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101.
102.
103.
J. W. Tomm H. Schmidt L. Werner K. H. Herrmann 《Crystal Research and Technology》1990,25(9):1069-1078
Material and structural parameters of narrow-gap p-type HgCdTe are investigated by infrared photoluminescence. The method is used for analyzing the energy gap, the carrier lifetime, and heterointerfaces and to monitor defects like inclusions. The spatial distribution of the quantities mentioned has been investigated by applying the mapping technique known for III – V semiconductors. The methods is a powerful tool for both crystal growth and device manufacturing. 相似文献
104.
Dr. Andreas A. Bastian Dr. Maria Bastian Dr. Manuel Jäger Mark Loznik Dr. Eliza M. Warszawik Xintong Yang Dr. Nabil Tahiri Dr. Peter Fodran Prof. Dr. Martin D. Witte Anne Thoma Dr. Jens Köhler Prof. Dr. Adriaan J. Minnaard Prof. Dr. Andreas Herrmann 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(36):e202200883
The continuous emergence of antimicrobial resistance is causing a threat to patients infected by multidrug-resistant pathogens. In particular, the clinical use of aminoglycoside antibiotics, broad-spectrum antibacterials of last resort, is limited due to rising bacterial resistance. One of the major resistance mechanisms in Gram-positive and Gram-negative bacteria is phosphorylation of these amino sugars at the 3’-position by O-phosphotransferases [APH(3’)s]. Structural alteration of these antibiotics at the 3’-position would be an obvious strategy to tackle this resistance mechanism. However, the access to such derivatives requires cumbersome multi-step synthesis, which is not appealing for pharma industry in this low-return-on-investment market. To overcome this obstacle and combat bacterial resistance mediated by APH(3’)s, we introduce a novel regioselective modification of aminoglycosides in the 3’-position via palladium-catalyzed oxidation. To underline the effectiveness of our method for structural modification of aminoglycosides, we have developed two novel antibiotic candidates overcoming APH(3’)s-mediated resistance employing only four synthetic steps. 相似文献
105.
Determination of pharmaceuticals, iodinated contrast media and musk fragrances in sludge by LC/tandem MS and GC/MS 总被引:1,自引:0,他引:1
Ternes TA Bonerz M Herrmann N Löffler D Keller E Lacida BB Alder AC 《Journal of chromatography. A》2005,1067(1-2):213-223
Analytical methods have been developed that allow for the determination of antiphlogistics, lipid regulators, the antiepileptic carbamazepine, cytostatic agents, the psychiatric drug diazepam and iodinated contrast media (ICM) as well as two major polycyclic musk fragrances HHCB (galaxolide) and AHTN (tonalide) in activated and digested sludge. The procedures consist of ultrasonic solvent extraction (USE) using methanol/acetone or pressurized liquid extraction (PLE) using 100% methanol. Clean-up was performed with C18ec material and silica gel followed by LC tandem MS (electrospray or atmospheric pressure chemical ionization) detection for pharmaceuticals and iodinated contrast media as well as GC/MS in the SIM mode for musk fragrances. Absolute recoveries from spiked activated sludge in general ranged from 88+/-4 to 119+/-20% for ICM and were 78+/-15 and 87+/-10% for the AHTN and HHCB, respectively. For the pharmaceuticals, absolute recoveries in activated sludge ranged between 43 and 78%. Subsequently, compensation of losses was carried out by using surrogate standards (acidic pharmaceuticals: fenoprop, neutral pharmaceuticals: dihydro-carbamazepine, musk fragrances: AHTN-D3). With one exception the recoveries were also adequate in digested sludge ranging from 43% to 120%. 相似文献
106.
107.
108.
W. A. Herrmann 《Nachrichten aus der Chemie》1988,36(11):1226-1227
109.
Damien Berthier Alain Trachsel Charles Fehr Lahoussine Ouali Andreas Herrmann 《Helvetica chimica acta》2005,88(12):3089-3108
Amphiphilic polystyrene‐ and polymethacrylate‐based β‐acyloxy ketones were investigated as potential delivery systems for the controlled release of damascones by retro‐1,4‐addition in applications of functional perfumery. A series of random copolymers being composed of the hydrophobic damascone‐release unit and a second hydrophilic monomer were obtained by radical polymerization in organic solution by using 2,2′‐azobis[2‐methylpropanenitrile] (AIBN) as the radical source (Schemes 2 and 3). A first evaluation of the polymer conjugates in acidic or alkaline buffered aqueous solution, and in the presence of a surfactant, showed that polymethacrylates and polystyrenes having a carboxylic acid function as hydrophilic group are particularly interesting for the targeted applications (Table 2). The release of δ‐damascone ( 1 ) from polymers with poly(methacrylic acid) and poly(vinylbenzoic acid) comonomers in different stoichiometric ratios was thus followed over several days at pH 4, 7, and 9 by comparison of fluorescence probing, solvent extraction, and particle‐size measurements (Tables 3 and 4). In acidic media, the polymers were found to be stable, and almost no δ‐damascone ( 1 ) was released. In neutral or alkaline solution, where the carboxylic acid functions are deprotonated, the concentration of 1 increased over time. In the case of the polymethacrylates, the fluorescence probing experiments showed an increasing hydrophilicity of the polymer backbone with increasing fragrance release, whereas in the case of the polystyrene support, the hydrophilicity of the environment remained constant. These results suggest that the nature of the polymer backbone may have a stronger influence on the fragrance release than the ratio of hydrophilic and hydrophobic monomers in the polymer chain. 相似文献
110.
J. N. Kavanagh F. J. Currell D. J. Timson M. H. Holzscheiter N. Bassler R. Herrmann K. M. Prise G. Schettino 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》2010,60(1):209-214
Radiotherapy employs ionizing radiation to induce lethal DNA lesions in
cancer cells while minimizing damage to healthy tissues. Due to their
pattern of energy deposition, better therapeutic outcomes can, in theory, be
achieved with ions compared to photons. Antiprotons have been proposed to
offer a further enhancement due to their annihilation at the end of the
path. The work presented here aimed to establish and validate an
experimental procedure for the quantification of plasmid and genomic DNA
damage resulting from antiproton exposure. Immunocytochemistry was used to
assess DNA damage in directly and indirectly exposed human fibroblasts
irradiated in both plateau and Bragg peak regions of a 126 MeV antiproton
beam at CERN. Cells were stained post irradiation with an anti-γ-H2AX antibody. Quantification of the
γ-H2AX foci-dose relationship is consistent with a linear increase in the Bragg peak region. A qualitative analysis of the
foci
detected in the Bragg peak and plateau
region indicates significant differences highlighting the different severity
of DNA lesions produced along the particle path. Irradiation of desalted
plasmid DNA with 5 Gy antiprotons at the Bragg peak resulted in a significant
portion of linear plasmid in the resultant solution. 相似文献