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11.
Boris Shivachev Rosica Petrova Petja Marinova Neyko Stoyanov Anife Ahmedova Mariana Mitewa 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(4):o211-o215
The crystal structures of four cycloalkanespiro‐4′‐imidazolidine‐2′,5′‐dithiones, namely cyclopentanespiro‐4′‐imidazolidine‐2′,5′‐dithione {systematic name: 1,3‐diazaspiro[4.4]nonane‐2,4‐dithione}, C7H10N2S2, cyclohexanespiro‐4′‐imidazolidine‐2′,5′‐dithione {systematic name: 1,3‐diazaspiro[4.5]decane‐2,4‐dithione}, C8H12N2S2, cycloheptanespiro‐4′‐imidazolidine‐2′,5′‐dithione {systematic name: 1,3‐diazaspiro[4.6]undecane‐2,4‐dithione}, C9H14N2S2, and cyclooctanespiro‐4′‐imidazolidine‐2′,5′‐dithione {systematic name: 1,3‐diazaspiro[4.7]dodecane‐2,4‐dithione}, C10H16N2S2, have been determined. The three‐dimensional packing in all of the structures is based on closely similar chains, in which hydantoin moieties are linked through N—H⋯S hydrogen bonding. The size of the cycloalkane moiety influences the degree of its deformation. In the cyclooctane compound, the cyclooctane ring assumes both boat–chair and boat–boat conformations. 相似文献
12.
Stefan Stoyanov Tatyana Stoyanova Pericles D. Akrivos Petros Karagiannidis Peter Nikolov 《Journal of heterocyclic chemistry》1996,33(3):927-931
The electronic absorption and emission spectra of some symmetrical heterocyclic disulfides are investigated. The reversible disulfide — thione transformation in water is discussed in view of the complex equilibrium processes present. UV irradiation and pH influence on the above transformation is also studied. The emission properties at room and low temperature are related to the computed molecular geometries of the ground and low excited states of the compounds. 相似文献
13.
V. M. Stoyanov M. M. El'chaninov A. M. Simonov A. F. Pozharskii 《Chemistry of Heterocyclic Compounds》1989,25(10):1168-1172
1-Methyl-2-(2-furyl)imidazole has been synthesized. Electrophilic attack (bromination, nitration, formylation, acylation, and hydroxymethylation) occurs in most cases at the free -position of the furan ring.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1396–1400, October, 1989. 相似文献
14.
V. Ya. Kustovskii I. A. Starostina O. V. Stoyanov 《Russian Journal of Applied Chemistry》2006,79(6):930-933
Free surface energy and acidity parameter of solid surfaces of polyepoxides used as anticorrosive coatings were measured. Formulations of epoxy resins with various curing agents were studied. The adhesion capacity of epoxy films to various metallic surfaces was evaluated. 相似文献
15.
Hydrolysis of 1,10-phenanthrolinopyrrole ethyl ester leads to the acid derivative which is unstable at room-temperature releasing CO(2) and forming 1,10-phenanthrolinopyrrole (php). The ligand reacts with ruthenium(II) to form a series of complexes of the general formula [Ru(php)(n)(bpy)(3-n)](2+), where bpy = 2,2'-bipyridine and n = 1-3. The photochemical properties reveal that the complexes have longer-lived excited states than the standard complex, [Ru(bpy)(3)](2+). Their emission lifetimes range from 9.04 micros (n = 1) to 35.5 micros (n = 3) at 77 K compared to 7.57 micros for the standard. Similarly, at room-temperature, emission lifetimes range from 1.20 micros (n = 1) to 1.70 micros (n = 3) relative to the standard (0.56 micros). The emission quantum yields also have higher values than the standard [Ru(bpy)(3)](2+) under similar conditions. The temperature-dependent studies for the complexes establish the distribution among the radiative, nonradiative, and (3)MLCT to (3)d-d decay channels and are in agreement with the energy gap law. 相似文献
16.
Pechkin A. A. El'chaninov M. M. Stoyanov V. M. 《Russian Journal of Organic Chemistry》2002,38(5):726-730
Condensation of 9,10-phenanthrenequinone with 2-furaldehyde and 2-thiophenecarbaldehyde in glacial acetic acid in the presence of ammonium acetate gave 2-(2-furyl)- and 2-(2-thienyl)phenanthro[9,10-d]imidazoles which were converted into the corresponding 1-methyl derivatives. The furan and thiophene rings in the products lose their acidophobic properties. Depending on the conditions, electrophilic substitution reactions in 2-(2-furyl)- and 2-(2-thienyl)phenanthro[9,10-d]imidazoles occur both at the furan (thiophene) and phenanthrene moieties. 相似文献
17.
Singlet ground-state geometry optimization of the monomer, four dimers, and the trimer of [Pt(bph)(CO)(2)], where bph = biphenyl dianion, was performed at the B3LYP level of density functional theory (DFT) with a mixed basis set (6-311G** on C, O, and H atoms; the Stuttgart/Dresden (SDD) effective core potential (ECP) on the Pt core; [6s5p3d] on the Pt valence shell). The aggregation was based on Pt[bond]Pt binding as well as on pi[bond]pi and electrostatic interactions. The lowest-lying triplet-state geometries of the monomer, one dimer, and the trimer of the complex were also optimized using the above theory. Significant shortening of the Pt[bond]Pt bond was recorded in the triplet state compared to the singlet one. A number of low-energy singlet and triplet allowed excited states were calculated using time-dependent density functional theory (TDDFT) and analyzed with respect to absorption, excitation, and emission spectra collected under various conditions. Simulated spectra of the monomer and dimer based on the singlet excited states were correlated with the absorption spectrum. The emission in concentrated solution was due to the triplet dimer, and the emitting states were (3)MLCT and Pt-centered states. 相似文献
18.
E. S. Stoyanov S. V. Chizhevskaya A. M. Chekmarev 《Journal of Structural Chemistry》1994,34(5):722-730
Using quantitative difference IR spectroscopy we have found that the tibutyl phosphate & acts of zirconium from 12–15 M HN03 contain ionic associates [(TBP)2H+]Zr(NO3)5
– (I) and [TBP· H30+ (H20)n]Zr(N03)5
– (II), where n = 1, 2, as well as the Zr(N03)4(TBP)2 complex at a lower concentration than (I) and (I.). The equilibrium I II is shifted toward II at higher CHNo
3
0 and lower cZr
0. The structure of associates I and II is discussed.Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, D. I. Mendeleev Moscow Chemical Technological Institute. Translated fromZhurnal Strukturnoi Khimii, Vol. 34, No. 5, pp. 80–89, September–October, 1993.Translated by L. Smolina 相似文献
19.
I. A. Starostina N. V. Sokorova O. V. Stoyanov Yu. N. Khakimullin 《Polymer Science Series D》2013,6(2):154-156
A quantitative estimate for the intensity of interphase acid-base interactions is proposed based on the acid and base parameters of the free surface energy of polymer adhesives and substrates of a different nature. An interaction between acid-base and strength characteristics of adhesive compounds is established. An increase in the adhesive strength with an increase in the difference between the surface acid and base properties of connected materials is revealed for a number of compounds (polyolefine-metal, rubber mixtures-brass, and Thiokol compounds-glass). 相似文献
20.