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131.
Etienne Airiau Thomas Spangenberg Nicolas Girard Dr. Angèle Schoenfelder Jessica Salvadori Maurizio Taddei Prof. André Mann Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2008,14(35):10938-10948
The development of hydroformylative domino reactions of easily accessible vinyl acetamides is described. Extremely regioselective hydroformylation of terminal double bounds provides a transient N‐acyliminium that can be trapped by various nucleophiles to give several aza‐heterocylic scaffolds in a diastereoselective manner. 相似文献
132.
W. Paul G. Gorbach F. Windhaber und Anna Maurizio 《Fresenius' Journal of Analytical Chemistry》1940,119(7-8):298-299
Ohne Zusammenfassung 相似文献
133.
M. Clara Gonçalves Luis M. Fortes Rui M. Almeida Alessandro Chiasera Andrea Chiappini Maurizio Ferrari Shivakiran Bhaktha 《Journal of Sol-Gel Science and Technology》2010,55(1):52-58
Er3+ photoluminescence (PL) and Yb3+ → Er3+ energy transfer (ET) phenomena in the near infrared (NIR) have been studied in three-dimensional (3-D) inverse opal (IO)
structures synthesized by a colloidal/sol–gel route, starting with the deposition of polystyrene microsphere (235 nm and 460 nm
diameter) direct opal templates by convective self-assembly, followed by infiltration of the interstices with Er3+/Yb3+-doped silica, titania and silica-titania sols and heat-removal of the polymeric template material. The crystalline quality
of the IOs has been optimized through suitable substrate treatments, plus the control of temperature and humidity during deposition
of the templates. The structural and optical properties of the 3-D opal and IO structures have been studied by field emission
scanning electron microscopy and visible-NIR reflection spectroscopy, in order to assess the relationship between microstructure
and the photonic properties obtained. Photonic bandgaps have been evidenced by the corresponding stop bands in the reflection
spectra. The shape and the intensity of the Er3+
4I13/2 → 4I15/2 transition at ~1.5 μm were modified in most IOs relatively to similar matrix deposits without a photonic crystal structure,
particularly in the case of pure silica and titania IOs, where the PL peak narrowed and intensified. It was not possible at
this stage to detect Yb3+ → Er3+ ET phenomena in the IOs structures. 相似文献
134.
Maurizio Benaglia Prof. Franco Cozzi Prof. Michele Mancinelli Dr. Andrea Mazzanti Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(25):7456-7468
Four thiophene‐ and furan‐containing [3.3]meta(heterocyclo)paracyclophanes were designed and synthesized to study the intramolecular interaction between standard heteroaromatic rings and tetra‐H‐ or tetra‐F‐substituted benzenes. A complete conformational analysis, carried out by DFT calculations and variable‐temperature NMR techniques, showed that, despite their structural similarity, these adducts have different conformational preferences and undergo different types of isomerizations depending on the nature of the heterocycle. The thiophene‐derived adducts adopted a parallel stacked arrangement of the aromatic systems in the ground‐state conformations. Their isomerization pathways involved a thiophene ring‐flip process passing through an edge‐to‐face arranged transition state in which the heterocycle is perpendicular to the benzene platform and its sulfur atom points toward the center of that ring. The threshold energy barrier to the ring‐flip process was higher by 10 kJ mol?1 in the case of the adduct featuring the perfluorinated benzene. This difference was rationalized by assuming that the ground‐state conformations of the H‐ and F‐substituted compounds have different stability. On the contrary, the furan‐derived adducts were shown by calculations and NMR spectroscopy to adopt, in their ground‐state conformations, a perpendicular edge‐to‐face disposition of the rings with the oxygen atom pointing toward the benzene platform. The adoption of this arrangement was confirmed by X‐ray crystallography. In the case of these compounds, the isomerization process involved distortion of the CH2SCH2 bridges connecting the aromatic systems and the adoption of transition‐state geometries for which the rings were arranged in a parallel‐stacked orientation. Once again a very nice agreement was observed between the predicted and the experimentally determined geometries and pathways. In the case of the furan‐containing compounds, the threshold barriers were found to be much lower in energy that those observed for the thiophene derivatives. Remarkably, they were virtually independent of the presence of fluorine atoms on the platform benzene ring. 相似文献
135.
2-Iodoxybenzoic acid (IBX), a mild and efficient hypervalent iodine oxidant, has been utilised in different reaction conditions to perform several efficient oxidative modifications of flavonoids. Fine-tuning of the reaction conditions allowed remarkably selective modifications of these compounds. At room temperature, IBX proved to be an excellent reagent for a highly regioselective aromatic hydroxylation of monohydroxylated flavanones and flavones, generating the corresponding catecholic derivatives showing high antioxidant activity. At 90 °C, IBX efficiently dehydrogenated a large panel of methoxylated flavanones to their corresponding flavones exhibiting anticancer activity. IBX polystyrene has also been utilised to increase the recovery of highly polar compounds. Following the first oxidation, the reagent was recovered and reused in several runs without loss of efficiency and selectivity. The first example of an application of IBX polystyrene in a dehydrogenation reaction has been described. 相似文献
136.
