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231.
Schnöller J Wiesinger R Kleber C Hilfrich U Schreiner M Hutter H 《Analytical and bioanalytical chemistry》2008,390(6):1543-1549
Silver-coated quartz crystal microbalance (QCM) disks were treated under different environmental conditions (including changes
in parameters such as relative humidity (%RH) and SO2/H2S content) in atmospheres of synthetic air and pure N2 for 24 h in a weathering chamber. The corroded surfaces were subjected to depth profiling by a time of flight (TOF) secondary
ion mass spectrometry (SIMS) instrument, equipped with a Bi+ analysis gun and Cs+ sputter gun. The evaluation of the in-depth distribution of several elements and species provides evidence for the formation
of a corrosion layer containing Ag2SO3, even in the absence of oxidizing agents, such as H2O2 or NO2. Furthermore it could be elucidated that the thickness of the formed Ag2SO3 layer does not depend on the SO2 concentration but rather on the humidity and oxygen content of the ambient atmosphere. In weathering experiments in atmospheres
composed of synthetic air, humidity, and H2S, the presence of different oxygen species (surface and bulk) and silver sulfide could be detected by TOF-SIMS depth profiling
experiments. The obtained results for both acidifying gases are in good correlation with the corresponding tapping mode atomic
force microscopy (TM-AFM) investigations and in situ QCM measurements. 相似文献
232.
Huang MD Becker-Ross H Florek S Heitmann U Okruss M Patz CD 《Analytical and bioanalytical chemistry》2008,390(1):361-367
A new method for the determination of sulfur forms in wine, i.e., free SO2, total SO2, bound SO2, total S, and sulfate, is presented. The method is based on the measurement of the carbon monosulfide (CS) molecular absorption
produced in a conventional air–acetylene flame using high-resolution continuum source absorption spectrometry. Individual
sulfur forms can be distinguished because of the different sensitivities of the corresponding CS molecular absorption. The
sensitivity of free SO2 is about three times higher than the value for bound SO2 and sulfate. The method makes use of procedures similar to those used in classic reference methods. Its performance is verified
by analyzing six wine samples. Relative standard deviations are between 5 and 13% for free SO2 and between 1 and 3% for total SO2. For the validation of the accuracy of the new method, the results are compared with those of reference methods. The agreement
of the values for total SO2 with values of the classic method is satisfactory: five out of six samples show deviations less than 16%. Due to the instability
of free SO2 in wine and the known problems of the used reference method, serious deviations of the free SO2 results are found for three samples. The evaluation of the limits of detection focuses on the value for free SO2, which is the sulfur form having by far the lowest concentration in wine. Here, the achievable limit of detection is 1.8 mg L−1.
Figure Detection of non-metal elements using continuum source flame absorption spectrometry 相似文献
233.
The effect of sodium carboxymethyl cellulose (Na-CMC) on the corrosion behavior of mild steel in 1.0 mol·L−1 HCl solution has been investigated by using weight loss (WL) measurement, potentiodynamic polarization, linear polarization resistance (LPR), and electrochemical impedance spectroscopy (EIS) methods. These results showed that the inhibition efficiency of Na-CMC increased with increasing the inhibitor concentration. Potentiodynamic polarization studies revealed that the Na-CMC was a mixed type inhibitor in 1.0 mol·L−1 HCl. The adsorption of the inhibitor on mild steel surface has been found to obey the Langmuir isotherm. The effect of temperature on the corrosion behavior of mild steel in 1.0 mol·L−1 HCl with addition of 0.04% of Na-CMC has been studied in the temperature range of 298–328 K. The associated apparent activation energy (E*a) of corrosion reaction has been determined. Scanning electron microscopy (SEM) has been applied to investigate the surface morphology of mild steel in the absence and presence of the inhibitor molecules. 相似文献
234.
Shen-Ming Chen Wen-Yan Chzo R. Thangamuthu 《Journal of Solid State Electrochemistry》2008,12(11):1487-1495
Electrochemically active hybrid coatings based on cationic films, didodecyldimethylammonium bromide (DDAB), and poly(diallyldimethylammonium
chloride) (PDDAC) are prepared on electrode surface by cycling the film-covered electrode repetitively in a pH 6.5 solution
containing Fe(CN)6
3− and Ru(CN)6
4− anions. Modified electrodes exhibited stable and reversible voltammetric responses corresponding to characteristics of Fe(CN)6
3−/4− and Ru(CN)6
4−/3− redox couples. The cyclic voltammetric features of hybrid coatings resemble that of electron transfer process of surface-confined
redox couple. Electrochemical quartz crystal microbalance results show that more amounts of electroactive anionic complexes
partitioned into DDAB coating than those doped into PDDAC coating from the same doping solution. Peak potentials of hybrid
film-bound redox couples showed a negative shift compared to those at bare electrode and this shift was more pronounced in
the case of DDAB. Finally, the advantages of hybrid coatings in electrocatalysis are demonstrated with sulfur oxoanions. 相似文献
235.
Adriana González Castro José Sánchez Costa Roberta Pievo Chiara Massera Ilpo Mutikainen Urho Turpeinen Patrick Gamez Jan Reedijk Prof. Dr. 《无机化学与普通化学杂志》2008,634(14):2477-2482
A new Schiff‐base ligand having a potentially coordinating thioether group (2‐quinoline‐N‐(2′‐methylthiophenyl)methyleneimine, qmtpm ) has been prepared. The synthesis, structure, UV‐Vis and EPR studies of one copper(II) and two cobalt(II) complexes from this ligand is reported. The X‐ray structures of the CuII and CoII chlorido complexes 1 and 2 reveal the metal atoms in highly distorted square‐pyramidal environments constituted of one tridentate ligand and two anions. On the other hand, the thiocyanato CoII compound 3 exhibits a distorted trigonal‐bipyramidal structure. These structural variations are apparently due to the different counter‐ions which leads to distinct lattice interactions. The spectroscopic data obtained by EPR and UV‐Vis investigations are in agreement with the solid‐state structures of the coordination compounds. 相似文献
236.
