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961.
Liquid chromatographic-mass spectrometric determination of post-harvest fungicides in citrus fruits 总被引:2,自引:0,他引:2
Liquid chromatography (LC)-atmospheric pressure ionisation (API)-mass spectrometry (MS) has been used to determine residues of five fungicides in oranges with a minimum sample cleanup. Atmospheric pressure chemical ionisation (APCI) and electrospray (ES) were compared and both gave similar results in terms of sensitivity and structural information. The main ions were [M+H]+ for carbendazim, imazalil, thiophanate methyl and thiabendazole, and [M+H-C4H9NHCO]+ for benomyl. Samples were extracted with sodium sulphate and ethyl acetate. Although benomyl and thiophanate methyl were transformed through the extraction procedure to carbendazim, the method showed good precision (<13%) and recovery (>70%), except for thiophanate methyl (50%), whilst also yielding limits of detection (<0.03 mg kg(-1)) that are adequate for the determination of the studied fungicides in oranges. 相似文献
962.
García AM Rodríguez MC Uria JE Sanz-Medel A 《Analytical and bioanalytical chemistry》1995,353(2):128-132
A sensitive, precise and automated non-chromatographic method for Sb(III) and Sb(V) analytical speciation based on a continuous tandem on-line separation device in connection with inductively coupled plasma-atomic emission (ICP-AES) detection is proposed. Two on-line successive separation steps are included into this method: a continuous liquid-liquid extraction of Sb(III) with ammonium pyrrolidine dithiocarbamate (APDC) into methylisobuthylketone (MIBK), followed by direct stibine generation from the organic phase. Both separation steps are carried out in a continuous mode and on-line with the ICP-AES detector. Optimization of experimental conditions for the tandem separation and ICP-AES detection are investigated in detail. Detection limits for Sb(III) were 3 ng.mL(-1) and for Sb(V) 8 ng.mL(-1). Precisions observed are in the range +/- 5%. The proposed methodology has been applied to Sb(III) and Sb(V) speciation in sea-water samples. 相似文献
963.
Robert Deschenaux Jean-Luc Marendaz Julio Santiago John W. Goodby 《Helvetica chimica acta》1995,78(5):1215-1218
The thermal properties of two ferrocene derivatives, substituted by either one or two cholesteryloxycarbonyl units, were investigated. While the monosubstituted ferrocene derivative 1 was found to be non-mesomorphic, the disubstituted ferrocene derivative 2 exhibited a crystal smectic-B phase. This result shows that ferrocene-containing thermotropic liquid crystals, despite the bulkiness of the metallocene core, are not limited to disordered calamitic phases. 相似文献
964.
Design and Synthesis of Aviram–Ratner‐Type Dyads and Rectification Studies in Langmuir–Blodgett (LB) Films 下载免费PDF全文
Dr. Govindasamy Jayamurugan Dr. Vijayendran Gowri David Hernández Prof. Dr. Santiago Martin Dr. Alejandro González‐Orive Dr. Cagatay Dengiz Dr. Oliver Dumele Prof. Dr. Francesc Pérez‐Murano Dr. Jean‐Paul Gisselbrecht Prof. Dr. Corinne Boudon Dr. W. Bernd Schweizer Dr. Benjamin Breiten Dr. Aaron D. Finke Prof. Dr. Gunnar Jeschke Dr. Bruno Bernet Prof. Dr. Laurent Ruhlmann Prof. Dr. Pilar Cea Prof. Dr. François Diederich 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(30):10539-10547
The design and synthesis of Aviram–Ratner‐type molecular rectifiers, featuring an anilino‐substituted extended tetracyanoquinodimethane (exTCNQ) acceptor, covalently linked by the σ‐spacer bicyclo[2.2.2]octane (BCO) to a tetrathiafulvalene (TTF) donor moiety, are described. The rigid BCO spacer keeps the TTF donor and exTCNQ acceptor moieties apart, as demonstrated by X‐ray analysis. The photophysical properties of the TTF‐BCO‐exTCNQ dyads were investigated by UV/Vis and EPR spectroscopy, electrochemical studies, and theoretical calculations. Langmuir–Blodgett films were prepared and used in the fabrication and electrical studies of junction devices. One dyad showed the asymmetric current–voltage (I–V) curve characteristic for rectification, unlike control compounds containing the TTF unit but not the exTCNQ moiety or comprising the exTCNQ acceptor moiety but lacking the donor TTF part, which both gave symmetric I–V curves. The direction of the observed rectification indicated that the preferred electron current flows from the exTCNQ acceptor to the TTF donor. 相似文献
965.
