Helix-sense-selective polymerization of poly(3-methyl-4vinylpyridine) have been carried out using the DPEDAHLi

Dendritic encapsulation of poly(phenyleneethynylene)s or PPEs has been shown to enhance photoluminescent quantum efficiency and facilitate energy transfer by funneling photonic energy absorbed on the dendron periphery efficiently to the conjugated polymeric core. The research presented herein focuses on incorporating degradable dendron onto PPEs, examining whether or not similar benefits were conferred upon the proposed system and controlling polymer luminescence through the elimination of the insulating macromolecules. PPEs appended with disassembling dendrons of various generation sizes were synthesized and their optical properties studied. Polymer luminescence was then quenched via chemical degradation of the disassembling dendrons. Furthermore, the macromolecules resulting from disassembly exhibited tunable luminescence properties upon manipulation of pH. Consequently, it was determined that polymer luminescence could be controlled upon forming phenolic moieties along the PPE backbone. Tunable emission was later realized in the thin film as well through the integration of crosslinkable dendrons onto the polymer core.Recently, helical synthetic linear polymers have demonstrated the ability to facilitate stereoselective processes such as catalysis, recognition and separation. Consequently, it has become increasingly desirable to develop new platforms capable of imparting asymmetry. The work presented herein describes the synthesis of a series of polymers based upon chiral hydrobenzoin and the subsequent conformational analysis performed on these materials. It was envisioned that these polymeric materials might inherently possess conformational asymmetry and as result could be able to impart configurationally chirality by introducing a diastereomeric bias for the formation of one enantiomer over the other during the course of the reaction.

Os estudos desenvolvidos nessa tese tiveram como objetivo principal o desenvolvimento de materiais que pudessem ser aplicados tanto para o reconhecimento de moléculas quirais quanto para catálise. A estrutura sugerida baseou-se em nanopartículas de ouro funcionalizadas com polímeros helicoidais ligados à superfície do metal através de um átomo de telúrio. O trabalho foi desenvolvido em quatro etapas, consistindo a primeira dos estudos de funcionalização de nanopartículas de ouro com os organoditeluretos, onde foi observado que a presença de diferentes grupos funcionais não interfere no processo. A segunda etapa foi a investigação da tolerância do catalisador de ródio, necessário para a polimerização, à presença do átomo de telúrio. Os resultados mostraram que a atividade do catalisador é inibida na presença do ditelureto, contudo, o mesmo não ocorre quando o composto está ligado à superfície da nanopartícula. A terceira e quarta etapas foram o desenvolvimento de polímeros helicoidais baseados em estruturas poli(fenilacetilênica)s, sendo uma delas desenvolvida no laboratório do Prof. Alcindo Dos Santos (terceira etapa - Brasil) e a outra no laboratório do Prof. Eiji Yashima (quarta etapa - Japão). Nos estudos da terceira etapa foi dado foco a preparação de um polímero que pudesse ser aplicado tanto para o reconhecimento de moléculas quirais quanto para catálise assimétrica, contudo, o material obtido foi bastante insolúvel na maioria dos solventes orgânicos e são necessárias modificações na estrutura do monômero para aumentar a solubilidade do respectivo polímero. Na última etapa foi investigada a influência da estrutura helicoidal em reações assimétricas, sendo preparados copolímeros constituídos por uma unidade quiral sem atividade catalítica e uma unidade aquiral com atividade catalítica. Os resultados mostraram que a unidade aquiral é capaz de promover transformações assimétricas quando presente em uma estrutura helicoidal com um sentido preferencial da hélice Com o trabalho desenvolvido determinou-se que é possível a preparação dos materiais desejados através do crescimento do polímero na superfície da nanopartícula. Preparou-se com sucesso o monômero que deverá ficar ancorado no metal, restando sintetizar um monômero de estrutura adequada para realizar o reconhecimento