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991.
A highly efficient synthetic strategy toward Michael addition of indoles to α,β‐unsaturated esters has been developed using Lewis acid InBr3 as catalyst. The reactions generated 3‐substituted indoles in high yields with excellent regio‐selectivity in the presence of catalytic amount of InBr3 under mild reaction conditions. The method is simple, efficient and practical. 相似文献
992.
采用高温固相反应法制备了质子导体BaCe0.8-xNbxGd0.2O3-δ(0≤x≤0.45)。结合XRD、SEM、EIS等技术对其物相、微观形貌、稳定性及电导率进行了研究。结果表明,在1600℃烧结5h制备的质子导体BaCe0.8-xNbxGd0.2O3-δ(0≤x≤0.45)均能保持主相为斜方晶的钙钛矿结构。Nb的加入可明显提高烧结样品的致密性及在CO2和水蒸气气氛下的稳定性。在湿润H2/Ar(0.4%,V/V)气氛中800℃下,x=0.1样品的电导率为5.73mS·cm-1,电导活化能为0.35eV,与x=0的样品相当。 相似文献
993.
Application of in-plasma catalysis and post-plasma catalysis for methane partial oxidation to methanol over a Fe2O3-CuO/γ-Al2O3 catalyst 总被引:1,自引:0,他引:1
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Methane partial oxidation to methanol (MPOM) using dielectric barrier discharge over a Fe2O3-CuO/γ-Al2O3 catalyst was performed. The multicomponent catalyst was combined with plasma in two different configurations, i.e., in-plasma catalysis (IPC) and post-plasma catalysis (PPC). It was found that the catalytic performance of the catalysts for MPOM was strongly dependent on the hybrid configuration. A better synergistic performance of plasma and catalysis was achieved in the IPC configuration, but the catalysts packed in the discharge zone showed lower stability than those connected to the discharge zone in sequence. Active species, such as ozone, atomic oxygen and methyl radicals, were produced from the plasma-catalysis process, and made a major contribution to methanol synthesis. These active species were identified by the means of in situ optical emission spectra, ozone measurement and FT-IR spectra. It was confirmed that the amount of active species in the IPC system was greater than that in the PPC system. The results of TG, XRD, and N2 adsorption-desorption revealed that carbon deposition on the spent catalyst surface was responsible for the catalyst deactivation in the IPC configuration. 相似文献
994.
Tetrahydrofuran (THF) hydrate was formed in bulk as well as in glass beads pack with a mean diameter of 3.0 mm by controlling the temperature under ambient pressure. Images of THF hydrate formation procedure were obtained using the magnetic resonance imaging (MRI) technique. The experiment results showed that MRI is an effective method for the detection of hydrate formation. Saturation of hydrate formed both in bulk and glass beads can be confirmed by intensity integration of MRI images. 相似文献
995.
996.
997.
膦系阻垢剂阻碳酸钙垢机理的研究 总被引:5,自引:0,他引:5
在模拟循环水中, 通过静态阻垢实验研究了HEDP, PBTCA, ATMP和EDTMP对碳酸钙的阻垢性能, 在相同的加药浓度下(按物质的量浓度计)阻垢性能的强弱顺序为HEDP>PBTCA>ATMP>EDTMP; 同时采用分子动力学方法, 模拟计算了阻垢剂负二价离子与方解石(104), (102), (202)和(113)面的相互作用. 结果表明: 阻垢剂分子中的膦酸基团和羧酸基团与碳酸钙中的Ca2+形成的离子键对吸附起到了主要作用, 同时阻垢剂与晶面间存在较弱的范德华力相互作用. 阻垢剂与各晶面的结合能强弱顺序为(113)≥(102)≥(202)>(104); 分子中的羟基易与垢晶面形成氢键而加强阻垢效果; 羧基的位置不同对阻垢作用的影响不同. 将静态阻垢的实验结果与分子动力学模拟结果进行了相关性分析, 发现阻垢剂在(104)面和(102)面上的吸附对阻垢作用的贡献较大. 相似文献
998.