Jorge Bravo Sandra Bolaño Luca Gonsalvi Maurizio Peruzzini 《Coordination chemistry reviews》2010,254(5-6):555-607
This review paper covers the recent developments (2004–2009) on the tailored synthetic modifications and related coordination chemistry of the water-soluble cage-like aminophosphine ligand 1,3,5-triaza-7-phosphatricyclo-[3.3.1.1]decane (PTA), together with the new applications in the fields of catalysis, material science and medicinal chemistry. 相似文献
137.
Stefano Gialanella Fabrizio Girardi Gloria Ischia Ivan Lonardelli Maurizio Mattarelli Maurizio Montagna 《Journal of Thermal Analysis and Calorimetry》2010,102(3):867-873
This study deals with some microstructural and crystallographic aspects of the thermally induced transformation of goethite
(α-FeOOH) into hematite (α-Fe2O3), occurring at about 300 °C. Powder specimens of goethite have been annealed in air at different temperatures, ranging from
200 °C up to 1,000 °C. The resulting products have been analyzed for a complete characterization of the changes brought about
by the thermal treatments, using a multianalytical approach, based on: thermogravimetry, differential thermal analysis, transmission
electron microscopy, Raman spectroscopy, and X-ray diffraction. At lower temperatures, the transition to hematite produces
no important changes in size and shape of the original goethite grains. Recrystallization, and partial sintering, occurs only
at temperatures in excess of 800 °C. The relevant evolution of pores present in both phases has been also considered, as it
may provide important indications on the actual formation mechanism of hematite. 相似文献
138.
This short review describes a breakthrough provided by the synthesis of d6 metal complexes containing the intact molecules P4 and P4S3. The coordinated cage molecules acquire unexpected reactivity and undergo dismutation reactions in mild conditions in the presence of water. The outcomings are obtained either in form of free or coordinated molecules; the former are hypophosphorous and phosphorous acids, the latter comprise, besides phosphine, PH3, such species as thiophosphinous acid, PH2SH, diphosphane, P2H4, 1-hydroxytriphosphane, PH(OH)PHPH2 and 1,1,4-tris-hydroxytetraphosphane, P(OH)2PHPHPH(OH), which are either unknown or extremely reactive as free molecules. The formation of the above molecules provides a clue to the hydrolytic activation of the P4 and P4S3 cage molecules. 相似文献
139.
Two different kinds of organoclays were prepared by mixing a pristine montmorillonite and a double‐chain ammonium salt in many different thermoplastic or elastomeric polymers. Independently of the chemical nature of the considered polymers, the obtained organoclays presented a basal spacing of 4 or 6 nm, when the mixing occurred in the absence or in the presence of a small amount of stearic acid (SA), respectively. X‐ray diffraction and Fourier transform infrared measurements support the hypothesis that these two kinds of organoclays correspond to paraffin‐type tilted and perpendicular bi‐layer intercalates, respectively. The co‐intercalation of SA molecules with the double‐chain amphiphile is suggested, to explain the observed expansion of the clay interlayer distance. The obtained results suggest an easy way to control the organoclay structure in polymer composites. Moreover, the authors on the basis of these results propose a criticism to the extensive literature that systematically explains most d basal spacing increase observed for clays in polymer with the penetration of apolar polymer chains in the clay interlayer space. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
140.
Cali F Ragalmuto A Chiavetta V Calabrese G Fichera M Vinci M Ruggeri G Schinocca P Sturnio M Romano S Romano V Elia M 《Experimental & molecular medicine》2010,42(12):842-848
Angelman syndrome (AS) is a severe neurobehavioural disorder caused by failure of expression of the maternal copy of the imprinted domain located on 15q11-q13. There are different mechanisms leading to AS: maternal microdeletion, uniparental disomy, defects in a putative imprinting centre, mutations of the E3 ubiquitin protein ligase (UBE3A) gene. However, some of suspected cases of AS are still scored negative to all the latter mutations. Recently, it has been shown that a proportion of negative cases bear large deletions overlapping one or more exons of the UBE3A gene. These deletions are difficult to detect by conventional gene-scanning methods due to the masking effect by the non-deleted allele. In this study, we have used for the first time multiplex ligation-dependent probe amplification (MLPA) and comparative multiplex dosage analysis (CMDA) to search for large deletions affecting the UBE3A gene. Using this approach, we identified a novel causative deletion involving exon 8 in an affected sibling. Based on our results, we propose the use of MLPA as a fast, accurate and inexpensive test to detect large deletions in the UBE3A gene in a small but significant percentage of AS patients. 相似文献