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1.
Gaston Casanova 《Advances in Applied Clifford Algebras》2004,14(2):249-252
We define analytic functions within Clifford Algebras CL, and study their trigonometric properties. We write the addition formulas when their arguments, A and B in CL, commute, this generalizes ordinary trigonometry. We examine in particular the case A2 = 1.
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Gaston Bocaz-BeneventiRosa Latorre Marta FarkováJosef Havel 《Analytica chimica acta》2002,452(1):47-63
The application of the combination of experimental design (ED) and artificial neural networks (ANNs) for the quantification of overlapped peaks in capillary zone electrophoresis is described. When the total separation cannot be achieved by separation techniques, the use of ED-ANN can be a suitable approach. The unstability of EOF causes peak shift that has to be corrected in order to apply ED-ANN methods. In this work, normalization procedure of electropherograms with consequent application of ANNs for quantification purpose was developed. Both, spectra and electropherograms can be used as multivariate data. In general, both kinds of data were found to be suitable for unresolved peaks quantification by ED-ANN approach. 相似文献
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The photochemical behaviour of twelve phenylmethylthiazole isomers is identical to that of non-methylated products. Thus, in order of decreasing reactivity we have: 2-phenylthiazole or 5-phenylisothiazole > 5-phenylthiazole or 3-phenylisothiazole > 4-phenylthiazole or 4-phenylisothiazole. The two latter undergo photoisomerization only to a slight extent.Most of the rearranged compounds (95%) are formed either by a valence bond isomerization mechanism via bicyclic intermediates where the phenyl group is conjugated to the cycle, or by the Kellogg mechanism, through a 180° rotation around the bonds adjacent to the sulphur atom.These results have furthermore allowed us to confirm the selective action of iodine in these isomerization reactions. 相似文献
7.
Eric W. Bohannan Xuerong Gao Kimberly R. Gaston Christopher D. Doss Chariklia Sotiriou-Leventis Nicholas Leventis 《Journal of Sol-Gel Science and Technology》2002,23(3):235-245
This study shows that conventional photolithography can be applied for patterning native or organic dye-doped silica films (0.5 m thick) obtained via a base-catalyzed sol-gel process. Photoresist was spin-coated onto high optical quality xerogel films, soft-baked, exposed to UV irradiation through a photomask, and developed with a commercial photoresist developing solution. Etching away of the photoresist-unprotected areas of the silica films was carried out with a dilute HF solution, while the remaining unexposed photoresist was removed with acetone. Interdigitated array patterns with features as small as 0.5 mm show a smooth surface and extremely sharp interfaces. Densification of the films at 550°C for 2 h decreases the film thickness by 11%, increases the refractive index from 1.420 to 1.456, and allows for well-defined patterning down to length scales of 10 m. Since the densification conditions are incompatible with organic dopants, it is demonstrated that sol-gel films can be doped after pattering (post-doping) by adsorption of cationic dyes from solution. Scanning electron microscopy reveals that the microstructure of patterned sol-gel films is similar to that of bulk monoliths, indicating that the photolithographic procedure is not harmful to the film quality. All patterned films demonstrate highly regular light diffraction patterns. 相似文献
8.
Philippe Milli Bernard Lvy Gaston Berthier 《International journal of quantum chemistry》1972,6(1):155-166
A first order perturbation treatment starting with SCF-MO 'S in canonical or equivalent quasi-localized form is presented for the hyperfine coupling constants of vinyl and methyl radicals. The spin-polarisation contribution to hyperfine splittings is found to be large, negative for the proton of the radical center in both radicals and positive for the β protons of vinyl. 相似文献
9.
Yves Ellinger André Rassat Robert Subra Gaston Berthier 《Theoretical chemistry accounts》1968,10(4):289-300
Résumé Une méthode de calcul dérivant des théories de champ self-consistant est utilisé pour l'étude des radicaux vinyle et cyclopropyle. L'énergie électronique et les écarts hyperfins dûs aux hydrogènes et au 13C ont été évalués en fonction de la géométrie du carbone radicalaire. L'angle C=-H du radical vinyle a été trouvé de l'ordre de 150°. Il est montré que les radicaux vinyle et cyclopropyle ont une structure électronique similaire qui ne peut être totalement expliquée ni par un modèle ni par un modèle classique, chaque radical présentant à la fois les deux caractères.
A method of calculation derived from self-consistent field theories is used for a study of vinyl and cyclopropyl radicals. Electronic energy, hydrogens and 13C hyperfine splittings are evaluated as a function of the carbon geometry. The C=-H bond angle is found to be about 150°. It is shown that vinyl and cyclopropyl radicals have a similar electronic structure which cannot be completely interpreted neither by a classical model nor by a one, each radical presenting both and character.
Zusammenfassung Nach einer auf dem SCF-Verfahren basierenden Methode werden Elektronenenergie, H- und 13C-Hyperfeinaufspaltung in Vinyl- und Cyclopropylradikalen in Abhängigkeit vom Bindungswinkel am berechnet, der sich im ersten Fall zu 150° ergibt. Es zeigt sich, daß die Elektronenstruktur der beiden behandelten Radikale ähnlich ist und daß sie weder durch ein reines - noch ein reines -Modell zu beschreiben ist.相似文献
10.
Ortica F Moustrou C Berthet J Favaro G Samat A Guglielmetti R Vermeersch G Mazzucato U 《Photochemistry and photobiology》2003,78(6):558-566
A photophysical and photochemical study of a biphotochromic compound where two naphthopyran units are linked by an acetylene-thiophene-acetylene bridge has been carried out in toluene. Both fluorescence and intersystem crossing to the triplet manifold were found to compete with the photocoloration process. Two photoproducts (transoid-trans and transoid-cis stereoisomers), absorbing at approximately 480 nm and corresponding to the opening of a single photochromic unit, were detected by spectrophotometric analysis after short irradiation time in diluted solution and identified by 1H-nuclear magnetic resonance (NMR) spectroscopy. After prolonged irradiation at 228 K of highly concentrated solutions (up to 3 x 10(-3) mol dm(-3)), two additional isomers, absorbing at approximately 550 nm, were formed. Their NMR spectra indicate the opening of both photochromic units. An interesting effect of selective vibronic excitation was found, showing that the photoreaction is favored at excited vibronic levels to the detriment of the radiative relaxation. 相似文献