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991.
Zusammenfassung Innerhalb der substituierten Selenoxide eignet sich Diphenylselenoxid, das in salzsaurer Lösung die Verbindung RhCl3·OSe(C6H5) bildet, zur extraktiv-photometrischen Bestimmung des Rhodiums besonders neben Co2+, Ni2+ und Fe3+.
Der Deutschen Forschungsgemeinsehaft und dem Fonds der chemischen Industrie danken wir für die Förderung unserer Arbeit durch Sachbeihilfen. 相似文献
Summary Among the substituted selenium oxides, diphenylselenium oxide, that in hydrochloric acid solution yields the compound RhCl3·OSe(C6H5)2, is especially suitable for the extractive-photometric determination of rhodium, particularly in the presence of Co2+, Ni2+ and Fe3+.
Résumé Dans le cadre des oxydes de sélénium substitués, le diphényloxyde de sélénium qui forme le composé RhCl3·OSe(C6H5) en solution chlorhydrique se prête au dosage photométrique par extraction du rhodium, en particulier en présence de Co2+, Ni2+ et Fe3+.
Der Deutschen Forschungsgemeinsehaft und dem Fonds der chemischen Industrie danken wir für die Förderung unserer Arbeit durch Sachbeihilfen. 相似文献
992.
In the course of this study, it has been attempted to give a precise definition of basic salts. These salts must be difterentiated from the adsorption compounds and even from the neutral salts correspondmg to an acid of which all the acidic functions have not been demonstrated.After havmg reviewed the principal techniques used up to now a potentiometric method is proposed, permitting the rapid determination of the basicity index of an insoluble basic salt. It consists, in principle, in precipitating the salt with an alkali hydroxide and deteminining the pH in the course of precipitation,Two measurements suffice theoretically to obtain the constitution of the salt studied. 相似文献
993.
Smith CB Stephens AK Wallwork KS Lincoln SF Taylor MR Wainwright KP 《Inorganic chemistry》2002,41(5):1093-1100
The ability of the pendant donor macrocyclic ligand 1,4,7,10-tetrakis((S)-2-hydroxy-3-phenoxypropyl)-1,4,7,10-tetraaza- cyclododecane((S)-thphpc12) (or [Cd((S)-thphpc12)](2+)) to act as a metal ion-dependent receptor for aromatic anions has been investigated in solution and in the solid state. [Cd((S)-thphpc12)](2+) adopts a stable conical conformation with a large hydrophobic cavity, which has been shown to contain, via complementary multiple hydrogen bonding, p-nitrophenolate, aromatic carboxylates, p-toluenesulfonate, certain aromatic amino acid anions, phenoxyacetate, and acetate. In the case of p-nitrophenolate only, one or two anions can be contained within the receptor cavity. The crystal structure of [Cd((S)-thphpc12)(p-nitrophenolate)(2)] shows a coplanar arrangement of the p-nitrophenolates, where each is retained in the cavity by a pair of hydrogen bonds to cis hydroxyl groups. The crystal structure of the p-aminobenzoate inclusion complex indicates retention of the guest via a pair of hydrogen bonds to each oxygen atom of the carboxylate moiety. The crystal structure of the (L)-phenylalaninate inclusion complex indicates that the amino acid is retained by five hydrogen bonds, two involving the nitrogen atom and three to the oxygen atoms of the carboxylate moiety. Binding constants (10(3)-10(5) M(-1)) for the inclusion of some of the aforementioned anions in [Cd((S)-thphpc12)](2+) and related receptors were measured by (1)H NMR titration in DMSO-d(6) at 298 K. 相似文献
994.
