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961.
有机电致发光(OLEDs)因其具有驱动电压低、主动发光、亮度高、视角宽、响应快、耐冲击与震动等特点,在平板显示与照明领域有着广阔的应用前景。磷光有机电致发光二极管(PhOLEDs)由于能够同时利用三重态和单重态激子,内量子效率从理论上可达到100%,从而克服了传统荧光OLEDs只利用单重态激子时效率25%的限制,在过去的几十年里受到业内人士的极大关注。但要实现三重态磷光,通常需要将重金属原子与主体材料进行掺杂,而重金属配合物的磷光寿命相对较长,容易引起浓度猝灭和三重态-三重态湮灭,所以需要找到合适的主体材料与重金属的磷光发射体进行掺杂来减少上述因素的影响从而得到高性能的电致磷光器件。本文综述了近年来国内外蓝色有机电致磷光主体材料的研究状况,并对空穴传输型、电子传输型和双极传输型的蓝色磷光主体材料按照官能团的不同进行了分类总结和评述,并对其光物理性质、热学性质、电化学性质及器件性能等作了详细归纳比较,最后展望了蓝色有机电致磷光主体材料的前景和发展趋势。 相似文献
962.
A novel non-coplanar aromatic diamine monomer,3,3'-ditertbutyl-4,4'-diaminodiphenyl-4'-naphthylmethane(TAPN) was synthesized by a condensation reaction of 2-tertbutylaniline and 1-naphthaldehyde under catalyst hydrochloric acid.The structure of the monomer was confirmed by FTIR,NMR,elementary analysis and mass spectrometry.A series of aromatic polyimides(PIs) were synthesized via conventional one-step polycondensation from TAPN and various commercial aromatic dianhydrides.All of the PIs exhibit excellent solubility in common organic solvents,even in low boiling point solvents such as chloroform(CHCl3),tetrahydrofuran(THF) and acetone.The PIs present outstanding thermal stability with the glass transition temperature(Tg) ranged from 299 °C to 350 °C,and the temperature at 10% weight loss ranged from 490 °C to 504 °C,and high optical transparency with the cutoff wavelengths of 306-356 nm.Moreover,the flexible and tough PI films have prominent mechanical properties with tensile strengths in the range of 77.6-90.5 MPa,tensile modulus in the range of 1.8-2.4 GPa and elongation at break in the range of 6.3%-9.5%,as well as lower dielectric constant(2.89-3.12 at 1 MHz) and lower moisture absorption(0.35%-0.66%). 相似文献
963.
Organic small molecules(TPA-BT3T,TPA-PT3T,and TPA-DFBT3T)using triphenylamine as a donor unit,terthiophene as a bridge,and benzo-2,1,3-thiadiazole(BT),[1,2,5]thiadiazolo[3,4-c]pyridine(PT)or 5,6-difluorobenzo[c][1,2,5]thiadiazole(DFBT)as an acceptor unit were designed and synthesized through Suzuki coupling reactions.These molecules exhibited good thermal stability with decomposition temperatures over 380°C and broad absorption from 300 to 700 nm.Photovoltaic devices were fabricated with these small molecules as donors and PC71BM as an acceptor.The TPA-BT3T based devices exhibited a power conversion efficiency of 2.89%,higher than those of the TPA-PT3T-and TPA-DFBT3T-based devices(1.34%and1.54%respectively).The effects of electron-withdrawing units on absorption,energy level,charge transport,morphology,and photovoltaic properties also were investigated. 相似文献
964.
以Keggin型铁取代杂多阴离子PW11O39Fe(III)(H2O)4- (PW11Fe)代替传统电芬顿(electro-Fenton)方法中的Fe3+作为电催化剂, 构成一个新颖的电催化体系并用于中性水溶液中硝基苯的降解. 结果表明, 含有1.0 mmol•L-1硝基苯和1.0 mmol•L-1 PW11Fe的混合磷酸盐溶液(pH 6.86), 在-0.5 V电位和60 mL•min-1 O2流速下反应100 min, 硝基苯便完全降解. 降解的准一级表观速率常数与硝基苯的初始浓度有关, 当硝基苯的初始浓度为1.0, 2.0和5.0 mmol•L-1时, kobs分别为7.18×10-2, 3.57×10-2和1.47×10-2 min-1. 降解反应100 min的TOC(有机碳总量)去除率约为35%, 表明硝基苯的降解过程伴随着矿化. 相似文献
965.
