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101.
Ruthenium‐Containing Linear Helicates and Mesocates with Tuneable p53‐Selective Cytotoxicity in Colorectal Cancer Cells
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Dr. Simon J. Allison Dr. David Cooke Francesca S. Davidson Prof. Paul I. P. Elliott Dr. Robert A. Faulkner Hollie B. S. Griffiths Owen J. Harper Omar Hussain Prof. P. Jane Owen‐Lynch Prof. Roger M. Phillips Prof. Craig R. Rice Samantha L. Shepherd Dr. Richard T. Wheelhouse 《Angewandte Chemie (International ed. in English)》2018,57(31):9799-9804
The ligands L1 and L2 both form separable dinuclear double‐stranded helicate and mesocate complexes with RuII. In contrast to clinically approved platinates, the helicate isomer of [Ru2( L1 )2]4+ was preferentially cytotoxic to isogenic cells (HCT116 p53?/?), which lack the critical tumour suppressor gene. The mesocate isomer shows the reverse selectivity, with the achiral isomer being preferentially cytotoxic towards HCT116 p53+/+. Other structurally similar RuII‐containing dinuclear complexes showed very little cytotoxic activity. This study demonstrates that alterations in ligand or isomer can have profound effects on cytotoxicity towards cancer cells of different p53 status and suggests that selectivity can be “tuned” to either genotype. In the search for compounds that can target difficult‐to‐treat tumours that lack the p53 tumour suppressor gene, [Ru2( L1 )2]4+ is a promising compound for further development. 相似文献
102.
103.
Griffiths DV Al-Jeboori MJ Cheong YK Duncanson P Harris JE Salt MC Taylor HV 《Organic & biomolecular chemistry》2008,6(3):577-585
Dialkyl heteroaroylphosphonates based on thiophene, pyrrole or furan have been prepared and their reactions with trimethyl phosphite investigated. Deoxygenation of the carbonyl groups in these heteroaroylphosphonates occurs to give carbene intermediates, which then undergo further reaction. In the case of the furan-3-oylphosphonates and those systems containing a thiophene or pyrrole ring, the major reaction pathway involves intermolecular trapping of the carbene intermediates by the trimethyl phosphite, leading to the formation of ylidic phosphonates that can be readily converted into the corresponding 1,1-bisphosphonates. However, in some furan-2-oylphosphonates the carbenes generated undergo ring-opening to initially give acyclic alkynylphosphonates which may react further to give other novel phosphorus compounds. The effects of substituents on the extent to which intermolecular trapping of the initially formed carbene competes with intramolecular rearrangement has been investigated. The latter process appears to be suppressed by a substituent at the 5-position of the furan ring, the resulting ylidic phosphonates being a rare example of an efficient intermolecular trapping of a furan-2-yl carbene. 相似文献
104.
Kieran?Griffiths Albert?EscuerView authors OrcID profile George?E.?KostakisEmail author 《Structural chemistry》2016,27(6):1703-1714
This article presents the syntheses, crystal structures, topological features and magnetic properties of two NiII/NaI coordination clusters formulated [Ni 3 II Na(L1)3(HL1)(MeOH)2] (1) and [Ni 6 II Na(L1)5(CO3)(MeO)(MeOH)3(H2O)3]·4(MeOH) 2(H2O) [2 4(MeOH) 2(H2O)] where H2L1 is the semi-rigid Schiff base ligand (E)-2-(2-hydroxy-3-methoxybenzylideneamino)-phenol). Compound 1 possesses a rare Ni 3 II NaI cubane (3M4-1) topology, and compound 2 is the first example in polynuclear Ni/Na chemistry that exhibits a 2,3,4M7-1 topology. 相似文献
105.
Martin Griffiths Surajit Rajagopal 《International Journal of Mathematical Education in Science & Technology》2016,47(1):139-144
In this article, we describe the outcome of a mathematical collaboration between a university lecturer and an undergraduate student. The resulting investigation concerned a particular divisibility property of the Fibonacci numbers, and indeed it seems that a new result was found in this regard. An interesting point to be made here is that, although the mathematical content was relatively straightforward, this joint exploration did, in a very modest sense, mirror certain key aspects of the research process. 相似文献
106.
