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91.
Formaggio F Barazza A Bertocco A Toniolo C Broxterman QB Kaptein B Brasola E Pengo P Pasquato L Scrimin P 《The Journal of organic chemistry》2004,69(11):3849-3856
In a recent series of papers, Miller and co-workers were able to show that His(pi-Me)-based, terminally protected peptides are potent catalysts of the asymmetric acyl transfer reaction, useful for the kinetic resolution of alcohols. In a structure-supporting solvent, one of the most active compounds, an Aib-containing tetrapeptide, is folded in a doubly intramolecularly H-bonded beta-hairpin motif incorporating a type-II' beta-turn conformation. In this work, we have expanded the study of the Miller tetrapeptide by examining a set of analogues and shorter sequences (dipeptide amides), characterized by chiral C(alpha)-tetrasubstituted alpha-amino acids of diverging bulkiness and optical configuration. Peptide synthesis in solution, conformational analysis by FT-IR absorption and (1)H NMR techniques, and screening of catalytic activity as well have been performed. Our results confirm the close relationship between the beta-hairpin 3D-structure and the catalytic activity of the peptides. A tetrapeptide analogue slightly more selective than the Miller compound has been found. However, the terminally protected, industrially more appealing, dipeptide amides are poorly effective. 相似文献
92.
Bartolo Gabriele Lucia Veltri Pierluigi Plastina Mirco Costa 《Tetrahedron letters》2010,51(13):1663-1786
A novel and convenient approach to furan-3-carboxylic esters 2 is presented, based on palladium-catalyzed direct oxidative carbonylation of readily available 3-yne-1,2-diols 1. The process, corresponding to a sequential combination between a 5-endo-dig heterocyclodehydration step and an oxidative alkoxycarbonylation stage, is catalyzed by PdI2 in conjunction with an excess of KI under relatively mild conditions (100 °C in ROH under 40 atm of a 4:1 mixture of CO-air). 相似文献
93.
A reversed-phase high-performance liquid chromatographic method for the determination of benzydamine hydrochloride and its impurities 3-dimethylaminopropyl 2-benzylaminobenzoate, 3-dimethylaminopropyl-2-aminobenzoate,1-benzyl-1H-indazol-3-ol, 1-benzyl-2-(3-dimethylaminopropyl)-1,2-dihydro-3H-indazol-3-one, and 1-benzyl-3-(3-(3-dimethylaminopropyl)-3-methylamino)propoxy-(1)H-indazole in a collutory formulation is developed. The separation is carried out on a Gemini C(18) (250 × 4.6 mm, 5 μm) column using acetonitrile-methanol-ammonium carbonate buffer (10 mM; pH 10.5) (37.5:37.5:25, v/v/v) as mobile phase at a flow rate of 1.0 mL/min, column temperature 30°C, and UV detection at 218 nm. Famotidine is used as an internal standard. The total run-time is less than 15 min. The analytical curves present coefficients of correlation greater than 0.99, and detection limits are calculated for all analytes. Excellent accuracy and precision are obtained for benzydamine hydrochloride. Recoveries vary from 98.25 to 102.8%, and intra- and inter-day precisions, calculated as the percent relative standard deviation, are lower than 2.2%. Specificity and robustness for benzydamine hydrochloride are also determined. The method allows the quantitative determination of benzydamine hydrochloride and its impurities, and it is suitable for routine analysis in quality control laboratories. 相似文献
94.
