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981.
Novel water-soluble amphiphilic graft copolymers (COS-g-PCL-b-MPEG) were synthesized by the coupling reaction between chitooligosaccharide (COS) and MPEG-b-PCL-COOH, which was synthesized via ring-opening polymerization of ε-caprolactone (CL) using MPEG as an initiator and subsequent carboxylation by succinic anhydride. The chemical composition of the graft copolymers was confirmed by 1H-NMR spectra and FT-IR spectrometry. The thermal properties and crystallinity of the copolymers were observed by DSC and XRD measurements, which showed the existence of separate backbone and graft chain phases in the copolymer. The micellar behavior via self-assembly of the graft copolymers in aqueous solution was studied using pyrene fluorescence dye technique. AFM measurements showed that the micelles had a spherical morphology at the critical micelle concentration (CMC) and ranged in size from 20–45 nm. The amphiphilic ternary biodegradable graft copolymer endows the hydrophilic outer shell of micelles with structural and functional diversification, which might be desirable for drug delivery applications. 相似文献
982.
U. Böhme W. Schmidt P. G. Dietrich A. Matschi F. Sacher H.-J. Brauch 《Analytical and bioanalytical chemistry》1997,357(6):629-634
The ion-chromatographic method for trace analysis of bromate and bromide presented in this paper is based on coating of reversed
phase (RP) material with an ionogenic agent, tetrakisdecylammonium bromide, to obtain a pseudo ion-exchange column. The analysis
is carried out with usual HPLC pump and UV-detection near 200 nm. Some commercially available RP materials were tested for
the coating procedure. The differences between the reversed phases are not significant. All HETP values are calculated between
0.02 and 0.14 mm. The calibration, the sensitivity of the method and the long-time stability of the coated column were tested
with one selected RP material. It is shown that the simultaneous trace analysis of bromate and bromide in surface and drinking
waters with chloride concentrations up to 50 mg/L is possible without any clean-up on Ag precolumns. A comparison of performance
data with a determination method for bromate and bromide employing a commercially available equipment demonstrates the efficiency
of the new technique.
Received: 23 February 1996/Received: 10 May 1996/Accepted: 14 May 1996 相似文献
983.
Applicability of surface-enhanced resonance Raman scattering for the direct discrimination of ballpoint pen inks 总被引:1,自引:0,他引:1
In situ surface-enhanced resonance Raman spectroscopy (SERRS) with excitation at 685 nm is suitable for the direct discrimination of blue and black ballpoint pen inks on paper. For black inks, shorter excitation wavelengths can also be used. For blue inks, SERRS at 514.5 and 457.9 nm does not provide adequate discriminative power. At these excitation wavelengths, the SERRS signals of the Methyl Violet derivatives present in inks easily dominate the overall spectrum because of resonance enhancement and preferential interaction with silver sol particles. At 685 nm, this problem is not encountered as the Methyl Violet derivatives do not show resonance enhancement, while other components may still exhibit resonance. Thirteen blue and thirteen black ink lines were examined. For the blue and black inks, on the basis of the 685 nm SERR spectra, eight and six groups of spectra, respectively, could be distinguished. This discrimination largely agrees with information from thin layer chromatography (TLC) experiments, although some differences in group compositions are found. The in situ SERR spectra show good repeatability with regard to the Raman frequencies, band shapes and relative intensities of the spectral bands. However, absolute intensities cannot be used for discrimination purposes. 相似文献
984.
Dzhemilev U. M. Khusnutdinov R. I. Atnabaeva A. M. Muslimov Z. S. Parfenova R. I. Tomilov Yu. V. 《Russian Chemical Bulletin》2001,50(7):1242-1247
The possibility of the cleavage of the C—C bond in acetylcyclopropane (ACP) under the action of water or alcohols in the presence of copper or palladium salts was demonstrated for the first time. At 175—180 °C, the reactions proceeded regioselectively with the cleavage of the C(1)—C(2) bond in the cyclopropane ring. The reaction of ACP with water afforded 5-hydroxypentan-2-one, bis(3-acetylpropyl) ether, and furan compounds, whereas the reactions with alcohols proceeded selectively to form 5-alkoxypentan-2-ones. The yields of the latter depend on the nature and structure of the alcohol, the maximum values (98%) being achieved in the case of primary alcohols. 相似文献
985.
