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1.
Science China Chemistry - Secrecy has received tremendous attention in modern information society. Innovative polymer-based fluorescent materials with multiple mode emission are quite desirable to... 相似文献
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Minxia Huang Beiyang Yao Manhua Jiang Fuzhou Sun Jinsong You Fangfang Huang Yanping Zhao Shuming Wu Xinqian He Xuezhi Song 《Journal of mass spectrometry : JMS》2022,57(4):e4821
Two unknown solution degradants were found during the dissolution testing in 0.1-M HCl for olmesartan medoxomil (OLM) tablets. The structure of the degradants was identified and characterized by liquid chromatography–ultraviolet (LC–UV), liquid chromatography with tandem mass spectrometry (LC–MS/MS), and nuclear magnetic resonance (NMR) and demonstrated to be cyclization of tetrazole and benzene in the olmesartan (OL) and OLM structures. A series of studies including stress studies, simulation studies, and mechanism-based studies were performed to reveal the potential mechanisms that lead to the formation of the unknown degradants. The study results demonstrated that the degradation was catalyzed with radicals that originated from the metal ions leached from the inner surface of high-performance liquid chromatography (HPLC) glass vials with dissolved oxygen under acidic condition. Prerinsing the glass vials with acidic solution dissolved with EDTA can effectively avoid the generation of such oxidative impurities. The present work provides new insights into the understanding of degradation pathways of OLM, which might support the development of OLM tablets. 相似文献
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Let L be a second order positive, elliptic differential operator that is self-adjoint with respect to some C~∞ density dx on a compact connected manifold M. We proved that if 0 α 1,α/2 s α and f ∈ H~s(M) then the fractional Schr?dinger propagator e~(it Lα/2) on M satisfies e~(it Lα/2) f(x)-f(x) = o(t~(s/α-ε)) almost everywhere as t → 0~+, for any ε 0. 相似文献
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In this paper, the authors study the multiplicity of solutions to the weighted p-Laplacian with isolated singularity and di?usion suppressed by convection ?div(|x|α|?u|p?2?u) + λ 1/|x|β |?u|p?2?u · x = |x|γg(|x|) in B \ {0} subject to nonlinear Robin boundary value condition |x|α|?u|p?2?u · ?n = A ? ρu on ?B,where λ > 0, B ? RN(N ≥ 2) is the unit ball centered at the origin, α > 0, p > 1, β ∈ R, γ > ?N, g ∈ C([0,1]) with g(0) > 0, A ∈ R, ρ > 0 and ?n is the unit outward normal. The same problem with di?usion promoted by convection, namely λ ≤ 0, has already been discussed by the last two authors (Song-Yin (2012)), where the existence, nonexistence and classi?cation of singularities for solutions are presented. Completely di?erent from [Song, H. J. and Yin, J. X., Removable isolated singularities of solutions to the weighted p-Laplacian with singular convection, Math. Meth. Appl. Sci., 35, 2012, 1089–1100], in the present case λ > 0, namely the di?usion is suppressed by the convection, non-singular solutions are not only existent but also may be in?nite which vary according only to the values of solutions at the isolated singular point. At the same time, the singular solutions may exist only if the di?usion dominates the convection. 相似文献
6.
Yi Lanhua Hu You Fei Junjie Li Juan Yang Chunguang Wang Xianyou 《Journal of Solid State Electrochemistry》2019,23(6):1739-1748
Journal of Solid State Electrochemistry - Pd/C and Pd-Co/C nanocatalysts are prepared via a simple and environmentally friendly method and are used as anodic catalyst for direct... 相似文献
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Marie‐Claire Giel Christopher J. Smedley Emily R. R. Mackie Taijie Guo Jiajia Dong Tatiana P. Soares da Costa John E. Moses 《Angewandte Chemie (International ed. in English)》2020,59(3):1181-1186
The boom in growth of 1,4‐disubstituted triazole products, in particular, since the early 2000’s, can be largely attributed to the birth of click chemistry and the discovery of the CuI‐catalyzed azide–alkyne cycloaddition (CuAAC). Yet the synthesis of relatively simple, albeit important, 1‐substituted‐1,2,3‐triazoles has been surprisingly more challenging. Reported here is a straightforward and scalable click‐inspired protocol for the synthesis of 1‐substituted‐1,2,3‐triazoles from organic azides and the bench stable acetylene surrogate ethenesulfonyl fluoride (ESF). The new transformation tolerates a wide selection of substrates and proceeds smoothly under metal‐free conditions to give the products in excellent yield. Under controlled acidic conditions, the 1‐substituted‐1,2,3‐triazole products undergo a Michael addition reaction with a second equivalent of ESF to give the unprecedented 1‐substituted triazolium sulfonyl fluoride salts. 相似文献
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Nature of Bonding in Bowl‐Like B36 Cluster Revisited: Concentric (6π+18π) Double Aromaticity and Reason for the Preference of a Hexagonal Hole in a Central Location 下载免费PDF全文
The bowl‐shaped C6v B36 cluster with a central hexagon hole is considered an ideal molecular model for low‐dimensional boron‐based nanosystems. Owing to the electron deficiency of boron, chemical bonding in the B36 cluster is intriguing, complicated, and has remained elusive despite a couple of papers in the literature. Herein, a bonding analysis is given through canonical molecular orbitals (CMOs) and adaptive natural density partitioning (AdNDP), further aided by natural bond orbital (NBO) analysis and orbital composition calculations. The concerted computational data establish the idea of concentric double π aromaticity for the B36 cluster, with inner 6π and outer 18π electron counting, which both conform to the (4n+2) Hückel rule. The updated bonding picture differs from existing knowledge of the system. A refined bonding model is also proposed for coronene, of which the B36 cluster is an inorganic analogue. It is further shown that concentric double π aromaticity in the B36 cluster is retained and spatially fixed, irrespective of the migration of the hexagonal hole; the latter process changes the system energetically. The hexagonal hole is a destabilizing factor for σ/π CMOs. The central hexagon hole affects substantially fewer CMOs, thus making the bowl‐shaped C6v B36 cluster the global minimum. 相似文献
10.
Joji Tanaka Satu Hkkinen Parker T. Boeck Yidan Cong Sbastien Perrier Sergei S. Sheiko Wei You 《Angewandte Chemie (International ed. in English)》2020,59(18):7203-7208
An orthogonal combination of cationic and radical RAFT polymerizations is used to synthesize bottlebrush polymers using two distinct RAFT agents. Selective consumption of the first RAFT agent is used to control the cationic RAFT polymerization of a vinyl ether monomer bearing a secondary dormant RAFT agent, which subsequently allows side‐chain polymers to be grafted from the pendant RAFT agent by a radical‐mediated RAFT polymerization of a different monomer, thus completing the synthesis of bottlebrush polymers. The high efficiency and selectivity of the cationic and radical RAFT polymerizations allow both polymerizations to be conducted in one‐pot tandem without intermediate purification. 相似文献