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71.
Ruben L. Mkrtchyan 《Letters in Mathematical Physics》2016,106(1):57-79
We define “population” of Vogel’s plane as points for which universal character of adjoint representation is regular in the finite plane of its argument. It is shown that they are given exactly by all solutions of seven Diophantine equations of third order on three variables. We find all their solutions: classical series of simple Lie algebras (including an “odd symplectic” one), \({D_{2,1,\lambda}}\) superalgebra, the line of sl(2) algebras, and a number of isolated solutions, including exceptional simple Lie algebras. One of these Diophantine equations, namely \({knm=4k+4n+2m+12,}\) contains all simple Lie algebras, except so\({(2N+1).}\) Among isolated solutions are, besides exceptional simple Lie algebras, so called \({\mathfrak{e}_{7\frac{1}{2}}}\) algebra and also two other similar unidentified objects with positive dimensions. In addition, there are 47 isolated solutions in “unphysical semiplane” with negative dimensions. Isolated solutions mainly belong to the few lines in Vogel plane, including some rows of Freudenthal magic square. Universal dimension formulae have an integer values on all these solutions at least for first three symmetric powers of adjoint representation. 相似文献
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Henriette de Loor Ruben Poesen Wout De Leger Wim Dehaen Patrick Augustijns Pieter Evenepoel Björn Meijers 《Analytica chimica acta》2016
Chronic kidney disease (CKD) is associated with an increased risk of mortality and cardiovascular disease, which is, at least partly, mediated by the accumulation of so-called uremic retention solutes. Although there has been an increasing interest in the behavior of these solutes, derived from both the endogenous and colonic microbial metabolism, methods to simultaneously and accurately measure a broad panel of relevant uremic retention solutes remain scarce. 相似文献
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Sharpe RB Burdinski D Huskens J Zandvliet HJ Reinhoudt DN Poelsema B 《Langmuir : the ACS journal of surfaces and colloids》2007,23(3):1141-1146
Self-assembled monolayers were investigated for their suitability as two-dimensional scaffolds for the selective growth of alkanethiol edge structures. Heterostructures with chemical contrast could be grown, whose dimensions were governed by both the initial pattern sizes and the process time. n-Octadecanethiol (ODT) was made to expand from the edges of 16-mercaptohexadecanoic acid (MHDA) monolayer patterns. Likewise, 11-mercaptoundecanol (MUD) was grown on MHDA and on ODT monolayer edges. The results of these experiments are in accordance with the moving boundary model for monolayer spreading. In addition to such surface-bound spreading, a vapor-phase contribution to lateral monolayer growth was identified. MUD was observed to be an excellent ink for creating chemical contrast by means of regioselective deposition from a vapor phase. As a proof of principle, ribbons of 11-mercaptoundecanol with submicrometer widths were grown on pentaerythritol-tetrakis(3-mercaptopropionate) edges, and submicrometer wide gold lines were produced by subsequent wet-chemical etching. 相似文献
76.
Aaron Moment Ruben Miranda Paula T. Hammond 《Macromolecular rapid communications》1998,19(11):573-579
The synthesis of a new liquid crystalline block copolymer consisting of a polystyrene block and a side-chain liquid crystalline siloxane block is reported. The synthetic approach described is based on the anionic polymerization of styrene and cyclic trimethyltrivinyltrisiloxane monomers, followed by functionalization of the siloxane block with side chain mesogens. The siloxane block has a Tg well below 25°C and is designed to exhibit a chiral smectic C* phase at room temperature. These block copolymers are the first side-chain liquid crystalline block copolymers which contain both a high Tg glassy block and a low Tg liquid crystalline block. 相似文献
77.
An efficient expansion method for the evaluation of VB matrix elements is introduced. The overlaps of VB wave functions of N electrons can be treated as algebrants, i.e., generalized determinants, of N × N matrices. An algebrant can be expanded with subalgebrants of lower orders in a successive way. By choosing Rumer spin bases and appropriately arranging the expansion, it is found that the number of unique subalgebrants involved in the expansion increases in a quite moderate way with N. In contrast to the traditional symmetric group approach, which explicitly utilizes all N! representation matrices, the new strategy incorporates the group theoretical factors in a simple way in the successive expansion. As only the unique subalgebrants are further expanded, the computational effort required by the new strategy scales in a very acceptable manner with the increasing number of electrons. © 1997 John Wiley & Sons, Inc. Int J Quant Chem 62: 245–259, 1997 相似文献
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ABSTRACTThe electronic rearrangements involved in Noyori hydrogenation reactions with double bonds (ethene and formaldehyde) are analysed using the bonding evolution theory. The study and analysis of the changes on the electron localisation function topology along a given reaction path reveals fluxes of electron density, allowing to unambiguously identify the main chemical events happening along the chemical reactions. This analysis shows that the first hydrogen transfer (with hydride character) occurs before the transition state (TS), while the second hydrogen transfer (with proton character) takes places after having reached the TS. The lower energy barrier found for formaldehyde over ethene is explained by two reasons. First, the hydride transfer is favoured for the C?=?O bond over C?=?C due to the electrophilic character of the carbon atom. Second, a negatively charged CH3–X (X?=?CH2, O) hidden intermediate is formed in the proximities of the TS region. The oxygen atom is able to stabilise this negatively charged species more effectively than the CH2 group due to its higher electronegativity and the presence of V(O) lone pairs. The obtained analysis explains and rationalises catalyst chemoselectivity (C?=?O vs. C?=?C). Finally, a curly arrow representation diagram accounting for the electronic rearrangements is proposed on the basis of BET results. 相似文献