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1.
2.
Thomas S Pookat G Nair SS Daniel M Dymerska B Liebig A Al-Harthi SH Ramanujan RV Anantharaman MR Fidler J Albrecht M 《J Phys Condens Matter》2012,24(25):256004
The magnetic properties of amorphous Fe-Ni-B based metallic glass nanostructures were investigated. The nanostructures underwent a spin-glass transition at temperatures below 100 K and revealed an irreversible temperature following the linear de Almeida-Thouless dependence. When the nanostructures were cooled below 25 K in a magnetic field, they exhibited an exchange bias effect with enhanced coercivity. The observed onset of exchange bias is associated with the coexistence of the spin-glass phase along with the appearance of another spin-glass phase formed by oxidation of the structurally disordered surface layer, displaying a distinct training effect and cooling field dependence. The latter showed a maximum in exchange bias field and coercivity, which is probably due to competing multiple equivalent spin configurations at the boundary between the two spin-glass phases. 相似文献
3.
We construct an explicit intertwining operator L{\mathcal L} between the Schr?dinger group eit \frac\triangle2{e^{it \frac\triangle2}} and the geodesic flow on certain Hilbert spaces of symbols on the cotangent bundle T*X Γ of a compact hyperbolic surface X Γ = Γ\D. We also define Γ-invariant eigendistributions of the geodesic flow PSj, k, nj,-nk{PS_{j, k, \nu_j,-\nu_k}} (Patterson-Sullivan distributions) out of pairs of \triangle{\triangle} -eigenfunctions, generalizing the diagonal case j = k treated in Anantharaman and Zelditch (Ann. Henri Poincaré 8(2):361–426, 2007). The operator L{\mathcal L} maps PSj, k, nj,-nk{PS_{j, k, \nu_j,-\nu_k}} to the Wigner distribution WGj,k{W^{\Gamma}_{j,k}} studied in quantum chaos. We define Hilbert spaces HPS{\mathcal H_{PS}} (whose dual is spanned by {PSj, k, nj,-nk{PS_{j, k, \nu_j,-\nu_k}}}), resp. HW{\mathcal H_W} (whose dual is spanned by {WGj,k}{\{W^{\Gamma}_{j,k}\}}), and show that L{\mathcal L} is a unitary isomorphism from HW ? HPS.{\mathcal H_{W} \to \mathcal H_{PS}.} 相似文献
4.
The stochastic behaviour of lifetimes of a two component system is often primarily influenced by the system structure and by the covariates shared by the components. Any meaningful attempt to model the lifetimes must take into consideration the factors affecting their stochastic behaviour. In particular, for a load share system, we describe a reliability model incorporating both the load share dependence and the effect of observed and unobserved covariates. The model includes a bivariate Weibull to characterize load share, a positive stable distribution to describe frailty, and also incorporates effects of observed covariates. We investigate various interesting reliability properties of this model using cross ratio functions and conditional survivor functions. We implement maximum likelihood estimation of the model parameters and discuss model adequacy and selection. We illustrate our approach using a simulation study. For a real data situation, we demonstrate the superiority of the proposed model that incorporates both load share and frailty effects over competing models that incorporate just one of these effects. An attractive and computationally simple cross‐validation technique is introduced to reconfirm the claim. We conclude with a summary and discussion. 相似文献
5.
The crystal structure of the paraelectric phase of rubidium hydrogen sulfate has been redetermined at room temperature to be monoclinic with a = 14.3503(14), b = 4.6187(4), c = 14.3933(14)?Å, β = 118.03(1)° (space group P21/n). Both the sulfate groups are found to be ordered, unlike in previous reports. The crystal structure of the ferroelectric phase at 200?K belongs to the noncentrosymmetric space group Pn with a = 14.2667(12), b = 4.5878(4), c = 14.2924(12)?Å, β = 118.01(1)°, with distorted sulfate groups. The change in the Rb coordination is discussed in terms of bond-valence-sum calculations. Variable-temperature powder X-ray diffraction patterns at temperatures above 393?K indicate a possible reduction in symmetry, suggesting a phase transition. 相似文献
6.
