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131.
Current work has evaluated uncertainty associated to quantification of several organic compounds present in particulate matter of atmospheric aerosols, setting out the stages of analytical procedure that contribute most to the global uncertainty. Several sources of uncertainty have been identified, which were clustered into five main contributions: sampling, extraction, clean-up, derivatization and analysis. A discussion of the main contributions to the overall uncertainty is reported, allowing authors to locate the largest ones and plan future improvements. Combined uncertainties ranged between 10-18% (alkanes), 12-16% (PAHs), 10-18% (alcohols) and 9-21% (acids). The analytical procedure was validated by analysing a standard reference material (SRM1649a, urban dust). Also, the proposed method was applied to the analysis of four samples of particulate matter. 相似文献
132.
García-Couceiro U Castillo O Cepeda J Lanchas M Luque A Pérez-Yáñez S Román P Vallejo-Sánchez D 《Inorganic chemistry》2010,49(24):11346-11361
We report herein the synthesis and physicochemical characterization of eight new manganese-oxalato compounds with 1,2-bis(4-pyridyl)ethylene (bpe): {(Hbpe)(2)[Mn(2)(μ-ox)(3)]·~0.8(C(2)H(5)OH)·~0.4(H(2)O)}(n) (1), {[Mn(μ-ox)(μ-bpe)]·xH(2)O}(n) (2), [Mn(2)(μ-ox)(2)(μ-bpe)(bpe)(2)](n) (3), [Mn(μ-ox)(μ-bpe)](n) (4a and 4b), and {[Mn(4)(μ-ox)(3)(μ-bpe)(4)(H(2)O)(4)]·(X)(2)·mY}(n) with X = NO(3)(-) (5a), Br(-) (5b), and ClO(4)(-) (5c) and Y = solvation molecules. The appropriate selection of the synthetic conditions allowed us to control the crystal structure and to design extended 2D and 3D frameworks. Compound 1 is obtained at acid pH values and its crystal structure consists of stacked [Mn(2)(μ-ox)(3)](2-) layers with cationic Hbpe(+) molecules intercalated among them. Compound 2 was obtained at basic pH values with a manganese/bpe ratio of 1:1, and the resulting 3D structure consists of an interpenetrating framework in which metal-oxalato chains are bridged by bpe ligands, leading to a microporous network that hosts a variable number of water molecules (between 0 and 1) depending on the synthetic conditions. Compound 3, synthesized with a manganese/bpe ratio of 1:3, shows a 2D framework in which linear metal-oxalato chains are joined by bis-monodentate 1,2-bis(4-pyridyl)ethylene ligands. The thermal treatment of compound 3 permits the release of one of the bpe molecules, giving rise to two new 2D crystalline phases of formula [Mn(μ-ox)(μ-bpe)](n) (4a and 4b) depending on the heating rate. The open structures of 5a-5c were synthesized in a medium with a high concentration of nitrate, perchlorate, or bromide salts (potassium or sodium as cations). These anions behave as templating agents directing the crystal growing toward a cationic porous network, in which the anions placed in the voids and channels of the structure present high mobility, as inferred from the ionic exchange experiments. Variable-temperature magnetic susceptibility measurements show an overall antiferromagnetic behavior for all compounds, which are discussed in detail. 相似文献
133.
Massimo Bietti Alessandra Calcagni Daniel Oscar Cicero Roberto Martella Michela Salamone 《Tetrahedron letters》2010,51(31):4129-1537
A product study on the reactivity of a 1,1-diarylalkoxyl radical bearing 2,2-diphenylcyclopropyl groups in the para-positions has been carried out. The exclusive formation of a product deriving from cyclopropyl ring-opening has been observed, indicating that 1,1-diarylalkoxyl radicals exist in equilibrium with a bridged 1-oxaspiro[2,5]octadienyl radical. This represents the first experimental evidence in support of the stepwise nature of the O-neophyl rearrangement of 1,1-diarylalkoxyl radicals. 相似文献
134.