J. Pablo Lamas Lucia Sanchez-PradoMarta Lores Carmen Garcia-JaresMaria Llompart 《Journal of chromatography. A》2010,1217(33):5307-5316
Exposure to fragrance substances is exponentially increasing in our daily life due to the enhanced use of scented products. Some fragrances are known to be important sensitizers, inhalation being an important exposure pathway in indoor environments. A simple and sensitive method based on solid-phase enrichment and solid-phase microextraction (SPME) followed by gas chromatography–mass spectrometry (GC–MS) has been developed for the analysis of 24 volatile fragrance allergens in indoor air. Suspected allergens present in the air (0.2 m3) were adsorbed onto a very small quantity of florisil (25 mg) and then transferred to a SPME fiber in the headspace mode (HS). To the best of our knowledge, this paper describes the first application of SPME for the determination of these compounds in air samples. The experimental parameters affecting the microextraction process have been optimized using a multifactor experimental design strategy. Accuracy, linearity, precision and detection limits (LODs) were evaluated to assess the performance of the proposed method. External calibration, using spiked sorbent standards, and not requiring the complete sampling process (only the SPME step), demonstrated to be suitable for the quantification of all suspected allergens. Recovery studies were performed at three concentration levels (0.04, 1.00 and 50 μg m−3), obtaining quantitative recoveries (≥85%) in most cases. LOD values at the low ng m−3 level were achieved for all the target compounds. The application of the method to daily home air samples demonstrated the ubiquity of this kind of fragrance ingredients in quotidian indoor environments, finding 18 of the 24 considered compounds in concentrations ranging from 0.01 to 56 μg m−3. Benzyl alcohol, linalool, citronellol, ionone and lilial were found in most analyzed samples. 相似文献
95.
Annemarie Huijser Dr. Alessandro Pezzella Dr. Jonas K. Hannestad Lucia Panzella Dr. Alessandra Napolitano Prof. Marco d'Ischia Prof. Villy Sundström Prof. 《Chemphyschem》2010,11(11):2424-2431
The UV‐dissipative mechanisms of the eumelanin building block 5,6‐dihydroxyindole‐2‐carboxylic acid (DHICA) and the 4,7‐dideutero derivative (DHICA‐d2) in buffered H2O or D2O have been characterized by using ultrafast time‐resolved fluorescence spectroscopy. Excitation of the carboxylate anion form, the dominating state at neutral pH, leads to dual fluorescence. The band peaking at λ=378 nm is caused by emission from the excited initial geometry. The second band around λ=450 nm is owed to a complex formed between the mono‐anion and specific buffer components. In the absence of complex formation, the mono‐anion solely decays non‐radiatively or by emission with a lifetime of about 2.1 ns. Excitation of the neutral carboxylic acid state, which dominates at acidic pH, leads to a weak emission around λ=427 nm with a short lifetime of 240 ps. This emission originates from the zwitterionic state, formed upon excitation of the neutral state by sub‐ps excited‐state intramolecular proton transfer (ESIPT) between the carboxylic acid group and the indole nitrogen. Future studies will unravel whether this also occurs in larger building blocks and ESIPT is a built‐in photoprotective mechanism in epidermal eumelanin. 相似文献
96.
Fernando C. Moraes Lucia H. Mascaro Sergio A. S. Machado Christopher M. A. Brett 《Electroanalysis》2010,22(14):1586-1591
A copper phthalocyanine/multiwalled carbon nanotube film‐modified glassy carbon electrode has been used for the determination of the herbicide glyphosate (Gly) at ?50 mV vs. SCE by electrochemical oxidation using differential pulse voltammetry (DPV). Cyclic voltammetry and electrochemical impedance spectroscopy showed that Gly is adsorbed on the metallic centre of the copper phthalocyanine molecule, with formation of Gly‐copper ion complexes. An analytical method was developed using DPV in pH 7.4 phosphate buffer solution, without any pretreatment steps: Gly was determined in the concentration range of 0.83–9.90 μmol L?1, with detection limit 12.2 nmol L?1 (2.02 μg L?1). 相似文献
97.
