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91.
Adam Tracz Jeremiasz Jeszka Iwona Kuciska Jean‐Paul Chapel Gisele Boiteux 《Macromolecular Symposia》2001,169(1):129-135
High density polyethylene (PE) was crystallised from the melt on freshly cleaved surface of highly oriented pyrolitic graphite (HOPG) or mica. Atomic force microscopy (AFM) studies of structure of the polymer surface adjacent to the graphite or mica were performed after peeling of from the substrate. Significant differences of crystalline structure on the interface were found between PE crystallised on graphite and mica. The surface of polyethylene crystallised on graphite shows large areas with regularly arranged rectangular structures. These objects (ca 20‐80 nm big) probably represent the nucleation centres of the lamellar growth. The surface of polyethylene crystallised at mica surface shows some dot‐like structures showing no particular arrangement. 相似文献
92.
Paulina Lewandowska Izabela Szczuka Iwona Bednarz-Misa Berenika M. Szczniak-Siga Katarzyna Neubauer Magdalena Mierzchaa-Pasierb Marek Zawadzki Wojciech Witkiewicz Magorzata Krzystek-Korpacka 《Molecules (Basel, Switzerland)》2021,26(23)
The mechanisms underlying the antineoplastic effects of oxicams have not been fully elucidated. We aimed to assess the effect of classic and novel oxicams on the expression/secretion of macrophage-associated chemokines (RTqPCR/Luminex xMAP) in colorectal adenocarcinoma cells, and on the expression of upstream the non-steroidal anti-inflammatory drug (NSAID)-activated genes NAG1, NFKBIA, MYD88, and RELA, as well as at the chemokine profiling in colorectal tumors. Meloxicam downregulated CCL4 9.9-fold, but otherwise the classic oxicams had a negligible/non-significant effect. Novel analogues with a thiazine ring substituted with arylpiperazine and benzoyl moieties significantly modulated chemokine expression to varying degree, upregulated NAG1 and NFKBIA, and downregulated MYD88. They inhibited CCL3 and CCL4, and their effect on CCL2 and CXCL2 depended on the dose and exposure. The propylene linker between thiazine and piperazine nitrogens and one arylpiperazine fluorine substituent characterized the most effective analogue. Only CCL19 and CXCL2 were not upregulated in tumors, nor was CXCL2 in tumor-adjacent tissue compared to normal mucosa. Compared to adjacent tissue, CCL4 and CXCL2 were upregulated, while CCL2, CCL8, and CCL19 were downregulated in tumors. Tumor CCL2 and CCL7 increased along with advancing T and CCL3, and CCL4 along with the N stage. The introduction of arylpiperazine and benzoyl moieties into the oxicam scaffold yields effective modulators of chemokine expression, which act by upregulating NAG1 and interfering with NF-κB signaling. 相似文献
93.
Andrzej Graja Iwona Olejniczak Boles?aw Barszcz John A. Schlueter 《Central European Journal of Physics》2009,7(4):663-667
Infrared and Raman investigations of two phases of bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) based organic conductors
with the same CF3CF2SO3− anion: β′-(BEDT-TTF)2CF3CF2SO3 and δ′-(BEDT-TTF)2CF3CF2SO3, are shortly reviewed and compared with the most typical infrared properties of the family of (BEDT-TTF)2RR′SO3 organic conductors, where R = SF5, CF3, and R′ are CH2, CF2, CHF, CHFCF2, and CH2CF2. The role of the molecular structur and spatial organization of the counterions is discussed.
Presented at 2-nd International Conference on Functional Materials and Devices, ICFMD 2008, June 16–19, 2008, Kuala Lumpur,
Malaysia 相似文献
94.
Chemically crosslinked polyimide organic–inorganic composite nanofiltration membranes suitable for application in harsh organic solvents were successfully prepared by phase inversion of dope solutions. TiO2 nanoparticles were dispersed in these dope solutions, comprising polyimide (PI) in N,N-dimethylformamide/1,4-dioxane. The impact of TiO2 on the resulting PI membranes was investigated using SEM, TGA, water contact angle, dope viscosity measurements and mechanical strength. The presence of TiO2 nanoparticles within the membrane matrix was proved by the detection of a peak characteristic of TiO2 in the WAXS pattern. SEM pictures of the cross-section of the PI/TiO2 membranes showed dramatically changed morphology compared to reference membranes with no TiO2 addition. Macrovoids present in reference membranes were suppressed by increasing loading of TiO2 nanoparticles, and eventually disappeared completely at a TiO2 loading above 3 wt.%. Decreasing water contact angle and an increase in ethanol flux indicated that hydrophilicity increased as nanoparticle loading increased. The effect of TiO2 on the functional performance of the membranes was evaluated by measuring flux and rejection using cross-flow filtration. Perhaps surprisingly, the presence of TiO2 improved the compaction resistance of the membranes, whereas rejection and steady flux were almost unaltered. 相似文献
95.
Let Λ be an algebraic set and let (n is even) be a polynomial mapping such that for each there is r(λ) > 0 such that the mapping g
λ = g(· , λ) restricted to the sphere S
n
(r) is an immersion for every 0 < r < r (λ), so that the intersection number I(g
λ|S
n
(r)) is defined. Then is an algebraically constructible function.
