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111.
112.
Jessica Orrego Hernandez Jaime Portilla Justo Cobo Christopher Glidewell 《Acta Crystallographica. Section C, Structural Chemistry》2015,71(5):363-368
Cyclohexylamine reacts with 5‐chloro‐3‐methyl‐1‐(pyridin‐2‐yl)‐1H‐pyrazole‐4‐carbaldehyde to give 5‐cyclohexylamino‐3‐methyl‐1‐(pyridin‐2‐yl)‐1H‐pyrazole‐4‐carbaldehyde, C16H20N4O, (I), formed by nucleophilic substitution, but with 5‐chloro‐3‐methyl‐1‐phenyl‐1H‐pyrazole‐4‐carbaldehyde the product is (Z)‐4‐[(cyclohexylamino)methylidene]‐3‐methyl‐1‐phenyl‐1H‐pyrazol‐5(4H)‐one, C17H21N3O, (II), formed by condensation followed by hydrolysis. Compound (II) crystallizes with Z′ = 2, and in one of the two independent molecular types the cyclohexylamine unit is disordered over two sets of atomic sites having occupancies of 0.65 (3) and 0.35 (3). The vinylogous amide portion in each compound shows evidence of electronic polarization, such that in each the O atom carries a partial negative charge and the N atom of the cyclohexylamine portion carries a partial positive charge. The molecules of (I) contain an intramolecular N—H...N hydrogen bond, and they are linked by C—H...O hydrogen bonds to form sheets. Each of the two independent molecules of (II) contains an intramolecular N—H...O hydrogen bond and each molecular type forms a centrosymmetric dimer containing one R22(4) ring and two inversion‐related S(6) rings. 相似文献
113.
Ying Zhang Yong-Guang Gao You-Di Shi Lian-Qian Tan Jessica S. Yue Zhong-Lin Lu 《中国化学快报》2015,26(7):894-898
A novel [12]aneN3-based BODIPY sensor 1 can be applied in the sequential recognition of Cu2 and ADP in aqueous solution and living cells with high selectivity and sensitivity 相似文献
114.
Brett D. Jones Jessica R. Chittum Sehmuz Akalin Asta B. Schram Jonathan Fink Christine Schnittka Michael A. Evans Carol Brandt 《School science and mathematics》2015,115(8):404-415
The primary purpose of this study was to examine the ways in which a 12‐week afterschool science and engineering program affected middle school students' motivation to engage in science and engineering activities. We used current motivation research and theory as a conceptual framework to assess 14 students' motivation through questionnaires, structured interviews, and observations. Students reported that during the activities they perceived that they were empowered to make choices in how to complete things, the activities were useful to them, they could succeed in the activities, they enjoyed and were interested in the hands‐on activities and some presentations, they felt cared for by the facilitators and received help when they were stuck or confused, and they put forth effort. Based on our examination of data across our three data sources, we identified motivating opportunities that were provided to students during the activities. These motivating opportunities can serve as examples to help both formal and informal science educators better connect motivation theory to practice so that they can create motivating opportunities for students. Furthermore, this study provides a methodological example of how students' motivation can be examined during the context of authentic science and engineering instruction. 相似文献
115.
Finn ST Strnad JA Barreto PD Fox ME Torres J Sweeney JD Barreto JC 《Photochemistry and photobiology》2011,87(5):1184-1188
We describe a screening methodology that can be used to quickly determine the effectiveness of newly synthesized photocatalysts. We were particularly interested in measuring the destruction of organic molecules painted onto a photocatalytic surface by spraying, with destruction proceeding in ambient air (as a model for airborne toxin destruction). Our method can utilize photocatalysts that are synthesized as powders (such as doped and undoped titanium oxide) and which are then calcined onto a glass substrate disk at 600°C. Herein, we used UV illumination of Aeroxide P-25 TiO(2), but the method is general and can accommodate any region of the light spectrum. 相似文献
116.
The hyphenation of lab-on-valve (LOV) and multisyringe flow analysis (MSFIA), coupled to a long path length liquid waveguide capillary cell (LWCC), allows the spectrophotometric determination of uranium in different types of environmental sample matrices, without any manual pre-treatment, and achieving high selectivity and sensitivity levels. On-line separation and preconcentration of uranium is carried out by means of UTEVA resin. The potential of the LOV-MSFIA makes possible the fully automation of the system by the in-line regeneration of the column. After elution, uranium(VI) is spectrophotometrically detected after reaction with arsenazo-III. The determination of levels of uranium present in environmental samples is required in order to establish an environmental control. Thus, we propose a rapid, cheap and fully automated method to determine uranium(VI) in environmental samples. The limit of detection reached is 1.9 ηg of uranium and depending on the preconcentrated volume; it results in ppt levels (10.3 ηg L−1). Different water sample matrices (seawater, well water, freshwater, tap water and mineral water) and a phosphogypsum sample (with natural uranium content) were satisfactorily analyzed. 相似文献
117.
