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1.
Nobuoki Eshima Claudio Giovanni Borroni Minoru Tabata Takeshi Kurosawa 《Entropy (Basel, Switzerland)》2021,23(2)
This paper proposes a method for deriving interpretable common factors based on canonical correlation analysis applied to the vectors of common factors and manifest variables in the factor analysis model. First, an entropy-based method for measuring factor contributions is reviewed. Second, the entropy-based contribution measure of the common-factor vector is decomposed into those of canonical common factors, and it is also shown that the importance order of factors is that of their canonical correlation coefficients. Third, the method is applied to derive interpretable common factors. Numerical examples are provided to demonstrate the usefulness of the present approach. 相似文献
2.
Prof. Nobutaka Fujieda Kyohei Umakoshi Yuta Ochi Dr. Yosuke Nishikawa Prof. Sachiko Yanagisawa Prof. Minoru Kubo Prof. Genji Kurisu Prof. Shinobu Itoh 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(32):13487-13492
The dinuclear copper enzyme, tyrosinase, activates O2 to form a (μ-η2:η2-peroxido)dicopper(II) species, which hydroxylates phenols to catechols. However, the exact mechanism of phenolase reaction in the catalytic site of tyrosinase is still under debate. We herein report the near atomic resolution X-ray crystal structures of the active tyrosinases with substrate l -tyrosine. At their catalytic sites, CuA moved toward l -tyrosine (CuA1 → CuA2), whose phenol oxygen directly coordinates to CuA2, involving the movement of CuB (CuB1 → CuB2). The crystal structures and spectroscopic analyses of the dioxygen-bound tyrosinases demonstrated that the peroxide ligand rotated, spontaneously weakening its O−O bond. Thus, the copper migration induced by the substrate-binding is accompanied by rearrangement of the bound peroxide species so as to provide one of the peroxide oxygen atoms with access to the phenol substrate's ϵ carbon atom. 相似文献
3.
Minoru Koyama Dr. Takafumi Kawakami Dr. Takashi Okazoe Prof. Dr. Kyoko Nozaki 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(46):10913-10917
Methacrylic esters, represented by methyl methacrylate (MMA), are widely used as commodity chemicals. Here, the one-pot synthesis of methacrylic esters from acetone, a haloform and alcohols in the presence of an organic base is described. Using DBU as the organic base for the reaction of acetone, chloroform and methanol in acetonitrile afforded MMA in 66 % yield. When the solvent was replaced by benzonitrile, the product MMA was successfully purified by distillation. Applicability of this process to various alcohols was also investigated to show ethyl, phenyl, CF3CH2, and n-C6F13CH2CH2 esters were obtained in moderate yields. The use of bromoform instead of chloroform resulted in the improvement of the yield, for example, methyl and n-C6F13CH2CH2 esters up to 81 and 70 %, respectively. The reaction with deuterated starting materials acetone-d6 and MeOH-d4, with DBU in acetonitrile afforded deuterated MMA (MMA-d8) in 70 % yield. 相似文献
4.
Minoru Yamamoto 《Geometriae Dedicata》2018,194(1):37-54
Let \(\mathrm{SM}_{2n}(S^1,\mathbb {R})\) be a set of stable Morse functions of an oriented circle such that the number of singular points is \(2n\in \mathbb {N}\) and the order of singular values satisfies the particular condition. For an orthogonal projection \(\pi :\mathbb {R}^2\rightarrow \mathbb {R}\), let \({\tilde{f}}_0\) and \({\tilde{f}}_1:S^1\rightarrow \mathbb {R}^2\) be embedding lifts of f. If there is an ambient isotopy \(\tilde{\varphi }_t:\mathbb {R}^2\rightarrow \mathbb {R}^2\) \((t\in [0,1])\) such that \({\pi \circ \tilde{\varphi }}_t(y_1,y_2)=y_1\) and \(\tilde{\varphi }_1\circ {\tilde{f}}_0={\tilde{f}}_1\), we say that \({\tilde{f}}_0\) and \({\tilde{f}}_1\) are height isotopic. We define a function \(I:\mathrm{SM}_{2n}(S^1,\mathbb {R})\rightarrow \mathbb {N}\) as follows: I(f) is the number of height isotopy classes of embeddings such that each rotation number is one. In this paper, we determine the maximal value of the function I equals the n-th Baxter number and the minimal value equals \(2^{n-1}\). 相似文献
5.
Dr. Ayumi Hirano‐Iwata Yutaka Ishinari Dr. Hideaki Yamamoto Prof. Michio Niwano 《化学:亚洲杂志》2015,10(6):1266-1274
Ion channel proteins provide gated pores that allow ions to passively flow across cell membranes. Owing to their crucial roles in regulating transmembrane ion flow, ion channel proteins have attracted the attention of pharmaceutical investigators as drug targets for use in the studies of both therapeutics and side effects. In this review, we discuss the current technologies that are used in the formation of ion channel‐integrated bilayer lipid membranes (BLMs) in microfabricated devices as a potential platform for next‐generation drug screening systems. Advances in BLM fabrication methodology have allowed the preparation of BLMs in sophisticated formats, such as microfluidic, automated, and/or array systems, which can be combined with channel current recordings. A much more critical step is the integration of the target channels into BLMs. Current technologies for the functional reconstitution of ion channel proteins are presented and discussed. Finally, the remaining issues of the BLM‐based methods for recording ion channel activities and their potential applications as drug screening systems are discussed. 相似文献
6.
