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241.
242.
Kojima T Nakanishi T Harada R Ohkubo K Yamauchi S Fukuzumi S 《Chemistry (Weinheim an der Bergstrasse, Germany)》2007,13(31):8714-8725
A doubly protonated hydrochloride salt of a saddle-distorted dodecaphenylporphyrin (H2DPP), [H4DPPP]Cl2, forms a porphyrin nanochannel (PNC). X-ray crystallography was used to determine the structure of the molecule, which revealed the inclusion of guest molecules within the PNC. Electron-donating molecules, such as p-hydroquinone and p-xylene, were selectively included within the PNC in sharp contrast to electron acceptors, such as the corresponding quinones, which were not encapsulated. This result indicates that the PNC can recognize the electronic character and steric hindrance of the guest molecules during the course of inclusion. ESR measurements (photoirradiation at lambda>340 nm at room temperature) of the PNC that contains p-hydroquinone, catechol, and tetrafluorohydroquinone guest molecules gave well-resolved signals, which were assigned to cation radicals formed without deprotonation based on results from computer simulations of the ESR spectra and density functional theory (DFT) calculations. The radicals are derived from photoinduced electron transfer from the guest molecules to the singlet state of H4DPP2+. Transient absorption spectroscopy by femtosecond laser flash photolysis allowed us to observe the formation of 1(H4DPP2+)*, which is converted to H4DPP+. by electron transfer from the guest molecules to 1(H4DPP2+)*, followed by fast disproportionation of H4DPP+., and charge recombination to give diamagnetic species and the triplet excited state 3(H4DPP2+)*, respectively. 相似文献
243.
Kojima T Kato F Teraoka R Matsuda Y Kitagawa S Tsuhako M 《Chemical & pharmaceutical bulletin》2007,55(3):407-411
Two novel pseudopolymorphs, methanolate and ethanolate of tamoxifen [(Z)-2-[4-(1,2-diphenyl-1-butenyl)phenoxy]-N,N-dimethylethylamine]citrate, were prepared in addition to forms A and B reported previously. Their crystalline forms were identified and characterized by powder and single crystal X-ray diffractometry, differential scanning calorimetry, thermogravimetric analysis, hot-stage microscopy, scanning electron microscopy and diffuse reflectance infrared Fourier-transform spectroscopy, and their physicochemical stability was also evaluated. The results of single crystal X-ray analysis and thermogravimetric analysis of methanolate and ethanolate suggested that the stoichiometry of tamoxifen citrate : methanol and tamoxifen citrate : ethanol could be composed of a 1 : 1 molecular ratio for both solvates. The results of physicochemical stability evaluations at 75 and 97% RH at 40 and 60 degrees C indicated that the metastable form A was quite stable for at least 2 months even under severe storage conditions, whereas methanolate immediately transformed to a crystalline mixture of forms A and B, and subsequently changed to the stable form B. 相似文献
244.
Hozumi A Kojima S Nagano S Seki T Shirahata N Kameyama T 《Langmuir : the ACS journal of surfaces and colloids》2007,23(6):3265-3272
A microfabrication technique is presented to fabricate a mesostructured inorganic/organic composite film, i.e., silica/cetyltrimethylammonium chloride (CTAC) film, with near-perfect site-selectivity on a large surface area based on a spatially regulated growth method. To precisely regulate the site-selective growth of this mesocomposite film at the solid/liquid interface, we designed a novel microtemplate consisting of a "dual-component" self-assembled monolayer (SAM) with alternating hydrophobic trifluorocarbon (CF3) and cationic amino (NH2) groups. First, (heptadecafluoro-1,1,2,2-tetrahydrodecyl)trimethoxysilane (FAS)-SAM was formed onto Si substrate covered with native oxide (SiO2/Si) from vapor phase. The substrate was then photolithographically micropatterned using 172 nm vacuum UV light. Finally, the micropatterned FAS-SAM was immersed in a solution of 1 vol % (aminoethylaminomethyl)phenethyltrimethoxysilane (AEAMPS) in absolute toluene. Due to these treatments, a dual-SAM microtemplate with CF3- and NH2-terminated surfaces was fabricated, as evidenced by lateral force microscopy, ellipsometry, and X-ray photoelectron spectroscopy. Using this template, the microfabrication of a mesocomposite film was demonstrated. As a control, the micropatterned hydrophobic FAS-SAM template (composed of CF3- and OH-terminated surfaces) was also treated under the same conditions. Optical microscopy and atomic force microscopy confirmed that the formation of the continuous mesocomposite film proceeded only on the FAS-SAM-covered regions, while the AEAMPS-SAM-covered regions remained free of deposits. This shielding effect also remained constant regardless of the pattern's geometry, i.e., the interval distance between the FAS-SAM-covered areas in the pattern. Through this approach, we were able to obtain well-defined 5-, 10-, and 20-mum wide mesocomposite microlines over the entire 10 x 10 mm2 area with high area-selectivity. On the other hand, when the SiO2 regions were not terminated with the cationic NH2 groups, cluster formation proceeded not only on the hydrophobic CF3 regions but also on the SiO2 regions, particularly with an increase in the pattern interval distance, resulting in lower final pattern resolution. 相似文献
245.
