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11.
Z. Rzączyńska A. Ostasz M. Sikorska-Iwan H. Głuchowska E. Olszewska S. Pikus 《Journal of Thermal Analysis and Calorimetry》2006,84(3):575-579
The complexes
of yttrium(III) and lanthanides(III) with 1,2,4,5-benzenetetracarboxylic acid
were prepared as crystalline solids of the general formula Ln4(C10H2O8)3⋅14H2O. They
are insoluble in water. On heating in air or inert gas atmosphere all compounds
lose water molecules; next anhydrous compounds decompose to oxides. The yttrium
complex and heavy lanthanide (from Ho to Lu) ones crystallize in monoclinic
crystal system. The dehydration does not change the crystal structure of the
compounds. 相似文献
12.
S. Görög 《Analytical and bioanalytical chemistry》1998,362(1):4-8
The present and past use of chemical derivatization reactions is overviewed with emphasis on the present role of derivatization
in chromatographic and electrophoretic methods with special respect to fluorogenic derivatization to increase the selectivity
and sensitivity, chiral derivatization to transform enantiomeric pairs to easily separable diastereomers, and GC/GC-MS derivatization.
Non-chromatographic derivatization is also discussed with emphasis on UV-VIS spectrophotometry, fluorimetry, and immunoassay
methods. The up-to-dateness of derivatization methods with negative examples mainly from the field of UV-VIS analysis are
also discussed. Finally, examples are given on how the experiences obtained in the course of old studies can be used to solve
current problems with the aid of chemical derivatization.
Received: 19 January 1998 / Revised: 2 March 1998 / Accepted: 6 March 1998 相似文献
13.
Wagner-Czauderna Elżbieta Orlik Marek Zajączkowska Agnieszka Kalinowski Marek K. 《Transition Metal Chemistry》2004,29(3):276-279
Microsolvation of the [Ni(acac)(tmen)]+ complex by a series of aliphatic n-alcohols (Solv) has been studied in ClCH2CH2Cl solutions by spectrophotometry. Based on the changes in the electronic spectrum of the afore-mentioned complex, observed under the influence of any alcohol, the equilibrium constants for the formation of the [Ni(acac)(tmen)Solv]+ and [Ni(acac)(tmen)Solv2]+ species have been computed according to the algorithm presented in this work. It was found that, in all the systems studied, the stability of five-coordinated [Ni(acac)(tmen)Solv]+ is higher than that of octahedral [Ni(acac)(tmen)Solv2]+. The resulting values are discussed in terms of the Lewis basicity of alcohols. 相似文献
14.
Åse Støg»rd 《Chemical physics letters》1975,36(3):357-360
Ab initio as well as semi-empirical SCF MO calculations are presented for ClCN and ONCl. The relative intensities for Cl Kβ emission in the two molecules were calculated. The calculated spectra from the ab initio wavefunctions are in excellent agreement with experiments. 相似文献
15.
The molecular electric dipole moments are reported for the series of tin-substituted tetracarbonyl cobalt compounds RnYm?nSn{Co(CO)4}4?m (m = 1–3; n ? m; R = alkyl, phenyl; Y = halogen). The effect of the substituents at the tin atom on the nature of the CoSn bond is established on calculating the (CO)4CoSn group dipole moments. It is shown that the charge transfer in the CoSn bond is mainly determined by the inductive properties of the ligands attached to tin. 相似文献
16.
A need for an elaboration of the methods for synthesis and characterization of activated carbons with a requisite porous structure has existed for a long time. One of the methods giving possibility for creating controlled mesopore and micropore structures deals with the steam gasification of various carbon materials. In this work the effects of calcium catalyst on the catalytic steam gasification of active carbons from plum stones and porous polymers are presented. Determination of micropores capacity and specific adsorption in mesopores have been performed by means of the
s
method, but adsorption on the heterogeneous solids was described by the integral equation with various local isotherms. This equation has been solved by the regularization method. Based on this method the changes in structural parameters of active carbons depending on the amount of calcium catalyst were estimated.Nomenclature
d
width of slit-like micropore
-
F(x)
distribution function of the half-width
-
p
vapor pressure of sorbate
-
p/p
N
relative pressure
- PSAC
Plum Stone Active Carbon
-
average pore radius, nm
-
S
1
relative limit of the validity of experimental point on the adsorption isotherm in the computations by means of regularization method
- SAC
Synthetic Active Carbon
-
S
BET
specific surface area calculated by means of BET method, m2/g
-
S
mes
mesopore surface area, m2/g
-
S
mic
micropore surface area, m2/g
-
T
absolute temperature, K
-
V
mes
sorption capacity of mesopores, cm3/g
-
V
mic
sorption capacity of micropores, cm3/g
-
V
p
sorption capacity of pores, cm3/g
- w/w
weight in weight concentration
-
x
half-width of slit-like micropore, nm
-
x
1
maximum of half-width of micropore slit, nm
-
average half-width of slit-like micropore, nm
-
X
min-X
max
integration limits of thex
Greek Letters Greek Letters
variance of average half-width of slit-like micropore, nm2
-
local relative filling of micropores
-
total relative filling of micropores 相似文献
17.
