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991.
Horst Kunz 《Angewandte Chemie (International ed. in English)》1987,26(4):294-308
Glycopeptides are partial structures of the connecting regions of glycoproteins and, like these, always contain glycosidic bonds between the carbohydrate and peptide parts. Glycoproteins are not only widely distributed but are also decisive factors in post-translational biological selectivity, especially in biological recognition. Targeted syntheses of glycopeptides require stereoselective formation of the glycosidic bonds between the carbohydrate and the peptide parts and protective group methods that enable selective deblocking of only one functional group in these polyfunctional molecules. These heavy demands have been met by the well-established use of benzylic protective groups, which can be removed by hydrogenolysis, combined with the use of base-labile 2-phosphonioethoxycarbonyl (Peoc) or 9-fluorenylmethoxycarbonyl (Fmoc) protective groups or of bromoethyl esters, which can be removed under neutral conditions. The acidolysis of tert-butyloxycarbonyl (Boc) groups and of tert-butyl esters has also been successfully used, although, under acidic conditions, anomerization or rupture of the glycosidic bonds may occur, especially when nucleophiles are present. The stable, two-stage 2-(pyridyl)ethoxycarbonyl (Pyoc) protective groups allow a more reliable synthesis of complex glycopeptides since they can be removed, after modifications, under mild conditions. Particularly suitable for the synthesis of sensitive glycopeptides are the stable allyl protective groups. They can be removed from the complex glycopeptides in a highly selective and effective manner by means of noble-metal catalysts under practically neutral conditions. These methods have been employed to synthesize glycopeptides corresponding to partial structures of interesting glycoproteins. Deprotected glyopeptides representing tumor-associated antigen structures can be coupled to bovine serum albumin, which serves as a biological carrier molecule, without the necessity of using an artificial coupling component (spacer). 相似文献
992.
Colloidal synthesis of organic-capped ZnO nanocrystals via a sequential reduction-oxidation reaction
A nonhydrolytic route to quantum-sized (d < 9 nm) ZnO nanocrystals in homogeneous organic solutions is presented. Nearly spherical ZnO nanocrystals were grown in a surfactant mixture of hexadecylamine and oleic acid (OLEA) by means of a two-step chemical process, based on the hot reduction (at 180-250 degrees C) of a zinc halide by superhydride (LiBEt3H) followed by oxidation of the resulting product. The experimental results suggested that the controlled growth of ZnO in the nanosized regime depended both on the OLEA-assisted generation of intermediate metallic nanoparticles and on the adjustment of their oxidation conditions by using a mild oxidant, trimethylamine-N-oxide, rather than molecular oxygen. The present synthetic approach demonstrates to be particularly suitable to prepare organic-soluble ultra-small ZnO nanocrystals of low size dispersion and of stable size, which are appealing for optoelectronic, catalytic, and sensing purposes. 相似文献
993.
Dickins RS Aime S Batsanov AS Beeby A Botta M Bruce JI Howard JA Love CS Parker D Peacock RD Puschmann H 《Journal of the American Chemical Society》2002,124(43):12697-12705
The nature of the ternary complexes formed in aqueous media at ambient pH on reversible binding of acetate, lactate, citrate, and selected amino acids and peptides to chiral diaqua europium, gadolinium, or ytterbium cationic complexes has been examined. Crystal structures of the chelated ytterbium acetate and lactate complexes have been defined in which the carboxylate oxygen occupies an "equatorial" site in the nine-coordinate adduct. The zwitterionic adduct of the citrate anion with [EuL1] was similar to the chelated lactate structure, with a 5-ring chelate involving the apical 3-hydroxy group and the alpha-carboxylate. Analysis of Eu and Yb emission CD spectra and lifetimes (H2O and D2O) for each ternary complex, in conjunction with 1H NMR analyses of Eu/Yb systems and 17O NMR and relaxometric studies of the Gd analogues, suggests that carbonate, oxalate, and malonate each form a chelated (q = 0) square-antiprismatic complex in which the dipolar NMR paramagnetic shift (Yb, Eu) and the emission circular polarization (gem for Eu) are primarily determined by the polarizability of the axial ligand. The ternary complexes with hydrogen phosphate, with fluoride, and with Phe, His, and Ser at pH 6 are suggested to be monoaqua systems with Eu/Gd with an apical bound water molecule. However, for the ternary complexes of simple amino acids with [YbL1]3+, the enhanced charge demand favors a chelate structure with the amine N in an apical position. Crystal structures of the Gly and Ser adducts confirm this. In peptides and proteins (e.g. albumin) containing Glu or Asp residues, the more basic side chain carboxylate may chelate to the Ln ion, displacing both waters. 相似文献
994.
