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71.
Pasi Huovinen Hannah Petersen 《The European Physical Journal A - Hadrons and Nuclei》2012,48(11):1-19
In hybrid models, which combine hydrodynamical and transport approaches to describe different stages of heavy-ion collisions, conversion of fluid to individual particles, particlization, is a non-trivial technical problem. We describe in detail how to find the particlization hypersurface in a 3+1 dimensional model, and how to sample the particle distributions evaluated using the Cooper-Frye procedure to create an ensemble of particles as an initial state for the transport stage. We also discuss the role and magnitude of the negative contributions in the Cooper-Frye procedure. 相似文献
72.
Steffen A. Bass Hannah Petersen Cory Quammen Hal Canary Christopher G. Healey Russell M. Taylor II 《Central European Journal of Physics》2012,10(6):1278-1281
We utilize an event-by-event relativistic hydrodynamic calculation performed at a number of different incident beam energies to investigate the creation of hot and dense QCD matter near the critical point. Using state-of-the-art analysis and visualization tools we demonstrate that each collision event probes QCD matter characterized by a wide range of temperatures and baryo-chemical potentials, making a dynamical response of the system to the vicinity of the critical point very difficult to isolate above the background. 相似文献
73.
Hannah E. Hackney Dr. Marco Paladino Hao Fu Prof. Dr. Dennis G. Hall 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(63):14324-14329
This study describes the synthesis, structure, and photophysical properties of a new luminescent polyaromatic boronic acid scaffold, diazaboryl-naphthyl-ketones (DNKs). These stable compounds display extremely bright fluorescence, aggregation-induced emission, positive solvatochromism, and solid-state fluorescence. DFT calculations and X-ray crystallographic study revealed notable electronic and structural differences between these compounds and the parent diaminonaphthalene (DAN) adducts. Acylation of the DAN system causes a localization of both HOMO and LUMO onto the DNK unit, which validates the negligible influence of the B-aryl substituent. The LUMO energy is lowered, and its shape significantly altered. Photophysical data in solution and the solid state revealed blue-shifted, narrowed, and intense emissions for DNKs (up to 89 % quantum yield). The potential utility of the fluorogenic DNK system was demonstrated with a proof-of-concept for the determination of trace boronic acid contaminants in solid samples, down to one-ppm level, using HPLC with fluorescence detection. This method could be useful in pharmaceutical development for the quantitation of difficult-to-detect and potentially mutagenic residual boronic acid from late cross-coupling reactions in drug syntheses. 相似文献
74.
Flexible and Hierarchical Metal–Organic Framework Composites for High‐Performance Catalysis
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Dr. Ning Huang Hannah Drake Jialuo Li Dr. Jiandong Pang Dr. Ying Wang Shuai Yuan Qi Wang Peiyu Cai Dr. Junsheng Qin Prof. Dr. Hong‐Cai Zhou 《Angewandte Chemie (International ed. in English)》2018,57(29):8916-8920
The development of porous composite materials is of great significance for their potentially improved performance over those of individual components and extensive applications in separation, energy storage, and heterogeneous catalysis. Now mesoporous metal–organic frameworks (MOFs) with macroporous melamine foam (MF) have been integrated using a one‐pot process, generating a series of MOF/MF composite materials with preserved crystallinity, hierarchical porosity, and increased stability over that of melamine foam. The MOF nanocrystals were threaded by the melamine foam networks, resembling a ball‐and‐stick model overall. The resulting MOF/MF composite materials were employed as an effective heterogeneous catalyst for the epoxidation of cholesteryl esters. Combining the advantages of interpenetrative mesoporous and macroporous structures, the MOF/melamine foam composite has higher dispersibility and more accessibility of catalytic sites, exhibiting excellent catalytic performance. 相似文献
75.
76.
John Hannah Richard L. Tolman John D. Karkas Richard Liou Helen C. Perry A. Kirk Field 《Journal of heterocyclic chemistry》1989,26(5):1261-1271
Ganciclovir 2 and 2′-carba-ganciclovir 5a are anti-viral agents differing structurally only in the replacement of an oxygen by a methylene group and yet expressing their biological properties along mechanistically independent pathways. Methoxy, hydroxy and fluoro derivatives of 2′-carba-ganciclovir were prepared to examine the effect of re-introducing a binding site close to that in the original oxa side chain. The cyclic phosphate of carba-ganciclovir was also prepared. 相似文献
77.
A polyclonal antiserum to pentachlorothiophenol-acetic acid-KLH was generated in sheep and assessed by solid phase ELISA. The assessment procedure included use of double checkerboard analysis in the absence and in the presence of analyte loads, estimation of cross reactivities of chlorophenol pesticides, assessment of the effect of pH, Tween 20, and Thames water matrix. The antiserum was highly specific for pentachlorophenol and enabled minimum detection limits of less than 0.2 ng mL–1 in river water matrix. Particularly important was the significant improvement of assay performance in the absence of Tween 20 and at pH 4 and the very low cross reactivity (less than 0.01%) for other commonly used chlorophenols—2,4,5-trichlorophenol and 2,4,6-trichlorophenol, 2-methyl-4-chlorophenoxyacetic acid, and 2,4-dichlorophenoxy acetic acid. The study re-affirms the importance of the judicious choice of hapten derivatives in the synthesis of immunogens and assay reagents for pentachlorophenol analysis by competitive immunoassays. 相似文献
78.
Hannah P. Ferguson Johns Emily E. Harrison Kyla J. Stingley Prof. Marcey L. Waters 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(22):6620-6644
Selective molecular recognition of hydrophilic guests in water plays a fundamental role in a vast number of biological processes, but synthetic mimicry of biomolecular recognition in water still proves challenging both in terms of achieving comparable affinities and selectivities. This Review highlights strategies that have been developed in the field of supramolecular chemistry to selectively and non-covalently bind three classes of biologically relevant molecules: nucleotides, carbohydrates, and amino acids. As several groups have systematically modified receptors for a specific guest, an evolutionary perspective is also provided in some cases. Trends in the most effective binding forces for each class are described, providing insight into selectivity and potential directions for future work. 相似文献
79.
Hannah G. Steeds Dr. Jonathan P. Knowles Dr. Wai L. Yu Dr. Jeffery Richardson Dr. Katie G. Cooper Prof. Kevin I. Booker-Milburn 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(63):14330-14334
A three-step synthesis of the 2-azabicyclo[3.3.1]nonane ring system from simple pyrroles, employing a combined photochemical/palladium-catalysed approach is reported. Substrate scope is broad, allowing the incorporation of a wide range of functionality relevant to medicinal chemistry. Mechanistic studies demonstrate that the process occurs by acid-assisted C−N bond cleavage followed by β-hydride elimination to form a reactive diene, demonstrating that efficient control of what might be considered off-cycle reactions can result in productive tandem catalytic processes. This represents a short and versatile route to the biologically important morphan scaffold. 相似文献