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851.
852.
Yaqin Fu Minghao Sun Yonggang Wu Zhishan Bo Dongge Ma 《Journal of polymer science. Part A, Polymer chemistry》2008,46(4):1349-1356
Conjugated polymers containing electron‐transporting, hole‐transporting, and blue light‐emitting units were synthesized by Suzuki polycondensation. These copolymers exhibited excellent thermal and optical stability. Optical investigation indicated that the incorporation of the spirobifluorene units in the polymer main chain could markedly increase the effective conjugation length of polymers. Electrochemical studies showed that the incorporation of spirobifluorene unit could raise the electrochemical stability and improve the electron‐ and hole‐injecting abilities. The electroluminescent results also showed that the introducing of spirobifluorene units could significantly improve the device performance. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1349–1356, 2008 相似文献
853.
Denis A. Svechkarev Ilya V. Bukatich Andrey O. Doroshenko 《Journal of photochemistry and photobiology. A, Chemistry》2008,200(2-3):426-431
Two novel 1,3,5-triphenyl-2-pyrazoline moiety containing derivatives of 3-hydroxychromone were synthesized and studied by 1H NMR, absorption and fluorescence spectroscopy. The prospects of practical application of these compounds exhibiting high solvatofluorochromism into analytical chemistry and biophysics as effective ratiometric polarity probes were discussed proceeding from the data on their fluorescent properties. 相似文献
854.
855.
Lifetime-based spectral decomposition using a frequency-domain phase/modulation technique has been developed on our UV confocal microspectrofluorimeter prototype. Examples of such an application are first given in the case of complex mixtures of three overlapping fluorescent components in solution. Preliminary results concerning cellular potential application are also reported in the case of Snarf-1 pH sensor. Limits and perspectives of such an approach at the subcellular level are discussed in view of future improvement. 相似文献
856.
Soo Kyung Bae Min‐Jung Kim Eon‐Jeong Shim Doo‐Yeoun Cho Ji‐Hong Shon Kwang‐Hyeon Liu Eun‐Young Kim Jae‐Gook Shin 《Biomedical chromatography : BMC》2009,23(6):568-572
A simple and rapid HPLC method using fluorescence detection was developed for determination of irbesartan in human plasma. Sample preparation was accomplished through a simple deproteinization procedure with 0.4 mL of acetonitrile containing 800 ng/mL of losartan (internal standard), and to a 0.1 mL plasma sample. Chromatographic separation was performed on a Zorbax Xclipse XDB C18 column (150 × 4.6 mm, i.d., 5 µm) at 40°C. An isocratic mobile phase, acetonitrile:0.1% formic acid (37:63, v/v), was run at a flow‐rate of 1.0 mL/min, and the column eluent was monitored using a fluorescence detector set at excitation and emission wavelengths of 250 and 370 nm, respectively. The retention times of irbesartan and losartan were 4.4 and 5.9 min, respectively. This assay was linear over a concentration range of 10–5000 ng/mL with a lower limit of quantification of 10 ng/mL. The coefficient of variation for this assay precision was less than 8.48%, and the accuracy exceeded 94.4%. The mean relative recoveries of irbesartan and losartan were 98.4 and 99.1%, respectively. This method was successfully applied for pharmacokinetic study after oral administration of irbesartan (300 mg) to 23 Korean healthy male volunteers. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
857.
858.
The effect of acceptor concentration on the energy transfer from Coumarin 30 (donor) to Rhodamine 6G (acceptor) has been studied.
The nature of energy transfer reaction has been studied through lifetime measurements by recording the time-resolved fluorescence
decay curves. The energy transfer parameters calculated were used to confirm the occurrence of energy transfer on the basis
of the emission-reabsorption effect. 相似文献
859.
Venkat R. Donuru Giri K. Vegesna Singaravelu Velayudham Ge Meng Haiying Liu 《Journal of polymer science. Part A, Polymer chemistry》2009,47(20):5354-5366
Novel deep‐red emissive poly(2,6‐BODIPY‐ethynylene)s bearing dodecyl side chains (polymers A , B , and C ) have been prepared by palladium‐catalyzed Sonogashira polymerization of 2,6‐diiodo‐functionalized BODIPY monomers with 2,6‐diethynyl‐functionalized BODIPY monomers. These polymers emit in the deep‐red region with emission maxima at up to 690 nm, and exhibit significant red shifts (up to 166 and 179 nm) of both absorption and emission maxima compared with their parent BODIPY dyes due to significant extension of π‐conjugation. These polymers possess good thermal stability with decomposition temperature between 270 and 360 °C. The polymers exhibit a little larger Stokes shifts and shorter lifetime than their corresponding BODIPY dyes. The solid state thin films of polymers A , B , and C emit in near‐infrared region between 723 and 743 nm, and show significantly red shifts (up to 57 nm) in absorption and emission maxima relative to their polymer solution. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 5354–5366, 2009 相似文献
860.
Zhi‐guo Zhang Ji‐bing Yuan Huai‐jun Tang Hao Tang Li‐na Wang Ke‐Li Zhang 《Journal of polymer science. Part A, Polymer chemistry》2009,47(1):210-221
A novel nonconjugated copolymer (PVKEu) with carbazole segments and phenanthroline [Eu(β‐diketonate)3] moieties was synthesized via free radical copolymerization, and characterized by FTIR, 1H NMR spectroscopy, GPC, ICP, and elemental analysis. The copolymer exhibited good solubility, as well as good thermal stability and high glass transition temperature. The photoluminescence (PL) of this polymer in solution and in solid film has been studied. A multi‐layer device with the configuration of ITO/PEDOT: PSS (40 nm)/PVKEu (70 nm)/BCP (15 nm)/AlQ3 (30 nm)/LiF/Al exhibited nearly monochromatic red emission at 615 nm and voltage‐independent spectral stability. Our results suggest that enhancing the ligand‐mediated energy transfer between the matrix polymer and europium complex is a potential method to improve the electroluminescence performance of the Eu‐chelated polymers. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 210–221, 2009 相似文献