<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-14T06:38:29Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/7800" metadataPrefix="dim">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/7800</identifier><datestamp>2023-09-09T22:00:53Z</datestamp><setSpec>com_10259_2699</setSpec><setSpec>col_10259_2727</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
<dim:field mdschema="dc" element="contributor" qualifier="advisor" authority="458" confidence="600" orcid_id="0000-0003-2764-7157">Quesada Pato, Roberto</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="advisor" authority="222" confidence="600" orcid_id="0000-0002-3990-8388">García Valverde, María</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" authority="fc3916df-6abf-4744-a527-397631146729" confidence="600" orcid_id="">Díaz Cabrera, Sandra</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="other" authority="48e5c491-04e9-472c-806a-a6077787bc75" confidence="600" orcid_id="">Universidad de Burgos. Departamento de Química. Área de Química Orgánica</dim:field>
<dim:field mdschema="dc" element="date" qualifier="accessioned">2023-09-07T11:46:43Z</dim:field>
<dim:field mdschema="dc" element="date" qualifier="available">2023-09-07T11:46:43Z</dim:field>
<dim:field mdschema="dc" element="date" qualifier="issued">2022</dim:field>
<dim:field mdschema="dc" element="date" qualifier="submitted">2022-04-29</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/10259/7800</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="doi">10.36443/10259/7800</dim:field>
<dim:field mdschema="dc" element="description" qualifier="abstract" lang="es">La relevancia de los compuestos heterocíclicos en áreas como la química orgánica o biológica&#xd;
hace que su estudio constituya un campo muy activo dentro de la química actual. En este&#xd;
contexto, el eje central de la presente Tesis Doctoral ha sido el estudio de derivados&#xd;
poliheterocíclicos conjugados, desde su síntesis al estudio de sus propiedades y su aplicación en&#xd;
distintas áreas. La tesis se ha estructurado en tres capítulos:&#xd;
En el primero, “Roseophilin derivatives”, se detalla la síntesis de nuevos compuestos, de tipo&#xd;
tambjamina y prodigiosina, basados en el núcleo del producto natural roseofilina. Estudio que&#xd;
ha permitido estudiar por primera vez la actividad anionofórica de sistemas con núcleo pirrolilfurano.&#xd;
En el segundo capítulo, denominado “Compuestos tetra(hetero)arílicos”, se han puesto a punto&#xd;
nuevas rutas sintéticas, basadas en la autocondensación de aldehídos pirrólicos, para la&#xd;
obtención de dipirrometenos simétricos α-sustituidos. Este capítulo se completa con el estudio&#xd;
de las propiedades fotofísicas y anionofóricas de estos sistemas, lo que ha permitido determinar&#xd;
la influencia de la sustitución en dichas propiedades.&#xd;
El tercer capítulo, “Derivados BODIPY”, se centra en el desarrollo de nuevas metodologías&#xd;
sintéticas para la obtención de meso-H BODIPYs 3,5-sustituidos. Además, para los BODIPYs&#xd;
sintetizados se han estudiado sus propiedades fotofísicas y espectroelectroquímicas,&#xd;
determinando especialmente cómo influyen los efectos electrónicos en ellas. Finalmente, se ha&#xd;
llevado a cabo el estudio de autoensamblaje supramolecular de BODIPYs con geometría angular,&#xd;
tratando de elucidar el mecanismo de agregación de estos sistemas y sus propiedades.</dim:field>
<dim:field mdschema="dc" element="description" qualifier="abstract" lang="en">Heterocyclic compounds represent key players in modern chemistry because of their&#xd;
relevance in many areas of organic and biological chemistry. This PhD dissertation is focused on&#xd;
the development of different synthetic methodologies to obtain conjugated polyheterocyclic&#xd;
derivatives, which contain pyrrole and furan units in their structures, as well as studying their&#xd;
properties and applications in different areas, such as the anions transport across lipid&#xd;
membranes or the preparation of fluorophores.&#xd;
Taking the natural product rosephilin as an inspiration, the first chapter of the dissertation&#xd;
details the results in the synthesis of compounds by mimicking this type of structure, with the&#xd;
final aim of evaluating the anionophore activity of these products in lipid vesicle models. Thus,&#xd;
it was determined the influence of the introduction of several heterocyclic rings at different&#xd;
molecular positions on their anionophoric activity. Additionally, these studies were extended to&#xd;
other compounds inspired by the structure of other alkaloids such as the tambjamines.&#xd;
Chapters two and three of this dissertation have been focused on the synthesis and study of&#xd;
