showed ~45% inhibition of Leishmania promastigotes proliferation. Analysis of inhibitor-NDK complexes reveals the mode of their binding, facilitating design of new compounds for optimization of activities as drugs against leishmaniasis. 相似文献
178.
Ram C. Maurya Deen D. Mishra Surendra K. Jaiswal Sudipta Mukherjee 《Transition Metal Chemistry》1992,17(5):381-383
Some new low-spin hexacoordinated cyanonitrosyl complexes of Cr1 of the type [Cr(NO)(CN)2(L)2(H2)], where L is an aromatic aldehyde oxime or Mannich base, have been prepared by the interaction or K3[Cr(NO)(CN)5]· H2O with L in aqueous AcOH, and characterized by a range of physico-chemical techniques, I.r. data suggest that all the oxime
derivatives and Mannich bases act as monodentate ligands by coordinating through the aromatic nitrogen.
TMC 2564 相似文献
179.
180.