Experimental and Theoretical Study of the Reactivity of Gold Nanoparticles Towards Benzimidazole‐2‐ylidene Ligands 下载免费PDF全文
Dr. María Rodríguez‐Castillo Gustavo Lugo‐Preciado Dr. Danielle Laurencin Dr. Frederik Tielens Dr. Arie van der Lee Dr. Sébastien Clément Dr. Yannick Guari Dr. José M. López‐de‐Luzuriaga Dr. Miguel Monge Dr. Françoise Remacle Dr. Sébastien Richeter 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(30):10446-10458
The reactivity of benzimidazol‐2‐ylidenes with respect to gold nanoparticles (AuNPs) has been investigated using a combined experimental and computational approach. First, the grafting of benzimidazol‐2‐ylidenes bearing benzyl groups on the nitrogen atoms is described, and comparisons are made with structurally similar N‐heterocyclic carbenes (NHCs) bearing other N‐groups. Similar reactivity was observed for all NHCs, with 1) the erosion of the AuNPs under the effect of the NHC and 2) the formation of bis(NHC) gold complexes. DFT calculations were performed to investigate the modes of grafting of such ligands, to determine adsorption energies, and to rationalize the spectroscopic data. Two types of computational models were developed to describe the grafting onto large or small AuNPs, with either periodic or cluster‐type DFT calculations. Calculations of NMR parameters were performed on some of these models, and discussed in light of the experimental data. 相似文献
966.
Rosa López Carmen Pérez Alfonso Femández-Mayoralas Santiago Conde 《Journal of carbohydrate chemistry》2013,32(2):165-171
Abstract The transesterification of some alkyl 2,3,4-tri-O-acyl-β-D-xylopyranosides catalysed by Pseudomonas cepacia lipase in organic solvents has been studied. In all the cases a unique regioisomeric product was obtained, the alkyl 2,3-di-O-acyl-β-D-xylopyranoside. The 2,3-di-O-acetyl derivative (2b) was obtained in 93% yield. These compounds thus obtained are useful intermediates in the synthesis of 4-O-β-D-galactopyranosyl-D-xylose. 相似文献
967.
968.
Ana Sánchez-Grande Dr. José I. Urgel Aleš Cahlík Dr. José Santos Shayan Edalatmanesh Eider Rodríguez-Sánchez Dr. Koen Lauwaet Dr. Pingo Mutombo Prof. Dana Nachtigallová Reed Nieman Prof. Hans Lischka Dr. Bruno de la Torre Prof. Rodolfo Miranda Dr. Oliver Gröning Prof. Nazario Martín Prof. Pavel Jelínek Prof. David Écija 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(40):17747-17752
We report on the synthesis and characterization of atomically precise one-dimensional diradical peripentacene polymers on a Au(111) surface. By means of high-resolution scanning probe microscopy complemented by theoretical simulations, we provide evidence of their magnetic properties, which arise from the presence of two unpaired spins at their termini. Additionally, we probe a transition of their magnetic properties related to the length of the polymer. Peripentacene dimers exhibit an antiferromagnetic (S=0) singlet ground state. They are characterized by singlet–triplet spin-flip inelastic excitations with an effective exchange coupling (Jeff) of 2.5 meV, whereas trimers and longer peripentacene polymers reveal a paramagnetic nature and feature Kondo fingerprints at each terminus due to the unpaired spin. Our work provides access to the precise fabrication of polymers featuring diradical character which are potentially useful in carbon-based optoelectronics and spintronics. 相似文献
969.
970.
Chukwuemeka P. Azubuike Héctor Rodríguez Augustine O. Okhamafe Robin D. Rogers 《Cellulose (London, England)》2012,19(2):425-433
Suitable α-cellulose and cellulose II powders for use in the pharmaceutical industry can be derived from maize cob. α-Cellulose
was extracted from an agricultural residue (maize cobs) using a non-dissolving method based on inorganic substances. Modification
of this α-cellulose was carried out by its dissolution in the ionic liquid 1-butyl-3-methylimidazolium chloride ([C4mim]Cl), and subsequent regeneration by addition of either water or acetone at room temperature, or of boiling water. X-ray
diffraction and infrared spectroscopy results showed that the regenerated celluloses had lower crystallinity, and proved that
the treatment with [C4mim]Cl led to the conversion of the crystalline structure of α-cellulose from cellulose I to cellulose II. Thermogravimetric
analysis and differential scanning calorimetry data showed quite similar thermal behavior for all cellulose samples, although
with somewhat lower stability for the regenerated celluloses, as expected. The comparison of physicochemical properties of
the regenerated celluloses and the native cellulose mainly suggests that the regenerated ones might have better flow properties.
For some of the characterizations carried out, it was generally observed that the sample regenerated with boiling water had
more similar characteristics to the α-cellulose sample, evidencing an influence of the regeneration strategy on the resulting
powder after the ionic liquid treatment. 相似文献