Lee CH McComb ME Bromirski M Jilkine A Ens W Standing KG Perreault H 《Rapid communications in mass spectrometry : RCM》2001,15(3):191-202
This article discusses the features of a newly developed matrix-assisted laser desorption/ionization quadrupole/time-of-flight (MALDI-QqTOF) mass spectrometer that is useful in the analysis of phosphorylated peptides. Aliquots of beta-casein, a commonly used phosphorylated protein standard, were digested with trypsin directly on a non-porous polyurethane membrane used as sample support in MALDI-QqTOF mass spectrometry (MS) experiments. Although a complete peptide map was obtained, it was difficult to obtain sequence information for some of the tryptic fragments, in particular T1-2, which bears four phosphate groups and is thus difficult to ionize in positive mode. This article focuses on the sequencing of this particular fragment by comparing MS/MS spectra obtained using different precursor ions. These precursors associated with T1-2 were [M + H](+), [M + H](2+), and [M + H - nH(3)PO(4)](+) ions. Typically, phosphorylated ions showed facile unimolecular losses of phosphoric acid moieties, and produced limited backbone fragmentation. The abundance of [M + H](2+) ions of T1-2 in the full mass spectrum was low relative to that of [M + H](+). [M + H - 4H(3)PO(4)](+) ions as MS/MS precursors underwent backbone fragmentations, with phosphoserine residues transformed into dehydroalanines or serines. Unusual b + 18 u fragments were observed, although only for segments with previously phosphorylated serines. These partly interfered with c-ions, and were noticeable due to overlapping isotopic envelopes. It was possible to establish the sequence of phosphorylated tryptic fragment T1-2 and the location of phosphate groups using the mass of dehydroalanine residues (69 Da) and b + 18 u fragments as markers. All MS and MS/MS spectra obtained with fully phosphorylated beta-casein were compared with spectra acquired with dephosphorylated beta-casein obtained commercially. These comparisons helped assess the spectral differences caused by the presence of phosphate groups. Also, they highlighted the potential usefulness of conducting dephosphorylation directly on the probe prior to MALDI analysis in future studies. 相似文献
986.
Gel analysis system purchasers have a large variety of digital imaging products to choose from today. Understanding the specifications presented by the manufacturers is important to ensure that the system fits the needs ofthe researcher using the system. The background information contained in this paper explains the terminology and many of the specifications along with their significance. 相似文献
987.
The theory for modeling vibronic interactions in bichromophores was introduced in sixties by Witkowski and Moffitt [J. Chem. Phys. 33, 872 (1960)] and extended by Fulton and Gouterman [J. Chem. Phys. 35, 1059 (1961)]. The present work describes extension of this vibronic model to describe bichromophores with broken vibrational symmetry such as partly deuterated molecules. Additionally, the model is extended to include inter-chromophore vibrational modes. The model can treat multiple vibrational modes by employing Lanczos diagonalization procedure of sparse matrices. The developed vibronic model is applied to simulation of vibronic spectra of flexible bichromophore diphenylmethane and compared to high-resolution experimental spectra [J. A. Stearns, N. R. Pillsbury, K. O. Douglass, C. W. Mu?ller, T. S. Zwier, and D. F. Plusquellic, J. Chem. Phys. 129, 224305 (2008)]. 相似文献
988.
Young Chul Kim Jun Young Lee Dong Young Kim Hyun Nam Cho Chung Yup Kim 《Macromolecular Symposia》1997,118(1):461-466
The optical transmittance of the film spin-cast from the polypyrrole(PPy) solution in chloroform depended on the thickness of the film. The film with 80% transmittance showed a surface resistivity of 23kΩ/□. A TN-LCD cell with rubbed PPy films as the LC alignment layers responded properly to an applied potential of 3.0V. Reflective mode cholesteric LCD cells made with black PPy film electrodes responded to AC fields to switch between the planar and focal conic states. PPy with imine structures introduced by deprotonation of doped PPy with NaOH solution was used as a diode material to exhibit a photo-current on exposing to light. 相似文献
989.
H. C. Eun Y. Z. Cho H. S. Park I. T. Kim H. S. Lee 《Journal of Radioanalytical and Nuclear Chemistry》2012,292(2):531-535
In this paper, a separation method of radionuclides (Ba, Sr) from LiCl salt wastes generated from the electroreduction process
of spent nuclear fuel was studied to recover pure LiCl salts and reduce radioactive wastes. The method consisted of chemical
conversion process of BaCl2 and SrCl2 in LiCl molten salts by using lithium compounds and vacuum distillation process of LiCl salts. In the chemical conversion,
BaCl2 and SrCl2 in LiCl molten salts were mainly converted into (Ba,Sr)CO3 or (Ba,Sr)SO4. Contents of Ba and Sr in LiCl salts recovered from the vacuum distillation process were equal to about 0.01 of initial concentrations
of Ba and Sr in LiCl molten salts. These results will be utilized to recycle the LiCl salt wastes. 相似文献
990.