{"id":86566,"date":"2018-03-10T00:11:12","date_gmt":"2018-03-10T00:11:12","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/complejos-con-ligandos-polifuncionalizados-sintesis-reactividad-y-estructura\/"},"modified":"2018-03-10T00:11:12","modified_gmt":"2018-03-10T00:11:12","slug":"complejos-con-ligandos-polifuncionalizados-sintesis-reactividad-y-estructura","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/complejos-con-ligandos-polifuncionalizados-sintesis-reactividad-y-estructura\/","title":{"rendered":"Complejos con ligandos polifuncionalizados: sintesis, reactividad y estructura"},"content":{"rendered":"<h2>Tesis doctoral de <strong>  Huertas De La Torre Sonia <\/strong><\/h2>\n<p>En esta memoria se recogen los resultados obtenidos en el estudio de la reactividad de distintos iones metalicos frente a ligandos polifuncionalizados. en particular se han seleccionado ligandos del tipo pysch2c(o)r y ditiolatos de los tipos {s2c=c{c(o)me}2}2- y {s2c=c(cn)r}2- (r=p-c6h4br,coo-p-c6h4br).  la memoria se ha dividido en dos capitulos, con objeto de presentar los resultados de una manera ordenada y sistematica:  en el primero se describen nuevos complejos mono- y polinucleares de oro y plata con el ligando 2-(fenaciltio) piridina, de los tipos [[m]{s(py-2)ch2c(o)ph}]n+[[m]=aupph3, n=1,[m]=ag (ocio3)pph3,n=0],[[m]2{s(py-2)ch2c(o)ph}]n+[[m]=aupph3,n=2, [m]=ag(ocio3)pph3,n=0], [[m]3{s(py-2)ch2c(o)ph}]n+[[m]=aupph3,n=3,[m]=ag(ocio3)pph3, n=0], [{ag(ocio3)}2{s(py-2)ch2c(o)ph}2] y [au{ch(spy-2){c(o)ph}}(pph3)], asi como nuevos complejos ciclometalados de au(iii) que resultan de la desprotonaci\u00f3n de los ligandos 2-(acetilmetilentio)piridina y 2-(metoxicarbonilmetilentio) piridina y que contienen el esqueleto [au]{py{schc(o)r}-2}(r=me, ome).  en el segundo capitulo se presentan nuevos complejos con los ligandos 2,2-diacetil-1,1-etilenoditiolato, 2-(4-bromofenil)-2-ciano-1,1-etilenoditiolato y 2-(4-bromofenoxicarbonil)-2-ciano-1,1-etilenoditiolato. algunos de estos complejos han sido tambien utilizados como ligandos frente a diversos centros metalicos.  los resultados incluidos en el capitulo i se publicaron en eur. J.Inorg. chem. 1998,511-516 y en organometallics 1999,18,753-757 y los del capitulo ii estan todavia pendientes de publicacion.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Complejos con ligandos polifuncionalizados: sintesis, reactividad y estructura<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Complejos con ligandos polifuncionalizados: sintesis, reactividad y estructura <\/li>\n<li><strong>Autor:<\/strong>\u00a0  Huertas De La Torre Sonia <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Murcia<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 26\/09\/2000<\/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> Vicente Soler Jos\u00e9 Jes\u00fas<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: mercedes Cano esquivel <\/li>\n<li>blanca Manzano manrique (vocal)<\/li>\n<li> Heras castello Jos\u00e9 vicente (vocal)<\/li>\n<li>f\u00e9lix angel Jal\u00f3n sot\u00e9s (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Huertas De La Torre Sonia En esta memoria se recogen los resultados obtenidos en el estudio de [&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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