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711.
712.
Julia G. Knapp Dr. Xijun Wang Dr. Andrew S. Rosen Xingjie Wang Dr. Xinyi Gong Dr. Matthew Schneider Dr. Tatyana Elkin Dr. Kent O. Kirlikovali Dr. Melissa Fairley Dr. Matthew D. Krzyaniak Prof. Michael R. Wasielewski Prof. Nathan C. Gianneschi Prof. Randall Q. Snurr Prof. Omar K. Farha 《Angewandte Chemie (International ed. in English)》2023,62(29):e202305526
The interactions between uranium and non-innocent organic species are an essential component of fundamental uranium redox chemistry. However, they have seldom been explored in the context of multidimensional, porous materials. Uranium-based metal–organic frameworks (MOFs) offer a new angle to study these interactions, as these self-assembled species stabilize uranium species through immobilization by organic linkers within a crystalline framework, while potentially providing a method for adjusting metal oxidation state through coordination of non-innocent linkers. We report the synthesis of the MOF NU-1700 , assembled from U4+-paddlewheel nodes and catecholate-based linkers. We propose this highly unusual structure, which contains two U4+ ions in a paddlewheel built from four linkers—a first among uranium materials—as a result of extensive characterization via powder X-ray diffraction (PXRD), sorption, transmission electron microscopy (TEM), and thermogravimetric analysis (TGA), in addition to density functional theory (DFT) calculations. 相似文献
713.
Dr. Raju Bej Dr. Chuanxiong Nie Dr. Kai Ludwig Dr. Vahid Ahmadi Dr. Jakob Trimpert Julia M. Adler Dr. Tatyana L. Povolotsky Dr. Katharina Achazi Marten Kagelmacher Ricardo Martin Vidal Dr. Jens Dernedde Dr. Benedikt B. Kaufer Prof. Dr. Rainer Haag 《Angewandte Chemie (International ed. in English)》2023,62(29):e202304010
Mucins are the key component of the defensive mucus barrier. They are extended fibers of very high molecular weight with diverse biological functions depending strongly on their specific structural parameters. Here, we present a mucin-inspired nanostructure, produced via a synthetic methodology to prepare methacrylate-based dendronized polysulfates ( MIP-1 ) on a multi gram-scale with high molecular weight (MW=450 kDa) and thiol end-functionalized mucin-inspired polymer ( MIP ) via RAFT polymerization. Cryo-electron tomography (Cryo-ET) analysis of MIP-1 confirmed a mucin-mimetic wormlike single-chain fiber structure (length=144±59 nm) in aqueous solution. This biocompatible fiber showed promising activity against SARS-CoV-2 and its mutant strain, with a remarkable low half maximal (IC50) inhibitory concentration (IC50=10.0 nM). Additionally, we investigate the impact of fiber length on SARS-CoV-2 inhibition by testing other functional polymers ( MIPs ) of varying fiber lengths. 相似文献
714.
715.
Boris I. Nakhmanovich Tatyana N. Prudskova Alexander A. Arest‐Yakubovich Axel H. E. Müller 《Macromolecular rapid communications》2001,22(15):1243-1248
Living potassium poly(N,N‐dimethylacrylamide) initiates the polymerization of styrene and butadiene, and adds 1,1‐diphenylethylene in THF solution. The model compound α‐potassio‐N,N‐dimethylpropionamide also polymerizes styrene and butadiene in contrast to esterenolates, which are known to be incapable of such reactions. The IR spectra and SEC traces of the polymers obtained unequivocally prove that styrene and butadiene initiation proceeds directly via the amidoenolate anion. Apparently, this is the first case observed where the polymerization of a nonpolar monomer can be initiated by the growing chain end of a polar polymer. 相似文献
716.
Eugene R. Zubarev Raissa V. Talroze Tatyana I. Yuranova Victor N. Vasilets Nicolai A. Plat 《Macromolecular rapid communications》1996,17(1):43-49
The influence of crosslinking conditions (γ-radiation-induced and chemical crosslinking above and below the clearing point) on the phase behavior of a liquid-crystalline polyacrylate-based elastomer is shown and discussed. The network formation in samples γ-irradiated in the nematic phase results in an increase of the clearing point Tn-i which does not depend on the crosslinking density expressed as the ratio of weight-average molecular weight over number-average molecular weight between crosslinks M w/M c within a wide M w/M c range. The distorting action of the crosslinking agent at the same temperature leads to the opposite tendency in the change of Tn-i. Crosslinking in the isotropic phase shows a strong decrease in Tn-i. 相似文献
717.
