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11.
Aspartate‐Based CXCR4 Chemokine Receptor Binding of Cross‐Bridged Tetraazamacrocyclic Copper(II) and Zinc(II) Complexes 下载免费PDF全文
Randall D. Maples Amy N. Cain Dr. Benjamin P. Burke Dr. Jon D. Silversides Dr. Ryan E. Mewis Thomas D'huys Prof. Dominique Schols Prof. Douglas P. Linder Prof. Stephen J. Archibald Prof. Timothy J. Hubin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(36):12916-12930
The CXCR4 chemokine receptor is implicated in a number of diseases including HIV infection and cancer development and metastasis. Previous studies have demonstrated that configurationally restricted bis‐tetraazamacrocyclic metal complexes are high‐affinity CXCR4 antagonists. Here, we present the synthesis of Cu2+ and Zn2+ acetate complexes of six cross‐bridged tetraazamacrocycles to mimic their coordination interaction with the aspartate side chains known to bind them to CXCR4. X‐ray crystal structures for three new Cu2+ acetate complexes and two new Zn2+ acetate complexes demonstrate metal‐ion‐dependent differences in the mode of binding the acetate ligand concomitantly with the requisite cis‐V‐configured cross‐bridged tetraazamacrocyle. Concurrent density functional theory molecular modelling studies produced an energetic rationale for the unexpected [Zn(OAc)(H2O)]+ coordination motif present in all of the Zn2+ cross‐bridged tetraazamacrocycle crystal structures, which differs from the chelating acetate [Zn(OAc)]+ structures of known unbridged and side‐bridged tetraazamacrocyclic Zn2+‐containing CXCR4 antagonists. 相似文献
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Distance geometry is a class of problems where the position of points in space is to be identified by using information about some relative distances between these points. Although continuous approaches are usually employed, problems belonging to this class can be discretized when some particular assumptions are satisfied. These assumptions strongly depend on the order in which the points to be positioned are considered. We discuss new discretization assumptions that are weaker than previously proposed ones, and present a greedy algorithm for an automatic identification of discretization orders. The use of these weaker assumptions motivates the development of a new method for computing point coordinates. Computational experiments show the effectiveness and efficiency of the proposed approaches when applied to protein instances. 相似文献
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A Visible‐Light‐Mediated Radical Smiles Rearrangement and its Application to the Synthesis of a Difluoro‐Substituted Spirocyclic ORL‐1 Antagonist 下载免费PDF全文
Dr. James J. Douglas Haley Albright Martin J. Sevrin Dr. Kevin P. Cole Prof. Corey R. J. Stephenson 《Angewandte Chemie (International ed. in English)》2015,54(49):14898-14902
A visible‐light‐mediated radical Smiles rearrangement has been developed to address the challenging synthesis of the gem‐difluoro group present in an opioid receptor‐like 1 (ORL‐1) antagonist that is currently in development for the treatment of depression and/or obesity. This method enables the direct and efficient introduction of the difluoroethanol motif into a range of aryl and heteroaryl systems, representing a new disconnection for the synthesis of this versatile moiety. When applied to the target compound, the photochemical step could be conducted on 15 g scale using industrially relevant [Ru(bpy)3Cl2] catalyst loadings of 0.01 mol %. This transformation is part of an overall five‐step route to the antagonist that compares favorably to the current synthetic sequence and demonstrates, in this specific case, a clear strategic benefit of photocatalysis. 相似文献
16.
Douglas W. Crandell Shivnath Mazumder P. Andrew Evans Mu-Hyun Baik 《Chemical science》2015,6(12):6896-6900
Density functional theory calculations demonstrate that the reversal of regiochemical outcome of the addition for substituted methyl propiolates in the rhodium-catalyzed [(2 + 2) + 2] carbocyclization with PPh3 and (S)-xyl-binap as ligands is both electronically and sterically controlled. For example, the ester functionality polarizes the alkyne π* orbital to favor overlap of the methyl-substituted terminus of the alkyne with the pπ-orbital of the alkenyl fragment of the rhodacycle during alkyne insertion with PPh3 as the ligand. In contrast, the sterically demanding xyl-binap ligand cannot accommodate the analogous alkyne orientation, thereby forcing insertion to occur at the sterically preferred ester terminus, overriding the electronically preferred orientation for alkyne insertion. 相似文献
17.
