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301.
Dragos Astanei François Faubert Stéphane Pellerin Bogdan Hnatiuc Maxime Wartel 《Plasma Chemistry and Plasma Processing》2018,38(5):1115-1132
The ignition sparks provided by the conventional spark plug do not always ensure a fast and complete combustion of the hydrocarbon-air mixture. For this reason, we offer a new type of plug with a double spark using two simultaneous discharges generated by a pulsed high voltage-power supply. This work presents the comparison of two spark plugs, a classical one and a double spark plug, by analyzing the unburned hydrocarbon gases from the exhaust pipe of the engine. For a first gasoline engine, we measure the oxygen concentration in the exhaust gases with a lambda probe and the unburned hydrocarbon by the use of GC–MS coupled with SPME extraction technique. We can observe a clear decrease of total unburned hydrocarbon (THC). For a second motor test bench, powered with propane, we complete measures in function of air/fuel ratio of the THC, NOx, CO2 and CO. These results confirm that we obtained a better combustion especially for leaner mixtures. 相似文献
302.
Well‐Defined Dinuclear Gold Complexes for Preorganization‐Induced Selective Dual Gold Catalysis
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Vincent Vreeken Dr. Daniël L. J. Broere Anne C. H. Jans Marianne Lankelma Prof. Dr. Joost N. H. Reek Dr. Maxime A. Siegler Dr. Jarl Ivar van der Vlugt 《Angewandte Chemie (International ed. in English)》2016,55(34):10042-10046
The synthesis, reactivity, and potential of well‐defined dinuclear gold complexes as precursors for dual gold catalysis are explored. Using the preorganizing abilities of the ditopic PNHPiPr ( LH ) ligand, dinuclear AuI–AuI complex 1 and mixed‐valent AuI–AuIII complex 2 provide access to structurally characterized chlorido‐bridged cationic species 3 and 4 upon halide abstraction. For 2 , this transformation involves unprecedented two‐electron oxidation of the redox‐active ligand, generating a highly rigidified environment for the Au2 core. Facile reaction with phenylacetylene affords the σ,π‐activated phenylacetylide complex 5 . When applied in the dual gold heterocycloaddition of a urea‐functionalized alkyne, well‐defined precatalyst 3 provides high regioselectivities for the anti‐Markovnikov product, even at low catalyst loadings, and outperforms common mononuclear AuI systems. This proof‐of‐concept demonstrates the benefit of preorganization of two gold centers to enforce selective non‐classical σ,π‐activation with bifunctional substrates. 相似文献
303.
Maxime Daigle Audrey Picard‐Lafond Eliane Soligo Prof. Jean‐François Morin 《Angewandte Chemie (International ed. in English)》2016,55(6):2042-2047
Novel nanographenes were prepared by a photochemical cyclodehydrochlorination (CDHC) reaction. Chlorinated precursors were irradiated in acetone in the presence of a base or in pure benzene and underwent multiple (up to four) regioselective cyclization reactions to provide rigid π‐conjugated molecules. Pure compounds were recovered in good yields by simple filtration at the end of the reaction. The CDHC reaction showed compatibility with both electron‐poor and electron‐rich substrates, thus allowing the synthesis of pyridine‐ and thiophene‐fused nanographenes. It also enabled the synthesis of sterically hindered contorted π‐conjugated molecules without causing full aromatization. A kinetic study showed that the CDHC reaction under the conditions used is a very fast process, and some reactions are completed within minutes. The CDHC reaction thus shows great potential as an alternative to other reactions involving harsher conditions for the preparation of nanographenes. 相似文献
304.
Maxime Beau Sunhee Lee Sooyeon Kim Won‐Sik Han Olivier Jeannin Marc Fourmigu Emmanuel Aubert Enrique Espinosa Ie‐Rang Jeon 《Angewandte Chemie (International ed. in English)》2021,60(1):366-370
Crystal engineering based on σ‐hole interactions is an emerging approach for realization of new materials with higher complexity. Neutral inorganic clusters derived from 1,2‐dicarba‐closo‐dodecaborane, substituted with ‐SeMe, ‐TeMe, and ‐I moieties on both skeletal carbon vertices are experimentally demonstrated herein as outstanding chalcogen‐ and halogen‐bond donors. In particular, these new molecules strongly interact with halide anions in the solid‐state. The halide ions are coordinated by one or two donor groups (μ1‐ and μ2‐coordinations), to stabilize a discrete monomer or dimer motifs to 1D supramolecular zig‐zag chains. Crucially, the observed chalcogen bond and halogen bond interactions feature remarkably short distances and high directionality. Electrostatic potential calculations further demonstrate the efficiency of the carborane derivatives, with Vs,max being similar or even superior to that of reference organic halogen‐bond donors, such as iodopentafluorobenzene. 相似文献
305.
Paiva Alexandre K. S. Pereira Wagner S. Lopes Jos M. Silva Leandro B. Carmo Alessander S. Tarre Ricardo M. Charles-Pierre Maxime Thalhofer Jardel L. Silva Ademir X. 《Journal of Radioanalytical and Nuclear Chemistry》2022,331(2):903-911
Journal of Radioanalytical and Nuclear Chemistry - Conventionally and organically grown vegetables were analyzed with gamma spectrometry, and its activity concentration were obtained for 40K,... 相似文献
306.