de moléculas e catálise, como desejado / The studies done in this PhD thesis aimed the preparation of a material that could be used in the recognition of chiral molecules and as catalysts. Its structure was based on gold nanoparticles that was functionalized with helical polymers containing a tellurium atom as an attach point. The presentation of the results was divided in four parts and the first one was the studies about the functionalization of gold nanoparticles with organoditellurides as a model material. It was observed that the presence of various functional groups in organic tellurides does not interfere into the process. The second part was the investigation of the tolerance of the rhodium catalyst, necessary for the polymerization, to the presence of the tellurium atom. The results showed that the activity of the catalyst was inhibited in the presence of a ditelluride, however, the polymerization occured when it was linked in the nanoparticle. The third and fourth parts consisted in the synthesis of the helical polymer based on oly(phenylacetilene)s structure, which one of them was prepared in professor Dos Santos\'s laboratory (third step - Brazil) and the other part in the professor Yashima\'s laboratory (fourth step - Japan). The studies of the third step was the preparation of polymers that could be applied for the recognition of chiral molecules and assymetric catalysis, however, the obtained material was too insoluble in many organic solvents and it is necessary to modify the structure of the monomer to increase the solubility of the respective polymer. In the last step was investigated the influence of the helicity in assymetric reactions. It was prepared copolymers constituted by a chiral unit without any catalytic activity and an achiral unit containing the catalytic functional group. The results showed that the achiral unit was capable to promote assymetric transformation when embebed in a preferred-handed helical structure. In this work was determined that is possible to prepare the suggested materials raising the polymer in the nanoparticle surface. The monomer that will be anchored in the metal was successfully prepared, remaining synthetize the monomer with an appropriate structure to perform the recognition of molecules and for catalysis

Nesta tese foram feitos estudos cujo objetivo principal foi centrado na síntese, caracterização e estudos da morfologia e das aplicações de polímeros helicoidais fenilacetilênicos contendo grupos laterais opticamente ativos. O trabalho foi dividido em 3 capítulos. O primeiro consistiu do estudo de inserção da fração acetilênica em núcleos aril- e piridil-oxazolínicos. Algumas limitações experimentais foram observadas em função da funcionalização das porções monoméricas sob as condições de polimerização. O segundo estudo consistiu do controle de crescimento das cadeias poliméricas, por ação de nanopartículas tipo core-shell (Au@Te-NP\'s). Foi observado que sob tais condições obtém-se cadeias poliméricas substancialmente menores do que na ausência dessas partículas. O terceiro capítulo consistiu no uso de polímeros helicoidais derivados de prolina para catálise assimétrica de reações do tipo aldol. Os resultados se mostraram promissores. Esses estudos não foram concluídos mas foi possível obter produtos com altos excessos enantio- e diastereoisomericos. / This thesis aimed the synthesis, characterization, morphology studies and applications of phenylacetilenic helical polymers containing optically active pendant groups. The results are presented in three chapters. The first was centered on the functionalization of aril- and pyridil-oxazolines with the acetylenic portion. Some experimental limitations were faced because of the functionalization of the monomers under polymerization conditions. The second chapter was dedicated to the utilization of core-shell nanoparticles (Au@Te-NP\'s) on the control of polymer chain growth. The presence of these NPs ensures the production of substantially smaller polymeric chains. The third chapter was dedicated to the employment of the optically active helical polymers as catalysts for aldol type reactions. These studies couldn\'t be concluded but where very promissory leading to products with high enantio- and diastereomeric excess.

