1000 resultados para State Funeral


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El presente trabajo busca analizar las diferentes instancias del funeral de Estado de Carlos Washington Lencinas, quien actuó en el escenario político mendocino durante la primera mitad del siglo XX. Lencinas integraba las filas de la Unión Cívica Radical, que estaba en tensión con el gobierno nacional de igual tinte político. El 10 de noviembre de 1929 Lencinas fue asesinado, provocando una profunda conmoción en la población local; no obstante, su muerte junto con las instancias del funeral colaboraron con la construcción de la imagen del caudillo popular. Esta labor se basa en artículos y fotografías de la prensa local de la época y en testimonios de la arquitectura funeraria.

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The South Carolina Board of Funeral Service publishes a newsletter of interest to funeral directors and morticians. Some topics covered are a message from the president of the South Carolina Board of Funeral Service, board meeting dates, information about new members, fines for inspection violations and continuing education.

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The South Carolina Board of Funeral Service publishes a newsletter of interest to funeral directors and morticians. Some topics covered are a message from the president of the South Carolina Board of Funeral Service, board meeting dates, information about new members, fines for inspection violations and continuing education.

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The South Carolina Board of Funeral Service publishes a newsletter of interest to funeral directors and morticians. Some topics covered are a message from the president of the South Carolina Board of Funeral Service, board meeting dates, information about new members, fines for inspection violations and continuing education.

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We report a theoretical study of the multiple oxidation states (1+, 0, 1−, and 2−) of a meso,meso-linked diporphyrin, namely bis[10,15,20-triphenylporphyrinatozinc(II)-5-yl]butadiyne (4), using Time-Dependent Density Functional Theory (TDDFT). The origin of electronic transitions of singlet excited states is discussed in comparison to experimental spectra for the corresponding oxidation states of the close analogue bis{10,15,20-tris[3‘,5‘-di-tert-butylphenyl]porphyrinatozinc(II)-5-yl}butadiyne (3). The latter were measured in previous work under in situ spectroelectrochemical conditions. Excitation energies and orbital compositions of the excited states were obtained for these large delocalized aromatic radicals, which are unique examples of organic mixed-valence systems. The radical cations and anions of butadiyne-bridged diporphyrins such as 3 display characteristic electronic absorption bands in the near-IR region, which have been successfully predicted with use of these computational methods. The radicals are clearly of the “fully delocalized” or Class III type. The key spectral features of the neutral and dianionic states were also reproduced, although due to the large size of these molecules, quantitative agreement of energies with observations is not as good in the blue end of the visible region. The TDDFT calculations are largely in accord with a previous empirical model for the spectra, which was based simplistically on one-electron transitions among the eight key frontier orbitals of the C4 (1,4-butadiyne) linked diporphyrins.