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991.
del Puerto E Sánchez-Cortés S García-Ramos JV Domingo C 《Chemical communications (Cambridge, England)》2011,47(6):1854-1856
A possibility of getting SERS spectra of insoluble aromatic compounds in colloidal silver solutions is described. The method tested for the organic pigment quinacridone quinone consists of dispersing it in calix[n]arenes. The potentials of such cavitands, both as dispersing and as silver functionalization agents, is reported as a function of the substitution in their lower rim and their cavity size. 相似文献
992.
Castelaín M Salavagione HJ Gómez R Segura JL 《Chemical communications (Cambridge, England)》2011,47(27):7677-7679
Hybrid materials composed of graphene and conjugated poly(fluorene-alt-phenylene) endowed with redox-active anthraquinone moieties are prepared. Remarkable changes in the electronic properties of the polymer are observed. Effective interactions among the pendant anthraquinone and graphene, likely due to π-π stacking, are confirmed. 相似文献
993.
Giust D Albasanz JL Martín M Marega R Delforge A Bonifazi D 《Chemical communications (Cambridge, England)》2011,47(38):10617-10619
Here we report on the surface immobilization of redox-active [60]fullerene derivatives and the consequent neuroprotective effects toward l-glutamate induced excitotoxicity in human derived undifferentiated neuroblastoma cells. 相似文献
994.
Pieters G Gaucher A Prim D Besson T Giner Planas J Teixidor F Viñas C Light ME Hursthouse MB 《Chemical communications (Cambridge, England)》2011,47(27):7725-7727
Valuable amino benzo[g,h,i]perylenes have been obtained through a one pot electrophilic aromatic substitution--Scholl reaction sequence. Novel molecular architectures combining 3D-o-carborane and planar amino benzo[g,h,i]perylene units are described. Photophysical properties of amino benzo[g,h,i]perylene and the carborane-appended derivatives are discussed. 相似文献
995.
Márquez JM Martínez-Castro E Gabrielli S López Ó Maya I Angulo M Álvarez E Fernández-Bolaños JG 《Chemical communications (Cambridge, England)》2011,47(19):5617-5619
We report the synthesis of the hitherto unknown zwitterionic alkoxyamino cyanoboranes by reduction of O-alkyloximes with sodium cyanoborohydride; unprecedented cyanoboronated N-alkoxyformamidines were also isolated as by-products. Boronated alkoxyamines were found to be efficient cyanoborane transfer agents towards more basic amines, including aminosugars; they were also successfully transformed into neoglycoconjugates by the neoglycorandomization reaction with reducing sugars. 相似文献
996.
Boudreau J Courtemanche MA Fontaine FG 《Chemical communications (Cambridge, England)》2011,47(39):11131-11133
Species R(2)PCH(2)AlMe(2) (R = Me, Ph) are stable Lewis adducts but still react with CO(2) both in solution and in the solid state. The CO(2) adducts undergo a rearrangement unprecedented for ambiphilic molecules to form aluminium carboxylates. A new spirocyclic compound was also obtained by double Lewis pair activation of CO(2). 相似文献
997.
Several pure and Ag-doped gold surfaces were used as models of nanoporous gold catalysts where O(2) was suggested to be activated. Density functional theory (DFT) calculations show that residual Ag on Au is able to promote adsorption and to dissociate thermodynamically favorable O(2) with high rate constants. 相似文献
998.
Rodrigo E Morales S Duce S Ruano JL Cid MB 《Chemical communications (Cambridge, England)》2011,47(40):11267-11269
Heteroarylvinyl sulfone 1 has been successfully used as a new sulfonyl Michael acceptor in aminocatalytic reactions with branched aldehydes. Subsequent one-pot Julia-Kocienski olefination allows the challenging preparation of enantiomerically pure α-allylated aldehydes bearing C-α quaternary carbons. 相似文献
999.
Blanca Rojas de Gáscue José Luis Prin Gilma Hernández Enrique M. Vallés Arnaldo T. Lorenzo Alejandro J. Müller 《Journal of Thermal Analysis and Calorimetry》2011,103(2):669-678
The application of the Successive Self-nucleation and Annealing (SSA) thermal fractionation technique can yield detailed information
of the structural changes induced in linear polyethylene by irradiation. The production of tertiary carbons during the crosslinking
reactions can be equivalent to the structural heterogeneity present in branched polyethylenes since in both cases interruption
of the linear crystallizable sequences occurs, and these are structural differences that can be easily detected by thermal
fractionation. We demonstrate how correlations between melting point and short chain branching content employed for branched
polymers can be useful to characterize the distribution of chain heterogeneity produced by crosslinking. As the radiation
dose is increased and the crosslinking content also increases, the distribution of chain heterogeneity gets broader as detected
by SSA. When the results are coupled with morphological observations made by transmission electron microscopy, valuable information
on the morphological changes produced by crosslinking can also be ascertained, since the distribution of lamellar thicknesses
substantially broadens with crosslinking. Such a broad distribution can also be predicted from SSA by simple calculations
performed employing a modified version of the Gibbs–Thomson equation and is expected on the basis of random crosslinking reactions. 相似文献
1000.
Machado AE Gomes WR Araújo DM Miglio HS Ueno LT De Paula R Cavaleiro JA Barbosa Neto NM 《Molecules (Basel, Switzerland)》2011,16(7):5807-5821
An imidazolium tetrasubstituted cationic porphyrin derivative (the free base and its Zn(II) complex) with five-membered heterocyclic groups in the meso-positions were synthesized using microwave irradiation, and the compounds obtained characterized by (1)H-NMR and mass spectrometry. We observed that under microwave irradiation the yield is similar to when the synthesis is performed under conventional heating, however, the time required to prepare the porphyrins decreases enormously. In order to investigate the electronic state of these compounds, we employed UV-Vis and fluorescence spectroscopy combined with quantum chemical calculations. The results reveal the presence, in both compounds, of a large number of electronic states involving the association between the Soret and a blue-shifted band. The Soret band in both compounds also shows a considerable solvent dependence. As for emission, these compounds present low quantum yield at room temperature and no solvent influence on the fluorescence spectra was observed. 相似文献