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91.
《印度化学会志》2021,98(10):100156
Corona virus disease 2019 (COVID-19) endemic has havoc on the world; the causative virus of the pandemic is SARS CoV-2. Pharmaceutical companies and academic institutes are in continuous efforts to identify anti-viral therapy or vaccines, but the most significant challenge faced is the highly evolving genome of SARS CoV-2, which is imparting evolutionary selective benefits to the virus. To understand the viral mutations, we have retrieved nine hundred and thirty-four samples from different states of India via the GISAID database and analyzed the frequency of all types of point mutation in all structural, non-structural proteins, and accessory factors of SARS CoV-2. Spike glycol protein, nsp3, nsp6, nsp12, N and NS3 were the most evolving proteins. High frequency point mutations were Q496P (nsp2), A380V (nsp4), A994D (nsp3), L37F (nsp6), P323L & A97V (nsp12), Q57H (ns3), D614G (S), P13L (N), R203K (N), G204R (N) and S194L (N). 相似文献
92.
在碱性介质中用分光光度法研究了二过碲酸合铜(Ⅲ)配离子(DTC)氧化乙二醇一乙醚(EGE)的反应动力学及机理。反应速率表明:反应对DTC为准一级,对EGE为分数级;在保持准一级条件([EGE]》[DTC])下,表观速率常数随着OH-浓度的增加而增大,随着TeO42-浓度的增加而减小;有负的盐效应。据此提出了包括配离子和EGE形成络合物的前期平衡的反应机理,由假设反应机理推出的速率方程能很好的解释全部实验现象,进一步求得速控步的速率常数和活化 相似文献
93.
V.?I.?VigdorovichEmail author L.?E.?Tsygankova O.?V.?Alekhina T.?P.?D'yachkova 《Russian Journal of Electrochemistry》2005,41(10):1046-1052
The effect of thiourea (0.5–10 mM) on the kinetics of the hydrogen evolution reaction (HER) at iron and the hydrogen transport through a steel membrane out of ethylene glycol (containing 2 and 10 wt % H2O) and aqueous solutions containing HCl (0.1–0.99 M) with a constant ionic strength equal to unity is studied in parallel experiments. The presence of 0.5 mM of thiourea in the solutions raises the overvoltage of hydrogen evolution, while a subsequent increase in its concentration does not effect the HER kinetics. The dependence of the flux of hydrogen diffusion through the membrane on the thiourea content passes through a maximum. 相似文献
94.
In this study, a simple method was developed to crosslink chitosan using poly(ethylene glycol) (PEG) with different molecular weights. Crosslinking of chitosan was confirmed by various spectral analyses. The differential scanning calorimetric (DSC) study indicated that the rigid crystalline structure of chitosan was decreased after crosslinking with PEG. The PEG-crosslinked chitosan (PEG-Ch) showed a pH-independent swelling behavior: swelled in both the simulated stomach (pH 1.1) and intestinal (pH 7.4) solutions. The swelling ratio of PEG-Ch increased significantly with a higher molecular weight of PEG used. In contrast, chitosan dissolved completely in a simulated stomach solution and showed a comparatively less swelling in a simulated intestinal solution. Thus, the prepared PEG-Ch could be a better biomaterial than chitosan in the development of orally sustained drug-delivery devices. 相似文献
95.
K.S. Morley N.V. Tokareva V.K. Popov J. Zhang S.M. Howdle 《European Polymer Journal》2007,43(2):307-314
A supercritical fluid (SCF) route for facile and homogeneous introduction of silver nanoparticles into polymer hosts is described. Our focus is on ultra-high molecular weight polyethylene (UHMWPE). We demonstrate that the metallic nanoparticles have a substantial effect upon the wear and tribochemical properties of the polymer substrate. 相似文献
96.
A simple high-performance liquid chromatographic method, using photodiode array detection was developed for the determination
of propylene glycol in human plasma and in the fluid retreived after continuous veno-venous hemofiltration. The method entailed
alkaline derivatization with benzoyl chloride and ethylene glycol as internal standard. The separation of the compounds, after
extraction with pentane, was carried out on a Pursuit C8 column with UV-detection at 230 nm. Validation samples were analyzed
with an accuracy between 95 and 105%, and intra- and inter-day coefficients of variation of less than 8%. The calibration
curve was linear over a concentration range of 5–100 mg L−1 with a detection limit of 1 mg L−1. Blood plasma samples of several patients were analysed by using the prescribed method with propylene glycol concentrations
varying from 5 to 98 mg L−1. Compared to previously described LC methods, this method is ten times more sensitive and thus suitable for use in pharmacokinetic
studies of propylene glycol. 相似文献
97.