Isabel C. Henao Castañeda Carlos O. Della Védova Oscar E. Piro Nils Metzler-Nolte Jorge L. Jios 《Polyhedron》2010
Structural and conformational properties of S-benzyl ferrocenecarbothioate (I) and S-(2-methoxyphenyl) ferrocenecarbothioate (II) are analyzed using data obtained from X-ray diffraction, vibrational data and theoretical calculations. According to chemical quantum calculations, the synperiplanar and antiperiplanar forms are found as the first and second more stable conformations, respectively, for the title compounds. The geometric parameters and normal modes of vibration were calculated using a density functional theory method (B3LYP) and the 6-31+G∗∗ basis set for all atoms except for iron. For this atom the calculations were carried out with the Lanl2dz basis set. The calculated parameters are in good agreement with the corresponding X-ray diffraction values. The combined experimental and theoretical approach allows a consistent assignment for most of the fundamental modes. 相似文献
135.
Garbiñe Álvarez Francisco Alcaide Oscar Miguel Laura Calvillo María Jesús Lázaro Jacob J. Quintana Juan Carlos Calderón Elena Pastor 《Journal of Solid State Electrochemistry》2010,14(6):1027-1034
This paper presents the behavior of ordered mesoporous carbon (OMC)-supported catalysts as anodes for direct methanol fuel
cells (DMFC), fed with an aqueous methanol solution. OMC samples were prepared by the nanocasting method from a polymerized
furan resin using mesoporous silica as a template. Pt and PtRu nanoparticles were supported on OMC with high dispersion, the
particle size being 2.4 nm at PtRu loading of 15 wt.%. The resulting catalysts were analyzed using carbon monoxide stripping
voltammetry, cyclic voltammetry, and chronoamperometry in three-electrode experiments and recording cell voltage vs. current
density curves in practical DMFC. It was found that PtRu-catalyzed technical electrodes exhibited good activity towards methanol
electrooxidation in half-cell experiments under fuel-cell-relevant conditions. Specifically, Pt85Ru15/OMC catalyst showed the highest catalytic enhancement compared to Pt/OMC for the steady-state electrooxidation of methanol
at 60 °C and 0.5 V, by a factor of 22 in 2-M MeOH solution. DMFC single cells yielded an open-circuit voltage of 0.625 V at
60 °C. Polarization curves indicate that DMFC with OMC-supported Pt85Ru15 catalyst at the anode exhibited the best performance. 相似文献
136.
Adam M. Hawkridge Rebecca B. Wysocky James N. Petitte Kenneth E. Anderson Paul E. Mozdziak Oscar J. Fletcher Jonathan M. Horowitz David C. Muddiman 《Analytical and bioanalytical chemistry》2010,398(2):737-749
The domestic chicken (Gallus domesticus) has emerged as a powerful experimental model for studying the onset and progression of spontaneous epithelial ovarian cancer
(EOC) with a disease prevalence that can exceed 35% between 2 and 7 years of age. An experimental strategy for biomarker discovery
is reported herein that combines the chicken model of EOC, longitudinal plasma sample collection with matched tissues, advanced
mass spectrometry-based proteomics, and concepts derived from the index of individuality (Harris, Clin Chem 20: 1535–1542,
1974). Blood was drawn from 148 age-matched chickens starting at 2.5 years of age every 3 months for 1 year. At the conclusion
of the 1 year sample collection period, the 73 birds that remained alive were euthanized, necropsied, and tissues were collected.
Pathological assessment of resected tissues from these 73 birds confirmed that five birds (6.8%) developed EOC. A proteomics
workflow including in-gel digestion, nanoLC coupled to high-performance mass spectrometry, and label-free (spectral counting)
quantification was used to measure the biological intra-individual variability (CVW) of the chicken plasma proteome. Longitudinal plasma sample sets from two birds within the 73-bird biorepository were selected
for this study; one bird was considered “healthy” and the second bird developed late-stage EOC. A total of 116 proteins from
un-depleted plasma were identified with 80 proteins shared among all sample sets. Analytical variability (CVA) of the label-free proteomics workflow was measured using a single plasma sample analyzed five times and was found to be
≥CVW in both birds for 16 proteins (20%) and in either bird for 25 proteins (31%). Ovomacroglobulin (ovostatin) was found to increase
(p < 0.001) over a 6 month period in the late-stage EOC bird providing an initial candidate protein for further investigation. 相似文献
137.