3-O-Acetyl-1,2-O-isopropylidene--D-allofuranose (2 b) was prepared from 1,2:5,6-di-O-isopropylidene--D-allofuranose (1 b). Treatment of2 b with triphenylphosphine-diethyl azodicarboxylate afforded regio- and stereospecifically the 5,6-epoxy--D-allo derivative (3). The other diastereomeric compound, 5,6-epoxy-1,2-O-isopropylidene--L-talofuranose (6) was also prepared stereoselectively from2 b
via the intermediates5 a and5 b. The epoxy sugars3 and6 were converted with lithium aluminum hydride to the corresponding 6-deoxy-1,2-O-isopropylidene--D-allofuranose (4 a) and --L-talofuranose (7 a) derivatives. Hydrolysis of4 a and7 a afforded 6-deoxy-D-allose and 6-deoxy-L-talose, respectively. The corresponding 3,5-di-O-acetyl- (4 b and7 b) and the 3,5-O-(tetraisopropyldisiloxane-1,3-diyl) derivatives (4 c and7 c) are also described. Selective removal of the isopropylidene group and subsequent acetylation offers a convenient route to prepare sugar derivatives containing furanose ring, like8 b, as a suitable precursor for nucleoside analogs.Herrn Prof. Dr.K. Komarek mit den besten Wünschen zum 60. Geburtstag gewidmet. 相似文献
18.
Claudia Mureşanu Lucian Copolovici Florina Pogącean 《Central European Journal of Chemistry》2005,3(4):592-604
The inhibitory effect of para-nitrophenol on the catalytic reaction of catalase was investigated. Michaelis-Menten kinetic parameters were determined from
Lineweaver-Burk plots obtained in the absence or in the presence of the inhibitor. The inhibitor pattern, revealed by the
Lineweaver-Burk plots, suggested a fully mixed inhibition mechanism. Spectrophotometric monitoring of the indicator reaction:
in conjunction with initial rate measurements was employed for the kinetic determination of the inhibitor. Calibration plots
of initial rate vs. para-nitrophenol concentration were linear in the concentration range 0.9·10−5–2.5·10−5 mol/L and the detection limit was 3·10−6 mol/L (417 μg/L) para-nitrophenol. Interferences from other phenolic compounds like orto-cresole, meta-and orto-nitrophenol were observed. 相似文献
19.
M. Iwan R. Łyszczek A. Ostasz Z. Rzączyńska 《Journal of Thermal Analysis and Calorimetry》2007,88(1):157-162
Properties of lanthanide 1,2,4-benzenetricarboxylates and lanthanide
1,2,4,5-benzenetetracarboxylates obtained by a classical synthesis method
and under hydrothermal conditions were compared. Solid 1,2,4-benzenetricarboxylates
and 1,2,4,5-benzenetetracarboxylates of cerium, neodymium and erbium were
prepared by a classical precipitation method. The same lanthanide compounds
were obtained also from hydrothermal reaction. All obtained products were
examined by elemental analysis. General formulae of complexes were: Ln(1,2,4-btc)·xH2O and Ln4(1,2,4,5-btec)3·yH2O. The thermal analysis
shows that hydrothermal conditions cause the coordination of less number of
water molecules to complex molecule. Because lanthanide ions exhibit the most
often the coordination number equal 8 or 9 one can conclude that the coordination
ability of carboxylic groups under hydrothermal conditions is different from
that under mild ones. Probably, in hydrothermal conditions the carboxylic
groups of 1,2,4-benzenetricarboxylate ions are able to form more coordination
bonds with lanthanide ions than under normal pressure. 相似文献
20.
Ion Association and Hydration in Aqueous Solutions of Nickel(II) and Cobalt(II) Sulfate 总被引:1,自引:0,他引:1
Ting?Chen Glenn?HefterEmail author Richard?Buchner 《Journal of solution chemistry》2005,34(9):1045-1066
Aqueous solutions of nickel(II) and cobalt(II) sulfate have been investigated at 25 ∘C by dielectric relaxation spectroscopy (DRS) over a wide range of frequencies (0.2 ≤ ν (GHz) ≤ 89) and salt concentrations
(0.025 ≤ c(mol-L−1) ≤ 1.4). The spectra indicate, as for MgSO4(aq) studied previously, the simultaneous presence of double solvent-separated, solvent-shared and contact ion pairs in both
NiSO4(aq) and CoSO4(aq). The stepwise formation constants for each ion-pair type and the overall association constant, obtained from the data
are in good agreement with ultrasonic relaxation and other estimates. The DR spectra at higher concentrations (c ≥ 0.5 mol-L−1) suggest the existence of a nonlinear triple ion M2SO42+(aq). Consistent with the very strong hydration of the salts, which have ‘effective’ hydration numbers approaching 27 at infinite
dilution, there are no significant differences in any of the relaxation or thermodynamic parameters for NiSO4(aq) and CoSO4(aq), except that the triple ion appears to be somewhat more stable for the latter. 相似文献