{"id":49316,"date":"2021-02-28T13:44:30","date_gmt":"2021-02-28T13:44:30","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/pares-ionicos-de-aminas-de-interes-farmaceutico-y-un-derivado-sulfonftaleinico-estudio-fisicoquimico-de-los-compuestos-en-disolucion-y-en-estado-solido\/"},"modified":"2021-02-28T13:44:30","modified_gmt":"2021-02-28T13:44:30","slug":"pares-ionicos-de-aminas-de-interes-farmaceutico-y-un-derivado-sulfonftaleinico-estudio-fisicoquimico-de-los-compuestos-en-disolucion-y-en-estado-solido","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/fisica\/pares-ionicos-de-aminas-de-interes-farmaceutico-y-un-derivado-sulfonftaleinico-estudio-fisicoquimico-de-los-compuestos-en-disolucion-y-en-estado-solido\/","title":{"rendered":"Pares ionicos de aminas de interes farmaceutico y un derivado sulfonftaleinico. estudio fisicoquimico de los compuestos en disolucion y en estado solido."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Alberto Hernandez Gainza <\/strong><\/h2>\n<p>Se ha evidenciado la interaccion de 26 aminas con un derivado sulfonftaleinico estudiando en disolucion clorofromica la espectroscopia de los pares ionicos formados  estequiometria  constantes de estabilidad efecto de la temperatura e interferencias de la reaccion.  posteriormente se han obtenido los complejos al estado solido investigando su solubilidad  espectroscopia v-uv e ir y a.T.D. Se han determinado los grupos de colorante y amina implicados en la reaccion. Tambien se han estudiado las propiedades de reparto de los pares ionicos entre cloroformo y agua calculando las constantes de extraccion y el efecto del ph en la extraccion de los complejos. Se han propuesto varias tecnicas de analisis de aminas utilizando su capacidad de formacion de pares ionicos con azul de bromotimol.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Pares ionicos de aminas de interes farmaceutico y un derivado sulfonftaleinico. estudio fisicoquimico de los compuestos en disolucion y en estado solido.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Pares ionicos de aminas de interes farmaceutico y un derivado sulfonftaleinico. estudio fisicoquimico de los compuestos en disolucion y en estado solido. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Alberto Hernandez Gainza <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Granada<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1982<\/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>Jes\u00fas Thomas Gomez<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Salvador Gonz\u00e1lez Garc\u00eda <\/li>\n<li>Antonio Cerezo Galan (vocal)<\/li>\n<li>Eugenio Sellez Flores (vocal)<\/li>\n<li>Jes\u00fas Thomas Gomez (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Alberto Hernandez Gainza Se ha evidenciado la interaccion de 26 aminas con un derivado sulfonftaleinico estudiando en [&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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