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141.
D'Archivio AA Galantini L Panatta A Tettamanti E 《The Journal of chemical physics》2004,120(10):4800-4807
Electron spin resonance (ESR) and quasielastic laser scattering (QELS) measurements have been carried out on sodium taurodeoxycholate (NaTDC) micellar aqueous solutions. Computer simulation of the ESR line shape has been used to quantitatively analyze the rotational dynamics of the cholestan-spin label (CSL) dissolved by the NaTDC micellar aggregates as a function of temperature and NaCl concentration. The local reorientation of CSL has been accounted for motionally-averaged g- and A-tensors assuming fast oscillation around the spin-probe long molecular axis. The overall Brownian tumbling of CSL-micelle complexes has been modeled by an axially symmetric rotational tensor. Good agreement with experimental spectra is obtained. Best-fit rotational parameters and QELS data suggest that, in the circumstance of large aggregation, NaTDC micelles have cylindrical shape and micellar growth occurs along the cylinder axis. 相似文献
142.
The UV. irradiation of 17β-acetoxy-4α, 5α-epoxy-2-oxaandrostan-3-one ( 7 ) yields 17β-acetoxy-2-oxa-10(5 → 4)abeo-4ζ (H)-androsta-3,5-dione ( 11 ). A non-photochemical synthesis of 11 , proceeding in lower yield, is also described. 相似文献
143.
Antonio Campiglio 《Mikrochimica acta》1977,68(1-2):71-80
Zusammenfassung Eine Methode zur Mikrobestimmung von Quecksilber in organischen Verbindungen wurde beschrieben. 3–5 mg Substanz werden in einem Sauerstoffkolben verbrannt und die Produkte in 4 ml konz. Salpetersäure absorbiert. Die Absorptionslösung wird dann für 6 min gekocht, wobei die vollständige Oxydation zu Quecksilber(II) abläuft. Dieses wird mit 0,005 M Kaliumjodidlösung potentiometrisch titriert. Zur Indikation des Endpunktes wird eine Meßkette aus einer ionenselektiven Elektrode für Jodid und einer Referenzelektrode mit KNO3-Zwischenelektrolyt verwendet. Die Resultate liegen innerhalb der üblichen Fehlergrenze von ± 0,30%.
Herrn Prof. Dr. Hans Lieb zum 90. Geburtstag gewidmet.
Frl. Mirella Piccinini hat an dem experimentellen Teil dieser Arbeit mitgeholfen, wofür ich bestens danke. 相似文献
Microassay of mercury in organic substances
Summary A method for microassay of mercury in organic compounds was described. 3–5 mg substance are combusted in an oxygen flask and the products absorbed in 4 ml conc. nitric acid. The absorption solution is then boiled for 6 minutes, during which complete oxidation to mercury(II) occurs. This is titrated potentiometrically with 0.005M potassium iodide solution. A measuring chain consisting of an ion-selective electrode for iodide and a reference electrode with KNO3 intermediate electrode was used to indicate the endpoint. The results are within the usual ±0.30% limit of error.
Herrn Prof. Dr. Hans Lieb zum 90. Geburtstag gewidmet.
Frl. Mirella Piccinini hat an dem experimentellen Teil dieser Arbeit mitgeholfen, wofür ich bestens danke. 相似文献
144.
Paired electrosynthesis of cyanoacetic acid 总被引:1,自引:0,他引:1
Batanero B Barba F Sánchez-Sánchez CM Aldaz A 《The Journal of organic chemistry》2004,69(7):2423-2426
Cyanoacetic acid is formed by cathodic reduction of CO(2) and anodic oxidation of the tetraalkylammonium salt anion; the process is conduced in acetonitrile using a divided cell with a medium porosity glass-frit diaphragm. A mechanism for this paired electrochemical reaction is proposed. 相似文献
145.
Imre T Schlosser G Pocsfalvi G Siciliano R Molnár-Szöllosi E Kremmer T Malorni A Vékey K 《Journal of mass spectrometry : JMS》2005,40(11):1472-1483
A new anionic surfactant (RapiGest SF) was successfully used for site-specific analysis of glycosylation in human alpha-1-acid glycoprotein (AGP). By means of this analytical approach combined with capillary HPLC-mass spectrometry (and tandem mass spectrometry), the N-linked glycosylation pattern of AGP was explored. On the basis of mass matching and MS/MS experiments ca 80 different AGP-derived glycopeptides were identified. Glycosylation shows a markedly different pattern for the various glycosylation sites. At sites I and II, triantennary complex-type oligosaccharides predominate and at sites III, IV and V, tetra-antennary complex-type oligosaccharides predominate. Sites IV and V show the presence of additional N-acetyl lactosamine (Gal-GlcNAc) units (even higher degree of branching and/or longer antennae are also present). 相似文献
146.
