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1.
Todd Rowland 《Complexity》2006,12(2):13-29
We present a network experiment that investigates the computational power of cellular automata on the simplest irregular lattice. One cellular automaton whose apparent complexity increased is Rule 60, the left neighbor Xor operator. It went from being nested to complex. That makes Xor a candidate for universal computational power. We present the evidence in terms of the size of cycle lengths, transients, and size of boolean expressions. © 2006 Wiley Periodicals, Inc. Complexity 12: 13–29, 2006 相似文献
2.
D. R. Rowland 《Optical and Quantum Electronics》1990,22(4):369-373
A geometrical method for determining the power transfer between piecewise uniform, alternating , twin-core linear directional couplers is presented. Phase space provides the basis for the method. 相似文献
3.
M.P. Irion W.D. Bowers R.L. Hunter F.S. Rowland R.T. McIver 《Chemical physics letters》1982,93(4):375-379
Ions produced by multiphoton ionization (MPI) of naphthalene, fluoranthene and triphenylene have been detected by Fourier-transform mass spectrometry (FT MS). Paret ions are produced very efficiently at 250 and 222 nm with pulse energies as low as 1 mJ. With FT MS a complete, high-resolution mass spectrum is obtained for each laser pulse. 相似文献
4.
The problem of defining N(E), the density of states, for molecular systems is discussed. It is shown that a numeric evaluation of N(E) is often only approximate, even for continuous data, and is not well defined for quantized systems. The application of the concept of density of states is discussed, particularly with regard to the RRKM theory of unimolecular reactions. The sum of states, W(E), and density of states curves are evaluated for several harmonic and anharmonic model systems and the results discussed in order to illustrate the foregoing considerations. 相似文献
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7.
S. P. Rowland V. O. Cirino A. L. Bullock 《Journal of polymer science. Part A, Polymer chemistry》1971,9(6):1677-1683
Cotton cellulose in fabric form was crosslinked with divinyl sulfone by catalysis with solutions of sodium hydroxide of normalities ranging from 0.1 to 4.0. The molecular chains of cellulose were hydrolyzed with sulfuric acid to yield hydrolyzates from which simple substituted glucoses (i.e., those bonded to a single unit of DVS), the simple crosslinked glucoses (i.e., those joined together by a single unit of DVS), and complex structures (i.e., those substituted or crosslinked with more than one unit of DVS in the chain) were isolated and measured. The fractions of the reagent residues in the forms of the structures noted above were found to change substantially with the concentration of base employed to catalyze the reaction. The constitution of the reagent residues resulting from reaction in 0.1N base was remarkably simple: 82% of the DVS residues in the form of simple crosslinks and 18% in the form of simple substituents. Complex structures accounted for as much as 70% of the DVS residues under other conditions of reaction. 相似文献
8.
Reaction of Cu(ClO(4))(2) x 6H(2)O with a racemic mixture of the novel chiral ligand N-(1,2-bis(2-pyridyl)ethyl)pyridine-2-carboxamide (PEAH) affords only the homochiral dimeric copper(II) complexes [Cu(2)((R)()PEA)(2)](ClO(4))(2) and [Cu(2)((S)()PEA)(2)](ClO(4))(2) in a 1:1 ratio. The phenomenon of molecular self-recognition is also observed when a racemic mixture of the monomeric copper(II) complex [Cu((R(S))()PEA)(Cl)(H(2)O)] is converted into the homochiral dimeric species [Cu(2)((R(S))()PEA)(2)](ClO(4))(2) via reaction with Ag(+) ion. This is the first report of direct conversion of a racemic mixture of a chiral monomeric copper(II) complex to a mixture of the homochiral dimers. 相似文献
9.
The novel tripodal ligand N-(bis(2-pyridyl)methyl)-2-pyridinecarboxamide (Py3AH) affords monomeric and dimeric copper(II) complexes with coordinated carboxamido nitrogens. Although many chloro-bridged dimeric copper(II) complexes are known, [Cu(Py3A)(Cl)] (1) remains monomeric and planar with a pendant pyridine and does not form either a chloro-bridged dimer or the ligand-shared dimeric complex [Cu(Py3A)(Cl)]2 (4) in solvents such as CH3CN. When 1 is dissolved in alcohols, square pyramidal alcohol adducts [Cu(Py3A)(Cl)(CH3OH)] (2) and [Cu(Py3A)(Cl)(C2H5OH)] (3) are readily formed. In 2 and 3, the ROH molecules are bound at axial site of copper(II) and the weak axial binding of the ROH molecule is strengthened by intramolecular hydrogen bonding between ROH and the pendant pyridine nitrogen. Two ligand-shared dimeric species [Cu(Py3A)(Cl)]2 (4) and [Cu(Py3A)]2(ClO4)2 (5) have also been synthesized in which the pendant pyridine of one [Cu(Py3A)] unit completes the coordination sphere of the other [Cu(Py3A)] neighbor. These ligand-shared dimers are obtained in aqueous solutions or in complete absence of chloride in the reaction mixtures. 相似文献
10.
The so-called imidazolines (2-alkyl-1-[ethylalkylamide]-2-imidazolines and 2-alkyl-1-ethylamine-2-imidazolines) are a group of surface-active compounds, complex mixtures of which are used by various industries as surfactants and corrosion inhibitors. Although their industrial synthesis was reported over 100 years ago, few methods for the determination of individual imidazolines in mixtures, including industrial matrices such as crude oils, have been reported. Here we demonstrate that spiking of crude oils with synthetic imidazolines followed by solid-phase extraction and liquid chromatography/electrospray ionisation multistage mass spectrometry (LC/ESI - MS(n)) allows an estimation of low (<10) parts per million concentrations of individual imidazolines in crude oils. Whilst non-optimised at present, the method is a significant advance and may prove useful not only for improving an understanding of the mechanisms of industrial imidazoline synthesis and for monitoring downhole and topside oilfield operations, but also for the determination of the fate of imidazoline-based oilfield corrosion inhibitors and surfactants in the environment. 相似文献