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1.
2.
The spectral structure of two parameter unbounded operator pencils of waveguide type is studied. Theorems on discreteness
of the spectrum for a fixed parameter are proved. Variational principles for real eigenvalues in some parts of the root zones
are established. In the case of n = 1 (quadratic pencils) domains containing the spectrum are described (see Fig. 1–3). Conditions in the definition of the
pencils of waveguide type arise naturally from physical problems and each of them has a physical meaning. In particular a
connection between the energetic stability condition and a perturbation problem for the coefficients is given. 相似文献
3.
Anshu Dandia Kapil Arya Meha Sati Pritima Sarawgi 《Journal of fluorine chemistry》2004,125(9):1273-1277
Reasonable pure fluorinated s-triazines were synthesized in quantitative yield (96-99%) in 2-3 min in aqueous medium under microwaves, by reaction of fluorinated anilines and aqueous formaldehyde. All synthesized compounds have been screened in vitro for their antifungal activity against Rhizoctonia solani, Fusarium oxysporum, and Collectotrichum capsici. 相似文献
4.
Spiro [3H-indole-3,2′-[4H] pyrido [3,2-e]-1,3-thiazine]-2,4′ (1H) diones, a class of previously unknown compound which does not form under conventional conditions, can be prepared by treatment of ‘in situ’ generated 3-indolylimine derivatives with 2-mercaptonicotinic acid under microwave irradiation in absence of any solvent or solid support in 85-92% yields in 3-8 min. The facile one pot reaction is generalized for a variety of ketones and amines to give pure pyrido [3,2-e] thiazine derivatives, which do not require further purification processes. 相似文献
5.
McGinn et al. [1] and Misra and Naik [2] studied the complexing capacity of maleic acid with metals. Edge [3] reported his findings on the pyrolysis of normal nickel maleato. This note is concerned with the estimation of kinetic parameters of the non-isothermal decomposition of acid maleato complexes of Co(II), Cu(II), Ni(II) and Cd(II). 相似文献
6.
Uzun O Sanyal A Nakade H Thibault RJ Rotello VM 《Journal of the American Chemical Society》2004,126(45):14773-14777
Polystyrene functionalized with diamidopyridine (DAP) recognition units self-assembles in nonpolar media to form thermally reversible micrometer-scale spherical aggregates. The size and the thermal stability of these microspheres can be controlled by the molecular weight of the polymer. The addition of thymine-functionalized polymer to these self-assembled microspheres converted them into vesicular aggregates with a controlled size. The morphology change was reversible: the addition of DAP-functionalized polymer converted the vesicles back to microspheres. 相似文献
7.
M. Emin Çorman Nilay Bereli Serpil Özkara Lokman Uzun Adil Denizli 《Biomedical chromatography : BMC》2013,27(11):1524-1531
As alternative hydrophobic adsorbent for DNA adsorption, supermacroporous cryogel disks were synthesized via free radical polymerization. In this study, we have prepared two kinds of cryogel disks: (i) poly(2‐hydroxyethyl methacrylate‐N‐methacryloyl‐l ‐tryptophan) [p(HEMA‐MATrp)] cryogel containing specific hydrophobic ligand MATrp; and (ii) monosize p(HEMA‐MATrp) particles synthesized via suspension polymerization embedded into p(HEMA) cryogel structure to obtain p(HEMA‐MATrp)/p(HEMA) composite cryogel disks. These cryogel disks containing hydrophobic functional group were characterized via swelling studies, Fourier transform infrared spectroscopy, elemental analysis, surface area measurements and scanning electron microscopy. DNA adsorption onto both p(HEMA‐MATrp) cryogel and p(HEMA‐MATrp)/p(HEMA) composite cryogels was investigated. Maximum adsorption of DNA on p(HEMA‐MATrp) cryogel was found to be 15 mg/g polymer. Otherwise, p(HEMA‐MATrp)/p(HEMA) composite cryogels significantly increased the DNA adsorption capacity to 38 mg/g polymer. Composite cryogels could be used repeatedly without significant loss on adsorption capacity after 10 repetitive adsorption–desorption cycles. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
8.
9.
The aim of this study is to prepare magnetic beads which can be used for the removal of heavy metal ions from synthetic solutions. Magnetic poly(ethylene glycol dimethacrylate‐vinyl imidazole) [m‐poly(EGDMA‐VIM)] beads were produced by suspension polymerization in the presence of magnetite Fe3O4 nano‐powder. The specific surface area of the m‐poly(EGDMA‐VIM) beads was found to be 63.1 m2/g with a size range of 150–200 µm in diameter and the swelling ratio was 85%. The average Fe3O4 content of the resulting m‐poly(EGDMA‐VIM) beads was 12.4%. The maximum binding capacities of the m‐poly(EGDMA‐VIM) beads were 32.4 mg/g for Cu2+, 45.8 mg/g for Zn2+, 84.2 mg/g for Cd2+and 134.5 mg/g for Pb2+. The affinity order on mass basis is Pb2+>Cd2+>Zn2+>Cu2+. Equilibrium data agreed well with the Langmuir model. pH significantly affected the binding capacity of the magnetic beads. Binding of heavy metal ions from synthetic wastewater was also studied. The binding capacities were 26.2 mg/g for Cu2+, 33.7 mg/g for Zn2+, 54.7 mg/g for Cd2+ and 108.4 mg/g for Pb2+. The magnetic beads could be regenerated up to about 97% by treating with 0.1 M HNO3. These features make m‐poly(EGDMA‐VIM) beads a potential candidate for support of heavy metal removal under magnetic field. 相似文献
10.
Demet Uzun 《Electroanalysis》2021,33(7):1699-1706
In this present study, to determine paracetamol, an electroanalytical method is presented using differential pulse voltammetry (DPV) at 3-amino-4H-1,2,4-triazole (3AT) coated glassy carbon (GC) electrode. The electrochemical characterization and electron transfer behavior of this prepared electrode in the mixture of K4[Fe(CN)6]/K3[Fe(CN)6] contains 0.1 M KCl was confirmed by using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) methods. Furthermore, scanning electron microscopy (SEM) was used to observe morphological structures of the bare and modified surfaces. The effect of pH was studied on the redox reaction of paracetamol in phosphate buffer in the range of pH 3.0–9.0. The limit of detection was 0.043 μM (3 s/m) for 3AT-GC electrode. The developed electrode was successfully utilized in pharmaceutical samples. 相似文献