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111.
测定了二(2,4,4-三甲基戊基)膦酸(BTMPPA)及其稀土配合物Ln(BTMPP)3在4000~50cm^-1光谱区内的FT-IR光谱和部分配合物的激光拉曼光谱,对其谱带进行了经验归属。发现稀土氧键具有较高的离子键特性。由Ln-O伸缩振动频率值算出其近似力常数约8m dyn/nm。 相似文献
112.
Using the connection between periodic complementary binary sequences and difference families given by Bömer and Antweiler [2], we use number theoretic techniques to obtain necessary conditions for their existence when two or three sequences are involved. Our results provide theoretical proof for the nonexistence of PCS3
20(a
i) and settle the open case PCS2
36(a
i) of [2], negatively.Research partially supported by National Security Agency grant #MDA 904-90-H-4008. 相似文献
113.
Xiang Liu 《The European Physical Journal C - Particles and Fields》2008,54(3):471-474
Very recently a new enhancement around 4.05 GeV was observed by the Belle experiment. We discuss some possible assignments
for this enhancement, i.e. the ψ(3S) and D*D̄* molecular states. In these two assignments, Y(4008) can decay into J/ψπ0π0 with a branching ratio comparable with that of Y(4008)→J/ψπ+π-. Thus, one suggests high energy experimentalists to look for Y(4008) in J/ψπ0π0 channel. Furthermore one proposes further experiments to search for the missing channels DD̄, DD̄*+h.c. and especially χcJπ+π-π0 and ηcπ+π-π0, which will be helpful to distinguish the ψ(3S) and D*D̄* molecular state assignments for this new enhancement.
PACS 13.30.Eg 13.75.Lb 相似文献
114.
115.
Tin is a typical residual element in steel and mainly originates from Sn-containing complex iron ore and steel scrap. The segregation of Sn in steel is harmful to the performances of steel. In this paper, the micro-segregation of residual element Sn during the solidification process of boiler and pressure vessel steel by micro-segregation model was studied. The results showed that the micro-segregation degree of Sn reduces apparently with the increase of cooling rate and remarkably deteriorates during the solidification process. When the initial content of C is higher than 0.1%, it will cause the solidification transform of the solid phase converting from the ferrite phase to austenite phase and the significant increase in the micro-segregation degree of Sn. However, increasing the initial contents of Si, Mn, P and S separately has non-significant effects on the micro-segregation degree of Sn. In addition, the improvement of initial content of Sn will lead to the micro-segregation degree decrease of Sn and has an inapparent impact on zero strength temperature and zero ductility temperature of the boiler and pressure vessel steel. 相似文献
116.
Huang Yingping Kun Yao Miaomiao Xiang Manke Jia Aiqing Zhang 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2019,93(6):1182-1191
Russian Journal of Physical Chemistry A - g-C3N4/BiOBr composites were obtained via solvothermal method. XRD, SEM, FTIR, UV–Vis DRS, BET, and BJH methods were used to characterize the... 相似文献
117.
Six new carbonate-bridged Zn2Ln2 cluster complexes derived from salen-type Schiff base ligands [H2La = N, N′-bis(3-methoxysalicylidene)-1,3-diaminopropane and H2Lb = N, N′-bis(3-methoxysalicylidene)- 1,2-diaminoethane] have been synthesized. The bis-imine chain in Schiff base ligands have an obvious influence on the cluster complexes' structures, magnetic and luminescence properties. The carbonate bridging ligand exactly comes from autoimmobilization of carbon dioxide, which may mediate ferromagnetic coupling between Ln3+ ions, favoring magnetocaloric effects and single molecule magnet (SMM) properties. Complexes Zn2Dy2(μ3-CO3)2(La)2(NO3)2(MeOH)2 ( 1 ) and [Zn2Dy2(μ3-CO3)2(Lb)2(NO3)2]·2MeOH ( 2) show field-induced SMM properties; complexes Zn2Tb2(μ3-CO3)2(La)2(NO3)2(MeOH)2 ( 3 ) and [Zn2Tb2(μ3-CO3)2(Lb)2(NO3)2]·2MeOH ( 4 ) display both luminescence and field-induced SMM behaviors; while complexes [Zn2Gd2(μ3-CO3)2(La)2(NO3)2]·2MeOH ( 5 ) and [Zn2Gd2(μ3-CO3)2(Lb)2(NO3)2]·2MeOH ( 6 ) exhibit medium magnetic entropy changes, which are candidates for cryogenic molecular magnetic refrigerants. 相似文献
118.
