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151.
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La, Ce(III), Pr, Nd and Sm(III) form very stable reddishviolet 1:1 complexes with 1-amino-4-hydroxyanthraquinone in methanol. The stability constants are very similar. 相似文献
154.
155.
Rajinder K. Tuli Purshotam Soni Kailash Chandra Rajendra K. Sharma Bhagawan S. Garg 《Transition Metal Chemistry》1980,5(1):145-148
Summary
N,N-Dialkyldithiocarbametohafnium(IV) complexes of the type -CpHf(S2CNR2)3, (R = Me or Et) have been prepared in nonaqueous media by reacting dichlorodicyclopentadienylhafnium(IV) with sodium salts of substituted dithiocarbamic acids. Conductance and i.r. studies show that these complexes are nonelectrolytes in which all of the dithiocarbamate ligands are bidentate. A coordination number of seven may be assigned to hafnium(IV) in these complexes, 'H n.m.r. spectra of the complexes in CDCI3 at ambient temperature (30°) indicate that the metal centered rearrangement and the S2C N bond rotation are both slow on the n.m.r. time scale. A capped octahedron configuration is suggested for these complexes.Author to whore all correspondence should be addressed. 相似文献
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157.
The paper describes the availability of crank-case manufacturing system in an automobile industry. The units discussed here fail either directly from normal working state or indirectly through partial failure state. The machines are subjected to both preventive and corrective maintenance. Failure and repair times of the units are independent. The problem is formulated using probability consideration and supplementary variable technique. The system of equations governing the working of system consists of ordinary as well as partial differential equations. Lagrange method and Runge–Kutta method is used to solve partial differential equation and ordinary differential equation respectively. The study reveals that successful program of preventive and routine maintenance will reduce equipment failures, extend the life of the equipment, and increase the system availability to considerable margin. 相似文献
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159.
Subhankar P. Mandal Aakriti Garg P. Prabitha Ashish D. Wadhwani Laxmi Adhikary B. R. Prashantha Kumar 《Chemistry Central journal》2018,12(1):141
Background
An alarming requirement for finding newer antidiabetic glitazones as agonists to PPARγ are on its utmost need from past few years as the side effects associated with the available drug therapy is dreadful. In this context, herein, we have made an attempt to develop some novel glitazones as PPARγ agonists, by rational and computer aided drug design approach by implementing the principles of bioisosterism. The designed glitazones are scored for similarity with the developed 3D pharmacophore model and subjected for docking studies against PPARγ proteins. Synthesized by adopting appropriate synthetic methodology and evaluated for in vitro cytotoxicity and glucose uptake assay. Illustrations about the molecular design of glitazones, synthesis, analysis, glucose uptake activity and SAR via 3D QSAR studies are reported.Results
The computationally designed and synthesized ligands such as 2-(4-((substituted phenylimino)methyl)phenoxy)acetic acid derivatives were analysed by IR, 1H-NMR, 13C-NMR and MS-spectral techniques. The synthesized compounds were evaluated for their in vitro cytotoxicity and glucose uptake assay on 3T3-L1 and L6 cells. Further the activity data was used to develop 3D QSAR model to establish structure activity relationships for glucose uptake activity via CoMSIA studies.Conclusion
The results of pharmacophore, molecular docking study and in vitro evaluation of synthesized compounds were found to be in good correlation. Specifically, CPD03, 07, 08, 18, 19, 21 and 24 are the candidate glitazones exhibited significant glucose uptake activity. 3D-QSAR model revealed the scope for possible further modifications as part of optimisation to find potent anti-diabetic agents.
160.
Simple, accurate, economical, and reproducible UV spectrophotometric and column high-performance liquid chromatographic (HPLC) methods were developed for simultaneous estimation of a 2-component drug mixture of metoprolol tartrate and hydrochlorothiazide in combined tablet dosage form. The first method used the simultaneous equation method with 7 mixed standards and the absorption maxima at 223 and 271 nm, respectively, for metoprolol tartrate and hydrochlorothiazide in methanol. Linearity was observed in the concentration ranges of 4-24 and 2-16 microg/mL for metoprolol tartrate and hydrochlorothiazide, respectively. The developed HPLC method used a reversed-phase C18 column and methanol-water (95 + 5) mobile phase at an ambient temperature of 27 +/- 2 degrees C and UV detection at 225 nm; the run time was 10 min, and quantification was based on peak area. The injection repeatability and intraday and interday repeatability were calculated. Paracetamol was used as an internal standard for the HPLC method, and linearity was observed in the concentration range of 5-50 microg/mL for metoprolol and 2-20 microg/mL for hydrochlorothiazide. The proposed methods were successfully applied for the determination of metoprolol tartrate and hydrochlorothiazide in bulk powder and dosage form. The results obtained were analyzed statistically, and there was no significant difference between the 2 methods. The validation was performed according to International Conference on Harmonization guidelines. 相似文献