Bonomo RP Cucinotta V Giuffrida A Impellizzeri G Magri A Pappalardo G Rizzarelli E Santoro AM Tabbi G Vagliasindi LI 《Dalton transactions (Cambridge, England : 2003)》2005,(1):150-158
An aqueous solution spectroscopic (Vis and EPR) study of the copper(II) complexes with the Ac-HGGG-NH2 and Ac-PHGGGWGQ-NH2 polypeptides (generically designated as L) suggests square base pyramids ascribable to [Cu(L)H(-2)] complex species, which contain three nitrogen donor atoms, arising from imidazole and peptide groups, in the equatorial plane and for a pseudo-octahedral geometry in the case of [CuLH-3]- and [Cu(L)H-4]2- which have four nitrogen donor atoms in their equatorial plane. The coordination sphere of the copper complex in the [Cu(L)H(-2)] species, which is present at neutral pH values, is completed by two oxygen donor atoms. ESI-MS spectra ascertained that water molecules are not present in the coordination equatorial plane of this latter species, in comparison with other copper(II) complexes with ligands bearing nitrogen and oxygen donor atoms and surely having equatorial water molecules. This indicates the coordination of a carbonyl oxygen atom in the equatorial plane has to be invoked. However, no direct proof about the involvement of a carbonyl group oxygen donor atom apically linked to copper was obtained, due to the flexibility of these structures at room temperature. Additionally, the low A(ll) value leads one to consider another oxygen atom of a carbonyl group being involved in the apical bond to copper in a fast exchange fashion. This apical interaction, which may also involve a water molecule, is more pronounced in the Cu-Ac-HGGG-NH2 than in the analogous Cu-Ac-PHGGGWGQ-NH2 system, probably because of the presence of tryptophan and proline in the polypeptide sequence. 相似文献
147.
The lithiation of trans- and cis-stilbene oxides (+/-)-1 and 8 has been investigated. While with 8, lithiation occurred exclusively at the benzylic position, with the trans isomer (+/-)-1, ortho-lithiation competed with alpha-lithiation depending upon the experimental conditions. The configurational stability of the alpha-lithiated cis- and trans-stilbene oxides (+/-)-2 and (+/-)-9, respectively, was proved as well as that of scalemic stilbene oxide (R,R)-2. 相似文献
148.
Micrometric BN powders used as catalyst support: influence of the precursor on the properties of the BN ceramic 总被引:1,自引:0,他引:1
Thin powders and foams of boron nitride have been prepared from molecular precursors for use as noble metal supports in the catalytic conversion of methane. Different precursors originating from borazines have been tested. The best results were obtained using a precursor derived from trichloroborazine (TCB) which, after reacting with ammonia at room temperature and then thermolyzing up to 1800°C, led to BN powders with a specific area of more than 300 m2 g−1 and a micrometric spherical texture. Comparable results were obtained using polyborazylene under similar conditions. Aminoborazine-derived precursors did not yield such high specific area ceramics but the BN microstructure resembled a foam with a crystallized skin and amorphous internal part. These differences were related to the chemical mechanism of the conversion of the precursor into BN. Polyhaloborazines and polyborazines yielded BN through gas-solid reactions whereas aminoborazine polymers could be kept waxy up to high temperatures, which favored the glassy foam. Catalysts composed of BN support and platinum have been prepared using two routes: from a mixture of precursor or by impregnation of a BN powder leading to very different catalysts. 相似文献
149.
[reaction: see text] 2,3-Disubstituted furo[3,2-b]pyridines, 2,3-disubstituted furo[2,3-b]pyridines, and 2,3-disubstituted furo[2,3-c]pyridines are readily prepared under mild conditions via the palladium-catalyzed cross-coupling of 1-alkynes with o-iodoacetoxy- or o-iodobenzyloxypyridines, followed by electrophilic cyclization by I(2) or by PdCl(2) under a balloon of carbon monoxide. 相似文献
150.
Antonio Da Settimo Giuliana Biagi Giampaolo Primofiore Pier Luigi Ferrarini Oreste Livi Anna Maria Marini 《Journal of heterocyclic chemistry》1980,17(6):1225-1229
The preparation of some 3,7-disubstituted-5,6-dihydroquino[3,2-c][1,8]naphthyridines ( 6 ) by the condensation of 7-substituted-2,3-dihydro-1,8-naphthyridin-4-(1H)ones ( 5 ) with o-aminoacetophenone or o-aminobenzophenone is described. All the 5,6-dihydroderivatives 6 were transformed into the fully aromatic compounds 7 by heating with nitrobenzene. Only a few quino[3,2-c][1,8]naphthyridines were previously described. 相似文献