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111.
Yan-Jun Yu Chen Zou Wan-Shan Shen Xiaopeng Zheng Qi-Sheng Tian You-Jun Yu Chun-Hao Chen Baodan Zhao Prof. Zhao-Kui Wang Prof. Dawei Di Prof. Osman M. Bakr Prof. Liang-Sheng Liao 《Angewandte Chemie (International ed. in English)》2023,62(22):e202302005
Perovskite nanocrystals (PeNCs) deliver size- and composition-tunable luminescence of high efficiency and color purity in the visible range. However, attaining efficient electroluminescence (EL) in the near-infrared (NIR) region from PeNCs is challenging, limiting their potential applications. Here we demonstrate a highly efficient NIR light-emitting diode (LED) by doping ytterbium ions into a PeNCs host (Yb3+ : PeNCs), extending the EL wavelengths toward 1000 nm, which is achieved through a direct sensitization of Yb3+ ions by the PeNC host. Efficient quantum-cutting processes enable high photoluminescence quantum yields (PLQYs) of up to 126 % from the Yb3+ : PeNCs. Through halide-composition engineering and surface passivation to improve both PLQY and charge-transport balance, we demonstrate an efficient NIR LED with a peak external quantum efficiency of 7.7 % at a central wavelength of 990 nm, representing the most efficient perovskite-based LEDs with emission wavelengths beyond 850 nm. 相似文献
112.
Aminomethylphosphine (P–C–N) type ligands, (Ph2PCH2)2NR R = –(CH2)3Si(OEt3)3 or –CH2CH2OH, and their Pd(II) complexes have been synthesized. All the compounds were characterized by 1H-, 31P-NMR, and elemental analysis. The complexes are proposed to have a square planar geometry. They were investigated as catalysts
for the Heck reaction of aryl halides (I, Br, Cl) with methyl acrylate. Both complexes showed high activity to give methyl
cinnamate in good yields, with the best turnover numbers found for [PdCl2(Ph2PCH2)2N(CH2)3Si(OEt)3]. 相似文献
113.
Hülya Kele Mustafa Kele lyas Dehri Osman Serinda 《Colloids and surfaces. A, Physicochemical and engineering aspects》2008,320(1-3):138-145
Electrochemical measurements were performed to investigate the effectiveness and adsorption behaviour of aminobiphenyl (Aph) and 2-(3-hydroxybenzylideneamino)biphenyl (Aph-S), as corrosion inhibitors for mild steel (MS) in 0.5 M HCl solution. Potentiodynamic polarization, linear polarization resistance (LP) and electrochemical impedance spectroscopy (EIS) techniques were applied to study the metal corrosion behaviour in the absence and presence of different concentrations of Aph and Aph-S. In order to gain more information about adsorption mechanism the AC impedance technique was used to evaluate the potential of zero charge (PZC) from polarization resistance (Rp) versus voltage (E) plot. Potentiodynamic polarization measurements showed that Aph act as cathodic type inhibitor where as Aph-S act mixed type. The inhibition efficiency (IE%) increases with increasing concentration of compounds and reached 92.6% for Aph and 97.2% for Aph-S at 5 × 10−3 M. Double layer capacitance (Cdl) and polarization resistance (Rp) values are derived from Nyquist plots obtained from AC impedance studies. The experimental data fit Langmuir isotherm for both Aph and Aph-S, and from the adsorption isotherm some thermodynamic data for the adsorption processes are calculated and discussed. The effect of exposure time on the corrosion behaviour of mild steel in the absence and presence of inhibitor over 168 h was also studied. 相似文献
114.
Julian R. Osman Joe A. Crayston Allin Pratt David T. Richens 《Journal of Sol-Gel Science and Technology》2008,46(2):126-132
Mixed IrO2–TiO2 oxides were prepared by the sol–gel method by adding an aqueous solution of an iridium(III) acetate precursor [Ir3O(OAc)6 (HOAc)3]OAc, to titanium tetraethoxide in ethanol. By using an acetylacetonate modifier to stabilize the hydrolysed titanium alkoxide
and by omitting a catalyst, gels were produced in all cases. Transmission electron microscopy and EDX analysis confirmed the
high dispersion of iridium in the dried gel material on the nanometre scale. The images also show spherical cage features
up to 20 nm in diameter. High mass losses of the gels in the TGA scans suggested low degrees of hydrolysis of the acetate
precursor, but calcination gave a crystalline, mixed oxide (TixIr1–xO2) solid solution. The precursor is also soluble in ethanol, which provides a slightly modified route to similar materials. 相似文献
115.