Xiaojuan Liu Qingqing Wen Prof. Dr. Li Xiang Dr. Xuebing Leng Prof. Dr. Yaofeng Chen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(24):5494-5499
The synthesis and catalytic applications of trivalent rare-earth metal alkyl complexes have been well developed, but the chemistry of divalent rare-earth metal alkyl complexes lagged much behind. Herein, we report the synthesis, structure, and catalytic applications of a samarium(II) monoalkyl complex supported by a β-diketiminato-based tetradentate ligand, [LSmCH(SiMe3)2] (L=[MeC(NDipp)CHC(Me)NCH2CH2N(Me)CH2CH2NMe2]−, Dipp=2,6-(iPr)2C6H3). This complex is synthesized by the salt metathesis reaction of samarium iodide [LSm(μ-I)]2 and KCH(SiMe3)2 in 63 % yield. Its structure is characterized by single-crystal X-ray diffraction, showing a distorted square-pyramid coordination geometry. This samarium(II) monoalkyl complex exhibits high catalytic activity in the hydrosilylation of aryl and methyl-substituted unsymmetrical internal alkynes with secondary hydrosilanes, selectively providing the α-(E) products in high yields. 相似文献
119.
Dr. Xiang Hao Kaixiang Yang Hairong Wang Prof. Feng Peng Prof. Haiyang Yang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(11):4344-4349
Non-Newtonian fluids are ubiquitous in daily life and industrial applications. Herein, we report an intelligent fluidic system integrating two distinct non-Newtonian rheological properties mediated by an autocatalytic enzyme reaction. Associative polyelectrolytes bearing a small amount of ionic and alkyl groups are engineered: by carefully balancing the charge density and the hydrophobic effect, the polymer solutions demonstrate a unique shear thickening property at low pH while shear thinning at high pH. The urea-urease clock reaction is utilized to program a feedback-induced pH change, leading to a strong upturn of the nonlinear viscoelastic properties. As long as the chemical fuel is supplied, two distinct non-Newtonian states can be achieved with a tunable lifetime span. As a proof of concept, we demonstrate how the physical energy-driven nonequilibrium properties can be manipulated by a chemical-fueled process. 相似文献
120.
Yunjie Xiang Suoping Peng Shaohui Zheng 《International journal of quantum chemistry》2020,120(1):e26047
Organic solar cell of silol dithiophene based D2-A-D1-A-D2/PC71BM (D: donor part; A: acceptor part; 1 and 2 denote different units) possesses promising power conversion efficiency. Researchers have studied D2-A-D1-A-D2 molecules carefully, including the effects of the different number of terminal thiophenes, the different central moiety (D1), and the length of the alkyl chain. However, there are few investigations, especially theoretical studies, on the influences of different A (acceptor) units on the properties of D2-A-D1-A-D2 molecule. In the present work, we have designed and modeled five new D2-A-D1-A-D2 (D2 = bithiophene and D1 = silol dithiophene) donors by changing A units (A = diketopyrrolopyrrole, naphtho[1,2-c:5,6-c′]bis[1,2,5]thiadiazole, 5-fluoro-2,1,3-benzoselenadiazole, benzobisthiadiazole, and thiazolo[5,4-d]thiazole). We have applied density functional theory (DFT) and time-dependent DFT to predict their ground-state electronic structures and the UV–vis spectra, and the open circuit voltages (Vocs) of organic solar cells of D2-A-D1-A-D2/PC71BM. Based on the calculated results, we find that bithiophene thiazolo[5,4-d]thiazole siloldithiophene (BTTS) (D2 = bithiophene, A = thiazolo[5,4-d]thiazole, D1 = silol dithiophene) possesses the highest lowest unoccupied molecular orbital (−2.60 eV) and the lowest highest occupied molecular orbital (−5.33 eV) energies, and the strongest absorption in the visible region. Besides, the solar cell of BTTS/PC71BM has the highest Voc of 1.02 V. These results indicate that it may be a promising donor. In contrast, bithiophene benzobisthiadiazole siloldithiophene (BBBS) (A = benzobisthiadiazole) has low absorption strength in the visible region, which indicates that it may not be a suitable donor material. 相似文献