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101.
102.
Gábor Dörnyei Marietta Bárczai-Beke Gábor Blaskó Péter Péchy Csaba Szántay 《Tetrahedron letters》1982,23(28):2913-2916
Regioselective demethylation of 3,4-dihydropapaveraldine (a) at 7 and 3' positions affords a properly substituted diphenolic key intermidiate (d) for the synthesis of reticuline and N-norreticuline. 相似文献
103.
104.
105.
Given a principal value convolution on the Heisenberg group Hn = Cn×R, we study the relation between its Laguerre expansion and the Fourier-Bessel expansion of its limit on Cn. We also calculate the Dirichlet kernel for the Laguerre expansion on the group Hn. 相似文献
106.
107.
I. M. Kolthoff S. R. Cooper V. J. Tulane F. Reimers H. A. J. Pieters K. Höppner V. H. Matula C. B. Macek W. N. Skworzow J. S. Schepelewa F. Čuta K. Kámen S. Cohen R. E. Oesper D. S. Narayanamurthi T. R. Seshadri H. M. State A. W. Kirssanow W. M. Tscherkassow D. M. Mukherjee T. Akiyama Y. Mine S. Yabe Y. Volmar M. Déribéré 《Analytical and bioanalytical chemistry》1937,111(5-6):192-197
108.
J.-C. Thomas L. Achouri J. Äystö R. Béraud B. Blank G. Canchel S. Czajkowski P. Dendooven A. Ensallem J. Giovinazzo N. Guillet J. Honkanen A. Jokinen A. Laird M. Lewitowicz C. Longour F. de Oliveira Santos K. Peräjärvi M. Stanoiu 《The European Physical Journal A - Hadrons and Nuclei》2004,21(3):419-435
109.
Dikandé A. M. 《The European Physical Journal B - Condensed Matter and Complex Systems》2004,42(2):247-253
Small and large-amplitude elastic deformations of the armchair structure of single-walled carbon nanotubes are investigated with emphasis on the cylindrical geometry. As starting model, we consider a discrete one-dimensional lattice of atoms interacting via a Lennard-Jones type two-body potential. In an expansion scheme using cylindrical coordinates where radial displacements are assumed negligible compared to the angular motions, a sine-lattice Hamiltonian is derived. In the limit of small-amplitude angular displacements, the dispersion spectrum of acoustic phonons is derived and the associate characteristic frequency is given as a function of parameters of the model. In the large-amplitude regime, lattice vibrations give rise to kink-type deformations which move undergoing lattice dispersion and lattice discreteness effects. The dispersion law of the kink motion is obtained and shown to lower the effect of lattice discreteness, giving rise to a vanishing Peierls stress for kink sizes of the order of a few lattice spacings. Implications of the coupling of two armchair structures on the stability of vibrational modes of an individual armchair nanotube are also discussed. A gap of forbidden modes is predicted in the phonon spectrum while the energy needed to create a kink deformation in individual nanotubes is shifted in the presence of a wall-to-wall interaction.Received: 2 August 2004, Published online: 14 December 2004PACS:
81.07.De Nanotubes - 62.30. + d Mechanical and elastic waves-vibrations - 63.22. + m Phonons in low-dimensional nanoscale materials - 63.20.Ry Anharmonic lattices modes 相似文献
110.
In order to investigate the relative effects of the differences between the structures and lipophilicities of 1, 10-dioxa-4, 7, 13, 16-tetra-azacyclo-octadecane (TA-18-crown-6) and the tetrabenzyl derivative of 1,10-dioxa-4, 7, 13, 16-tetra-azacyclo-octadecane (TBTA-18-crown-6) on their extraction-abilities and -selectivities for transition metal cations, constants of the overall extraction (logK
ex) of 1:1 (M:L) complexes, the distribution (K
D) for two diluents (CH2Cl2 and CHCl3) with different dielectric constants have been determined at 25 ± 0.1 °C. The magnitude of logK
ex is largely determined by that of K
D. The equilibrium constants of TA-18-crown-6 have been compared with those of TBTA-18-crown-6. It is found that:(i) logK
ex sequences of TA-18-crown-6 and TBTA-18-crown-6 for transition metals in CH2Cl2 lie in order: Fe3+ > Cu2+ > Mn2+ > Co2+ > Cd2+ > Ni2+ > Zn2+ and Fe3+ > Cu2+ > Co2+ > Mn2+ > Ni2+ > Cd2+ > Zn2+ respectively; (ii) the stability sequences of two types of tetra-aza-crown ethers with the transition metal cations in CHCl3 are the same as follows: Fe3+ > Ni2+ > Cu2+ > Co2+ > Zn2+ > Cd2+ > Mn2+, and (iii) unusual selectivities are observed for transition metal-tetra-aza-crowns, e.g. the high Fe3+/M
n+ selectivity factors (Sf) of TA-18-crown-6, except for the competitive-extractions for the special case in CHCl3 of TBTA-18-crown-6, it was found that the Mn2+/M
n+ values were relatively higher according to the other transition metal cations. A systematic sequence in these two types of solvents is not found for a given transition metal cation in terms of the variation of selectivity with the tetra-aza-crown ethers. The results provide alternatives for the rational design of other specific ligands on the transition metal cations. 相似文献