We studied vitamin K(1)(20), vitamin K(1)(25), and vitamin K(1) epoxide in n-hexane and ethanol solutions by gas chromatography/mass spectrometry (GC/MS) utilizing a DB-5 MS fused-silica capillary column. In ethanol solutions of K(1), we observed an extra peak eluting from the GC column with somewhat longer retention time than K(1)(20). A similar peak following K(1)(25) was also found. These peaks were not found in n-hexane solutions of K(1). A close examination of the mass spectra of these peaks indicated that they were vitamin K(1) variants containing a base peak at m/z 225 characteristic of the methylnaphthoquinone ring with a four-carbon side chain. In addition, they contained the molecular ions of K(1)(20) and K(1)(25), respectively. We conclude that K(1)(20) and K(1)(25), but not K(1) epoxide, might undergo rearrangements in ethanol involving an intramolecular proton transfer and a shift of the beta,gamma-double bond on the phytyl side chain toward the ring. The conjugation of the phytyl double bond with the quinone ring is probably the driving force of the rearrangement. We emphasize, however, that our conclusion is based only on mass spectral analysis and would require further investigation by other spectroscopic methods. 相似文献
116.
A series of discrete compounds and supramolecular polymers were synthesized by self-assembly of dithioether building blocks and HAuCl4.3H2O. In complexes 1 {[AuL(1-Me)Cl], where L(1-Me) is bis(methylthio)methane} and 2 {[Au2L(2-Ph)Cl2], where L(2-Ph) is 1,2-bis(phenylthio)ethane}, adjacent units are connected via aurophilic interactions. Complex 1, a one-dimensional (1D) supramolecular polymer, and complex 2, a two-dimensional supramolecular network, both feature nearly linear [Au-Au-](infinity) chains. Complexes 4a, 4b, and 4c, all of which contain 1,3-bis(phenylthio)propane (L(3-Ph)), are polymorphs having the composition [Au2L(3-Ph)Cl2]. Complex 3 {[Au2L(1-Ph)Cl2], where L(1-Ph) is bis(phenylthio)methane}and complexes 4a and 4b consist of nearly identical 1D supramolecular polymers formed through Au-Au interactions. The third polymorph, 4c, is a molecular complex, as it does not have metal-metal interactions. Complex 5 {[Au2L(4-Ph)Cl2], where L(4-Ph) is 1,4-bis(phenylthio)butane} is also molecular. UV-vis spectra showed that the absorption bands of these complexes are allowed ligand-centered transitions between 230 and 260 nm. Complexes 1, 2, and 6 {[AuL(3-Me)Cl], where L(3-Me) is 1,3-bis(methylthio)propane} exhibited solid-state luminescence at 5 K with vibronic progressions and band maxima at approximately 570 nm. It is suggested that complex 6 contains [Au-Au-](infinity) chains. 相似文献
117.
Osman Zeki Okuyucu Önder Gökmen Yıldız Murat Tosun 《Advances in Applied Clifford Algebras》2016,26(4):1341-1348
In this paper, we study spinor Frenet equations in three dimensional Lie groups with a bi-invariant metric. Also, we obtain spinor Frenet equations for some special cases of three dimensional Lie groups. 相似文献
118.
Mohamed R. Shaaban Ahmad M. Farag Tamer S. Saleh Fayez H. Osman 《Journal of heterocyclic chemistry》2007,44(1):177-181
2‐Acetyl‐1‐methyl‐1H‐benzimidazole reacts with dimethylformamide‐dimethyl‐acetal (DMF‐DMA) to afford the corresponding E‐1‐(1‐methyl‐1H‐benzimidazol‐2‐yl)‐3‐N,N‐dimethylaminoprop‐2‐enone. The latter compound reacts regioselectively with some nitrilimines and nitrile oxides to afford the corresponding pyrazole and isoxazole derivatives, respectively. These reaction products react with hydrazine hydrate to give the novel pyrazolo[3,4‐d]pyridazine and isoxazolo[3,4‐d]pyridazine derivatives, respectively. 相似文献
119.
Nonlinear Dynamics - A variety of new types of nonautonomous combined multi-wave solutions of the ( $$2+1$$ )-dimensional variable coefficients KdV equation is derived by means of the generalized... 相似文献
120.
Osman Akba Feyyaz Durap Ak?n Baysal Saim Özkar 《Journal of organometallic chemistry》2009,694(5):731-18
Oxidation of N,N,N′,N′-tetrakis(diphenylphosphino)ethylendiamine (1) with elemental sulfur and selenium gives the corresponding sulfide and selenide, respectively, [(Ph2P(E))2NCH2CH2N(P(E)Ph2)2] (E: S 1a, Se 1b). Complexes of 1 [(M2Cl4){(Ph2P)2NCH2CH2N(PPh2)2}] (M: Ni(II) 1c, Pd(II) 1d, Pt(II) 1e) were prepared by the reaction of 1 with NiCl2 or [MCl2(COD)] (M = Pd, Pt). The new compounds were characterized by NMR, IR spectroscopy and elemental analysis. The catalytic activity of Pd(II) complex 1d was tested in the Suzuki coupling reaction and Heck reaction. The palladium complex 1d catalyses the Heck reaction between styrene and aryl bromides as well as Suzuki coupling reaction between phenylboronic acid and arylbromides affording stilbenes and biphenyls in high yield, respectively. 相似文献