Nesta tese foram feitos estudos cujo objetivo principal foi centrado na síntese, caracterização e estudos da morfologia e das aplicações de polímeros helicoidais fenilacetilênicos contendo grupos laterais opticamente ativos. O trabalho foi dividido em 3 capítulos. O primeiro consistiu do estudo de inserção da fração acetilênica em núcleos aril- e piridil-oxazolínicos. Algumas limitações experimentais foram observadas em função da funcionalização das porções monoméricas sob as condições de polimerização. O segundo estudo consistiu do controle de crescimento das cadeias poliméricas, por ação de nanopartículas tipo core-shell (Au@Te-NP\'s). Foi observado que sob tais condições obtém-se cadeias poliméricas substancialmente menores do que na ausência dessas partículas. O terceiro capítulo consistiu no uso de polímeros helicoidais derivados de prolina para catálise assimétrica de reações do tipo aldol. Os resultados se mostraram promissores. Esses estudos não foram concluídos mas foi possível obter produtos com altos excessos enantio- e diastereoisomericos. / This thesis aimed the synthesis, characterization, morphology studies and applications of phenylacetilenic helical polymers containing optically active pendant groups. The results are presented in three chapters. The first was centered on the functionalization of aril- and pyridil-oxazolines with the acetylenic portion. Some experimental limitations were faced because of the functionalization of the monomers under polymerization conditions. The second chapter was dedicated to the utilization of core-shell nanoparticles (Au@Te-NP\'s) on the control of polymer chain growth. The presence of these NPs ensures the production of substantially smaller polymeric chains. The third chapter was dedicated to the employment of the optically active helical polymers as catalysts for aldol type reactions. These studies couldn\'t be concluded but where very promissory leading to products with high enantio- and diastereomeric excess.

Os estudos desenvolvidos nessa tese tiveram como objetivo principal o desenvolvimento de materiais que pudessem ser aplicados tanto para o reconhecimento de moléculas quirais quanto para catálise. A estrutura sugerida baseou-se em nanopartículas de ouro funcionalizadas com polímeros helicoidais ligados à superfície do metal através de um átomo de telúrio. O trabalho foi desenvolvido em quatro etapas, consistindo a primeira dos estudos de funcionalização de nanopartículas de ouro com os organoditeluretos, onde foi observado que a presença de diferentes grupos funcionais não interfere no processo. A segunda etapa foi a investigação da tolerância do catalisador de ródio, necessário para a polimerização, à presença do átomo de telúrio. Os resultados mostraram que a atividade do catalisador é inibida na presença do ditelureto, contudo, o mesmo não ocorre quando o composto está ligado à superfície da nanopartícula. A terceira e quarta etapas foram o desenvolvimento de polímeros helicoidais baseados em estruturas poli(fenilacetilênica)s, sendo uma delas desenvolvida no laboratório do Prof. Alcindo Dos Santos (terceira etapa - Brasil) e a outra no laboratório do Prof. Eiji Yashima (quarta etapa - Japão). Nos estudos da terceira etapa foi dado foco a preparação de um polímero que pudesse ser aplicado tanto para o reconhecimento de moléculas quirais quanto para catálise assimétrica, contudo, o material obtido foi bastante insolúvel na maioria dos solventes orgânicos e são necessárias modificações na estrutura do monômero para aumentar a solubilidade do respectivo polímero. Na última etapa foi investigada a influência da estrutura helicoidal em reações assimétricas, sendo preparados copolímeros constituídos por uma unidade quiral sem atividade catalítica e uma unidade aquiral com atividade catalítica. Os resultados mostraram que a unidade aquiral é capaz de promover transformações assimétricas quando presente em uma estrutura helicoidal com um sentido preferencial da hélice Com o trabalho desenvolvido determinou-se que é possível a preparação dos materiais desejados através do crescimento do polímero na superfície da nanopartícula. Preparou-se com sucesso o monômero que deverá ficar ancorado no metal, restando sintetizar um monômero de estrutura adequada para realizar o reconhecimento de moléculas e catálise, como desejado / The studies done in this PhD thesis aimed the preparation of a material that could be used in the recognition of chiral molecules and as catalysts. Its structure was based on gold nanoparticles that was functionalized with helical polymers containing a