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171.
Superstructures of temporarily stabilized nanocrystalline CaCO3 particles: morphological control via water surface tension variation 总被引:1,自引:0,他引:1
In this paper, the formation of different complex morphologies of nanocrystalline CaCO3 under the control of double hydrophilic block copolymers (DHBCs) carrying phosphate groups is described. The DHBCs consist of a poly(ethylene glycol) (PEG) block and a pendant poly[2-(2-hydroxy ethyl)ethylene] block with different degrees of phosphorylation up to 40%, some of which show surface activity. The polymers furthermore temporarily stabilize CaCO3 nanocrystals, which are formed by slow CO2 evaporation from a supersaturated Ca(HCO3)2 solution (Kitano method). The polymers are active down to concentrations of 10(-4) g/L. In dependence of the nature and concentration of the DHBC, tunable complex shuttlecock flowerlike and other superstructures are formed, which are aggregates of CaCO3 vaterite nanoparticles with an enhanced stability of at least 2 months. It is shown that the aggregation starts around template CO2 gas bubbles at the air/water interface. The size and morphology of the growing aggregates depends on the polymer concentration, phosphorylation degree, and water surface tension. The latter determines when the aggregate sinks to the bottom, interrupting the further growth process. Variation of the water surface tension by addition of the nonionic surfactant Antharox CO880 also allows a variation of the aggregate morphology, thus implying the described method as simple and versatile for the generation of complex CaCO3 morphologies. 相似文献
172.
Synthesis of the Stannatetraphospholanes (tBuP)4SnR2 (R = tBu, nBu, C6H5) and (tBuP)4Sn(Cl)nBu Molecular and Crystal Structure of (tBuP)4Sn(tBu)2 The reaction of the diphosphide K2[tBuP-(tBuP)2-PtBu] 4 with the halogenostannanes (tBu)2SnCl2, (nBu)2SnCl2, (C6H5)2SnCl2 or nBuSnCl3 in a molar ratio of 1 : 1 leads via a [4 + 1]-cyclocondensation reaction to the stannatetraphospholanes (tBuP)4SnR2 3 b–3 d and (tBuP)4Sn(Cl)nBu 3 e , respectively, with the binary 5-membered P4Sn ring system. 3 b was characterized by a single crystal structure analysis; the 5-membered ring exists in a planar conformation. The compounds 3 b–3 e were identified by NMR and also by mass spectroscopy; the 31P{1H}-NMR spectra of 3 b–3 d showed an AA′MM′ (AA′MM′X), 3 e on the other hand an ABCD (ABCDX) spin system. 相似文献
173.
Thin layers of basic zinc carbonate can be used with good results for separation and multiple identification of carbamate and phenylurea pesticides. Five important substances could be separated by one-dimension TLC. The best results were obtained by the following developing solvents: a) benzene, b) a mixture of benzene/petroleum ether/chloroform (6∶1∶1). The substances are either recognisable in short-wave UV-light, when a fluorescence indicator (F 254 nm) is added, or in day-light, after spraying a solution of 0.1 N AgNO3 in 3 N HNO3, followed by an UV-exposure for about 4 min. 相似文献
174.
Sigmar Spauszus Claus Schwarz und Hans -Jürgen Weigel 《Fresenius' Journal of Analytical Chemistry》1961,182(3):184-192
Zusammenfassung Einige der üblichen Methoden zur Phosphorbestimmung in wolframlegierten Stählen werden unter Anwendung von 185W und 32P einer Nachprüfung unterzogen. Dabei erweisen sich die Phosphorverluste durch Adsorption an dem Wolframsäureniederschlag als gering, so daß sie bei weniger anspruchsvollen Bestimmungen unberücksichtigt bleiben können. Erheblich größer sind dagegen die Fehler, die durch Mitfällung von Wolframsäure mit dem Ammoniummolybdatophosphatniederschlag entstehen können. Es werden zwei Methoden angegeben, nach denen eine quantitative Abtrennung des Wolframs und damit eine sichere Bestimmung des Phosphors möglich ist.Herr Prof. Dr.-Ing. K. Schwabe ermöglichte es uns freundlicherweise, die Untersuchungen mit radioaktivem Wolfram und Phosphor im Zentralinstitut für Kernphysik Rossendorf, Bereich Radiochemie, durchzuführen. Ihm sei auch an dieser Stelle herzlichst gedankt. 相似文献
175.
Summary Examples are given of the application of higher-order derivative spectrophotometry to microanalytical problems, including the increase in sensitivity for estimation of Zn and Cd dithizonates and the quantitative detection of arenes, aniline and phenols. We also describe the estimation of saccharin in soft drinks, and the characterization and estimation of dyes in solution and after absorption on a thin layer of alumina. Only ng-g amounts of substance are needed.
Presented at the 8th International Microchemical Symposium, Graz, August 25–30, 1980. 相似文献
Hochauflösende UV/VIS-Derivativspektrophotometrie höherer Ordnung in der Mikroanalytik
Zusammenfassung Einige Beispiele für die Anwendung der Derivativspektrophotometrie höherer Ordnung in der Mikroanalyse wurden angegeben. Im besonderen wurden die Erhöhung der Empfindlichkeit der Zn- und Cd-Dithizonat-Bestimmung, die quantitative Bestimmung von Arenen, Anilin, Phenol, die Erfassung von Saccharin in Limonaden und sowohl die Charakterisierung als auch die quantitative Bestimmung von Farbstoffen in Lösung oder adsorbiert an einer dünnen Schicht Aluminiumoxid beschrieben. Es werden nur einige Mikrogramm bis Nanogramm Substanz für die Untersuchungen benötigt.
