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951.
Pradeep Mathur Raj Kumar Joshi Amrendra K. Singh 《Journal of organometallic chemistry》2010,695(24):2687-2694
A facile, one pot, high yield synthesis of α,β-vinylester (1-14) and alkoxy substituted γ-lactones (15-28) has been achieved by the photochemical reaction of terminal acetylene (ferrocenyl phenyl trimethylsillyl, hexyl and cyclohexyl) with alcohol (methanol, ethanol and isopropanol) and carbon monoxide in presence of iron pentacarbonyl as a catalyst. The selectivity of the compounds depends on the time of photolysis of the reaction as well as the solvent used. A stable reaction intermediate ferrole was isolated, and further photolysis with alcohols, resulted in the formation of α,β-vinylester. All the compounds were fully characterised by spectroscopic methods and the molecular structures of compounds 1, 16, 17 and 20 were established crystallographically. 相似文献
952.
K.K. Bhasin Rishu Sukhjinder Singh H. Kumar S.K. Mehta 《Journal of organometallic chemistry》2010,695(5):648-2013
The present work reports an efficient one-pot synthesis of symmetrical pyridyl monoselenides by the reaction of bromo-/iodopyridines with the isopropylmagnesium chloride, iPrMgCl followed by quenching with selenyl chloride, SeCl2. The current methodology constitutes a convenient synthesis of bis(5-bromo-2-pyridyl) selenide (I), bis(2-bromo-5-pyridyl) selenide (II) and bis(2,5-dibromo-3-pyridyl) selenide (III) under cryogenic conditions requiring shorter time duration to give satisfactory yields. The hitherto unknown compounds have been characterized by elemental analysis and various spectroscopic techniques i.e., 1H NMR, 13C NMR, FT-IR, mass spectrometry and X-ray crystallography. 相似文献
953.
954.
Munish Puri Aneet Kaur Ram Sarup Singh Anubhav Singh 《Applied biochemistry and biotechnology》2010,162(1):181-191
Response surface methodology was used to optimize the fermentation medium for enhancing naringinase production by Staphylococcus xylosus. The first step of this process involved the individual adjustment and optimization of various medium components at shake
flask level. Sources of carbon (sucrose) and nitrogen (sodium nitrate), as well as an inducer (naringin) and pH levels were
all found to be the important factors significantly affecting naringinase production. In the second step, a 22 full factorial
central composite design was applied to determine the optimal levels of each of the significant variables. A second-order
polynomial was derived by multiple regression analysis on the experimental data. Using this methodology, the optimum values
for the critical components were obtained as follows: sucrose, 10.0%; sodium nitrate, 10.0%; pH 5.6; biomass concentration,
1.58%; and naringin, 0.50% (w/v), respectively. Under optimal conditions, the experimental naringinase production was 8.45 U/mL. The determination coefficients
(R
2) were 0.9908 and 0.9950 for naringinase activity and biomass production, respectively, indicating an adequate degree of reliability
in the model. 相似文献
955.
This paper describes the synthesis and characterization of aromatic diimide–diacids (DIDAS) obtained by reacting pyromellitic
dianhydride (PMDA), 4,4′-oxo diphthalic anhydride (ODA), 1,4,5,8-naphthalene tetra carboxylic dianhydride (NTDA) with excess
of 4-aminobutyric acid (B) or 6-aminohexanoic acid (H) using N,N-dimethyl formamide (DMF) as solvent. The synthesized compounds were used as curing agents to investigate the effect of structure
on the curing and thermal behaviour of diglycidyl ether of bisphenol-A (DGEBA). Structural characterization of DIDAS was done
by using FTIR, 1H-NMR, 13C-NMR spectroscopy and elemental analysis. Curing behaviour of DGEBA in the presence of aromatic DIDAS was investigated by
differential scanning calorimetry (DSC). The peak exotherm temperature (T
P) was low in the case of DIDAS synthesized from ODA and high in the case of DIDAS synthesized from NTDA. Thermal stability
of the isothermally cured DGEBA with DIDAS was investigated using dynamic thermogravimetry in nitrogen atmosphere. The char
yield was highest for resin cured with DIDAS containing NTDA. 相似文献
956.
Bruno Fabre Soraya Ababou-Girard Prabhpreet Singh Jitendra Kumar Sandeep Verma Alberto Bianco 《Electrochemistry communications》2010,12(6):831-834
Redox-active ferrocene was assembled on gold surfaces through the hydrogen bonding interactions between adenine-substituted ferrocene and a uracil-terminated organothiol monolayer. The surface coverage of ferrocene Γ could be varied from ca. 4 × 10? 11 to 2.0 × 10? 10 mol cm? 2 by diluting the thiol-modified uracil derivative with inert 1-octanethiol. A decrease in the apparent electron transfer rate constant for ferrocene, kapp, from ca. 50 to 10 s? 1 was observed upon increasing Γ. 相似文献
957.
