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排序方式: 共有7985条查询结果,搜索用时 15 毫秒
981.
Abulimiti B Zhu R Long J Xu Y Liu Y Ghazal AY Yang M Zhang B 《The Journal of chemical physics》2011,134(23):234301
The dynamics of electronically excited states in 2-picoline is studied using femtosecond time-resolved photoelectron imaging spectroscopy. The internal conversion from the S(2) state to the vibrationally excited S(1) state is observed in real time. The secondarily populated high vibronic S(1) state deactivates further to the S(0) state. Photoelectron energy and angular distributions reveal the feature of ionization from the singlet 3p Rydberg states. In addition, variation of time-dependent anisotropy parameters indicates the rotational coherence of the molecule. 相似文献
982.
Vanadate(V)-templated Dawson-type capsules {V(IV)M(VI)(17)(VO(4))(2)} (M = Mo, W; 1-2) have been synthesized and investigated by electrochemical methods in aqueous and organic media using spectroscopic techniques, EPR, UV-vis/NIR, IR, and CSI-MS (cryospray ionization mass spec.), and the clusters have been examined in the solid state by magnetic studies. The collision-induced dissociation (CID-MS) studies confirmed the solution structures as well as helped pinpoint the position of the vanadium ion on the {VM(17)}-type shell, which was corroborated by EPR and theoretical studies. 相似文献
983.
Two nanotubular metal-organic frameworks (MOFs), {Cu(L1)·2H(2)O·1.5DMF}(∞) (1) and {Cu(2)(L2)(2)(H(2)O)(2)·7H(2)O·3DMF}(∞) (2), with novel topologies have been constructed based on Cu(2+), 5-(pyridin-4-yl)isophthalic acid (L1) and 5-(pyridin-3-yl)isophthalic acid (L2), respectively. Two MOFs were characterized by IR spectroscopy, thermogravimetry, single-crystal, and powder X-ray diffraction methods. Network analysis reveals a two-nodal (3,6)-connected (4·6(2))(2)(4(2)·6(10)·8(3)) net and a three-nodal (3,4)-connected (4·8(2))(4)(4(2)·8(2)·10(2))(2)(8(4)·12(2)) net. Interpenetration is inherently prevented by both of the topologies of the frameworks. The porosity of MOF 1 was confirmed by N(2) and CO(2) gas adsorption investigations. MOF 1 exhibits remarkable hydrogen sorption hysteresis at low pressure and a H(2) uptake capacity of 1.05 wt% at 77 K and 1 atm. 相似文献
984.
Mass spectra were recorded for (2 + n) resonance enhanced multiphoton ionization (REMPI) of HCl as a function of resonance excitation energy in the 88865-89285 cm(-1) region to obtain two-dimensional REMPI data. Band spectra due to two-photon resonance transitions to number of Rydberg states (Ω' = 0, 1, and 2) and the ion-pair state V((1)Σ(+)(Ω' = 0)) for H(35)Cl and H(37)Cl were identified, assigned, and analyzed with respect to Rydberg to ion-pair interactions. Perturbations show as line-, hence energy level-, shifts, as well as ion signal intensity variations with rotational quantum numbers, J', which, together, allowed determination of parameters relevant to the nature and strength of the state interactions as well as dissociation and ionization processes. Whereas near-resonance, level-to-level, interactions are found to be dominant in heterogeneous state interactions (ΔΩ ≠ 0) significant off-resonance interactions are observed in homogeneous interactions (ΔΩ = 0). The alterations in Cl(+) and HCl(+) signal intensities prove to be very useful for spectra assignments. Data relevant to excitations to the j(3)Σ(0(+)) Rydberg states and comparison with (3 + n) REMPI spectra allowed reassignment of corresponding spectra peaks. A band previously assigned to an Ω = 0 Rydberg state was reassigned to an Ω = 2 state (ν(0) = 88957.6 cm(-1)). 相似文献
985.
The nature of the lowest energy optical transition for the complexes (η(6)-naphthalene)Cr(CO)(3) and (η(6)-phenanthrene)Cr(CO)(3) in the solid state has been investigated by Raman spectroscopy using a range of different excitation wavelengths progressively approaching the resonant condition. Examination of the resonantly enhanced Raman modes confirms that the first absorption is attributed predominantly to a metal-to-arene charge transfer transition for both complexes. A notable difference in the photochemistry of the two complexes was observed. In the case of the phenanthrene complex, population of the lowest energy excited state leads to a photochemical process which resulted in the loss of the arene ligand and formation of Cr(CO)(6). 相似文献
986.
Zheng H Wang Q Long Y Zhang H Huang X Zhu R 《Chemical communications (Cambridge, England)》2011,47(38):10650-10652
Blue luminescent reduced state carbon dots were prepared by reducing carbon dots with NaBH(4). The quantum yield of the reduced state carbon dots increased from 2% to 24% and the maximum emission wavelength shifted from 520 to 450 nm. This offers a simple pathway to enhance the luminescence of carbon dots. 相似文献
987.
Cheng X Jia H Long T Feng J Qin J Li Z 《Chemical communications (Cambridge, England)》2011,47(43):11978-11980
A new design strategy for the development of fluorescent turn-on chemodosimeters toward OCl(-) was proposed by the removal, but not the general inhibition, of the C=N isomerization. Accordingly, Flu-1 was prepared, which, as shown in the fluorescent picture, exhibited the off-on response for OCl(-), sensitively and selectively. 相似文献
988.
Shi W Wang Q Long Y Cheng Z Chen S Zheng H Huang Y 《Chemical communications (Cambridge, England)》2011,47(23):6695-6697
Carbon nanodots (C-Dots) were found to possess intrinsic peroxidase-like activity, and could catalytically oxidize 3,3',5,5'-tetramethylbenzidine (TMB) by H(2)O(2) to produce a colour reaction. This offers a simple, sensitive and selective colorimetric method for glucose determination in serum. 相似文献
989.
Zheng X Zhang L Li J Luo S Cheng JP 《Chemical communications (Cambridge, England)》2011,47(45):12325-12327
Magnetic polyoxometalates (POMs) are obtained by a simple sonication between functionalized magnetic nanoparticles and polyoxometalates. This material can be used not only as a highly active acid catalyst, but also as a catalyst support for chiral amines. 相似文献
990.
Li D Yang Z Zhao G Long Y Lv B Li C Hiew S Ng MT Guo J Tan H Zhang H Li T 《Chemical communications (Cambridge, England)》2011,47(26):7479-7481
It is demonstrated that the shapes and magnitudes of DNA writhe can be precisely manipulated solely through maneuvering the nucleotide sequence of DNA and without the assistance of topoisomerases. 相似文献