Donehue JE Varnavski OP Cemborski R Iyoda M Goodson T 《Journal of the American Chemical Society》2011,133(13):4819-4828
A series of π-extended cyclic thiophene oligomers of 12, 18, 24, and 30 repeat units have been studied using methods of ultrafast time-resolved absorption, fluorescence upconversion, and three-pulse photon echo. These measurements were conducted in order to examine the structure-function relationships that may affect the coherence between chromophores within the organic macrocycles. Our results indicate that an initial delocalized state can be seen upon excitation of the cyclic thiophenes. Anisotropy measurements show that this delocalized state decays on an ultrafast time scale and is followed by the presence of incoherent hopping. From the use of a phenomenological model, we conclude that our ultrafast anisotropy decay measurements suggest that the system does not reside in the Fo?rster regime and coherence within the system must be considered. Three-pulse photon echo peak shift experiments reveal a clear dependence of initial peak shift with ring size, indicating a weaker coupling to the bath (and stronger intramolecular interactions) as the ring size is increased. Our results suggest that the initial delocalized state increases with ring size to distances (and number of chromophores) comparable to the natural light-harvesting system. 相似文献
118.
119.
Koshevoy IO Smirnova ES Haukka M Laguna A Chueca JC Pakkanen TA Tunik SP Ospino I Crespo O 《Dalton transactions (Cambridge, England : 2003)》2011,40(28):7412-7422
A series of luminescent dinuclear neutral complexes of stoichiometry [(AuSPh)(2)(PPh(2)-(C(6)H(4))(n)-PPh(2))] (n = 1, 2, 3) as well as their tetranuclear cationic derivatives [(Au(2)SPh)(2)(PPh(2)-(C(6)H(4))(n)-PPh(2))(2)](PF(6))(2) are reported. Their crystal structures have been elucidated by X-ray studies. These studies indicate that, for the dinuclear species, only when n = 1 the molecules exhibit intermolecular aurophilic interactions. None of the tetranuclear species crystallizes in their molecular form, due to the formation of aggregates through Au···Au interactions. The origin of the luminescence has been analyzed by computational studies indicating that the presence or absence of aurophilic interactions does not affect the luminescent behavior and that intraligand charge transfer processes which involve the thiolate and the diphosphine are responsible for the emissions. The result is in contrast with the thiolate-gold charge transfer processes which dominate the photophysics of gold-thiolate compounds and reveals the influence of the phenylene spacers in the emissive behavior of these compounds. 相似文献
120.
Serrano A Sousa MM Hallett J Lopes JA Oliveira MC 《Analytical and bioanalytical chemistry》2011,401(2):735-743
A new analytical approach based on high-performance liquid chromatography with diode array detector (HPLC-DAD) and multivariate
data analysis was applied and assessed for analyzing the red dye extracted from cochineal insects, used in precious historical
textiles. The most widely used method of analysis involves quantification of specific minor compounds (markers), using HPLC-DAD.
However, variation in the cochineal markers concentration, use of aggressive dye extraction methods and poor resolution of
HPLC chromatograms can compromise the identification of the precise insect species used in the textiles. In this study, a
soft extraction method combined with a new dye recovery treatment was developed, capable of yielding HPLC chromatograms with
good resolution, for the first time, for historical cochineal-dyed textiles. After principal components analysis (PCA) and
mass spectrometry (MS), it was possible to identify the cochineal species used in these textiles, in contrast to the accepted
method of analysis. In order to compare both methodologies, 7 cochineal species and 63 historical cochineal insect specimens
were analyzed using the two approaches, and then compared with the results for 15 historical textiles in order to assess their
applicability to real complex samples. The methodology developed here was shown to provide more accurate and consistent information
than the traditional method. Almost all of the historical textiles were dyed with Porphyrophora sp. insects. These results emphasize the importance of adopting the proposed methodology for future research on cochineal
(and related red dyes). Mild extraction methods and HPLC-DAD/MSn analysis yield distinctive profiles, which, in combination with a PCA reference database, are a powerful tool for identifying
red insect dyes. 相似文献