{"id":1564,"date":"1994-01-01T00:00:00","date_gmt":"1994-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/1994\/01\/01\/sintesis-de-nuevos-complejos-organometalicos-quirales-de-rhi-soportados-sobre-zeolitas-y-estudio-de-su-perfil-catalitico-en-reacciones-de-hidrogenacion\/"},"modified":"1994-01-01T00:00:00","modified_gmt":"1994-01-01T00:00:00","slug":"sintesis-de-nuevos-complejos-organometalicos-quirales-de-rhi-soportados-sobre-zeolitas-y-estudio-de-su-perfil-catalitico-en-reacciones-de-hidrogenacion","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/sintesis-de-nuevos-complejos-organometalicos-quirales-de-rhi-soportados-sobre-zeolitas-y-estudio-de-su-perfil-catalitico-en-reacciones-de-hidrogenacion\/","title":{"rendered":"Sintesis de nuevos complejos organometalicos quirales de rh(i) soportados sobre zeolitas y estudio de su perfil catalitico en reacciones de hidrogenacion."},"content":{"rendered":"<h2>Tesis doctoral de <strong>  Mohino Aldeanueva Federico Jes\u00fas <\/strong><\/h2>\n<p>El trabajo de tesis doctoral esta dividido en cuatro partes diferenciadas: 1 sintesis de nuevos ligandos quirales a partir de 4-hidroxiprolina, 2 preparacion de complejos organometalicos neutros y cationicos de rh (i) con los ligandos quirales mencionados anteriormente, y con diferentes coligandos, 3 su anclaje a traves de un enlace covalente a soportes inorganicos (silice y zeolita hy), y, finalmente, el estudio de dichos organometalicos heterogeneizados en comparacion a sus correspondientes complejos homogeneos, como catalizadores en reacciones de hidrogenacion, evaluando el papel del soporte, el tipo de ligando y la distancia entre el punto de anclaje en el soporte y el centro catalitico en relacion a la reactividad y selectividad de la reaccion.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Sintesis de nuevos complejos organometalicos quirales de rh(i) soportados sobre zeolitas y estudio de su perfil catalitico en reacciones de hidrogenacion.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Sintesis de nuevos complejos organometalicos quirales de rh(i) soportados sobre zeolitas y estudio de su perfil catalitico en reacciones de hidrogenacion. <\/li>\n<li><strong>Autor:<\/strong>\u00a0  Mohino Aldeanueva Federico Jes\u00fas <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Complutense de Madrid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1994<\/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>Felix Sanchez Alonso<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal:  Soto Camara Jos\u00e9 Luis <\/li>\n<li>Tom\u00e1s Torres Cebada (vocal)<\/li>\n<li>Moises Moran Horrillo (vocal)<\/li>\n<li>Jaime Primo Millo (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Mohino Aldeanueva Federico Jes\u00fas El trabajo de tesis doctoral esta dividido en cuatro partes diferenciadas: 1 sintesis [&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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