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91.
Daria Larowska Dr. Aleksandra Wojcik Dr. Marta Mazurkiewicz-Pawlicka Dr. Artur Malolepszy Dr. Leszek Stobiński Prof. Bronislaw Marciniak Dr. Anna Lewandowska-Andralojc 《Chemphyschem》2019,20(8):1054-1066
Non-covalent nanohybrids composed of cationic 5,10,15,20-tetra(4-trimethylammoniophenyl)porphyrin tetra(p-toluenesulfonate) (TMAP) and the graphene oxide sheets were prepared under two pH values (6.2 vs. 1.8). The TMAP molecule was positively charged, regardless of the pH value during preparation. However, protonation of the imino nitrogens increased the overall charge of the porphyrin molecule from +4 to +6 (TMAP4+ and TMAP6+). It was found that at acidic pH, interaction of TMAP6+ with GO was largely suppressed. On the other hand, results of FTIR, Raman spectroscopy, thermogravimetric analysis, atomic force microscopy (AFM) and elemental analysis confirmed effective non-covalent functionalization of graphene oxide with cationic porphyrin at pH 6.2. The TMAP4+-GO hybrids exhibited well defined structure with a monolayer of TMAP4+ on the GO sheets as confirmed by AFM. Formation of the ground-state TMAP4+-GO complex in solution was monitored by the red-shift of the porphyrin Soret absorption band. This ground-state interaction between TMAP4+ and GO is responsible for the static quenching of the porphyrin emission. Fluorescence was not detected for the nanohybrid which indicated that a very fast deactivation process had to take place. Ultrafast time-resolved transient absorption spectroscopy clearly demonstrated the occurrence of electron transfer from the photoexcited TMAP4+ singlet state to GO sheets, as proven by the formation of a porphyrin radical cation. 相似文献
92.
Joanna Brzeska Magda Morawska Aleksandra Heimowska Wanda Sikorska Wojciech Wałach Anna Hercog Marek Kowalczuk Maria Rutkowska 《Chemical Papers》2018,72(5):1249-1256
The surface morphology and thermal properties of polyurethanes can be correlated to their chemical composition. The hydrophilicity, surface morphology, and thermal properties of polyurethanes (differed in soft segments and in linear/cross-linked structure) were investigated. The influence of poly([R,S]-3-hydroxybutyrate) presence in soft segments and blending of polyurethane with polylactide on surface topography were also estimated. The linear polyurethanes (partially crystalline) had the granular surface, whereas the surface of cross-linked polyurethanes (almost amorphous) was smooth. Round aggregates of polylactide un-uniformly distributed in matrix of polyurethane were clearly visible. It was concluded that some modification of soft segment (by mixing of poly([R,S]-3-hydroxybutyrate) with different polydiols and polytriol) and blending of polyurethanes with small amount of polylactide influence on crystallinity and surface topography of obtained polyurethanes. 相似文献
93.
Iwona E. Głowacka Dorota G. Piotrowska Andrzej E. Wróblewski Aleksandra Trocha 《Tetrahedron: Asymmetry》2017,28(11):1602-1607
A simple and efficient synthetic strategy to all four enantiomerically pure diethyl 1,2-di(N-Boc-amino)propylphosphonates has been elaborated starting from the corresponding N-[(R)-(1-phenylethyl)]aziridine-(2S)- and N-[(S)-(1-phenylethyl)]aziridine-(2R)-carboxaldehydes, employing a one-pot three-components Kabachnik-Fields reaction followed by the hydrogenolytic removal of the chiral auxiliary and aziridine ring opening with simultaneous protection of the amino groups as the N-Boc derivatives. 相似文献
94.
Aleksandra Mielewczyk-Gryn Tomasz Lendze Katarzyna Gdula-Kasica Piotr Jasinski Andrzej Krupa Boguslaw Kusz Maria Gazda 《Central European Journal of Physics》2013,11(2):213-218
A composite of CaTi0.9Fe0.1O3 and electrolyte material, i.e. magnesium doped La0.98Mg0.02NbO4 was prepared and studied. The phase content and the sample microstructure was examined by an X-ray diffraction method and scanning electron microscopy. EDS measurements were done both for composite samples and the diffusion couple. The electrical properties were studied by four terminal DC method. The high-temperature interaction between the two components of the composite has been observed. It has been suggested that lanthanum diffused into the perovskite phase and substituted for calcium whereas calcium and niobium formed the Ca2Nb2O7 pyrochlore phase. At 1500°C very large crystallites of the pyrochlore were observed. Regardless of strong interaction between the composite components, its total conductivity was weakly dependent on the sintering temperature. 相似文献
95.