Shiori Komai Mitsuhiro Hirano Naofumi Ohtsu 《Surface and interface analysis : SIA》2020,52(12):823-828
The Sr 3d X-ray photoelectron spectroscopy (XPS) spectrum of Sr-containing hydroxyapatite (SHAp) overlaps completely with the P 2p spectrum. Thus, the chemical state identification of Sr in SHAp is a challenging task. In this work, the Sr 3d spectrum was isolated from the overlapping spectra for analyzing the chemical state of Sr using a generic peak-fitting method. The SHAp layers containing various Sr concentrations were produced on a Ti substrate using a chemical treatment process with a calcium phosphate slurry that included Sr (NO3)2. The distribution of the constituent elements changed according to the Sr concentration, implying that the chemical state of Sr varied with concentration. The isolation of the Sr 3d XPS spectrum was conducted via spectral deconvolution using the P 2p spectrum corresponding to HAp. The isolated Sr 3d spectrum revealed that the chemical state of Sr was in SrO and Sr-substituted HAp states, and their ratio varied with the Sr concentration in the layer. The SrO to Sr-substituted HAp ratios affected the Sr ion releasing behavior from the SHAp layer, supporting the validity of the obtained analytical results. 相似文献
7.
Raku Watanabe Dr. Nobuki Kato Kengo Hayashi Sho Tozawa Dr. Yusuke Ogura Prof. Shigefumi Kuwahara Prof. Minoru Ueda 《ChemistryOpen》2020,9(10):1008-1017
An efficient and stereoselective syntheses of all the possible stereoisomers of coronafacic acid (CFA) has been developed. The stereochemistries of C3a and C7a were controlled in a diastereoselective Diels-Alder type cycloaddition using a chiral auxiliary. CFA and 6-epi-CFA were synthesized by hydrogenation of a common intermediate. During the synthesis of 6-epi-CFA, we established that its cis-fused configuration is important for the introduction of C4-C5 double bond by dehydration. This report is the first practical synthesis of both 6-epi-CFA, and its enantiomer. 相似文献
8.
Shofu Matsuda Yuuki Okuda Yoshiki Obu Norio Nagayama Minoru Umeda 《Electroanalysis》2019,31(12):2466-2471
With the objective of understanding the kinetic redox properties of triphenylamine derivatives in association with chemical reactions, for their future application in functional organic semiconductor devices, the electrochemical characteristics of 4‐(2,2‐diphenylethenyl)‐N,N‐bis(4‐methylphenyl)‐benzenamine (TPA) were evaluated. Based on cyclic voltammograms of TPA on Pt disk electrodes with diameters of 300 μm and 10 μm at slow and fast scan rates in an acetonitrile solution, the TPA.+ is stable, while the TPA2+ is unstable. Importantly, the unstable TPA2+ appears to break down by a subsequent chemical reaction. A Cottrell plot analysis from chronoamperometry of a solution containing TPA reveals that both the first and second oxidations are one‐electron reactions. Concerning the stabilization mechanism of the first oxidation state of TPA, the results of molecular orbital calculations indicate that the electrons of the HOMO level are distributed in the triphenylamine group, which induces a resonance‐stabilized TPA.+. Based on these results, TPA/TPA.+ is suggested to have a sufficient stability for further application in organic semiconductor devices. 相似文献
9.
Shibo Xu Kazutaka Takamatsu Prof. Dr. Koji Hirano Prof. Dr. Masahiro Miura 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(40):9400-9404
A NiCl2(PEt3)2-catalyzed regioselective C−H coupling of 8-aminoquinoline-derived benzamides with oxetanes has been developed. The reaction proceeds with concomitant removal of the 8-aminoquinoline auxiliary to directly form the corresponding seven-membered benzolactones, which frequently occur in natural products and bioactive molecules. Additionally, no stereochemical erosion is observed during the course of the reaction, and the use of enantioenriched and substituted oxetane thus provides a new avenue to the optically active benzolactone. 相似文献
10.
Treatment of a meso‐diarylporphyrin with PhI(OAc)2 in the presence of BF3 ? OEt2 and propionic acid affords the corresponding porphyrinquinone in a high yield (91%). A novel quinone derived from meso‐meso β–β doubly‐fused diporphyrin was obtained as the sole byproduct (16% yield), which exhibits strong panchromatic absorption between 300 and 1000 nm. It has a low HOMO‐LUMO gap owing to expanded and low‐symmetry π‐planes. 相似文献