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91.
In §2, we prove that if a 2-group G and all its nonabelian maximal sub-groups are two-generator, then G is either metacyclic or minimal non-abelian. In §3, we consider a similar question for p > 2. In §4 the 2-groups all of whose minimal nonabelian subgroups have order 16 and a cyclic subgroup of index 2, are classified.
It is proved, in §5, that if G is a nonmetacyclic two-generator 2-group and A, B, C are all its maximal subgroups with d(A) ≤ d(B) ≤ d(C), then d(C) = 3 and either d(A) = d(B) = 3 (this occurs if and only if G/G′ has no cyclic subgroup of index 2) or else d(A) = d(B) = 2. Some information on the last case is obtained in Theorem 5.3. 相似文献
92.
93.
We study the liquid-crystalline phase behavior of a concentrated suspension of helical flagella isolated from Salmonella typhimurium. Flagella are prepared with different polymorphic states, some of which have a pronounced helical character while others assume a rodlike shape. We show that the static phase behavior and dynamics of chiral helices are very different when compared to simpler achiral hard rods. With increasing concentration, helical flagella undergo an entropy-driven first order phase transition to a liquid-crystalline state having a novel chiral symmetry. 相似文献
94.
Z. olji und V. Marjanovi 《Fresenius' Journal of Analytical Chemistry》1968,242(4):245-246
Ohne Zusammenfassung
Separation of indium from iron, aluminium, gallium and titanium by thin-layer chromatography相似文献
95.
The problem of intrinsic Lewis acidities of simple boron compounds (BH3-mXm, m = 0-3, X = F, Cl, Br, CH3, and OH) is assessed by their gas-phase hydride affinities (HAs). A simple and intuitively appealing picture of the interaction process including detachment of an electron from the hydride ion H-, capture of the pruned electron to the investigated Lewis acid (LA), and subsequent formation of the homolytic chemical bond between two newly created radicals is proposed. It enables transparent and straightforward dissection of the initial and final state effects, which taken together with the intermediate relaxation stabilization determine the trend of changes in the hydride affinities. The former effect is reflected in the electron affinities of the neutral Lewis acids given within Koopmans' approximation, while the final state effect involves properties of the formed Lewis acid-base adducts mirrored in the bond dissociation energy of the formed [LA-H]- chemical bond. It is demonstrated that unexpectedly low Lewis acidity of fluoroboranes relative to the corresponding chlorine and bromine derivatives can be traced down to the unfavorable Koopmans' electron affinities. Hence, it is a consequence of the initial state effect. In contrast, chloroboranes are more potent Lewis acids than fluoroboranes, because the relaxation and final state effects decisively influence their Lewis acidity. Finally, bromine-substituted borane compounds provide the most powerful studied Lewis acids. Their hydride affinities are result of a synergic interplay of the initial state, intermediate stabilization via relaxation, and final state effects. It is shown that Pearson's global hardness indices defined within his hard and soft acid-base (HSAB) principle fail to adequately predict and interpret the calculated hydride affinities. 相似文献
96.
Kubícek V Rudovský J Kotek J Hermann P Vander Elst L Muller RN Kolar ZI Wolterbeek HT Peters JA Lukes I 《Journal of the American Chemical Society》2005,127(47):16477-16485
A new macrocyclic DOTA-like ligand (BPAMD) for bone imaging and therapy containing a monoamide bis(phosphonic acid) bone-seeking group was designed and synthesized. Its lanthanide(III) complexes were prepared and characterized by 1H and 31P NMR spectroscopy. The Gd(III)-BPAMD complex was investigated in detail by 1H and 17O relaxometric studies to inspect parameters relevant for its potential application as an MRI contrast agent. Sorption experiments were conducted with Gd(III) and Tb(III) complexes using hydroxyapatite (HA) as a model of bone surface. Very effective uptake of the Gd-BPAMD complex by the HA surface was observed in NMR experiments. Radiochemical studies with the (160Tb-BPAMD)-HA system proved the sorption to be remarkably fast and strong on one hand and fully reversible on the other hand. The strong (Gd-BPAMD)-HA interaction was also supported by 1H NMRD measurements in the presence of a hydroxyapatite slurry, which showed an increase of the rotational correlation time upon adsorption of the complex on the HA surface, resulting in a significant relaxivity enhancement. The amide-bis(phosphonate) moiety is the only factor responsible for the binding of the complex to HA. 相似文献
97.
Summary The separation of diazepam, N-desmethyl diazepam, oxazepam and temazepam by thin-layer chromatography has been investigated. Satisfactory results have been obtained. 相似文献
98.
99.
100.
The structure and aromatic properties of Rees hydrocarbons 7bH-cyclopent[cd]indene and its benzo-annelated derivative 1a and 2a, respectively, are examined by the B3LYP/6−31+G(d) calculations employing HOMA criterion of Krygowski and coworkers. It is
shown that 1a possesses strong π-electron delocalization over the perimeter of the CC bonds, thus forming a quasi-[10]annulene pattern.
Its aromatic character is determined to be 83%. In contrast, 2a is less convenient model system for [14]annulene. The reason behind is that the perimeter network of the potentially aromatic
14π-electrons is supplemented by two additional more local aromatic patterns involving 10π and 6π electrons. Consequently,
the π-electron delocalization over the molecular rim is incomplete being thus diminished. The aromatic character of the peripheral
bonds in both 1a
−
and 2a
−
anions formed upon deprotonation of the central C–H bond is decreased, since the role of the smaller rings in forming aromatic
subsystems is increasing. Finally, polycyano substitution of 1a and 2a decreases aromaticity due to the price paid for the resonance effect taking place between the carbocyclic π-network and the
double bonds of the CN groups. The resonance effect is particularly strong in anions derived by heterolytic cleavage of the
C–H bond emanating from the central sp
3 carbon atom.
Dedicated to Professor T. M. Krygowski for his outstanding scientific achievements on the occasion of his 70th birthday. 相似文献