基于香豆素和苯并吡啶基团,构建了用于二氧化硫(SO_(2))高效检测的荧光探针P1,其化学结构通过核磁氢谱(^(1)H NMR)、碳谱(^(13)C NMR)和高分辨质谱(HR-MS)确证。在缓冲溶液体系中,单独的探针P1具有微弱的荧光,识别SO_(2)后荧光发射强度明显增强,能够实现对SO_(2)的专一性裸眼识别,检出限为126 nmol/L。生物应用实验结果表明,该探针具有较低的细胞毒性,可用于生物活细胞中外源性SO_(2)的荧光成像。 相似文献
237.
Pengcheng Liu Dean Yen Bairav S. Vishnugopi Varun R. Kankanallu Doğa Gürsoy Mingyuan Ge John Watt Partha P. Mukherjee Yu-chen Karen Chen-Wiegart David Mitlin 《Angewandte Chemie (International ed. in English)》2023,62(23):e202300943
Combined synchrotron X-ray nanotomography imaging, cryogenic electron microscopy (cryo-EM) and modeling elucidate how potassium (K) metal-support energetics influence electrodeposit microstructure. Three model supports are employed: O-functionalized carbon cloth (potassiophilic, fully-wetted), non-functionalized cloth and Cu foil (potassiophobic, nonwetted). Nanotomography and focused ion beam (cryo-FIB) cross-sections yield complementary three-dimensional (3D) maps of cycled electrodeposits. Electrodeposit on potassiophobic support is a triphasic sponge, with fibrous dendrites covered by solid electrolyte interphase (SEI) and interspersed with nanopores (sub-10 nm to 100 nm scale). Lage cracks and voids are also a key feature. On potassiophilic support, the deposit is dense and pore-free, with uniform surface and SEI morphology. Mesoscale modeling captures the critical role of substrate-metal interaction on K metal film nucleation and growth, as well as the associated stress state. 相似文献
238.
Helian Li Yongxin Zhang Xiaoxiao Yang Zhenxi Deng Zhimin Zhu Pan Zhou Xinke Ouyang Yuting Yuan Xi Chen Lingyue Yang Meng Liu Prof. Dr. Chao Shu 《Angewandte Chemie (International ed. in English)》2023,62(15):e202300159
Despite the significance of sultines in synthesis, medicine, and materials science, the chemistry of sultines has remained unexplored due to their inaccessibility. Herein, we demonstrate the development of a photoredox-catalyzed multifluoromethyl radical addition/SO2 incorporation/polar cyclization cascade approach to multifluoromethylated γ-sultines. The reactions proceed by single electron transfer induced multifluoromethyl radical addition to an alkene followed by SO2 incorporation, and single-electron reduction for polar 5-exo-tet cyclization. Key to the success of the protocol is the use of easily oxidizable multifluoroalkanesulfinates as bifunctional reagents. The reactions proceed with excellent functional-group tolerance to deliver γ-sultines in moderate to excellent yields. 相似文献
239.
The kinetic study of in-situ eopolymerization of aniline with o- and p-methylaniline by ammonium persulfate (APS) has been carried out. UV-vis spectroscopic method was used to investigate the course of copolymerization. Structural characterization was studied by PT-IR spectral analysis. The electronic spectra of the copolymers poly(aniline-co-p-toluidine) and poly(aniline-co-o- toluidine) show blue shift. The shift has been observed in the bands corresponding to π→π^* transition as well as in the exciton transition. The increase in absorbance recorded during the reaction for different concentration of aniline, o- and p-toluidine at various intervals of time of polymerization reaction indicates a growth in the polymer formation. The resulting first-order rate constant was used to calculate the rate of copolymer formation using the rate equation -d[A]/dt = kc^n. 相似文献
240.
Dr. Trapti Aggarwal Kenshiro Hada Yusuke Murata Dr. Yuji Sumii Kazuhiro Tanagawa Kiyoteru Niina Soichiro Mori Dr. Jorge Escorihuela Prof. Dr. Norio Shibata 《Angewandte Chemie (International ed. in English)》2023,62(33):e202307090
Alkyne hydroamination is an effective approach for the production of enamines and enamine-containing N-heterocycles. However, stereoselectivity control is a considerable challenge in this reaction because of the electronic repulsion between an incoming nitrogen lone pair and the alkyne π-system. Herein, we propose a methodology involving β-regio- and Z-selective alkyne hydroamination by using tetrafluoro-λ6-sulfanyl (SF4) alkynes under superbasic, naked anion conditions. The reaction is compatible with a wide variety of N-heterocycles, including indoles, carbazoles, pyrazoles, and imidazoles, and selectively furnishes SF4-linked Z-vinyl enamines with β-regioselectively. Moreover, the method can be extended to the β- and Z-controlled, base-mediated alkyne hydrophenoxylation with phenols to provide SF4-linked Z-vinyl ethers in high yields. As the SF4 unit has attracted attention as a bioisostere for alkynes, p-benzenes, bicyclo[1.1.1]pentyl (BCP) groups, and cubanes in medicinal chemistry, this chemistry represents an effective approach to creating novel drug candidates incorporating SF4-containing molecules. 相似文献