We study the asymptotic behavior of solutions of the fourth Painlevé equation as the independent variable goes to infinity in its space of (complex) initial values, which is a generalization of phase space described by Okamoto. We show that the limit set of each solution is compact and connected and, moreover, that any solution that is not rational has an infinite number of poles and infinite number of zeros. 相似文献
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8.
A. Stephen K. Hashmi Prof. Dr. Christian Lothschütz Dipl.‐Chem. Martin Ackermann Dipl.‐Chem. René Doepp Dipl.‐Chem. Sankaran Anantharaman Benjamin Marchetti Dipl.‐Chem. Helmut Bertagnolli Prof. Dr. Frank Rominger Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(27):8012-8019
Gold complexes were prepared and investigated as catalysts for the oxidative esterification of aldehydes. Stabilisation by pyridine ligands gave good conversions and the in situ extended X‐ray absorption fine structure (EXAFS) study of the reactions indicated that the reaction mixtures contained only mononuclear gold species. Thus, this is the first proof for a homogeneous gold‐catalysed oxidation reaction; the presence of nanoparticles could be excluded experimentally. 相似文献
9.
R. Murugavel G. Anantharaman D. Krishnamurthy M. Sathiyendiran M. G. Walawalkar 《Journal of Chemical Sciences》2000,112(3):273-290
This article describes the recent results obtained in our laboratory on the interaction of polyfunctional ligands with divalent
alkaline earth metal ions and a few divalent transition metal ions. Treatment of MC12·nH2O (M = Mg, Ca, Sr or Ba) with 2-amino benzoic acid leads to the formation of complexes [Mg(2-aba)2] (1), [Ca(2-aba)2(OH2)3]∞ (2), [Sr(2-aba)2(OH2)2
2·H2O)]∞ (3), [Ba(2-aba)2(OH2)]∞ (4), respectively. While the calcium ions in2 are hepta-coordinated, the strontium and barium ions in3 and4 reveal a coordination number of nine apart from additional metal-metal interactions. Apart from the carboxylate functionality,
the amino group also binds to the metal centres in the case of strontium and barium complexes3 and4. Complexes [Mg(H2O)6(4-aba)2·2H2O] (5), [Ca(4-aba)2(H2O)2] (6) prepared from 4-aminobenzoic acid reveal more open or layered structures. Interaction of 2-mercaptobenzoic acid with MCl2·6H2O (M = Mg, Ca), however, leads to the oxidation of the thiol group resulting in the disulphide 2,2′ -dithiobis(benzoic acid).
New metal-organic framework based hydrogen-bonded porous solids [M(btec) (OH2)4
n·n(C4H12N2)·4nH2O] (btec = 1,2,4,5-benzene tetracarboxylate) (M = Co9; Ni10; Zn11) have been synthesized from 1,2,4,5-benzene tetracarboxylic acid in the presence of piperazine. These compounds are made up
of extensively hydrogen-bonded alternating layers of anionic M-btec co-ordination polymer and piperazinium cations. Compounds2- 11 described herein form polymeric networks in the solid-state with the aid of different coordinating capabilities of the carboxylate
anions hydrogen bonding interactions. 相似文献
10.
The rate constants of O2(1Δg) with aliphatic alcohols, terpenes, unsaturated hydrocarbons, chlorinated hydrocarbons, oxygen, and diamines have been studied in thepresence of NO2. The rate constants for oxygen, 1,2-ethane diamine, and 1,2-propane diamine are (9.9 ± 0.4) × 102, (8.7 ± 0.7) × 104, and (1.4 ± 0.3) × 104 1/mol/s, respectively. The rate constants for all other compounds are less than the oxygen rate constant. 相似文献