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101.
Malvi B Panda C Dhar BB Gupta SS 《Chemical communications (Cambridge, England)》2012,48(43):5289-5291
An [Fe(III)(biuret-amide)] complex has been immobilized onto mesoporous silica nanoparticles via Cu(I) catalyzed azide-alkyne click chemistry. This hybrid material functions as an efficient peroxidase mimic and was successfully used for the quantitative determination of hydrogen peroxide and glucose via a one-pot colorimetric assay. 相似文献
102.
J Mondal A Modak A Dutta S Basu SN Jha D Bhattacharyya A Bhaumik 《Chemical communications (Cambridge, England)》2012,48(64):8000-8002
Surface functionalization of SBA-15 followed by its reaction with Cu(OAc)(2) has been carried out to develop a new Cu-grafted functionalized mesoporous material, which catalyzes one-pot three component coupling of different aryl halides with thiourea and benzyl bromide in aqueous medium to produce aryl thioethers in very good yields (80-88%). 相似文献
103.
Singh AK Chawla R Rai A Yadav LD 《Chemical communications (Cambridge, England)》2012,48(31):3766-3768
NHC-catalysed azalactone ring-opening and piperidine ring-closing cascade with α,β-unsaturated aldehydes (enals) in a one-pot operation is reported. The present reaction cascade offers a convenient method for a highly diastereoselective synthesis of multifunctionalised piperidines in excellent yields under mild conditions. 相似文献
104.
We present some solutions in a modified theory of gravity with R 2 and \frac1R\frac{1}{R} terms in the Einstein-Hilbert action with an ideal fluid in FLRW spacetime. Graceful exit from early inflation to radiation dominated era is obtained in the strong curvature regime preceding a fluctuation of effective equation of state parameter at the end of inflation. In the weak curvature regime the universe evolves through a radiation era that subsequently turns to a matter era and finally transits to late time accelerating era. 相似文献
105.
Rohit Verma R. Dhar M.C. Rath S.K. Sarkar R. Dabrowski 《Journal of Physics and Chemistry of Solids》2012,73(2):288-295
Dielectric and electro-optical studies of a pure and electron beam irradiated liquid crystalline compound 4-(trans-4′-n-hexylcyclohexyl) isothiocyanatobenzoate have been carried out. Dielectric anisotropy, relaxation frequency, activation energy and distribution parameter of an observed non-collective mode corresponding to the molecular rotation about the short axes have been determined as a function of temperature and irradiation dose whereas threshold and switching voltages, splay elastic constant are determined as a function of irradiation dose. The relaxation frequencies initially decrease up to an irradiation dose of 40 kGy but thereafter increase due to irradiation. The activation energies are increased up to irradiation dose of 40 kGy but around 60 kGy dose of irradiation, we found decrease in the activation energy. Electro-optical measurements show the lowering of the threshold voltage with sufficient improvement in the steepness of the transmission voltage curves due to irradiation. The observed changes in the dielectric and electro-optical properties are related with the cis–trans isomerization due to electron beam irradiation. 相似文献
106.
Arsenic(III) sorption on nanostructured cerium incorporated manganese oxide (NCMO): a physical insight into the mechanistic pathway 总被引:1,自引:0,他引:1
Gupta K Bhattacharya S Nandi D Dhar A Maity A Mukhopadhyay A Chattopadhyay DJ Ray NR Sen P Ghosh UC 《Journal of colloid and interface science》2012,377(1):269-276
Arsenic(III) sorption was investigated with nanostructured cerium incorporated manganese oxide (NCMO). The pH between 6.0 and 8.0 was optimized for the arsenic(III) sorption. Kinetics and equilibrium data (pH=7.0±0.2, T=303±1.6 K, and I=0.01 M) of arsenic(III) sorption by NCMO described, respectively, the pseudo-second order and the Freundlich isotherm equations well. The sorption process was somewhat complicated in nature and divided into two different segments, initially very fast sorption followed by slow intraparticle diffusion process. Sorption reaction of arsenic(III) on NCMO was endothermic (ΔH°=+13.46 kJ mol(-1)) and spontaneous (ΔG°=-24.75 to -30.15 kJ mol(-1) at T=283-323 K), which took place with increasing entropy (ΔS°=+0.14 kJ mol(-1)K(-1)) at solid-liquid interface. Energy of arsenic(III) sorption estimated by analyzing the equilibrium data using the D-R isotherm model was 15.4 kJ mol(-1), indicating the ion-exchange type mechanism. Raman, FT-IR, pH effect, desorption, etc. studies indicated that arsenic(III) was oxidized to arsenic(V) during the sorption process. 相似文献
107.
108.
Arghyadeep Paul Siddhartha Mukherjee Jayabrata Dhar Sandip Ghosal Suman Chakraborty 《Electrophoresis》2020,41(7-8):607-614
Screened repulsion between uniformly charged plates with an intervening electrolyte is analyzed for strongly overlapped electrical double layers (EDL), accounting for the steric effect of ions and their expulsion from EDL edges into the surrounding solution. As a generalization of a study by Philipse et al. which does not account for these effects, an analytical expression is derived for the repulsion pressure in the limit of infinitely long plates with a zero-field assumption, which agrees closely with the corresponding numerical solution at low inter-plate separations. Our results show an augmented repulsive pressure for finite-sized ions at strong EDL overlaps. For plates with a finite lateral size, we demonstrate a further extended domain of low inter-plate gaps where the repulsion pressure increases with ion size due to a strong interplay between the steric interaction of ions and the EDL overspill phenomenon, considered earlier in a study by Ghosal & Sherwood limited to the linear Debye-Hückel regime (which cannot account for the steric effect of ions). This investigation on a simple model should enhance our understanding of the interaction between charged particles in electrophoresis, nanoscale self-assembly, active particles, and various other electrokinetic systems. 相似文献
109.
P. S. Kulkarni V. N. Gogte A. S. Modak S. D. Sahasrabudhe B. D. Tilak 《Journal of mass spectrometry : JMS》1985,20(7):454-457
The chemical ionization mass spectra of some substituted heterocyclic systems, viz. tetrahydro-1,3,2-oxazaphosphorin-2-oxides, reveal polar cycloreversion reactions. The zwitterion intermediate formed by the heterolysis of the C? O bond undergoes stepwise clean heterolysis further resulting in the expulsion of the potential nucleophilic and electrophilic groups. The competitive and consecutive heterolysis of the ring bonds leads to the formation of the protonated phenylimine ions. Competing with heterolysis, elimination reactions involving hydrogen transfer leading to the formation of α-phenylethyl ions are also observed. The chemical ionization mass spectrometry of the heterocyclic system shows many features of the Grob type of fragmentation mechanism. 相似文献
110.
We work out the non-equilibrium steady state properties of a harmonic lattice which is connected to heat reservoirs at different temperatures. The heat reservoirs are themselves modeled as harmonic systems. Our approach is to write quantum Langevin equations for the system and solve these to obtain steady state properties such as currents and other second moments involving the position and momentum operators. The resulting expressions will be seen to be similar in form to results obtained for electronic transport using the non-equilibrium Green’s function formalism. As an application of the formalism we discuss heat conduction in a harmonic chain connected to self-consistent reservoirs. We obtain a temperature dependent thermal conductivity which, in the high-temperature classical limit, reproduces the exact result on this model obtained recently by Bonetto, Lebowitz and Lukkarinen. 相似文献