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131.
E. N. Brown R. B. Willms G. T. Gray III P. J. Rae C. M. Cady K. S. Vecchio J. Flowers M. Y. Martinez 《Experimental Mechanics》2007,47(3):381-393
The current work presents the characterization and comparison of the mechanical response of three different industrial forms
of polyethylene. Specifically, high-density polyethylene (HDPE), ultra high molecular weight polyethylene (UHMWPE), and cross-linked
polyethylene (PEX) were tested in compression as a function of temperature (−75 to 100°C) and strain-rate (10−4 to 2,600 s−1). The responses of UHMWPE and PEX are very similar, whereas HDPE exhibits some differences. The HDPE samples display a significantly
higher yield stress followed by a flat flow behavior. Conversely UHMWPE and PEX both exhibit significant strain hardening
after yield. The temperature and strain-rate dependence are captured by simple linear and logarithmic fits over the full range
of conditions investigated. The yield behavior is presented in terms of an empirical mapping function that is extended to
analytically solve for the mapping constant. The power-law dependence on strain-rate observed in some polymers is explained
using this mapping function. 相似文献
132.
Lancaster KM Sproules S Palmer JH Richards JH Gray HB 《Journal of the American Chemical Society》2010,132(41):14590-14595
Redox and spectroscopic (electronic absorption, multifrequency electron paramagnetic resonance (EPR), and X-ray absorption) properties together with X-ray crystal structures are reported for the type 2 Cu(II) C112D/M121E variant of Pseudomonas aeruginosa azurin. The results suggest that Cu(II) is constrained from interaction with the proximal glutamate; this structural frustration implies a "rack" mechanism for the 290 mV (vs NHE) reduction potential measured at neutral pH. At high pH (~9), hydrogen bonding in the outer coordination sphere is perturbed to allow axial glutamate ligation to Cu(II), with a decrease in potential to 119 mV. These results highlight the role played by outer-sphere interactions, and the structural constraints they impose, in determining the redox behavior of transition metal protein cofactors. 相似文献
133.
Matthew R. Hartings Igor V. Kurnikov Alexander R. Dunn Jay R. Winkler Harry B. Gray Mark A. Ratner 《Coordination chemistry reviews》2010,254(3-4):248-253
We report a quantitative theoretical analysis of long-range electron transfer through sensitizer wires bound in the active-site channel of cytochrome P450cam. Each sensitizer wire consists of a substrate group with high binding affinity for the enzyme active site connected to a ruthenium-diimine through a bridging aliphatic or aromatic chain. Experiments have revealed a dramatic dependence of electron transfer rates on the chemical composition of both the bridging group and the substrate. Using combined molecular dynamics simulations and electronic coupling calculations, we show that electron tunneling through perfluorinated aromatic bridges is promoted by enhanced superexchange coupling through virtual reduced states. In contrast, electron flow through aliphatic bridges occurs by hole-mediated superexchange. We have found that a small number of wire conformations with strong donor–acceptor couplings can account for the observed electron tunneling rates for sensitizer wires terminated with either ethylbenzene or adamantane. In these instances, the rate is dependent not only on electronic coupling of the donor and acceptor but also on the nuclear motion of the sensitizer wire, necessitating the calculation of average rates over the course of a molecular dynamics simulation. These calculations along with related recent findings have made it possible to analyze the results of many other sensitizer-wire experiments that in turn point to new directions in our attempts to observe reactive intermediates in the catalytic cycles of P450 and other heme enzymes. 相似文献
134.
Benjamin M. Gray Andrew L. Hector William Levason Gillian Reid Michael Webster Wenjian Zhang Marek Jura 《Polyhedron》2010
The reaction of o-C6H4(AsMe2)2 with VCl4 in anhydrous CCl4 produces orange eight-coordinate [VCl4{o-C6H4(AsMe2)2}2], whilst in CH2Cl2 the product is the brown, six-coordinate [VCl4{o-C6H4(AsMe2)2}]. In dilute CH2Cl2 solution slow decomposition occurs to form the VIII complex [V2Cl6{o-C6H4(AsMe2)2}2]. Six-coordination is also found in [VCl4{MeC(CH2AsMe2)3}] and [VCl4{Et3As)2]. Hydrolysis of these complexes occurs readily to form vanadyl (VO2+) species, pure samples of which are obtained by reaction of [VOCl2(thf)2(H2O)] with the arsines to form green [VOCl2{o-C6H4(AsMe2)2}], [VOCl2{MeC(CH2AsMe2)3}(H2O)] and [VOCl2(Et3As)2]. Green [VOCl2(o-C6H4(PMe2)2}] is formed from [VOCl2(thf)2(H2O)] and the ligand. The [VOCl2{o-C6H4(PMe2)2}] decomposes in thf solution open to air to form the diphosphine dioxide complex [VO{o-C6H4(P(O)Me2)2}2(H2O)]Cl2, but in contrast, the products formed from similar treatment of [VCl4{o-C6H4(AsMe2)2}x] or [VOCl2{o-C6H4(AsMe2)2}] contain the novel arsenic(V) cation [o-C6H4(AsMe2Cl)(μ-O)(AsMe2)]+. X-ray crystal structures are reported for [V2Cl6{o-C6H4(AsMe2)2}2], [VO(H2O){o-C6H4(P(O)Me2)2}2]Cl2, [o-C6H4(AsMe2Cl)(μ-O)(AsMe2)]Cl·[VO(H2O)3Cl2] and powder neutron diffraction data for [VCl4{o-C6H4(AsMe2)2}2]. 相似文献
135.