Simultaneous Measurement of Individual ATPase and Mechanical Reactions by a Single Myosin Molecule at Work 总被引:1,自引:0,他引:1
Based on techniques for single molecule imaging and nanomanipulation by optical tweezers, we have developed a new technique that allows simultaneous measurement of individual ATPase and mechanical reactions from a single myosin molecule during force generation. We show how the ATPase reaction couples to the mechanical reaction directly at the single molecule level. The results show that the myosin head can produce force even after releasing the bound nucleotide, probably ADP, suggesting that the chemical energy driven by ATP hydrolysis can be hysteretically stored in the myosin molecule. This view does not support a widely accepted hypothesis in which the force generation is tightly coupled to ligand dissociation.This paper was originally presented as an invited paper at the seventh Meeting on Near Field Optics, which was held on July 1, 1998 at Nagoya University, Nagoya, organized by the Research Group on Near Field Optics of the Optical Society of Japan, an affiliate of the Japan Society of Applied Physics. 相似文献
246.
Shunji Aoki Kouichi Higuchi Ai Kato Nobutoshi Murakami Motomasa Kobayashi 《Tetrahedron》1999,55(52):621-14870
Novel mono-O-alkyl-diglycosylglycerols named myrmekiosides A (1) and B (2) were isolated from a marine sponge of Myrmekioderma sp. and their absolute stereostructures were elucidated on the basis of chemical and physicochemical evidence. Myrmekiosides A (1) and B (2) reversed the phenotype of melanoma H-ras transformed NIH3T3 cells at 5 μg/ml. 相似文献
247.
T. Kojima H. Tachibana N. Haneda I. Kawashima P. H. G. Sharpe 《Radiation Physics and Chemistry》1999,54(6):12-626
The uncertainties in 60Co gamma-ray dosimetry at JAERI have been estimated by reviewing irradiation and calibration procedures. The uncertainty in dose delivered by the JAERI calibration system has been estimated to be 2.2% (2σ) and the uncertainty in dose measurement using JAERI alanine/ESR transfer dosimeters has been estimated to be 3.4% (2σ). A two-way dose intercomparison study between NPL and JAERI employing alanine-PS, alanine-paraffin, and dichromate dosimeters as transfer dosimeters was performed to confirm the estimated uncertainty over the dose range 1–50 kGy. Dose intercomparison results using both alanine and dichromate dosimeters show agreement within about 2%, which gives confidence in the estimated uncertainty in 60Co gamma-ray dosimetry at JAERI. 相似文献
248.
249.
T. Muroyama A. Shinohara T. Saito A. Yokoyama K. Takamiya S. Morimoto K. Nakanishi H. Baba T. Miura Y. Hamajima T. Kaneko H. Muramatsu S. Kojima M. Furukawa 《Journal of Radioanalytical and Nuclear Chemistry》1999,239(1):159-163
Annihilation γ-rays of π0 and pionic X-rays were measured in the gas mixtures of H2+Z and CH4+Z systems (Z=He, Ne, Ar and Kr). Pion capture probability of hydrogen atom was obtained from the annihilation γ-ray counts
and the capture probability of Z atom was obtained from the pionic X-ray intensities. Transfer rates were determined from
the data based on a combined large mesomolecular model. The transfer rates obtained were smaller than the systematics of the
Russian group. Difference in the transfer rate between the gas and the liquid phases was found by a comparison of the present
results with our previous ones. 相似文献
250.
Kimihisa Yamamoto Masayoshi Higuchi Kumiko Uchida Yojiro Kojima 《Macromolecular rapid communications》2001,22(4):266-270
Triphenylamines with thienyl groups are electro‐oxidatively polymerized to yield the corresponding branched polymers on an electrode. The resulting polymers show significantly better redox properties, such as redox activity, catalytic activity, and conductivity when compared with for example the linear polymeric analog. The good properties of the branched polymers are based on the higher electronic conductivity (2–6 S/cm), since the branching provides multiple routes for charge carriers. The redox‐active polymers show high capacity (ca. 40 mC/cm2) and catalytic activity for the electron transfer of ferrocene on the electrode. 相似文献