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41.
Ina Heckelmann Zifei Lu Dr. Joseph C. A. Prentice Dr. Florian Auras Dr. Tanya K. Ronson Prof. Dr. Richard H. Friend Prof. Dr. Jonathan R. Nitschke Dr. Sascha Feldmann 《Angewandte Chemie (International ed. in English)》2023,62(12):e202301806
Organic semiconductors are promising for efficient, printable optoelectronics. However, strong excited-state quenching due to uncontrolled aggregation limits their use in devices. We report on the self-assembly of a supramolecular pseudo-cube formed from six perylene diimides (PDIs). The rigid, shape-persistent cage sets the distance and orientation of the PDIs and suppresses intramolecular rotations and vibrations, leading to non-aggregated, monomer-like properties in solution and the solid state, in contrast to the fast fluorescence quenching in the free ligand. The stabilized excited state and electronic purity in the cage enables the observation of delayed fluorescence due to a bright excited multimer, acting as excited-state reservoir in a rare case of benign inter-chromophore interactions in the cage. We show that self-assembly provides a powerful tool for retaining and controlling the electronic properties of chromophores, and to bring molecular electronics devices within reach. 相似文献
42.
Patrick H. Maag Dr. Florian Feist Dr. Vinh X. Truong Dr. Hendrik Frisch Prof. Peter W. Roesky Prof. Christopher Barner-Kowollik 《Angewandte Chemie (International ed. in English)》2023,62(37):e202309259
We introduce a class of single-chain nanoparticles (SCNPs) that respond to visible light (λmax=415 nm) with complete unfolding from their compact structure into linear chain analogues. The initial folding is achieved by a simple esterification reaction of the polymer backbone constituted of acrylic acid and polyethylene glycol carrying monomer units, introducing bimane moieties, which allow for the photochemical unfolding, reversing the ester-bond formation. The compaction and the light driven unfolding proceed cleanly and are readily followed by size exclusion chromatography (SEC) and diffusion ordered NMR spectroscopy (DOSY), monitoring the change in the hydrodynamic radius (RH). Importantly, the folding reaction and the light-induced unfolding are reversible, supported by the high conversion of the photo cleavage. As the unfolding reaction occurs in aqueous systems, the system holds promise for controlling the unfolding of SCNPs in biological environments. 相似文献
43.
Florian J. Stadler Tatsuhiro Takahashi Koichiro Yonetake 《European Polymer Journal》2011,(5):1048-1053
Ethene-/α-olefin copolymers having a wide range of comonomers between 8 and 26 carbon atoms in length were characterized by wide angle X-ray diffraction (WAXD). It was found that the crystallinities for the shorter comonomers (C8, C12) matched fairly well with the crystallinities from DSC and volumetric measurements, while for the longer comonomers (C18, C26) distinct differences between the three methods were found. This was explained by the presence of an additional crystalline phase of the side chains slightly deforming the amorphous peak. 相似文献
44.
Auneau F Michel C Delbecq F Pinel C Sautet P 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(50):14288-14299
We report herein a detailed and accurate study of the mechanism of rhodium-catalysed conversion of glycerol into 1,2-propanediol and lactic acid. The first step of the reaction is particularly debated, as it can be either dehydration or dehydrogenation. It is expected that these elementary reactions can be influenced by pH variations and by the nature of the gas phase. These parameters were consequently investigated experimentally. On the other hand, there was a lack of knowledge about the behaviour of glycerol at the surface of the metallic catalyst. A theoretical approach on a model Rh(111) surface was thus implemented in the framework of density functional theory (DFT) to describe the above-mentioned elementary reactions and to calculate the corresponding transition states. The combination of experiment and theory shows that the dehydrogenation into glyceraldehyde is the first step for the glycerol transformation on the Rh/C catalyst in basic media under He or H(2) atmosphere. 相似文献
45.
In natural gas dehydration units, rich TEG solutions are decompressed before the TEG regeneration stage and the direction of the temperature change during the decompression has been debated. The temperature change from an isenthalpic expansion from (7000 kPa to 440 kPa was measured for the following aqueous mixtures: pure water, 99% pure triethylene glycol (TEG), aqueous TEG (99 wt% TEG + 1% water), aqueous TEG saturated with methane, aqueous TEG saturated with n-pentane, and aqueous TEG saturated with n-heptane. In all cases, the temperature increased upon expansion with the magnitude of the temperature change ranging from 1.4 K for pure water to 2.4 K for TEG. A simple equation of state model predicted the correct direction for the temperature change and the predicted values were within ±1 K of the experimental data. 相似文献
46.
