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排序方式: 共有249条查询结果,搜索用时 562 毫秒
1.
Algebras and Representation Theory - We introduce and study the category of twisted modules over a triangular differential graded bocs. We show that in this category idempotents split, that it... 相似文献
2.
To Professor Guillermo Torres on the occasion of his 70th birthday. 相似文献
3.
4.
Jesús Valdés-Martínez Ruben A. Toscano Roberto Salcedo Raymundo Cea-Olivares Adrian Meléndez 《Monatshefte für Chemie / Chemical Monthly》1990,121(8-9):641-647
Summary The crystal and molecular structure of salicylaldehyde semicarbazone was obtained by single crystal X-ray diffraction. The O atom of the semicarbazone fragment isanti to the N atom of the hydrazinic group. The distribution of bond lengths in the semicarbazone fragment indicates delocalization of the -electrons. The crystal structure is stabilized by intra- and intermolecular hydrogen bonds.
Semicarbazone und Thiosemicarbazone, 12. Mitt.: Die Kristallstruktur des Salicylaldehyd-Semicarbazons
Zusammenfassung Die Kristallstruktur und die molekulare Struktur des Salicylaldehyd-Semicarbazons wurde über Einkristall-Röntgenstreuung ermittelt. Das O-Atom des Semicarbazonteils stehtanti zum N-Atom der Hydrazin-Gruppierung. Die Bindungslängen in der Semicarbazoneinheit zeigen eine Delokalisierung der -Elektronen an. Die Geometrie der Verbindung wird durch stabilisierende intra- und intermolekulare Wasserstoffbrückenbindungen bestimmt.相似文献
5.
M. A. Bautista C. Pérez Sirvent I. López García M. Hernández Córdoba 《Fresenius' Journal of Analytical Chemistry》1994,350(6):359-364
A flame atomic absorption spectrometric procedure for the rapid determination of manganese, lead, zinc, calcium, magnesium, iron, sodium and potassium in cements is described. For minor components, slurries are prepared in the 0.05–0.25% m/v range by direct suspension of the samples in a medium containing 2% v/v nitric acid, 2% hydrofluoric acid and 30% v/v glycerol. 50–200 l aliquots are injected in a simple flow injection manifold using water as the carrier. When determining major components, the FI manifold includes an easy-to-construct variable volume chamber allowing the on-line dilution of the suspensions. The degree of dilution can be easily modified to obtain signals within the linear response range of the instrument. Aqueous standards are used for calibration. The data obtained for six cements agree with those obtained by conventional procedures based on the compl
M
v£e
w
ete dissolution of the samples. 相似文献
6.
M. Garcia-Vargas J. M. Bautista Rodriguez S. Avila NovsR. Coy-Yll 《Microchemical Journal》1982,27(4):519-529
The formation and extraction into chloroform of iron complex with PASH (λmax = 640 nm) was studied. Beer's law is obeyed between 2.7 and 16.0 μg · ml−1 of iron, in organic phase (10 ml). The method can be applied to volume ratios Vaq.:Vorg. from 1:1 to 20:1. The minimum concentration determinable in aqueous phase is 135 ng ml−1 of iron. The interferences of 73 species were evaluated and eliminated when it was possible. The extraction method of the green complex was applied for the spectrophotometric determination of iron(II) in several standard, geochemical, and bromatological samples. A procedure based on the standard addition method was applied satisfactorily to the determination of as little as 25 ng of iron(II) per milliliter. 相似文献
7.
F. M. Bautista J. M. Campelo A. Garcia D. Luna J. M. Marinas A. A. Romero M. R. Urbano 《Reaction Kinetics and Catalysis Letters》1997,62(1):47-54
The vapor-phase catalytic alkylation of phenol with methanol and dimethyl carbonate on a series of differently prepared CrPO4 (Cr/P=1) and CrPO4-AlPO4 (CrAIP) catalysts, has been studied at different temperatures (473–673 K). The reaction is first order in phenol, giving
a mixture of O- and C-alkylated products (C-alkylation taking place preferentially at theortho-position). Moreover, dimethyl carbonate is a better methylating agent than methanol. 相似文献
8.