Novel zirconium silicalite‐1 zeolite membrane was hydrothermally prepared on the mullite porous support at 150–185°C for 40–72 h by an "in situ" method using tetraethyl orthosilicate (TEOS), zirconium butoxide (ZBOT) and tetrapropylammonium hydroxide (TPAOH) as silica source, zirconium source and organic structure directing agent, respectively. X‐ray diffraction (XRD) patterns, fourier transformed infrared (FT‐IR) spectra, and inductively coupled plasma‐atomic emission spectrometry (ICP) of the accompanying zeolite powder confirmed that the zirconium was isomorphously incorporated into the zeolite framework. The surface chemical compositions of the obtained membrane were measured with an energy‐dispersive X‐ray spectral analyzer (EDS), and the membrane morphologies were observed by a scanning electron microscope (SEM). The results showed that the zeolite crystals growing on the support were zirconium silicalite‐1 zeolites, and the dense membrane layer was composed of the well inter‐growing zeolite crystals. The zirconium silicalite‐1 zeolite membrane, which was derived from the synthesis solution having a molar ratio of 1.00SiO2:0.01ZrO2:0.17TPAOH:120H2O, showed high ethanol permselectivity with a flux of 1.01 kg/(m2·h) accompanied with a separation factor of 73 for ethanol/water (5/95, w/w) system under a pervaporation condition at 60°C. Moreover, this membrane displayed pervaporation‐aided catalysis activity for iso‐propanol oxidation with hydrogen peroxide as oxidant, and the corresponding iso‐propanol conversion was 35%. 相似文献
966.
A pre-column derivatized high-performance liquid chromatographic (HPLC) method with ultraviolet-visible detection was developed
to measure the concentrations of spectinomycin in fermentation broth. Derivatization reagents, 2,4-dinitrophenylhydrazine
in acetonitrile (5 mg mL−1) and trifluoroacetic acid in acetonitrile (0.8 mol L−1), were added to an aliquot of the fermentation broth, and the mixture was incubated for 60 min at 70°C. The resulting derivative
was separated from other compounds by isocratic elution in a reversed-phase column Zorbax SB-C18 (250 mm × 4.6 mm, 5 μm).
Mobile phase consisted of acetonitrile, tetrahydrofuran, and water (φ
r = 40: 35: 25) and the flow rate was 1.0 mL min−1. The detection wavelength was 415 nm. The standard curve for spectinomycin sulfate was linear with correlation coefficients
of 0.9997 in the range of 25 μg mL−1 to 600 μg mL−1. The relative standard deviation values ranged from 0.43 % to 2.18 % depending on the concentration of samples. The average
recovery was 101.5 %. The limit of detection was 50 ng mL−1. 相似文献
967.
Two discrete lanthanide complexes with bulky aromatic mixed‐ligands, {[La2(na)6(phen)2]·[La2(na)6(phen)2]} ( 1 ) and [La2(na)6(2,2′‐bipy)2] ( 2 ) (Hna = 1‐naphthoic acid, phen = 1,10‐phenanthroline, and 2,2′‐bipy = 2,2′‐bipyridine), have been synthesized under hydrothermal conditions and fully characterized by single‐crystal X‐ray crystallography, IR, elemental analysis, TG‐DTA and fluorescence spectra. Structure determination reveals that 1 contains two separate binuclear [La2(na)6(phen)2] units, in which both crystallographically LaIII ions are nine‐coordinated with tricapped trigonal prism polyhedron for La1 and a distorted monocapped square antiprism arrangement for La2; whereas 2 has a binuclear structure bridged by carboxylate groups of four na anions. Due to the introduction of bulky aromatic ligands, non‐classical C–H···O H–bonds and π – involved stacking interactions become the dominantly driving forces for the supramolecular structure. The two solid complexes exhibit intense fluorescent emissions at room temperature resulted from the ligand‐to‐metal charge transfer. 相似文献
968.
Huiyong Wang Jianji Wang Prof. Dr. Sheli Zhang Yuanchao Pei Dr. Kelei Zhuo Prof. Dr. 《Chemphyschem》2009,10(14):2516-2523
Considering the ionic nature of ionic liquids (ILs), ionic association is expected to be essential in solutions of ILs and to have an important influence on their applications. Although numerous studies have been reported for the ionic association behavior of ILs in solution, quantitative results are quite scarce. Herein, the conductivities of the ILs [Cnmim]Br (n=4, 6, 8, 10, 12), [C4mim][BF4], and [C4mim][PF6] in various molecular solvents (water, methanol, 1‐propanol, 1‐pentanol, acetonitrile, and acetone) are determined at 298.15 K as a function of IL concentration. The conductance data are analyzed by the Lee–Wheaton conductivity equation in terms of the ionic association constant (KA) and the limiting molar conductance (Λm0). Combined with the values for the Br? anion reported in the literature, the limiting molar conductivities and the transference numbers of the cations and [BF4]? and [PF6]? anions are calculated in the molecular solvents. It is shown that the alkyl chain length of the cations and type of anion affect the ionic association constants and limiting molar conductivities of the ILs. For a given anion (Br?), the Λm0 values decrease with increasing alkyl chain length of the cations in all the molecular solvents, whereas the KA values of the ILs decrease in organic solvents but increase in water as the alkyl chain length of the cations increases. For the [C4mim]+ cation, the limiting molar conductivities of the ILs decrease in the order Br?>[BF4]?>[PF6]?, and their ionic association constants follow the order [BF4]?>[PF6]?>Br? in water, acetone, and acetonitrile. Furthermore, and similar to the classical electrolytes, a linear relationship is observed between ln KA of the ILs and the reciprocal of the dielectric constants of the molecular solvents. The ILs are solvated to a different extent by the molecular solvents, and ionic association is affected significantly by ionic solvation. This information is expected to be useful for the modulation of the IL conductance by the alkyl chain length of the cations, type of anion, and physical properties of the molecular solvents. 相似文献
969.
970.