Testosterone metabolism revisited: discovery of new metabolites 总被引:1,自引:0,他引:1
Oscar J. Pozo Josep Marcos Rosa Ventura Andreu Fabregat Jordi Segura 《Analytical and bioanalytical chemistry》2010,398(4):1759-1770
The metabolism of testosterone is revisited. Four previously unreported metabolites were detected in urine after hydrolysis
with KOH using a liquid chromatography–tandem mass spectrometry method and precursor ion scan mode. The metabolites were characterized
by a product ion scan obtained with accurate mass measurements. Androsta-4,6-dien-3,17-dione, androsta-1,4-dien-3,17-dione,
17-hydroxy-androsta-4,6-dien-3-one and 15-androsten-3,17-dione were proposed as feasible structures for these metabolites
on the basis of the mass spectrometry data. The proposed structures were confirmed by analysis of synthetic reference compounds.
Only 15-androsten-3,17-dione could not be confirmed, owing to the lack of a commercially available standard. That all four
compounds are testosterone metabolites was confirmed by the qualitative analysis of several urine samples collected before
and after administration of testosterone undecanoate. The metabolite androsta-1,4-dien-3,17-dione has a structure analogous
to that of the exogenous anabolic steroid boldenone. Specific transitions for boldenone and its metabolite 17β-hydroxy-5β-androst-1-en-3-one
were also monitored. Both compounds were also detected after KOH treatment, suggesting that this metabolic pathway is involved
in the endogenous detection of boldenone previously reported by several authors. 相似文献
138.
Javier Mazuela Alexander Paptchikhine Oscar Pàmies Pher G. Andersson Montserrat Diéguez 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(15):4567-4576
A library of readily available phosphite–oxazole/thiazole ligands ( L1 a – g – L7 a – g ) was applied in the Ir‐catalyzed asymmetric hydrogenation of several largely unfunctionalized E‐ and Z‐trisubstituted and 1,1‐disubstituted terminal alkenes. The ability of the catalysts to transfer chiral information to the product could be tuned by choosing suitable ligand components (bridge length, the substituents in the heterocyclic ring and the alkyl backbone chain, the configuration of the ligand backbone, and the substituents/configurations in the biaryl phosphite moiety), so that enantioselectivities could be maximized for each substrate as required. Enantioselectivities were therefore excellent (enantiomeric excess (ee) values up to >99 %) for a wide range of E‐ and Z‐trisubstituted and 1,1‐disubstituted terminal alkenes. The biaryl phosphite moiety was a very advantageous ligand component in terms of substrate versatility. 相似文献
139.
The present paper deals with the formulation of minimal loading conditions for the application of numerical homogenisation techniques, namely the FE2 methodology. Based on the set of volume averaging rules connecting the heterogeneous micro and the homogeneous macro scale, the minimal constraints on the deformation of a micro volume are derived for a classical Cauchy continuum as well as for a micromorphic continuum theory. For both cases, numerical studies are included highlighting the main aspects of the proposed procedure within the context of small deformations. (© 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
140.
J. Oscar Gonz??lez-Cervantes M. E. Luna-Elizarrar??s M. Shapiro 《Complex Analysis and Operator Theory》2011,5(1):237-251
This is a continuation of our work (González-Cervantes et al. in On the Bergman theory for solenoidal and irrotational vector
fields. I. General theory. Operator theory: advances and applications. Birkhauser, accepted) where for solenoidal and irrotational
vector fields theory as well as for the Moisil–Théodoresco quaternionic analysis we introduced the notions of the Bergman
space and the Bergman reproducing kernel and studied their main properties. In particular, we described the behavior of the
Bergman theory for a given domain whenever the domain is transformed by a conformal map. The formulas obtained hint that the
corresponding objects (spaces, operators, etc.) can be characterized as conformally covariant or invariant, and in the present
paper we construct a series of categories and functors which allow us to give such characterizations in precise terms. 相似文献