Mir Ali Farajzadeh Mortaza Ebrahimi Ali Ranji Elham Feyz Vali Bejani Amir Abbas Matin 《Mikrochimica acta》2006,153(1-2):73-78
High performance liquid chromatography (HPLC) and gas chromatography (GC) are introduced for analysis of polymer lubricants
(stearamide, oleamide and erucamide). In the HPLC method, a reverse phase octadecylsilane (ODS) column along with acetonitrile/methanol
(60:40) as a mobile phase were used. Detection of analytes was performed by a UV detector at 202 nm. The analysis time was
less than 8 min. In the GC method, polar capillary column and flame ionization detector (FID) were used for separations and
detection, respectively. The analysis time by GC was longer than HPLC and was about 30 min. Limits of detection, linear range
and repeatability of both methods are similar, but determination of oleamide in real samples by HPLC method is difficult due
to complexity of the initial part of HPLC chromatogram in polyethylene samples. That problem is not observed in the GC method.
Detection limits in both methods for all analytes are lower than 0.003% which are much lower than the amount of lubricants
in commercial polymers (0.05–0.2%). 相似文献
98.
Polyethylene glycols can be immobilized in glass capillary columns by a new procedure involving covering the glass walls with a layer of graphitized carbon black and by flowing a mixture of the stationary phase and dicumyl peroxide. After curing and conditioning the column is ready for use. Excellent performance is reported for Carbowax 20 M and high molecular weight glycols. For other glycols the immobilized layer is less stable and can be washed out. 相似文献
99.
100.
Barry R. Lentz 《Journal of fluorescence》1995,5(1):29-38
An important process in the life of a cell is fusion between cellular membranes. This is the process by which two cellular compartments surrounded by different membranes join to become a single compartment surrounded by a single membrane, without significant loss of compartment contents. To demonstrate fusion, the cell biophysicist must demonstrate all three critical aspects of the process: (1) mixing of membrane components, (2) mixing of compartment contents; and (3) retention of compartment contents. Most commonly, accomplishing this involves the use of fluorescence probes. The general theme to the methods described involves some form of concentration-dependent quenching. An unique method developed in our laboratory utilizes the concentration dependence of the fluorescence lifetime of a phosphatidylcholine containing carboxyethyl diphenylhexatriene at position 2 and palmitic acid at position 1 of glycerol (DPHpPC). The fluorescence lifetime of this molecule and that of its parent fluorophore diphenylhexatriene (DPH) shorten dramatically as their two-dimensional concentrations in a membrane increase. This lifetime quenching can be described by dimer formation that reduces the symmetry of the DPH excited state. This phenomenon allows one to use the fluorescence lifetime to gain insight into the local concentration of probe in microscopic regions of a membrane. One application of this is in distinguishing lipid transfer between the outer leaflets of two contacting membrane bilayers from fusion between these membranes that leads to mixing of lipids in both the inner and outer leaflets of the membrane bilayers. This allows a single measurement to demonstrate fusion between membrane pairs.Abbreviations PEG
poly(ethylene glycol)
- Na2EDTA
ethyiene-diamine-tetraacedic acid, disodium salt
- LUV
large, unilamellar vesicles made by rapid extrusion technique
- DPH
1,6-diphenyl-trans-1,3,5-hexatriene
- DPHpPC
1-palmitoyl-2-[[[2-[4- (phenyl-trans-1,3,5-hexatrienyl)phenyl]ethyl]oxy]carbonyl]-3-sn-phosphatidylcholine
- DPPC
1,2-dipalmitoyl-3-sn-phosphatidylcholine
- PA
palmitic acid
- NBD-PE
N-(7-nitro-2,1,3-benzoxadiazol-4-yl)-PE
- Rh-PE
N-(lissamine Rhodamine B sulfoyl)-PE
- R18
octadecyl Rhodamine B chloride
- ANTS
1-aminonaphthalene-3,6,8-trisulfonic acid
- DPX
N,N-p-xylylene-bis(pyradinium bromide) 相似文献