Presented at the 8th International Microchemical Symposium, Graz, August 25–30, 1980. 相似文献
176.
Helmut Schneider 《The Journal of the Operational Research Society》1978,29(12):1181-193
This paper deals with a periodic review inventory system. Methods are discussed for determining the re-order point s of an (s, S) order policy, when a certain service level is required. The results differ from those presented for a (Q, s) model which is usually considered in literature and implemented in practice. Methods are discussed for determining the re-order point of an (s, S) policy when demand is normal or gamma distributed. A numerical investigation demonstrates the applicability of the described methods. In particular, it is shown that these methods are superior to a formula that is implemented in many inventory control systems. 相似文献
177.
Helmut Röhrl 《manuscripta mathematica》1978,25(4):359-390
In [3] it was shown that a polynomial of degree n with coefficients in an associative division algebra, which is d-dimensional over its center, has either infinitely many or at most nd zeros. In this paper we raise the same question for arbitrary m-ary F-algebras A which are d-dimensional over the algebraically closed field F. Our main result states that in the affine space of m-ary algebras of dimension d there is a non-empty Zariski-open set whose elements A have the following property: in the space of polynomial of precise degree n with coefficients in A there is a non-empty Zariski-open set whose elements have precisely nd zeros. It is shown that all simple algebras, all semi-simple associative algebras, all semisimple Jordan algebras (char F2), all semi-simple Lie algebras (char F=0), and the generic algebra possess this property. 相似文献
178.
Helmut Karzel 《Aequationes Mathematicae》1978,17(1):83-90
A permutation set (M, I) consisting of a setM and a set of permutations ofM, is calledsymmetric, if for any two permutations, the existence of anx M with (x) (x) and
–1
(x) =
–1
(x) implies
–1
=
–1
, andsharply 3-transitive, if for any two triples (x
1,x
2,x
3), (y
1,y
2,y
3) M
3 with|{x
1,x
2,x
3
}| = |{y
1,y
2,y
3
}| = 3 there is exactly one permutation with(x
1) =y
1,(x
2) =y
2,(x
3) =y
3. The following theorem will be proved.THEOREM.Let (M, ) be a sharply 3-transitive symmetric permutation set with |M|3, such that contains the identity. Then is a group and there is a commutative field K such that and the projective linear group PGL(2, K) are isomorphic. 相似文献
179.
Erich Dubler Helmut W. Schmalle Frdric Arod Alain Schneider 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(2):m111-m115
The syntheses and structures of two mixed‐ligand complexes of platinum(II) with deprotonated oxopurine bases and triphenylphosphine are reported, namely the theophyllinate complex cis‐bis(1,2,3,6‐tetrahydro‐1,3‐dimethylpurine‐2,6‐dionato‐κN7)bis(triphenylphosphine‐κP)platinum(II), [Pt(C7H7N4O2)2(C18H15P)2], (I), and the theobrominate complex cis‐chloro(1,2,3,6‐tetrahydro‐3,7‐dimethylpurine‐2,6‐dionato‐κN1)bis(triphenylphosphine‐κP)platinum(II) ethanol hemisolvate, [PtCl(C7H7N4O2)(C18H15P)2]·0.5C2H5OH, (II). In (I), the coordination geometry of Pt is square planar, formed by the two coordinating N atoms of the theophyllinate anions in a cis arrangement and two P atoms from the triphenylphosphine groups. In (II), there are two crystallographically independent molecules. They both exhibit a square‐planar coordination geometry around Pt involving one Cl atom, the coordinating N atom of the theobrominate anion and two P atoms from the triphenylphosphine groups. The two triphenylphosphine groups are arranged in a cis configuration in both structures. The heterocyclic rings are rotated with respect to the coordination plane of the metal by 82.99 (8) and 88.09 (8)° in complex (I), and by 85.91 (16) and 88.14 (18)° in complex (II). Both structures are stabilized by intramolecular stacking interactions involving the purine rings and the phenyl rings of adjacent triphenylphosphine moieties. 相似文献
180.
Pentacarbonyl(diethylaminocarbyne)chromium tetrafluoroborate, [(CO)5− CrCNEt2]BF4 (I), reacts with PPh3 with substitution of CO and formation of trans-tetracarbonyl(diethylaminocarbyne)triphenylphosphanechromium tetra-fluoroborate, trans-[PPh3(CO)4CrCNEt2]BF4 (III). Substitution of CO by PPh3 in neutral trans-tetracarbonyl(halo)(diethylaminocarbyne)chromium complexes, trans-X(CO)4CrCNEt2 (IVa: X = Br, IVb: X = I), leads in a reversible reaction to the corresponding tricarbonyl complexes, mer-X(PPh3)(CO)3− CrNEt2 (V), PPh3 occupying the cis-position to the carbyne ligand. With PPh3 in large excess both reactions follow a first-order rate law. This as well as the activation parameters (ΔH≠ = 104–113 kJ mol−1, ΔS≠ = 64–71 J mol−1 K−1) indicate a dissociative mechanism. 相似文献