Simple, selective and sensitive isotachophoretic methods for the analysis of ionic liquid (IL) compartments were developed in this study. A leading electrolyte containing 10 mM L ‐histidine + 10 mM histidine hydrochloride and a terminating electrolyte containing 5 mM glutamic acid + 5 mM L ‐histidine were selected to separate nitrate(V), chlorate(V), hexafluorophosphate, dicyanimide, trifluoromethanesulfonate, phosphate(V) and bis(trifluoromethanesulfonyl)imide in anionic mode. In contrast, seven short‐chain alkylimidazolium, alkylpyrrolidinium, alkylpyridinium and non‐chromophoric tetraalkylammonium and tetraalkylphosphonium IL cations were separated with 10 mM potassium hydroxide + 10 mM acetic acid as leading electrolyte, and 10 mM β‐alanine + 10 mM acetate as terminating electrolyte. Both methods were optimized and validated with good analytical performance parameters. LOD was about 3–5 μM, and the repeatability lay in the range of 1.06–5.59%. These methods were evaluated for their applicability to the analysis of soil samples and freshwater contaminated with ILs. In light of hitherto the absence of reports on the determination of non‐chromophoric IL cations, this study delivers for the first time a universal method enabling analysis of these species. Moreover, as there is still significant lack of methodologies of IL anion analysis, the obtained results offer an interesting alternative in that matter. 相似文献
96.
Conventional sol-gels are rather hydrophilic. A more hydrophobic material is obtained preparing organically modified siloxanes (ormosils). The polarity-sensitive probe Nile Red (NR) was doped in various sol-gels to probe their micro-polarity. The experiments show that the NR is an excellent probe and sensitive to the polarity of its microenvironment. Spectroscopic studies reveal remarkable changes in the absorption band positions and intensities as a function of the polarity of the sol-gel, which depends on the different precursors used. Furthermore, sol aging, gelation and temporal stability as a function of different ormosils have been investigated. 相似文献
97.
Novel Mechanism of Bioluminescence: Oxidative Decarboxylation of a Moiety Adjacent to the Light Emitter of Fridericia Luciferin 下载免费PDF全文
Maxim A. Dubinnyi Zinaida M. Kaskova Natalja S. Rodionova Mikhail S. Baranov Andrey Yu. Gorokhovatsky Alexey Kotlobay Kyril M. Solntsev Aleksandra S. Tsarkova Valentin N. Petushkov Ilia V. Yampolsky 《Angewandte Chemie (International ed. in English)》2015,54(24):7065-7067
A novel luciferin from a bioluminescent Siberian earthworm Fridericia heliota was recently described. In this study, the Fridericia oxyluciferin was isolated and its structure elucidated. The results provide insight into a novel bioluminescence mechanism in nature. Oxidative decarboxylation of a lysine fragment of the luciferin supplies energy for light generation, while a fluorescent CompX moiety remains intact and serves as the light emitter. 相似文献
98.
99.
Aleksandra Radoičić Radivoj Petronijević Filip Andrić Živoslav Tešić 《液相色谱法及相关技术杂志》2017,40(5-6):297-303
ABSTRACTA new method for the extraction and quantitative determination of amygdalin has been proposed. Accelerated solvent extraction was applied for the extraction, and reversed-phase high-performance thin-layer chromatography method was developed, validated, and applied for the determination of amygdalin in the extracts of apricot, plum, almond, and peach kernels. The chromatographic system used was RP-18 silica, as stationary phase and acetonitrile/water (50:50, v/v), as mobile phase. Densitometric scanning was performed at 210 nm. The method was validated with respect to specificity, linearity, precision, and accuracy. The results showed that the peak area responses were linear within the concentration range of 2.5–50.0 µg/spot (R2 = 0.9984). The limit of quantification was 4.28 µg/spot, and the detection limit 1.28 µg/spot. The intra-day and inter-day reproducibility, in terms of %RSD, were in the range of 0.81–1.15 and 1.32–1.89, respectively. The accuracy data were in the range from 99.98 to 100.56%. The method is linear, quantitative and reproducible, and could be used as an efficient and economical green chromatographic procedure for the determination of amygdalin in the fruit kernel. 相似文献
100.
Schmidt H Böttcher C Trampczynska A Clemens S 《Analytical and bioanalytical chemistry》2011,399(3):1355-1361
Nicotianamine (NA) is an important metal chelator, implicated in the intra- and intercellular trafficking of several transition
metal ions in plants. To decipher its roles in physiological processes such as micronutrient acquisition, distribution or
storage, fast and sensitive analytical techniques for quantification of this non-proteinogenic amino acid will be required.
The use of a recombinant Schizosaccharomyces pombe strain expressing a nicotianamine synthase (NAS) gene allowed for the production of [15N3]-NA, which was enriched from cell extracts through cation exchange and used for stable isotope dilution analysis of NA. Such
an approach should be widely applicable to important bioanalytes that are difficult to synthesize. The analytical procedure
comprises mild aqueous extraction and rapid Fmoc derivatization, followed by fast separation using ultra-performance liquid
chromatography (UPLC) and sensitive detection by positive ion electrospray ionization time-of-flight mass spectrometry (ESI-TOF-MS)
with a chromatographic cycle time of only 8 min. Derivatization was optimized with respect to incubation time and species
suitable for quantification. The limit of detection was 0.14 to 0.23 pmol in biological matrices with the response being linear
up to 42 pmol. Recovery rates were between 83% and 104% in various biological matrices including fission yeast cells, fungal
mycelium, plant leaves and roots. 相似文献