Hari Ji Singh Bhupesh Kumar Mishra Nand Kishor Gour 《Theoretical chemistry accounts》2010,125(1-2):57-64
The unimolecular decomposition reaction of CF3CCl2O radical has been investigated using theoretical methods. Two most important channels of decomposition occurring via C–C bond scission and Cl elimination have been considered during the present investigation. Ab initio quantum mechanical calculations are performed to get optimized structure and vibrational frequencies at DFT and MP2 levels of theory. Energetics are further refined by the application of a modified Gaussian-2 method, G2M(CC,MP2). The thermal rate constants for the decomposition reactions involved are evaluated using Canonical Transition State Theory (CTST) utilizing the ab initio data. Rate constants for C–C bond scission and Cl elimination are found to be 6.7 × 106 and 1.1 × 108 s?1, respectively, at 298 K and 1 atm pressure with an energy barrier of 8.6 and 6.5 kcal/mol, respectively. These values suggest that Cl elimination is the dominant process during the decomposition of the CF3CCl2O radical. Transition states are searched on the potential energy surface of the decomposition reactions involved and are characterized by the existence of only one imaginary frequency (NIMAG = 1) during frequency calculation. The existence of transition states on the corresponding potential energy surface is further ascertained by performing intrinsic reaction coordinate (IRC) calculation. 相似文献
958.
Manish Pratap Singh Rajendra Kumar Singh Dr. Suresh Chandra Prof. 《Chemphyschem》2010,11(9):2036-2043
Porous silica matrices of different pore sizes with confined ionic liquid (1‐butyl‐3‐methylimidazolium hexafluorophosphate) [BMIM] [PF6] were prepared by sol‐gel technique using a tetraethyl orthosilicate (TEOS) precursor with an aim to study the changes in physico‐chemical properties of ionic liquid on confinement. It is found that on confinement 1) melting point decreases, 2) fluorescence spectra shows a red shift and 3) the vibrational bands are affected particularly those of imadazolium ring, which interacts more with the walls of the silica matrix. Preliminary theoretical calculations suggest that SiO2 matrix interact more with the heterocyclic group of [BMIM] cation than the tail alkyl chain end group resulting in significant changes in the aromatic vibrations. 相似文献
959.
Nanocrystalline Ce(1-x)Fe(x)O(2-δ) (0 ≤ x ≤ 0.45) and Ce(0.65)Fe(0.33)Pd(0.02)O(2-δ) of ~4 nm sizes were synthesized by a sonochemical method using diethyletriamine (DETA) as a complexing agent. Compounds were characterized by powder X-ray diffraction (XRD), X-ray photo-electron spectroscopy (XPS) and transmission electron microscopy (TEM). Ce(1-x)Fe(x)O(2-δ) (0 ≤ x ≤ 0.45) and Ce(0.65)Fe(0.33)Pd(0.02)O(2-δ) crystallize in fluorite structure where Fe is in +3, Ce is in +4 and Pd is in +2 oxidation state. Due to substitution of smaller Fe(3+) ion in CeO(2), lattice oxygen is activated and 33% Fe substituted CeO(2)i.e. Ce(0.67)Fe(0.33)O(1.835) reversibly releases 0.31[O] up to 600 °C which is higher or comparable to the oxygen storage capacity of CeO(2)-ZrO(2) based solid solutions (Catal. Today 2002, 74, 225-234). Due to interaction of redox potentials of Pd(2+/0)(0.89 V) and Fe(3+/2+) (0.77 V) with Ce(4+/3+) (1.61 V), Pd ion accelerates the electron transfer from Fe(2+) to Ce(4+) in Ce(0.65)Fe(0.33)Pd(0.02)O(1.815), making it a high oxygen storage material as well as a highly active catalyst for CO oxidation and water gas shift reaction. The activation energy for CO oxidation with Ce(0.65)Fe(0.33)Pd(0.02)O(1.815) is found to be as low as 38 kJ mol(-1). Ce(0.67)Fe(0.33)O(1.835) and Ce(0.65)Fe(0.33)Pd(0.02)O(1.815) have also shown high activity for the water gas shift reaction. CO conversion to CO(2) is 100% H(2) specific with these catalysts and conversion rate was found to be as high 27.2 μmoles g(-1) s(-1) and the activation energy was found to be 46.4 kJ mol(-1) for Ce(0.65)Fe(0.33)Pd(0.02)O(1.815). 相似文献
960.
D. P. Singh V. Malik R. Kumar K. Kumar 《Russian Journal of Coordination Chemistry》2010,36(3):220-225
The condensation reaction of succinyldihydrazide with glyoxal in the presence of divalent metal ions (1: 1: 1) results in
the formation of the complexes of type [M(C6H8N4O2)X2], where M = Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and X = Cl−, NO3−, CH3COO−. The complexes have been characterized with the aid of elemental analyses, conductance measurements and electronic, NMR,
infrared spectral studies. On the basis of these studies, a six-coordinated distorted octahedral geometry in which two nitrogen
and two carbonyl oxygen atoms are suitably placed for coordination toward metal ion, has been proposed for all the complexes.
The complexes were tested for their in vitro antibacterial activity. Some of the complexes showed remarkable antibacterial
activities against some selected bacterial strains. 相似文献