I. Karolkiewicz and A. Nowel supported by the grant BW/5100-5-0286-7. 相似文献
96.
Fita P Luzina E Dziembowska T Radzewicz C Grabowska A 《The Journal of chemical physics》2006,125(18):184508
The two structurally related Schiff bases, 2-hydroxynaphthylidene-(8-aminoquinoline) (HNAQ) and 2-hydroxynaphthylidene-1(')-naphthylamine (HNAN), were studied by means of steady-state and time resolved optical spectroscopies as well as time-dependent density functional theory (TDDFT) calculations. The first one, HNAQ, is stable as a keto tautomer in the ground state and in the excited state in solutions, therefore it was used as a model of a keto tautomer of HNAN which exists mainly in its enol form in the ground state at room temperature. Excited state intramolecular proton transfer in the HNAN molecule leads to a very weak (quantum yield of the order of 10(-4)) strongly Stokes-shifted fluorescence. The characteristic time of the proton transfer (about 30 fs) was estimated from femtosecond transient absorption data supported by global analysis and deconvolution techniques. Approximately 35% of excited molecules create a photochromic form whose lifetime was beyond the time window of the experiment (2 ns). The remaining ones reach the relaxed S(1) state (of a lifetime of approximately 4 ps), whose emission is present in the decay associated difference spectra. Some evidence for the back proton transfer from the ground state of the keto form with the characteristic time of approximately 13 ps was also found. The energies and orbital characteristics of main electronic transitions in both molecules calculated by TDDFT method are also discussed. 相似文献
97.
Quantitative EPR study on free radicals in the natural polyphenols interacting with metal ions and other environmental pollutants 总被引:1,自引:0,他引:1
Jezierski A Czechowski F Jerzykiewicz M Golonka I Drozd J Bylinska E Chen Y Seaward MR 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2002,58(6):1293-1300
Quantitative electron paramagnetic resonance (EPR) method was applied to characterise radicals stabilised in polyphenolic matrices of various biogenic materials: lichens, mosses, composts, soils, peats, brown coals and sewage sludge sediments. The investigations were carried out on raw materials and extracted fractions of humic acids (HA). General trends of g value and spin concentration changes were found. These parameters in lichens strongly depend on lichen species and air pollution. Determination of the g value and semiquinone spin concentration allows to assess degree of transformation of organic matter in compost, soil, peat and lignite. Application of gaseous ammonia as a base penetrating the organic matrices extends the possibilities and usefulness of the method. Interaction of metal ions with humic materials is illustrated by interaction of VO2+ ion with peat and lignite HA as well as demineralised (raw and carbonised) brown coal. Our investigations demonstrate that quantitative EPR is a rapid and effective monitoring method to study the influence of various environmental factors on substances containing polyphenolic matrices. 相似文献
98.
Bury W Justyniak I Prochowicz D Wróbel Z Lewiński J 《Chemical communications (Cambridge, England)》2012,48(59):7362-7364
Two unique adducts of an oxozinc carboxylate cluster with H(2)O and THF were isolated and structurally characterized, [Zn(4)(μ(4)-O)(O(2)CR)(6)(H(2)O)(THF)]·2(THF) and [Zn(4)(μ(4)-O)(O(2)CR')(6)(THF)(3)] (where R = benzoate and R' = 9-antracenecarboxylate anion). The study shows that the zinc centers of the Zn(4)O core can easily form unique coordination environments without breaking of the Zn-O(carboxylate) bonds. 相似文献
99.
Kamila Malecka Iwona Grabowska Jerzy Radecki Anna Stachyra Anna Góra‐Sochacka Agnieszka Sirko Hanna Radecka 《Electroanalysis》2012,24(2):439-446
The working principle of a genosensor is based on the mechanism of ion‐channel mimetic sensors. The analytical signals generated upon hybridization processes were recorded by a redox active marker [Fe(CN)6]3?/4? present in the sample solution using voltammetric techniques. The developed genosensor was suitable for determination of 20‐mer complementary oligonucleotide sequence, and also of the PCR products containing the complementary 20‐mer sequence in various positions, with detection limits in the 10 pM range. The noncomplementary 20‐mer oligonucleotide sequence as well as the PCR product without complementary region generated very weak response. The good discrimination of the position of the complementary part in the PCR products was observed. 相似文献
100.
Bury W Justyniak I Prochowicz D Rola-Noworyta A Lewiński J 《Inorganic chemistry》2012,51(13):7410-7414
An atom-efficient and mild synthesis of a series of oxozinc carboxylates [Zn(4)(μ(4)-O)(O(2)CR)(6)] [where R = Ph (2a), p-PhC(6)H(4) (2b), p-MeC(6)H(4) (2c), and p-MeSC(6)H(4) (2d)] from well-defined alkylzinc precursors and H(2)O is described. The molecular and crystal structures of the resulting complexes have been determined by single-crystal X-ray diffraction. A closer examination of their crystal structure provides a direct picture of the effect of the nature of substituents on the molecular self-assembly of the octahedral oxozinc through noncovalent interactions. It was revealed that these discrete oxozinc clusters can form diverse types of noncovalent assemblies ranging from structures representing zeolitic topologies in the case of 2a to soft porous materials with gated voids or open channels for the remaining molecular clusters. 相似文献