Christopher Hoffman Douglas Rizzolo Erik Slivken 《Random Structures and Algorithms》2017,50(3):394-419
Permutations that avoid given patterns are among the most classical objects in combinatorics and have strong connections to many fields of mathematics, computer science and biology. In this paper we study the scaling limits of a random permutation avoiding a pattern of length 3 and their relations to Brownian excursion. Exploring this connection to Brownian excursion allows us to strengthen the recent results of Madras and Pehlivan [25] and Miner and Pak [29] as well as to understand many of the interesting phenomena that had previously gone unexplained. © 2016 Wiley Periodicals, Inc. Random Struct. Alg., 50, 394–419, 2017 相似文献
18.
Hyehwang Kim Dr. Zheng-wang Qu Prof. Dr. Stefan Grimme Nahil Al-Zuhaika Prof. Dr. Douglas W. Stephan 《Angewandte Chemie (International ed. in English)》2023,62(43):e202312587
The phosphino-phosphonium cations of the form [R3PPR′2]+ are labile and provide access to the constituent Lewis acidic and Lewis basic fragments. This permits frustrated Lewis pair-type addition reactions to alkynes, affording unprecedented phosphino-phosphination reactions and giving cations of the form [cis-R3PCHC(R′′)PR′2]+. This reactivity is further adapted to prepare several examples of a rare class of dissymmetric cis-olefin-linked bidentate phosphines. 相似文献
19.
Dr. Soumendu Roy Laura Gravener Prof. Dr. Douglas Philp Dr. Euan R. Kay 《Angewandte Chemie (International ed. in English)》2023,62(22):e202217613
Transient states maintained by energy dissipation are an essential feature of dynamic systems where structures and functions are regulated by fluxes of energy and matter through chemical reaction networks. Perfected in biology, chemically fueled dissipative networks incorporating nanoscale components allow the unique properties of nanomaterials to be bestowed with spatiotemporal adaptability and chemical responsiveness. We report the transient dispersion of gold nanoparticles in water, powered by dissipation of a chemical fuel. A dispersed state that is generated under non-equilibrium conditions permits fully reversible solid–liquid or liquid–liquid phase transfer. The molecular basis of the out-of-equilibrium process is reversible covalent modification of nanoparticle-bound ligands by a simple inorganic activator. Activator consumption by a coupled dissipative reaction network leads to autonomous cycling between phases. The out-of-equilibrium lifetime is tunable by adjusting the pH value, and reversible phase cycling is reproducible over several cycles. 相似文献
20.
Douglas M. Sartore Deyber A. Vargas Medina Marcio D. Bocelli Marcela Jordan-Sinisterra Álvaro J. Santos-Neto Fernando M. Lanças 《Journal of separation science》2023,46(15):2300215
Sample preparation frequently is considered the most critical stage of the analytical workflow. It affects the analytical throughput and costs; moreover, it is the primary source of error and possible sample contamination. To increase efficiency, productivity, and reliability, while minimizing costs and environmental impacts, miniaturization and automation of sample preparation are necessary. Nowadays, several types of liquid-phase and solid-phase microextractions are available, as well as different automatization strategies. Thus, this review summarizes recent developments in automated microextractions coupled with liquid chromatography, from 2016 to 2022. Therefore, outstanding technologies and their main outcomes, as well as miniaturization and automation of sample preparation, are critically analyzed. Focus is given to main microextraction automation strategies, such as flow techniques, robotic systems, and column-switching approaches, reviewing their applications to the determination of small organic molecules in biological, environmental, and food/beverage samples. 相似文献