Thermoresponsive copolymer nanofilms for controlling cell adhesion, growth, and detachment 总被引:1,自引:0,他引:1
Yang L Pan F Zhao X Yaseen M Padia F Coffey P Freund A Yang L Liu T Ma X Lu JR 《Langmuir : the ACS journal of surfaces and colloids》2010,26(22):17304-17314
This study reports the development and use of a novel thermoresponsive polymeric nanofilm for controlling cell adhesion and growth at 37 °C, and then cell detachment for cell recovery by subsequent temperature drop to the ambient temperature, without enzymatic cleavage or mechanical scraping. A copolymer, poly(N-isopropylacrylamide-co-hydroxypropyl methacrylate-co-3-(trimethoxysilyl)propyl methacrylate) (abbreviated PNIPAAm copolymer), was synthesized by free radical polymerization. The thermoresponses of the copolymer in aqueous solution were demonstrated by dynamic light scattering (DLS) through detecting the sensitive changes of copolymer aggregation against temperature. The DLS measurements revealed the lower critical solution temperature (LCST) at approximately 30 °C. The PNIPAAm film stability and robustness was provided through silyl cross-linking within the film and with the hydroxyl groups on the substrate surface. Film thickness, stability, and reversibility with respect to temperature switches were examined by spectroscopic ellipsometry (SE), atomic force microscopy (AFM), and contact angle measurements. The results confirmed the high extent of thermosensitivity and structural restoration based on the alterations of film thickness and surface wettability. The effective control of adhesion, growth, and detachment of HeLa and HEK293 cells demonstrated the physical controllability and cellular compatibility of the copolymer nanofilms. These PNIPAAm copolymer nanofilms could open up a convenient interfacial mediation for cell film production and cell expansion by nonenzymatic and nonmechanical cell recovery. 相似文献
999.
Xinsheng Xu Lixia Jia Lei Shi Xuehan Ji Zhifeng Cui 《Research on Chemical Intermediates》2010,36(3):269-275
Chemically induced dynamic electron polarization (CIDEP) is one of the important research fields of dynamic spin chemistry.
In the present work, with ethylene glycol, 1,2-propanol and their mixtures with different ratios in volume as solvents and
duroquinone as photosensitive molecule, the influence of solvent viscosity on the CIDEP of photolyzed duroquinone radicals
has been studied experimentally. In each solvent, duroquinone neutral radicals are observed. Duroquinone neutral radicals
are generated through hydrogen transfer reaction from hydrogen-donor solvent molecules to excited duroquinone triplet. The
CIDEP mechanism is mainly triplet mechanism. The CIDEP intensity of duroquinone neutral radicals decreases with the increase
in the solvent viscosity, and the variation was rapid in low-viscosity range and slow in high-viscosity range. 相似文献
1000.
Dr. Xiao Liu Dr. Peiyuan Wang Dr. Lei Zhang Dr. Jie Yang Prof. Dr. Can Li Prof. Dr. Qihua Yang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(42):12727-12735
(R)‐(+)‐1,1′‐Bi‐2‐naphthol ((R)‐(+)‐Binol)‐functionalized (Binol=2,2′‐dihydroxy‐1,1′‐binaphthyl) chiral mesoporous organosilica nanospheres with uniform particle size (100 to 300 nm) have been synthesized by co‐condensation of tetraethoxysilane and (R)‐2,2′‐di(methoxymethyl)oxy‐6,6′‐di(1‐propyl trimethoxysilyl)‐1,1′‐binaphthyl in a basic medium with cetyltrimethylammonium bromide as the template. Nanospheres with a radiative 2D hexagonal channel arrangement exhibit higher enantioselectivity and turnover frequency than those with a penetrating 2D hexagonal channel arrangement (94 versus 88 % and 43 versus 15 h?1, respectively) in the asymmetric addition of diethylzinc to aldehydes. In addition, under similar conditions, the enantioselectivity of the nanospheres can be greatly improved as the structural order of the framework increases. These results clearly show that the structural order of nanospheres affects enantioselective reactions. The enantioselectivity of the nanospheres synthesized by the co‐condensation method is higher than that of nanospheres prepared by a grafting method and even higher than that of their homogeneous counterpart. These results indicate that the bite angle of (R)‐(+)‐Binol bridging in a more rigid porous network is in a more favorable position for achieving higher enantioselectivity. The efficiency of a co‐condensation method for the synthesis of high‐performance heterogeneous asymmetric catalysts is also reported. 相似文献