different -functionalized dipyrromethenic compounds. Dipyrromethenes are complex&#xd;
chromophoric systems with interesting properties and precursors of BODIPY-type fluorophores&#xd;
(4,4-difluoro-4-bora-3a, 4a-diaza-s-indacenes).&#xd;
Thereby, in the second chapter, two synthetic routes were designed, based on the selfcondensation of pyrrolic aldehydes, to obtain -substituted symmetric dipyrromethenes. The&#xd;
products obtained proved to have good photophysical properties, tunable through structural&#xd;
variations of the compounds, modifying their protonation state and by the effect of the&#xd;
concentration or the solvent. In addition, the anionophore activity of some of them was also&#xd;
demonstrated.&#xd;
On the other hand, the third chapter of the report has been oriented to the development of&#xd;
new methodologies for obtaining 3,5-substituted meso-H BODIPYs. First, the complexation&#xd;
reaction of -prefunctionalized dipyrromethenes was studied to obtain BODIPYs with groups of&#xd;
different nature in the C3/C5 positions. In addition, the scope of cross-coupling and nucleophilic&#xd;
aromatic substitution (SNAr) reactions was explored as strategies for the post-functionalization&#xd;
of BODIPYs through the derivatization of a 3,5-dibromo BODIPY. Thus, the use of cross-coupling&#xd;
reactions allowed to maximize the overall yield of the corresponding BODIPYs with respect to&#xd;
the prefunctionalization methodologies. On the other hand, the combination of SNAr with&#xd;
copper(I)-catalyzed azide alkyne cycloaddition (CuAAC) reactions facilitated the access to&#xd;
different regioisomers of symmetric click-BODIPYs. Likewise, by using amines as nucleophiles,&#xd;
asymmetric amino-BODIPYs, precursors of more complex products such as tambjamineBODIPYs, were isolated too.&#xd;
Some of the most important properties of synthesized BODIPYs were also explored in this&#xd;
chapter. In addition to the photophysical properties, similar to those that characterizing this&#xd;
type of fluorophores; the spectroelectrochemical properties of two -aryl BODIPYs were also&#xd;
studied, study that revealed their redox activity and the differences due to the different&#xd;
electronic nature of the substituents on the fluorophores. Finally, the application of some of the&#xd;
BODIPY derivatives as anion transporters was explored and, besides, derivatives of this type&#xd;
were prepared and studied considering a special design focused on the construction of&#xd;
supramolecular polymers through supramolecular self-assembly processes.</dim:field>
<dim:field mdschema="dc" element="format" qualifier="mimetype">application/pdf</dim:field>
<dim:field mdschema="dc" element="language" qualifier="iso" lang="es">spa</dim:field>
<dim:field mdschema="dc" element="rights" lang="*">Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="uri" lang="*">http://creativecommons.org/licenses/by-nc-nd/4.0/</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="holder">Este documento está sujeto a una licencia de uso Creative Commons, por la cual está permitido hacer copia, distribuir y comunicar públicamente la obra siempre que se cite al autor original y no se haga de él uso comercial ni obra derivada</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="accessRights" lang="es">info:eu-repo/semantics/openAccess</dim:field>
<dim:field mdschema="dc" element="subject" lang="es">Dipirrometeno</dim:field>
<dim:field mdschema="dc" element="subject" lang="es">BODIPY</dim:field>
<dim:field mdschema="dc" element="subject" lang="es">Roseofilina</dim:field>
<dim:field mdschema="dc" element="subject" lang="es">Sistema poliheterocíclico</dim:field>
<dim:field mdschema="dc" element="subject" lang="es">Reacción de autocondensación</dim:field>
<dim:field mdschema="dc" element="subject" lang="en">Dipyrromethene</dim:field>
<dim:field mdschema="dc" element="subject" lang="en">Roseophilin</dim:field>
<dim:field mdschema="dc" element="subject" lang="en">Poliheterocyclic system</dim:field>
<dim:field mdschema="dc" element="subject" lang="en">Self-condensation reaction</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="other" lang="es">Química orgánica</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="other" lang="en">Chemistry, Organic</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="unesco" lang="es">23 Química</dim:field>
<dim:field mdschema="dc" element="title" lang="es">Síntesis y estudio de las propiedades de sistemas poliheterocíclicos conjugados y BODIPYs α-sustituidos</dim:field>
<dim:field mdschema="dc" element="type" lang="es">info:eu-repo/semantics/doctoralThesis</dim:field>
<dim:field mdschema="dc" element="type" qualifier="hasVersion" lang="es">info:eu-repo/semantics/acceptedVersion</dim:field>
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