Katsonis N Marchenko A Taillemite S Fichou D Chouraqui G Aubert C Malacria M 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(11):2574-2581
We recently discovered that a linear multifunctional trimethylsilylacetylene (TMSA) compound forms long-range and highly stable self-assembled monolayers (SAMs) on reconstructed Au(111). To better understand the interactions governing self-assembly in this new system, we synthesized a series of homologue organosilanes and performed scanning tunneling microscopy (STM) measurements at the Au(111)/n-tetradecane interface. The four TMSA-terminated linear silanes that we synthesized self-assemble in similar ways on gold, with the molecules standing upright on the surface. In contrast, compounds with a slightly modified terminal group but the same polyunsaturated linear chain above the TMSA head do not self-assemble. In particular, substituting a methyl group of TMSA with a more bulky one prevents self-assembly. Removing the C triple bond C triple bond of TMSA or substituting the Si atom by a C atom also hinders self-assembly. Finally, substituting one methyl group of TMSA by a hydrogen atom induces self-assembly but in a different geometry, with the molecules lying flat on the gold surface in a quasi-epitaxy mode. Our molecular approach demonstrates the key role played by the TMSA head in self-assembly, its origin being twofold: 1) the TMSA layers are commensurate to the Au(111) adlattice along the <112> direction, and 2) the C triple bond C triple bond of TMSA activates the Si atom and induces the creation of a surface Si-Au chemical bond. The highly stable TMSA-based SAMs appear then as promising materials for applications in surface modification. 相似文献
995.
Max Vecchi Willy Walther Ernst Glinz Thomas Netscher Rudolf Schmid Michel Lalonde Walter Vetter 《Helvetica chimica acta》1990,73(4):782-789
Separation and Quantitation of All Eight Stereoisomers of α-Tocopherol by Chromatography The results of the analysis of several derivatives of (all-rac)-α-tocopherol by HPLC on a chiral stationary phase and by capillary GC on a achiral stationary phase are reported. Consecutive application of both methods to the ethyl-ether derivative allows the separation and quantification of all eight possible stereoisomers of (all-rac)-α-tocopherol. 相似文献
996.
Zusammenfassung Lösungen von Kartoffelamylopektin und Kartoffelamylosen zeigen in einer Apparatur, welche die Empfindlichkeit= 1 besitzt, keine Strömungsdoppelbrechung. Durch Vergleich der Rotationsdiffusionskonstante, welche aus der durch die Empfindlichkeit der Apparatur geschätzten Maxwellschen Konstante folgt, und des für kugelige Teilchen berechneten Wertes findet man, daß sowohl das Amylopektin wie auch die Amylose Moleküle besitzen, die nicht wesentlich von der Kugelgestalt abweichen. 相似文献
997.
Isolation and Structure Elucidation of 36 Diterpenoids from Leaf-Glands of Plectranthus edulis (VATKE ) T.T. AYE Analysis of the polar diterpenoids from the yellow glands of the title plant from Kenya and Abyssinia led to the identification of several novel abietanoids. Main compound is the known edulon A ( 40 ), a 5(4→3) abeo-abietane. Minor compounds include 6 different royleanones, 15 spirocoleons, 3 vinylogous quinones, 8 acylhydroquinones (as their 6,7-dioxo compounds or the tautomeric disophenols), 2 naphthaquinones (as the 1,10-seco-abietanoids), and deacetyledulon A. The known coleon-A-lactone (37) now has also been found in Plectranthus edulis. The intermediacy of the γ-enollactol 44 , combined with a leaving group on C(3) is postulted to explain the biogenesis of the unusual 4H-5-oxaaceanthrylen skeleton of edulon A. 相似文献
998.
999.
1000.
Robert K. Müller Kurt Bernhard Hans Mayer August Rüttimann Max Vecchi 《Helvetica chimica acta》1980,63(6):1654-1664
Contribution to the Analytical Separation and the Synthesis of 3-Hydroxy-4-oxocarotenoids (3RS,3′RS)-Astaxanthin (= 3,3′-dihydroxy-β,β-carotene-4,4′-dione, 1:1-mixture of racemate and meso-form; 1 ) can be separated into its optical isomers (3S,3′S)- 1a , (3R,3′R)- 1b and meso-(3R,3′S)- 1c via the corresponding diastereomeric di-(?)-camphanates. Some aspects of the configurational stability of astaxanthin are discussed. - HPLC. analysis of the (?)-camphanates of 3-hydroxy-4-oxocarotenoids provides, in suitable cases and supported by spectroscopic data, an analytical method for the simultaneous determination of constitution and chirality. 相似文献