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81.
CuAl2O4 powder synthesis by sol-gel method and its photodegradation property under visible light irradiation 总被引:1,自引:0,他引:1
Jiang Yanyan Li Jinggang Sui Xiaotao Ning Guiling Wang Chengyu Gu Xiumei 《Journal of Sol-Gel Science and Technology》2007,42(1):41-45
Nanocrystalline spinel CuAl2O4 powders were prepared by sol-gel method from nitrate Cu(NO3)2·3H2O, Al(NO3)3·9H2O and complex C6H8O7·H2O. Sintering was carried out at 400, 500, 600, 700, 800°C respectively for 2 h in air. The XRD patterns started to appear
CuAl2O4 peaks after sintering of 500°C and consist of only CuAl2O4 peaks as spinel crystal after sintering of 700°C. The powders were analyzed by TEM and UV-vis diffuse reflectance spectrum
to be round, about 10–30 nm in size and Eg=1.77 eV. Photodegradation property of nanocrystalline CuAl2O4 powders was investigated by using methyl orange as model pollutant and mercury lamp (λ>400 nm) as energy source. The results
indicated that CuAl2O4 powders sintered at 700°C had the excellent visible photocatalytic property. Under the irradiation of visible light, methyl
orange could be degraded 97% in 120 min. 相似文献
82.
Hong‐Ze Gao Zhong‐Min Su Chun‐Sheng Qin Ri‐Gen Mo Yu‐He Kan 《International journal of quantum chemistry》2004,97(6):992-1001
Bis(2‐methyl‐8‐quinolinolato)aluminum(III) hydroxide complex (AlMq2OH) is used in organic light‐emitting diodes (OLEDs) as an electron transport material and emitting layer. By means of ab initio Hartree–Fock (HF) and density functional theory (DFT) B3LYP methods, the structure of AlMq2OH was optimized. The frontier molecular orbital characteristics and energy levels of AlMq2OH have been analyzed systematically to study the electronic transition mechanism in AlMq2OH. For comparison and calibration, bis(8‐quinolinolato)aluminum(III) hydroxide complex (Alq2OH) has also been examined with these methods using the same basis sets. The lowest singlet excited state (S1) of AlMq2OH has been studied by the singles configuration interaction (CIS) method and time‐dependent DFT (TD‐DFT) using a hybrid functional, B3‐LYP, and the 6‐31G* basis set. The lowest singlet electronic transition (S0 → S1) of AlMq2OH is π → π* electronic transitions and primarily localized on the different quinolate ligands. The emission of AlMq2OH is due to the electron transitions from a phenoxide donor to a pyridyl acceptor from another quinolate ligand including C → C and O → N transference. Two possible electron transfer pathways are presented, one by carbon, oxygen, and nitrogen atoms and the other via metal cation Al3+. The comparison between the CIS‐optimized excited‐state structure with the HF ground‐state structure indicates that the geometric shift is mainly confined to the one quinolate and these changes can be easily understood in terms of the nodal patterns of the highest occupied and lowest unoccupied molecular orbitals. On the basis of the CIS‐optimized structure of the excited state, TD‐B3‐LYP calculations predict an emission wavelength of 499.78 nm. An absorption wavelength at 380.79 nm on the optimized structure of B3LYP/6‐31G* was predicted. They are comparable to AlMq2OH 485 and 390 nm observed experimentally for photoluminescence and UV‐vis absorption spectra of AlMq2OH solid thin film on quartz, respectively. Lending theoretical corroboration to recent experimental observations and supposition, the reasons for the blue‐shift of AlMq2OH were revealed. © 2003 Wiley Periodicals, Inc. Int J Quantum Chem, 2004 相似文献
83.
84.
Anton Dmitrienko Prof. Melanie Pilkington Prof. Georgii I. Nikonov 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(18):5730-5736
The AlI compound NacNacAl ( 1 , NacNac = [ArNC(Me)CHC(Me)NAr]−, Ar = 2,6-iPr2C6H3) serves as a template for the chemoselective coupling between carbonyls (benzophenone, fenchone, isophorone, p-tolyl benzoate, N,N-dimethylbenzamide, (1-phenylethylidene)aniline) and pyridine. With the CH-acidic ketone (1R)-(+) camphor, the reaction affords a hydrido alkoxide compound of Al, formed as the result of enolization, whereas an enolizable imine, (1-phenylethylidene)aniline, and the bulky ketone isophorone, still chemoselectively couple with pyridine. In contrast, reaction with the ester p-tolyl benzoate results in cleavage of the ester bond together with replacement of the alkoxy group by a hydrogen atom of the pyridine moiety. This study demonstrates that for carbonyl substrates featuring phenyl substituents, the reaction proceeds via intermediate formation of η2(C,X)-coordinated (X = O, N) carbonyl adducts, whereas the reaction of 1 with (R)-(−)-fenchone in the absence of pyridine leads to CH activation in the pendant isopropyl group of the Ar substituent of the NacNac ligand. 相似文献
85.