Pentafluorosulfanylamines and Sulfanylammonium Salts . From the addition of HF to sulfurtetrafluorideimides N-alkylpentafluorosulfanylamines RNHSF5(2a, 2b: R=CH3, C2H5) are obtained in quantitative yield. N, N-dialkylpentafluorosuIfanylamines Et2NSF5(5a) and pip-SF5 (5b) are isolated from the reaction of the appropriate sulfurdifluoronitridearnides NSF2NR2 and HF/SF4. Protonation of the amines with the superacidic system HF/AsF5 gives stable pentafluorosulfanyl-ammonium salts SF5NHRR′. AsF6 (12: R = R′ = CH3; 14: R=R′=H; 10: R=CH3, R′ = H). Under the same conditions the adduct AsF5· NSF2CF(CF3)2 (15) forms a cation with hexacoordinated sulfur (trans-H3NSF4CF(CF3)2?AsF66: 16), while with Asp5 · NSF2NMe2 (17) the reaction stops at tetracoordination (HNSF2NMe2+AsF6 : 18). 相似文献
995.
Polymethines are chain molecules with equal bond-lengths and charge alteration along the chain. They embrace three classes of compounds with (N - 1)π, Nπ, or (N + 1)π electrons on N atoms. The MO-theoretical characteristics of the (N - 1)π, Nπ, and (N + 1 )π polymethines are strongly related, and the eigenvalues can be derived by a mnemonic technique. The theoretical results establish the particular position of the polymethines among the π-systems and allow a rationalization of experimental findings within the framework of the one electron theory. 相似文献
996.
Zusammenfassung Proben aus Polyäthylen hoher Dichte wurden bei Raumtemperatur mit verschiedenen Geschwindigkeitenv
ver auf einer Zugprüfmaschine verstreckt. Beiv
ver 10 mm/min beobachtet man eine fast isotherm verlaufende inhomogene Deformation, die zu Verstreckungsgraden=8–13 und mittleren Dichten = 0.80 g/cm3 in den verstreckten Probenbereichen führt. Die bei höherenv
ver bis zu 50 mm/min eintretende adiabatische Erwähnung ergibt höhere Verstreckungsgrade=13–18 und geringere Dichten = 0.64 g/cm3. Es existiert kein natürlicher Verstreckungsgrad. Der Dichteabfall mit zunehmendem kann durch eine Gerade repräsentiert werden; der ElastizitätsmodulE ergibt eine mit zunehmende Kurve.Nach einer Druckbehandlung der Proben mit 5600 bar bei Raumtemperatur erreichte ihre Dichte fast wieder den Anfangswert vor der Verstreckung, wobei keine Abhängigkeit von oder anderen Parametern zeigte. Der ModulE hatte zugenommen, aber nicht proportional zur Dichte. Der Vergleich von undE verstreckter Proben vor und nach der Druckbehandlung weist auf den Netzwerkcharakter von kaltverstrecktem Polyäthylen hin.Herrn Prof. Dr. K. Ueberreiter zum 70. Geburtstag gewidmet. 相似文献
997.
Wyss HM Tervoort E Meier LP Müller M Gauckler LJ 《Journal of colloid and interface science》2004,273(2):455-462
We produce concentrated (40 vol%) gels of uniformly sized silica particles by an in situ process, based on the enzyme-catalyzed hydrolysis of urea in the liquid phase of electrostatically stabilized suspensions. Two different methods are used: Either the pH of the suspensions is shifted toward the isoelectric point of the particles (delta pH method), or the ionic strength is continuously increased at constant pH (deltaI method). We compare the two kinds of gels in terms of elastic and yield behavior as well as microstructure by using rheological measurements in oscillation and high-pressure freezing in combination with cryo-SEM, respectively. Results suggest a strong increase of elastic and yield properties in concentrated particle gels with decreasing homogeneity of their microstructures. 相似文献
998.
Analytical and Bioanalytical Chemistry - Zink kann in Abwesenheit von Eisen mit Kaliumferrocyanid mit Hilfe eines photoelektrischen Colorimeters bis zur maximalen Trübung titriert werden.... 相似文献
999.
Zusammenfassung Die Aufl?sung von Azetylzellulose in Zyklohexanon, ?thylazetat, Methylphtalat, Diazetonalkohol, Benzylalkohol und Methyl?thylketon
wurde kinetisch untersucht. Neben normalen Geschwindigkeitskurven ergaben sich auch verwickeitere Formen, z. B. zweiteilige
Kurvenformen, die im Sinne früherer Ausführungen als „Autopeptisationskurven“ gedeutet wurden. Wartet man nicht den Endzustand
der Aufl?sung ab, so ergaben sich abnorme Kurven der Bodenk?rperabh?ngigkeit der L?slichkeit. 相似文献
1000.