Austin Nevin Daniela Comelli Iacopo Osticioli Lucia Toniolo Gianluca Valentini Rinaldo Cubeddu 《Analytical and bioanalytical chemistry》2009,395(7):2139-2149
The assessment of the influence of natural and artificial ageing on the spectrofluorescence of triterpenoid varnishes dammar
and mastic is the focus of this work. Both Fourier transform infrared (FTIR) microscopy using attenuated total reflectance
and Raman spectroscopy have been employed for complementary molecular analysis of samples. Synchronous fluorescence spectroscopy,
excitation emission spectroscopy, and statistical analysis of data have been used to monitor changes in the optical properties
of varnish samples. Assessment of naturally and artificially aged samples using excitation emission spectroscopy suggests
that extensive exposure to visible light does not lead to easily appreciable differences in the fluorescence of mastic and
dammar; cluster analysis has been used to assess changes, which occur with artificial ageing under visible light, indicating
that differences in the fluorescence spectra of aged triterpenoids may be insufficient for their discrimination. The results
highlight significant differences between the initial fluorescence of films of dammar and mastic and the fluorescence, which
develops with ageing and oxidation, and specific markers, which change with ageing in FTIR and Raman spectra, have been identified. 相似文献
98.
Sebastian Dresen Merja Gergov Lucia Politi Claudia Halter Wolfgang Weinmann 《Analytical and bioanalytical chemistry》2009,395(8):2521-2526
An electrospray ionization tandem mass spectrometry (ESI-MS/MS) library which contains over 5,600 spectra of 1,253 compounds
relevant in clinical and forensic toxicology has been developed using a hybrid tandem mass spectrometer with a linear ion
trap. Pure compound solutions—in some cases solutions made of tablets—were prepared and 1 to 2,000 ng of each compound were
injected into the system using standard reversed-phase analytical columns with gradient elution. To obtain maximum mass spectral
information enhanced product ion spectra were acquired with positive and/or negative ionization at low, medium, and high collision
energies and additionally applying collision energy spread. In this mode, all product ions generated by the different collision
energies are trapped in the linear ion trap prior to their detection. The applicability of the library for other types of
hybrid tandem mass spectrometers with a linear ion trap of the same manufacturer as well as a standard triple-quadrupole tandem
mass spectrometer has been investigated with a selection of compounds. The spectra of the developed library can be used to
create methods for target analysis, either screening methods or quantitative procedures by generating transitions for multiple
reaction monitoring. For those procedures, suitable transitions and convenient collision energies are selected from the library.
It also has been utilized to identify compounds with a multi target screening approach for clinical and forensic toxicology
with a standardized and automated system. The novel aspects compared to our former library produced with a standard triple-quadrupole
mass spectrometer are the enlargement of the ESI-MS/MS library and the additional acquisition of spectra with collision energy
spread. 相似文献
99.
Cellulose composites were produced by culturing Acetobacter aceti subsp. xylinum (ATCC 53524, agitation tolerant strain) under shaking and agitating conditions in the presence of 2% pine or beech Björkman lignin-carbohydrate complexes (LCCs) or six different types of hemicellulosic polysaccharides including glucuronoxylan, glucomannan, O-acetyl-glucuronoxylan, arabinoglucuronoxylan, arabinogalactan and xyloglucan. Hemicellulosic polysaccharide contents in cellulose composites were similar in spite of the differences in culture, shaking and agitating conditions. On the basis of hemicellulosic polysaccharide contents and X-ray diffraction patterns after extraction by dilute NaOH solution, glucomannan family polysaccharides were found to have the highest affinity to bacterial cellulose. Composites with neutral and acidic LCCs were resistant against alkali while high lability of their delignified carbohydrates against alkali indicates the importance of lignin for formation of cellulose-hemicellulose-lignin framework of plant secondary cell-walls. 相似文献
100.
Aires da Conceição Silva Lucia C.S. Aguiar Andréa Luzia F. de Souza Luiz Fernando Brum Malta 《Tetrahedron letters》2010,51(30):3883-6491
In this work, we present ligand-free Suzuki cross-coupling reactions in PEG 300 under thermal conditions at 55 °C with good yields of conversion; better results were obtained with low reaction time. In 1 hour, 1-iodo-4-nitrobenzene and phenylboronic acid reached 98% of the yield and 9700 of TON. Better results were obtained with Pd(0) sources. The reaction system was recycled up to three times with good activity. 相似文献