M. C. Mahedero A. Muñoz De La Peña A. Bautista J.J. Aaron 《Journal of inclusion phenomena and macrocyclic chemistry》2002,42(1-2):61-70
The effect of -cyclodextrin (-CD) and hydroxypropyl--cyclodextrin (HP--CD) upon the photochemically-induced fluorescence (PIF) properties of four phenylurea herbicides, including linuron, diuron, isoproturon and neburon has been studied. Photochemical conversion of these nonfluorescent herbicides into strongly fluorescent photoproducts was shown to occur in -CD and HP--CD aqueous media. The influence of pH, UV irradiation time and photoproduct stability on the fluorescence intensity was also investigated. In addition, the stoichiometry and formation constants of the complexes formed between herbicides and -cyclodextrin (-CD) or 2-hydroxypropyl--cyclodextrin (HP--CD) were determined. The formation constant values, ranging from 184 ± 40 to 1498 ± 245 M-1, were calculated by applying the iterative nonlinear regression (NLR) approach to the PIF data. Linear calibrations graphs were established in the interval 1–12 g/mL, for diuron, linuron and neburon. The IUPAC limits of detection ranged between 580 and 700 ng/mL, according to the compound. Application to the analysis of phenylurea herbicides in spiked river water was also described. 相似文献
9.
Raymundo Cea-Olivares Jesús Wingartz Elsa Ríos Jesús Valdés-Martinez 《Monatshefte für Chemie / Chemical Monthly》1990,121(5):377-383
Summary The heterocyclic compounds ClMS2 (CH2)2 (M = As, Sb) are tested by first time as source of starting materials in the synthesis of complexes. The preparation and characterization of heterocyclic dithiocarbamatesR
2NCS2
MS2 (CH2)2, (M = As, Sb;R =Me,Et,i-Pr) is reported. Spectroscopic and analytical data suggest a bidentate behavior of the dithiocarbamate entity and the presence of aMS4 core.
Die Koordinationsfähigkeit der Heterocyclen 1,3-Dithia-2-arsa- und-stiba-cyclopentan gegenüber Schwefel enthaltenden Liganden, I. Dialkyldithiocarbamat-Komplexe
Zusammenfassung Die heterocyclischen Verbindungen ClMS2 (CH2)2 (M = As, Sb) werden erstmals als Quelle für Ausgangsmaterial zur Synthese von Komplexen herangezogen. Es wird über die Herstellung und Charakterisierung der heterocyclischen DithiocarbamateR 2NCS2 MS2 (CH2)2 (M = As, Sb;R =Me,Et,i-Pr) berichtet. Spektroskopische und analytische Daten sprechen für ein bidentates Verhalten der Dithiocarbamat-Einheit und der Präsenz einerMS4-Anordnung im Komplex.相似文献
10.
Kirmaier C Bautista JA Laible PD Hanson DK Holten D 《The journal of physical chemistry. B》2005,109(50):24160-24172
Subpicosecond transient absorption studies are reported for a set of Rhodobacter (R.) capsulatus bacterial photosynthetic reaction centers (RCs) designed to probe the origins of the unidirectionality of charge separation via one of two electron transport chains in the native pigment-protein complex. All of the RCs have been engineered to contain a heterodimeric primary electron donor (D) consisting of a bacteriochlorophyll (BChl) and a bacteriopheophytin (BPh). The BPh component of the M heterodimer (Mhd) or L heterodimer (Lhd) is introduced by substituting a Leu for His M200 or His L173, respectively. Previous work on primary charge separation in heterodimer mutants has not included the Lhd RC from R. capsulatus, which we report for the first time. The Lhd and Mhd RCs are used as controls against which we assess RCs that combine the heterodimer mutations with a second mutation (His substituted for Leu at M212) that results in replacement of the native L-side BPh acceptor with a BChl (beta). The transient absorption spectra reveal clear evidence for charge separation to the normally inactive M-side BPh acceptor (H(M)) in Lhd-beta RCs to form D+H(M)- with a yield of approximately 6%. This state also forms in Mhd-beta RCs but with about one-quarter the yield. In both RCs, deactivation to the ground state is the predominant pathway of D decay, as it is in the Mhd and Lhd single mutants. Analysis of the results indicates an upper limit ofV2L/V2m < or = 4 for the contribution of the electronic coupling elements to the relative rates of electron transfer to the L versus M sides of the wild-type RC. In comparison to the L/M rate ratio (kL/kM) approximately 30 for wild-type RCs, our findings indicate that electronic factors contribute approximately 35% at most to directionality with the other 65% deriving from energetic considerations, which includes differences in free energies, reorganization energies, and contributions of one- and two-step mechanisms on the two sides of the RC. 相似文献