Loukiani Savva Dr. Mathieu Fossépré Odysseas Keramidas Alexandros Themistokleous Natalia Rizeq Dr. Nikos Panagiotou Dr. Maxime Leclercq Eliana Nicolaidou Dr. Mathieu Surin Dr. Sophia C. Hayes Dr. Savvas N. Georgiades 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(54):e202201497
Organometallic molecules offer some of the most promising scaffolds for interaction with G-quadruplex nucleic acids. We report the efficient synthesis of a family of organoplatinum(II) complexes, featuring a 2-([2,2′-bipyridin]-6-yl)phenyl tridentate (N∧N∧C) ligand, that incorporates peripheral side-chains aiming at enhancing and diversifying its interaction capabilities. These include a di-isopropyl carbamoyl amide, a morpholine ethylenamide, two enantiomeric proline imides and an oxazole. The binding affinities of the Pt-complexes were evaluated via UV-vis and fluorescence titrations, against 5 topologically-distinct DNA structures, including c-myc G-quadruplex, two telomeric (22AG) G-quadruplexes, a duplex (ds26) and a single-stranded (polyT) DNA. All compounds exhibited binding selectivity in favour of c-myc, with association constants (Ka) in the range of 2–5×105 M−1, lower affinity for both folds of 22AG and for ds26 and negligible affinity for polyT. Remarkable emission enhancements (up to 200-fold) upon addition of excess DNA were demonstrated by a subset of the compounds with c-myc, providing a basis for optical selectivity, since optical response to all other tested DNAs was low. A c-myc DNA-melting experiment showed significant stabilizing abilities for all compounds, with the most potent binder, the morpholine-Pt-complex, exhibiting a ΔTm>30 °C, at 1 : 5 DNA-to-ligand molar ratio. The same study implied contributions of the diverse side-chains to helix stabilization. To gain direct evidence of the nature of the interactions, mixtures of c-myc with the four most promising compounds were studied via UV Resonance Raman (UVRR) spectroscopy, which revealed end-stacking binding mode, combined with interactions of side-chains with loop nucleobase residues. Docking simulations were conducted to provide insights into the binding modes for the same four Pt-compounds, suggesting that the binding preference for two alternative orientations of the c-myc G-quadruplex thymine ‘cap’ (‘open’ vs. ‘closed’), as well as the relative contributions to affinity from end-stacking and H-bonding, are highly dependent on the nature of the interacting Pt-complex side-chain. 相似文献
307.
CH Activation of Benzene by a Photoactivated NiII(azide): Formation of a Transient Nickel Nitrido Complex
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Vincent Vreeken Dr. Maxime A. Siegler Prof. Dr. Bas de Bruin Prof. Dr. Joost N. H. Reek Dr. Martin Lutz Dr. Ir. Jarl Ivar van der Vlugt 《Angewandte Chemie (International ed. in English)》2015,54(24):7055-7059
Photochemical activation of nickel‐azido complex 2 [Ni(N3)(PNP)] (PNHP=2,2′‐di(isopropylphosphino)‐4,4′‐ditolylamine) in neat benzene produces diamagnetic complex 3 [Ni(Ph)(PNPNH)], which is crystallographically characterized. DFT calculations support photoinitiated N2‐loss of the azido complex to generate a rare, transient NiIV nitrido species, which bears significant nitridyl radical character. Subsequent trapping of this nitrido through insertion into the Ni? P bond generates a coordinatively unsaturated NiII imidophosphorane P?N donor. This species shows unprecedented reactivity toward 1,2‐addition of a C? H bond of benzene to form 3 . The structurally characterized chlorido complex 4 [Ni(Cl)(PNPNH)] is generated by reaction of 3 with HCl or by direct photolysis of 2 in chlorobenzene. This is the first report of aromatic C? H bond activation by a trapped transient nitrido species of a late transition metal. 相似文献
308.
We propose a new approximate Bayesian computation (ABC) algorithm that aims at minimizing the number of model runs for reaching a given quality of the posterior approximation. This algorithm automatically determines its sequence of tolerance levels and makes use of an easily interpretable stopping criterion. Moreover, it avoids the problem of particle duplication found when using a MCMC kernel. When applied to a toy example and to a complex social model, our algorithm is 2–8 times faster than the three main sequential ABC algorithms currently available. 相似文献
309.
John A. Medford Jeremiah W. Hubbard François Orange Maxime J.-F. Guinel Barbara O. Calcagno Carlos Rinaldi 《Colloid and polymer science》2014,292(6):1429-1437
We report on the magnetothermal repair of a thermoplastic magnetic nanocomposite consisting of iron oxide nanoparticles embedded in poly(methyl methacrylate) (PMMA). The nanoparticles responded to an applied alternating magnetic field by dissipating heat, raising the nanocomposite temperature to above the glass transition temperature and resulting in the repair of the nanocomposite. This was demonstrated by cutting the nanocomposite and subsequently joining two pieces together under the action of an alternating magnetic field. Examination by optical and transmission electron microscopy of the region where the two pieces were joined demonstrated the healing and disappearance of the interface between both pieces down to the nanoscale. 相似文献