Nataliya Kutsevol Tatyana Zheltonozhskaya Nataliya Melnik Jean-Michel Guenet Vladimir Syromyatnikov 《Macromolecular Symposia》2003,203(1):201-206
Conformational changes have been studied in intramolecular polymer-polymer complexes (intraPC) of graft copolymers of poly(acrylamide) and poly(vinyl alcohol) (PVA-g-PAA) with various numbers of grafts (4-42) per molecule as a function of temperature and copolymer concentration. It is shown that the magnitude of conformational change depends on the grafts content while the temperature range over which the conformation changes occur is essentially determined by copolymer concentration. The conformational changes are reversible on heating and cooling. 相似文献
718.
Natalya Permyakova Tatyana Zheltonozhskaya Nikolay Strilchyk Nina Zagdanskaya Lesya Momot Vladimir Syromyatnikov 《Macromolecular Symposia》2003,203(1):247-258
Complex formation in the model three-component system, including polymer-polymer complex of poly(styrene-alt-maleic acid) (PSMA) and poly(ethylene oxide) (PEO), and also silica sol (SiO2) in aqueous solution as a function of molecular weight of PEO and the order of component mixing, were investigated. The degree of binding of PSMA links with PEO and SiO2 as well as the Gibbs energy of formation of the polymer-polymer complex and polymer-colloid complexes were defined. It was shown that the main factor of stabilization of the structure is hydrogen bonds. The conditions of three-component polymer-colloid system are practically independent of the order of component mixing. The spontaneous formation of polymer-colloid complexes between chemically complementary polymers and small dispersed particles is considered as the main reason for the abnormally high binding ability of colloid particles to the polymer-polymer complex. 相似文献
719.
Tatyana S. Zyubina Alexander S. Zyubin Lyubov A. Frolova Rostislav V. Pisarev Anna V. Pisareva Yury A. Dobrovolsky 《中国化学会会志》2023,70(3):432-438
The influence of the composition of oxides supports on the specific electroactive surface area of Pt in the catalysts, the platinum nanoparticles dispersion, and Pt contents in the catalysts was studied. The Sb-doped SnO2 oxides with various Sb-doping levels were prepared as a supports of platinum catalysts in polymer electrolyte membrane fuel cells. Density functional theory simulation of Ti, Sb, and Ru doping of tin dioxide and interaction of the doped surfaces with platinum cluster Pt19 have been carried out. All calculations were performed in PBE exchange–correlation functional, with periodic boundary conditions and projector-augmented waves (PAW) basis set. The calculation results were compared with the experimental data X-ray diffraction and transmission electron microscopy (TEM). It was shown that Sb doping of tin dioxide (in quantity of less than 10%, that is, the quantity which cannot provoke significant defects of crystal structure of the supports) leads to a significant increase in a number of platinum clusters adsorbed from the colloidal solution onto the supports surface which results to an increase of the platinum cluster interaction with the supports. The calculated and experimental results are in close fit. 相似文献
720.
Ol'ga Demchenko Nataliya Kutsevol Tatyana Zheltonozhskaya Vladimir Syromyatnikov 《Macromolecular Symposia》2001,166(1):117-122
The issue of applying the usual concepts of polymer compatibility to nonstoichiometric PVA/PAA mixtures of chemically complementary poly(vinyl alcohol) and poly(acrylamide), which form in water solution InterPC (intermolecular polymer complex) stabilyzed by H‐bonds, and PAA to PVA graft copolymers (PVA‐PAAN) with different grafted chains number N, that are IntraPC (intramolecular polymer complexes) is discussed. PVA and PAA are compatible on molecular level. At the same time PVA/PAA mixture (50/50 W/W) is characterized by heterogeneous structure consists of InterPC with ϕchar=9gPVA/gPAA and the excess of unconnected PAA. In the case of IntraPC, yet, only PVA‐PAAN, where N=25, is characterized by a single glass transition temperature (Tg). At larger values of N separate PAA domains form giving rise to the corresponding Tg. These results are discussed in view of IntraPC structure peculiarities as a function of N investigated by IR spectroscopy. 相似文献