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11.
Marina Sicignano Dr. Rosaria Schettini Luisa Sica Giovanni Pierri Prof. Dr. Francesco De Riccardis Prof. Dr. Irene Izzo Dr. Bholanath Maity Dr. Yury Minenkov Prof. Dr. Luigi Cavallo Dr. Giorgio Della Sala 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(29):7131-7141
The first highly enantioselective arylogous Michael reaction (AMR) of 3-unsubstituted phthalides has been described. This phase-transfer methodology, which uses catalytic amounts of KOH/18-crown-6 catalyst in mesitylene in the presence of N,O-bis(trimethylsilyl)acetamide (BSA), gives access to a broad range of 3-monosubstituted phthalides with high levels of syn diastereoselectivity and good yields, starting from 3-unsubstituted derivatives and diverse α,β-unsaturated carbonyl compounds. The reaction also applies to unactivated 3-alkyl phthalides to afford 3,3-dialkyl derivatives. A plausible mechanism has been suggested. DFT analysis of possible transition states gives a rationale of the high syn diastereoselectivity observed and its correlation with the solvent's dielectric constant. 相似文献
12.
13.
Maria Luisa Spreafico Dip. Matematica 《Annali di Matematica Pura ed Applicata》2001,179(1):295-307
Given a smooth k-variety Y (where k is a field of arbitrary characteristic) and a linear systemL on Y we study the dimension of the singular locus of the general element ofL, both inside and outside the base locus B ofL. We interpret these results from the point of view of the transversality theory, and we improve a result by Speiser about
the not too ramified morphisms. Moreover, we show that our results can be applied in some cases where a criterion by Zhang,
for the smoothness of the general element ofL, fails.
Entrata in Redazione il 15 settembre 1997, e in versione definitiva il 28 ottobre 1999. 相似文献
14.
Luisa Beghin 《Stochastic Processes and their Applications》2018,128(7):2427-2447
We deal with some extensions of the space-fractional diffusion equation, which is satisfied by the density of a stable process (see Mainardi et al. (2001)): the first equation considered here is obtained by adding an exponential differential (or shift) operator expressed in terms of the Riesz–Feller derivative. We prove that this produces a random component in the time-argument of the corresponding stable process, which is represented by the so-called Poisson process with drift. Analogously, if we add, to the space-fractional diffusion equation, a logarithmic differential operator involving the Riesz-derivative, we obtain, as a solution, the transition semigroup of a stable process subordinated by an independent gamma subordinator with drift. Finally, we show that an extension of the space-fractional diffusion equation, containing both the fractional shift operator and the Feller integral, is satisfied by the transition density of the process obtained by time-changing the stable process with an independent linear birth process with drift. 相似文献
15.
Alberto de Juan Dr. Yann Pouillon Dr. Luisa Ruiz‐González Dr. Almudena Torres‐Pardo Dr. Santiago Casado Prof. Dr. Nazario Martín Prof. Dr. Ángel Rubio Dr. Emilio M. Pérez 《Angewandte Chemie (International ed. in English)》2014,53(21):5394-5400
Extensive research has been devoted to the chemical manipulation of carbon nanotubes. The attachment of molecular fragments through covalent‐bond formation produces kinetically stable products, but implies the saturation of some of the C? C double bonds of the nanotubes. Supramolecular modification maintains the structure of the SWNTs but yields labile species. Herein, we present a strategy for the synthesis of mechanically interlocked derivatives of SWNTs (MINTs). In the key rotaxane‐forming step, we employed macrocycle precursors equipped with two π‐extended tetrathiafulvalene SWNT recognition units and terminated with bisalkenes that were closed around the nanotubes through ring‐closing metathesis (RCM). The mechanically interlocked nature of the derivatives was probed by analytical, spectroscopic, and microscopic techniques, as well as by appropriate control experiments. Individual macrocycles were observed by HR STEM to circumscribe the nanotubes. 相似文献
16.
We have studied the ability of an alpha-imino glyoxylamide derived from (S, S)-(+)-pseudoephedrine as a valuable chiral electrophile for the preparation of alpha-amino carbonyl compounds. In this context, the addition of Grignard reagents to the azomethine moiety of this chiral electrophile afforded the expected alpha-amino amide adducts in good yields and diastereoselectivities. Moreover, these adducts have been transformed into enantioenriched alpha-amino ketones by exploiting the ability of pseudoephedrine amides to undergo selective monoaddition to the carbamoyl group with organolithium reagents. 相似文献
17.
Danilo Sciarrone Luisa Schipilliti Carla Ragonese Peter Quinto Tranchida Paola Dugo Giovanni Dugo Luigi Mondello 《Journal of chromatography. A》2010,1217(7):1101-1105
The present research is focused on the determination of the enantiomeric distribution of chiral compounds, contained in mandarin essential oils, by means of conventional chiral gas chromatography with flame ionization detection (enantio-GC-FID); the results attained were compared with those derived from heart-cutting multidimensional GC-mass spectrometry (MDGC/MS), to evaluate the reliability of the monodimensional technique as a tool for quality control. The Deans-switch MDGC system was equipped with two GC ovens, which were connected via a heated transfer line, a flame ionization detector (FID1) in the first dimension and a quadrupole MS as second-dimension detector. The a priori knowledge of potential co-elutions concerning target compounds (an enantiomer and an interfering compound), when using enantio-GC-FID, could enable the use of corrected enantiomer excess values. Correction factors could be calculated through a preliminary GC-FID analysis (using an apolar column), considering the peak areas of the known interferences. The method used for the calculation of a so-called “coelution correction factor” is described, along with some examples. 相似文献
18.
Ramachandra S Schuermann KC Edafe F Belser P Nijhuis CA Reus WF Whitesides GM De Cola L 《Inorganic chemistry》2011,50(5):1581-1591
Two luminescent ruthenium complexes containing tripod-type end groups linked through a rigid spacer to a phenanthroline derivative, able to confer an axial geometry to the complexes, are described. One of the compounds is functionalized with thioacetate groups in order to link the metal complex to metallic surfaces. The photophysical and electrochemical behavior of the complexes are studied in solution and on conductive substrates and, furthermore, self-assembled monolayers are investigated in a junction using gold and an indium gallium eutectic, as electrodes, and by time-resolved confocal microscopy. The results show that the complexes form very stable and well-ordered monolayers because of the tripod system, which can anchor the complex almost perpendicular to the surfaces. 相似文献
19.
20.
Sofia Pessanha Maria Luisa Carvalho Maria Becker Alex von Bohlen 《Spectrochimica Acta Part B: Atomic Spectroscopy》2010
The purpose of this study is to determine the elemental content, namely heavy metals, of samples of vine-leaves, grapes must and wine. In order to assess the influence of the vineyard age on the elemental content throughout the several stages of wine production, elemental determinations of trace elements were made on products obtained from two vineyards aged 6 and 14 years from Douro region. The elemental content of vine-leaves and grapes was determined by Energy Dispersive X-Ray Fluorescence (EDXRF), while analysis of the must and wine was performed by Total Reflection X-ray Fluorescence (TXRF). 相似文献