Chakhalian J Rondinelli JM Liu J Gray BA Kareev M Moon EJ Prasai N Cohn JL Varela M Tung IC Bedzyk MJ Altendorf SG Strigari F Dabrowski B Tjeng LH Ryan PJ Freeland JW 《Physical review letters》2011,107(11):116805
Using resonant x-ray spectroscopies combined with density functional calculations, we find an asymmetric biaxial strain-induced d-orbital response in ultrathin films of the correlated metal LaNiO3 which are not accessible in the bulk. The sign of the misfit strain governs the stability of an octahedral "breathing" distortion, which, in turn, produces an emergent charge-ordered ground state with an altered ligand-hole density and bond covalency. Control of this new mechanism opens a pathway to rational orbital engineering, providing a platform for artificially designed Mott materials. 相似文献
136.
S.D. Gopal Ram G. Ravi MR. Manikandan T. Mahalingam M. Anbu Kulandainathan 《Superlattices and Microstructures》2011,50(4):296-302
In the present work, a controlled growth of ZnO nanostructures by manipulating Zn metal ion concentration by the chelating action of ethylene diaminetetra acetic acid in hydrothermal method is studied. EDTA produces metal–chelate complex by the formation of bidentate ligand with Zn2+ in the solution and diminishes the reactivity of Zn metal cations. Concentration of EDTA in the mother solution was varied in different ranges like 3, 5 and 10 mM while retaining the zinc metal salt and the NaOH concentration the same. Three different morphologies of wurtzite structured ZnO nanostructures such as nanorods-bunch, separate/discrete uniformly sized hexagonal nanorods and tapered flower petals like shapes are achieved by 3, 5 and 10 mM strengths of EDTA, respectively. The medium concentration 5 mM of EDTA is found to have moderate control over producing ZnO nanostructures of uniform diameter and a high aspect (length to diameter) ratio. An array of vertically aligned free standing ZnO nanorods with uniform spacing is successfully achieved by the addition of 5 mM of EDTA in the mother solution and the same is studied for its fluorescence property at an excitation of 325 nm and it has exhibited a characteristic UV emission of ZnO around 383 nm. 相似文献
137.
J. R. A. Gray 《Applied Categorical Structures》2014,22(5-6):981-1007
We introduce the notion of normalizer as motivated by the classical notion in the category of groups. We show for a semi-abelian category ? that the following conditions are equivalent:
- ? is action representable and normalizers exist in ?;
- the category Mono(?) of monomorphisms in ? is action representable;
- the category ?2 of morphisms in ? is action representable;
- for each category \(\mathbb {D}\) with a finite number of morphisms the category \({\mathbb {C}} ^{\mathbb {D}}\) is action representable.
- ? satisfies the amalgamation property for protosplit normal monomorphism and ? satisfies the axiom of normality of unions;
- for each small category \(\mathbb {D}\) , the category \({\mathbb {C}} ^{\mathbb {D}}\) is action representable.
138.
139.
The present paper begins by deriving an instantaneous formulation for the backward-looking (reinforcement based learning) satisfaction balance model of Gray and Tallman (1984). This model is then used to generate interactional data from four simulated agents in a network interaction experiment. Because this initial model does not generate stable interaction structures in the network experiment, it is altered step by step in the direction of a forward-looking (agent with goals) model that has been shown to generate such stable interaction structures. The purpose of the modifications are to learn what aspects of the forward-looking model are needed to evolve a stable interaction structure, and to learn how these aspects may be incorporated into a model that remains essentially reinforcement based. 相似文献
140.
Joshua P. Gray Md. Nasir Uddin Rajan Chaudhari Margie N. Sutton Hailing Yang Philip Rask Hannah Locke Brian J. Engel Nefeli Batistatou Jing Wang Brian J. Grindel Pratip Bhattacharya Seth T. Gammon Shuxing Zhang David Piwnica-Worms Joshua A. Kritzer Zhen Lu Robert C. Bast Jr. Steven W. Millward 《Chemical science》2021,12(10):3526
In recent decades it has become increasingly clear that induction of autophagy plays an important role in the development of treatment resistance and dormancy in many cancer types. Unfortunately, chloroquine (CQ) and hydroxychloroquine (HCQ), two autophagy inhibitors in clinical trials, suffer from poor pharmacokinetics and high toxicity at therapeutic dosages. This has prompted intense interest in the development of targeted autophagy inhibitors to re-sensitize disease to treatment with minimal impact on normal tissue. We utilized Scanning Unnatural Protease Resistant (SUPR) mRNA display to develop macrocyclic peptides targeting the autophagy protein LC3. The resulting peptides bound LC3A and LC3B—two essential components of the autophagosome maturation machinery—with mid-nanomolar affinities and disrupted protein–protein interactions (PPIs) between LC3 and its binding partners in vitro. The most promising LC3-binding SUPR peptide accessed the cytosol at low micromolar concentrations as measured by chloroalkane penetration assay (CAPA) and inhibited starvation-mediated GFP-LC3 puncta formation in a concentration-dependent manner. LC3-binding SUPR peptides re-sensitized platinum-resistant ovarian cancer cells to cisplatin treatment and triggered accumulation of the adapter protein p62 suggesting decreased autophagic flux through successful disruption of LC3 PPIs in cell culture. In mouse models of metastatic ovarian cancer, treatment with LC3-binding SUPR peptides and carboplatin resulted in almost complete inhibition of tumor growth after four weeks of treatment. These results indicate that SUPR peptide mRNA display can be used to develop cell-penetrating macrocyclic peptides that target and disrupt the autophagic machinery in vitro and in vivo.SUPR peptide mRNA display was used to evolve a cell-permeable, macrocyclic peptide for autophagy inhibition. 相似文献