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991.
Fairlamb IJ Lynam JM Moulton BE Taylor IE Duhme-Klair AK Sawle P Motterlini R 《Dalton transactions (Cambridge, England : 2003)》2007,(33):3603-3605
An evaluation of the CO releasing ability of iron(II) and molybdenum(II) complexes has facilitated the discovery of the most rapid CO releaser, namely [Mo(CO)(3)(eta(5)-C(5)H(5))(eta(1)-{O}-C{=O}-O-CMe=CH-COMe=CBr)]BF(4) (CORM-F10), reported to date. The rate of CO release is related to the overall solution phase stability of the transition metal carbonyl complex. The cytotoxicity and vasodilatory properties of CORM-F10 have been determined. 相似文献
992.
Schmiege BM Carney MJ Small BL Gerlach DL Halfen JA 《Dalton transactions (Cambridge, England : 2003)》2007,(24):2547-2562
This report describes the synthesis and characterization of metal halide complexes (M = Mn, Fe, Co) supported by a new family of pendant donor-modified alpha-diimine ligands. The donor (N, O, P, S) substituent is linked to the alpha-diimine by a short hydrocarbon spacer forming a tridentate, mer-coordinating ligand structure. The tridentate ligands are assembled from monoimine precursors, the latter being synthesized by selective reaction with one carbonyl group of the alpha-dione. While attempts to separately isolate tridentate ligands in pure form were unsuccessful, metal complexes supported by the tridentate ligand are readily synthesized in-situ, by forming the ligand in the presence of the metal halide, resulting in a metal complex which subsequently crystallizes out of the reaction mixture. Metal complexes with NNN, NNO, NNP and NNS donor sets have been prepared and examples supported by NNN, NNP and NNS ligands have been structurally characterized. In the solid state, NNN and NNP ligands coordinate in a mer fashion and the metal complexes possess distorted square pyramidal structures and high spin (S = 2) electronic configurations. Compounds with NNS coordination environments display a variety of solid state structures, ranging from those with unbound sulfur atoms, including chloride bridged and solvent ligated species, to those with sulfur weakly bound to the metal center. The extent of sulfur ligation depends on the donor ability of the crystallization solvent and the substitution pattern of the arylthioether substituent. 相似文献
993.
One-step synthesis of oxazoline and dihydrooxazine libraries 总被引:1,自引:0,他引:1
Chaudhry P Schoenen F Neuenswander B Lushington GH Aubé J 《Journal of combinatorial chemistry》2007,9(3):473-476
The reactions of 1,2- and 1,3-hydroxyalkyl azides and aldehydes in the presence of Lewis acid result in the one-step construction of oxazolines and dihydrooxazines, respectively. The reaction was adapted to parallel synthesis using a polymer-bound phosphine to scavenge excess hydroxyalkyl azide. Thus, a 60-member library of various disubstituted oxazolines and di- and trisubstituted dihydrooxazines was generated. 相似文献
994.
Antioxidant and Anti-Inflammatory Effects of Peganum harmala Extracts: An In Vitro and In Vivo Study
Malik Waseem Abbas Mazhar Hussain Muhammad Qamar Sajed Ali Zahid Shafiq Polrat Wilairatana Mohammad S. Mubarak 《Molecules (Basel, Switzerland)》2021,26(19)
Peganum harmala (P. harmala) belongs to the family Zygophyllaceae, and is utilized in the traditional medicinal systems of Pakistan, China, Morocco, Algeria, and Spain to treat several chronic health disorders. The aim of the present study was to identify the chemical constituents and to evaluate the antioxidant, anti-inflammatory, and toxicity effects of P. harmala extracts both in vitro and in vivo. Sequential crude extracts including 100% dichloromethane, 100% methanol, and 70% aqueous methanol were obtained and their antioxidant and anti-inflammatory effects evaluated both in vitro and in vivo. The anti-inflammatory effect of the extract was investigated using the carrageenan-induced paw edema method in mice, whereas the toxicity of the most active extract was evaluated using an acute and subacute toxicity rat model. In addition, we have used the bioassay-guided approach to obtain potent fractions, using solvent–solvent partitioning and reversed phase high performance liquid chromatography from active crude extracts; identification and quantification of compounds from the active fractions was achieved using electrospray ionization mass spectrometry and high performance liquid chromatography techniques. Results revealed that the 100% methanol extract of P. harmala exhibits significant in vitro antioxidant activity in DPPH assay with an IC50 of 49 µg/mL as compared to the standard quercetin with an IC50 of 25.4 µg/mL. The same extract exhibited 63.0% inhibition against serum albumin denaturation as compared to 97% inhibition by the standard diclofenac sodium in an in vitro anti-inflammatory assay, and in vivo anti-inflammatory against carrageenan-induced paw edema (75.14% inhibition) as compared to 86.1% inhibition caused by the standard indomethacin. Furthermore, this extract was not toxic during a 14 day trial of acute toxicity when given at a dose of 3 g/kg, indicating that the lethal dose (LD50) of P. harmala methanol extract was greater than 3 g/kg. P. harmala methanolic fraction 2 obtained using bioassay-guided fractionation showed the presence of quinic acid, peganine, harmol, harmaline, and harmine, confirmed by electrospray ionization mass spectrometry and quantified using external standards on high performance liquid chromatography. Taken all together, the current investigation further confirms the antioxidant, anti-inflammatory, and safety aspects of P. harmala, which justifies its use in folk medicine. 相似文献
995.
We construct quasi-Hopf algebras quantizing double extensions of the Manin pairs of Drinfeld, associated to a curve with a
meromorphic differential, and the Lie algebrasl
2. This construction makes use of an analysis of the vertex relations for the quantum groups obtained in our earlier work,
PBW-type results and computation ofR-matrices for them; its key step is a factorization of the twist operator relating “conjugated” versions of these quantum
groups. 相似文献
996.
Basis- and partition identification for quadratic programming and linear complementarity problems 总被引:1,自引:0,他引:1
Arjan B. Berkelaar Benjamin Jansen Kees Roos Tamás Terlaky 《Mathematical Programming》1999,86(2):261-282
Optimal solutions of interior point algorithms for linear and quadratic programming and linear complementarity problems provide
maximally complementary solutions. Maximally complementary solutions can be characterized by optimal partitions. On the other
hand, the solutions provided by simplex–based pivot algorithms are given in terms of complementary bases. A basis identification
algorithm is an algorithm which generates a complementary basis, starting from any complementary solution. A partition identification
algorithm is an algorithm which generates a maximally complementary solution (and its corresponding partition), starting from
any complementary solution. In linear programming such algorithms were respectively proposed by Megiddo in 1991 and Balinski
and Tucker in 1969. In this paper we will present identification algorithms for quadratic programming and linear complementarity
problems with sufficient matrices. The presented algorithms are based on the principal pivot transform and the orthogonality
property of basis tableaus.
Received April 9, 1996 / Revised version received April 27, 1998?
Published online May 12, 1999 相似文献
997.
When examined by fluorescence microscopy, tumor cells loaded with a zinc benzochlorin iminium salt showed a very faint deep-red fluorescence that was rapidly transformed to a substantially brighter red-orange fluorescence. Fourier transfer spectroscopy analysis with a red-sensitive detection system revealed that an initial fluorescence at 770 nm was gradually converted to 640 nm fluorescence during excitation. Image analysis showed that photoproduct formation was accompanied by a change in the site of drug localization from the cytoplasm to the nucleus. These studies illustrate the power of interferometry for the characterization of photoproducts and changes in sensitizer localization during photoproduct formation. 相似文献
998.
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