The generation of a hidden Br?nsted acid as a true catalytic species in hydroalkoxylation reactions from metal precatalysts has been clarified in case studies. The mechanism of triflic acid (CF(3)SO(3)H or HOTf) generation starting either from AgOTf in 1,2-dichloroethane (DCE) or from a Cp*RuCl(2)/AgOTf/phosphane combination in toluene has been elucidated. The deliberate and controlled generation of HOTf from AgOTf and cocatalytic amounts of tert-butyl chloride in the cold or from AgOTf in DCE at elevated temperatures results in a hidden Br?nsted acid catalyst useful for mechanistic control experiments or for synthetic applications. 相似文献
47.
André R Tahir MN Link T Jochum FD Kolb U Theato P Berger R Wiens M Schröder HC Müller WE Tremel W 《Langmuir : the ACS journal of surfaces and colloids》2011,27(9):5464-5471
In nature, mineralization of hard tissues occurs due to the synergistic effect of components present in the organic matrix of these tissues, with templating and catalytic effects. In Suberites domuncula, a well-studied example of the class of demosponges, silica formation is mediated and templated by an axial proteinaceous filament with silicatein-α, one of the main components. But so far, the effect of other organic constituents from the proteinaceous filament on the catalytic effect of silicatein-α has not been studied in detail. Here we describe the synthesis of core-shell TiO(2)@SiO(2) and TiO(2)@ZrO(2) nanofibers via grafting of silicatein-α onto a TiO(2) nanowire backbone followed by a coassembly of silintaphin-1 through its specifically interacting domains. We show for the first time a linker-free, one-step funtionalization of metal oxides with silicatein-α using glutamate tag. In the presence of silintaphin-1 silicatein-α facilitates the formation of a dense layer of SiO(2) or ZrO(2) on the TiO(2)@protein backbone template. The immobilization of silicatein-α onto TiO(2) probes was characterized by atomic force microscopy (AFM), optical light microscopy, and high-resolution transmission electron microscopy (HRTEM). The coassembly of silicatein-α and silintaphin-1 may contribute to biomimetic approaches that pursue a controlled formation of patterned biosilica-based biomaterials. 相似文献
48.
Mercey G Verdelet T Saint-André G Gillon E Wagner A Baati R Jean L Nachon F Renard PY 《Chemical communications (Cambridge, England)》2011,47(18):5295-5297
Nerve agents are highly toxic organophosphorus compounds with strong inhibition potency against acetylcholinesterase (AChE). Herein, we describe two first extremely promising uncharged reactivators for poisoned human AChE with a superior or similar in vitro ability to reactivate the enzyme as compared to that of HI-6, obidoxime, TMB-4 and HL?-7. 相似文献
49.
High sensitive matrix-free mass spectrometry analysis of peptides using silicon nanowires-based digital microfluidic device 总被引:1,自引:0,他引:1
Lapierre F Piret G Drobecq H Melnyk O Coffinier Y Thomy V Boukherroub R 《Lab on a chip》2011,11(9):1620-1628
We present for the first time an electrowetting on dielectric (EWOD) microfluidic system coupled to a surface-assisted laser desorption-ionization (SALDI) silicon nanowire-based interface for mass spectrometry (MS) analysis of small biomolecules. Here, the transfer of analytes has been achieved on specific locations on the SALDI interface followed by their subsequent mass spectrometry analysis without the use of an organic matrix. To achieve this purpose, a device comprising a digital microfluidic system and a patterned superhydrophobic/superhydrophilic silicon nanowire interface was developed. The digital microfluidic system serves for the displacement of the droplets containing analytes, via an electrowetting actuation, inside the superhydrophilic patterns. The nanostructured silicon interface acts as an inorganic target for matrix-free laser desorption-ionization mass spectrometry analysis of the dried analytes. The proposed device can be easily used to realize several basic operations of a Lab-on-Chip such as analyte displacement and rinsing prior to MS analysis. We have demonstrated that the analysis of low molecular weight compounds (700 m/z) can be achieved with a very high sensitivity (down to 10 fmol μL(-1)). 相似文献
50.
Casadevall i Solvas X Geier FM Leroi AM Bundy JG Edel JB DeMello AJ 《Chemical communications (Cambridge, England)》2011,47(35):9801-9803
We present a passive microfluidic strategy for sorting adult C. elegans nematodes on the basis of age and size. The separation mechanism takes advantage of phenotypic differences between 'adult' and 'juvenile' organisms and their behaviour in microfluidic architectures. In brief, the microfluidic device allows worms to sort themselves in a passive manner. 相似文献