Yu-Liang Lin Yu-Hsuan Tseng Jhih-Hao Ho Yi-Fan Chen Prof. Jiun-Tai Chen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(60):14981-14988
Composite polymer electrolytes (CPEs) with smart, stimuli-responsive characteristics have gained considerable attention owing to their noninvasive manipulation and applications in future technologies. To address this potential, in this work, we demonstrate photoresponsive composite polymer electrolytes, consisting of gel polymer electrolyte (GPE) and spiropyran-immobilized nanoporous anodic aluminum oxide (SP-AAO) templates. Under UV irradiation, the close SP form isomerizes to the open merocyanine (MC) form, creating extremely polarized AAO surfaces; whereas, under visible light irradiation, the MC form reverts to the SP form, creating neutral surface conditions. The electrostatic interactions between ions and AAO surfaces are investigated by attenuated total reflection Fourier-transform infrared (ATR-FTIR) spectroscopy. Moreover, the behavior of ionic conductivity of the GPE@SP-AAO is found to be consistent with the kinetics of isomerization tracked by UV-Vis spectroscopy. This work provides a promising platform for developing next-generation photoelectronic smart devices. 相似文献
86.
LIU QingMing BAI ChunHua JIANG Li DAI WenXi & NIU Fang State Key Lab of Explosion Science Technology Beijing Institute of Technology Beijing China 《中国科学:物理学 力学 天文学(英文版)》2011,(3)
The deflagration-to-detonation transitions (DDTs) for clouds of spherical aluminum dust (SAD) mixed with air or epoxypropane mist (EPM) and air were investigated in a 29.6-m-long experimental tube of 199 mm in diameter. The clouds formed through the injection of SAD and SAD/liquid epoxypropane samples into the experimental tube. Explosions of the SAD/air mixture were initiated using a 7-m-long EPM/air cloud explosion ignited by a 40-J electric spark. Explosions in SAD/EPM/air clouds were initiated using a 1... 相似文献
87.
Selective Oxidation of Alcohols with a New Reagent: Iron(III) Nitrate Supported on Aluminum Silicate
A selective and effective oxidation of alcohols, except aliphatic alcohols, such as 1‐hexanol or 1‐octyl alcohol, to the corresponding aldehydes and ketones using a new reagent, iron(III) nitrate supported on aluminum silicate, under heterogeneous conditions with reflux with 85–98% yield is described. 相似文献
88.
《Analytical letters》2012,45(2):209-219
ABSTRACT Indirect differential pulse voltammetric (DPV) determination of aluminum in the presence of 3, 4-dihydroxyphenylalanine (L-dopa) with glass carbon electrode as working electrode has been described. The method relies on the decrease of DPV anodic peak current of L-dopa with the addition of AlIII The decreasing value of the peak current is linear with the increase of AlIII concentration. Under the optimum experimental conditions (pH 4.8, 6×10?4 M L-dopa, 0.06M NaAc - HAc 1buffer solution), the linear ranges are 4.0×10?7 - 5.2×10?6 M and 7.2×10?6 - 4.5×10?5 M. The relative standard deviation for 8×10?6 M aluminum is 1.0% (n = 8) and the detection limit is 3.5×10?7 M. A number of foreign species for interference have been studied. The method has been applied to determine aluminum in drinking water, synthetic renal dialysate and urine samples. 相似文献
89.
Frontispiece: Irreversible Denaturation of Proteins through Aluminum‐Induced Formation of Backbone Ring Structures 下载免费PDF全文
90.
A series of aluminum dimethyl complexes 1 – 6 bearing N‐[2‐(pyrrolidinyl)benzyl]anilido ligands were synthesized and well characterized. The molecular structure of complex 1 determined by an X‐ray diffraction study indicates the bidentate chelating mode of the pyrrolidinyl‐anilido ligand. In the absence of a coinitiator, these complexes exhibited excellent control toward the polymerizations of ε‐caprolactone and rac‐lactide, affording polyesters with quite narrow molecular weight distributions (Mw/Mn = 1.04–1.26). The end group analysis of ε?CL oligomer via 1H NMR and ESI‐TOF MS methods gave strong support to the hypothesis that the polymerization catalyzed by these aluminum complexes proceeds via a coordination‐insertion mechanism involving a unique Al? N (amido) bond initiation. Via 1H NMR scale oligomerization studies, it is suggested that the insertion of the first lactide monomer into Al? N bond of the complex is much easier than the insertion of lactide monomer into the newly formed Al? O (lactate) bond and might also be easier than the insertion of the first ε?CL monomer into Al? N bond. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3096–3106 相似文献