Martin Griffiths Jonny Griffiths 《International Journal of Mathematical Education in Science & Technology》2016,47(2):291-298
We study here a pair of sequences of polynomials that arise from a particular iterated mapping on the plane. We show how these sequences come about, and give some of their interesting mathematical properties. 相似文献
107.
Gonzalo Fiz Pontiveros Simon Griffiths Robert Morris David Saxton Jozef Skokan 《Combinatorica》2016,36(1):71-89
The Ramsey number r(K 3,Q n ) is the smallest integer N such that every red-blue colouring of the edges of the complete graph K N contains either a red n-dimensional hypercube, or a blue triangle. Almost thirty years ago, Burr and Erd?s conjectured that r(K 3,Q n )=2 n+1?1 for every n∈?, but the first non-trivial upper bound was obtained only recently, by Conlon, Fox, Lee and Sudakov, who proved that r(K 3,Q n )?7000·2 n . Here we show that r(K 3,Q n )=(1+o(1))2 n+1 as n→∞. 相似文献
108.
We consider the flavour non-singlet Reggeon within the context of perturbative QCD. This consists of ladders built out of
“reggeized” quarks. We propose a method for the numerical solution of the integro-differential equation for the amplitude
describing the exchange of such a Reggeon. The solution is known to have a sharp rise at low values of Bjorken-x when applied to non-singlet quantities in deep-inelastic scattering. We show that when the running of the coupling is taken
into account this sharp rise is further enhanced, although the dependence is suppressed by the introduction of the running coupling. We also investigate the effects of simulating non-perturbative
physics by introducing a constituent mass for the soft quarks and an effective mass for the soft gluons exchanged in the t-channel.
Received: 30 June 1999 / Published online: 16 November 1999 相似文献
109.
David F. Griffiths 《国际流体数值方法杂志》1997,24(4):393-411
We use a one-dimensional model problem of advection– diffusion to investigate the treatment recently advocated by Papanastasiou and colleagues to deal with boundary conditions at artificial outflow boundaries. Using finite elements of degree p, we show that their treatment is equivalent to imposing the condition that the (p+1 )st derivative of the dependent variable should vanish at a point close to the outflow. This is then shown to lead to errors of order 𝒪((h+1/Pe)1.6p+1) in the numerical solutions (where h is the maximum element size and Pe is the global Peclet number), which is superior to the errors of order 𝒪(hp+1+1/Pe) obtained using a standard no-flux outflow condition. These findings are verified by numerical experiments. © 1997 by John Wiley and Sons, Ltd. 相似文献
110.
NO dissociation and subsequent N2 production in the presence of co-adsorbed S18O2 and D2 on the surface of stepped Pt(3 3 2) were studied using Fourier transform infra red reflection–absorption spectroscopy (FTIR-RAS) combined with thermal desorption spectroscopy (TDS). Reduction of NO by D (D2 is adsorbed dissociatively on Pt surfaces) proceeds to a limited extent, because this reaction is rate-controlled by NO dissociation and the supply of D atoms at the higher surface temperatures at which NO dissociation becomes significant (350 K and higher). NO–D reaction is suppressed in the presence of S18O2, depending significantly on the S18O2 coverage and the competition between the reactions NO–D and S18O2–D. When the supply of D2 is limited, e.g., 0.1 L in this study, the presence of S18O2 suppresses the NO–D reaction. With a sufficient supply of D2, e.g., 0.4 L and higher, D-atom competing reactions do not play a role any more because the reactions of both NO and S18O2 with D proceed only to a very limited extent. As such, generation of O atoms from S18O2 dissociation is the main reaction that leads to the suppression in NO dissociation and consequently, N2 production.It is also concluded that the presence of S18O2 does not seriously poison the active sites on the Pt surface, providing that there is a sufficient D supply to remove O atoms from both NO dissociation and S18O2 dissociation. 相似文献