{"id":57895,"date":"2007-11-04T00:00:00","date_gmt":"2007-11-04T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/capacidad-coordinate-de-ligandos-derivados-de-2-tiazolina-e-hidrazona-frente-a-iones-metalicos-de-transicion\/"},"modified":"2007-11-04T00:00:00","modified_gmt":"2007-11-04T00:00:00","slug":"capacidad-coordinate-de-ligandos-derivados-de-2-tiazolina-e-hidrazona-frente-a-iones-metalicos-de-transicion","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/extremadura\/capacidad-coordinate-de-ligandos-derivados-de-2-tiazolina-e-hidrazona-frente-a-iones-metalicos-de-transicion\/","title":{"rendered":"Capacidad coordinate de ligandos derivados de 2-tiazolina e hidrazona frente a iones met\u00e1licos de transici\u00f3n"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Emilio Vi\u00f1uelas Zahinos <\/strong><\/h2>\n<p>Resumen:     en este trabajo se ha realizado la s\u00edntesis de (2-acetil-2-tiazolina) hidrazona (ath), n-(2-acetil-2-tiazolina)-n#-(2-tiazolid\u00edn-2-ona) azina (athtd), (2-acetil-2-tiazolina) tiosemicarbazona (hattsc), (2-acetil-2-tiazolina) semicarbazona (atsc) y (2-acetil-2-tiazolina) acetilhidrazona (athac). Estos compuestos se han caracterizado tanto en disoluci\u00f3n como en estado s\u00f3lido mediante las t\u00e9cnicas de an\u00e1lisis elemental, difracci\u00f3n de rayos x de monocristal, espectroscopia infrarroja, resonancia magn\u00e9tica nuclear y espectroscopia. Asimismo, se ha realizado la s\u00edntesis y caracterizaci\u00f3n de las fases s\u00f3lidas resultantes de la reacci\u00f3n de ath con co(ii), ni(ii), cu(ii) y cd(ii), de athtd con ni(ii), cu(ii), zn(ii) y cd(ii), de hattsc con co(ii), ni(ii), zn(ii) y cd(ii), de atsc con ni(ii) y cu(ii) y de athac con ni(ii). Las fases s\u00f3lidas obtenidas de la reacci\u00f3n de los ligandos estudiados en este trabajo con las sales de los metales de transici\u00f3n mencionados han sido caracterizas mediante an\u00e1lisis elemental, difracci\u00f3n de rayos x de monocristal, espectroscopia electr\u00f3nica, medida de la susceptibilidad magn\u00e9tica, resonancia de esp\u00edn electr\u00f3nico, espectroscopia ir y espectrometr\u00eda de masas. Asimismo se ha estudiado la actividad antimicrobiana de los ligando, algunos de los complejos obtenidos y las sales met\u00e1licas utilizadas en la s\u00edntesis de los complejos con el fin de determinar si la actividad que presentan los ligandos y las sales met\u00e1licas se ve afectada con la coordinaci\u00f3n<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Capacidad coordinate de ligandos derivados de 2-tiazolina e hidrazona frente a iones met\u00e1licos de transici\u00f3n<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Capacidad coordinate de ligandos derivados de 2-tiazolina e hidrazona frente a iones met\u00e1licos de transici\u00f3n <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Emilio Vi\u00f1uelas Zahinos <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Extremadura<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 11\/04\/2007<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li>Fernando Jos\u00e9 Barros Garc\u00eda<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: cristobal Valenzuela calahorro <\/li>\n<li>gregorio L\u00f3pez l\u00f3pez (vocal)<\/li>\n<li>\u00e1lvaro Bernalte Garc\u00eda (vocal)<\/li>\n<li>Jos\u00e9 Manuel Vila abad (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Emilio Vi\u00f1uelas Zahinos Resumen: en este trabajo se ha realizado la s\u00edntesis de (2-acetil-2-tiazolina) hidrazona (ath), n-(2-acetil-2-tiazolina)-n#-(2-tiazolid\u00edn-2-ona) [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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