tellurium atom as an attach point. The presentation of the results was divided in four parts and the first one was the studies about the functionalization of gold nanoparticles with organoditellurides as a model material. It was observed that the presence of various functional groups in organic tellurides does not interfere into the process. The second part was the investigation of the tolerance of the rhodium catalyst, necessary for the polymerization, to the presence of the tellurium atom. The results showed that the activity of the catalyst was inhibited in the presence of a ditelluride, however, the polymerization occured when it was linked in the nanoparticle. The third and fourth parts consisted in the synthesis of the helical polymer based on oly(phenylacetilene)s structure, which one of them was prepared in professor Dos Santos\'s laboratory (third step - Brazil) and the other part in the professor Yashima\'s laboratory (fourth step - Japan). The studies of the third step was the preparation of polymers that could be applied for the recognition of chiral molecules and assymetric catalysis, however, the obtained material was too insoluble in many organic solvents and it is necessary to modify the structure of the monomer to increase the solubility of the respective polymer. In the last step was investigated the influence of the helicity in assymetric reactions. It was prepared copolymers constituted by a chiral unit without any catalytic activity and an achiral unit containing the catalytic functional group. The results showed that the achiral unit was capable to promote assymetric transformation when embebed in a preferred-handed helical structure. In this work was determined that is possible to prepare the suggested materials raising the polymer in the nanoparticle surface. The monomer that will be anchored in the metal was successfully prepared, remaining synthetize the monomer with an appropriate structure to perform the recognition of molecules and for catalysis

Ein Ansatz der Darstellung von neuartigen funktionalen Materialien basiert auf der Synthese von Foldameren mit charakteristischen Eigenschaften, die eine Kontrolle über Formgebung und Gestaltung der Makromoleküle und derer Aggregate zulassen. Bislang sind gerade größere Foldamerstrukturen definierter Größe und Form meist schwer darstellbar und eine strukturelle Modifizierbarkeit nicht ohne weiteres möglich. In dieser Arbeit konnte gezeigt werden, dass die hohe Effizienz der seit 2002 bekannten Kupfer(I)-katalysierten 1,3-dipolaren Azid-Alkin-Cycloaddition, kurz “Klick“-Reaktion genannt, verwendet werden kann, um neuartige heteroaromatische Gerüste für die Konstruktion von diversen (makromolekularen) Strukturen zu generieren. Hierbei wird der bei der Reaktion entstehende Triazol-Ring gezielt als funktionale und strukturgebende Einheit genutzt. Zunächst wurden auf einfache und hochmodulare Weise 2,6-Bis(1-aryl-1,2,3-triazol-4-yl)pyridine (BTPs) dargestellt, die in einer hufeisenförmigen, planaren Konformation vorliegen und sich daher als helikogene Einheiten für die Konstruktion von helikalen aromatischen Foldameren eignen. Zudem stellen die BTP-Strukturen eine neue Klasse von pyridinzentrierten, tridentaten Liganden dar. Sie koordinieren an eine Vielzahl von Übergangsmetallionen unter Ausbildung von Metallkomplexen, die über interessante magnetische und lumineszierende Eigenschaften verfügen. Durch die Koordination, aber auch bei Protonierung, lassen sich die BTP-Gerüste von der gebeugten anti-anti-Konformation in eine gestreckte syn-syn-Konformation schalten. Dies wurde in Lösung, im kristallinen Festkörper und an der Flüssig-Fest-Grenzfläche zu Graphit untersucht. Über Selbstorganisation großflächig ausgebildete hochgeordnete BTP-Monoschichten an der Graphitoberfläche lassen sich mit Hilfe der Rastertunnel-Mikroskopie visualisieren und durch oben genannte externe Stimuli umstrukturieren. Eine neue Klasse von (BTP-basierten) responsiven heteroaromatischen oligomeren und polymeren Foldameren wurde mit Hilfe der „Klick“-Reaktion generiert. Die Oligomeren, sogenannte ”Klickamere“, mit einer Länge von 17 aromatischen Ringen zeigen in polaren Lösungsmitteln ein ausgeprägtes helikales Faltungsverhalten. Ein aus 17 aromatischen Ringen bestehender Foldamerstrang ist gegenüber Chloridionen responsiv, wobei es durch die Wechselwirkung mit diesem achiralen Stimulus bemerkenswerter Weise zu einer Helixinversion kommt. Die entsprechenden responsiven Polymere falten in eine stabile helikale Konformation, die bei Zugabe von Metallionen aufbricht und zu der Bildung von koordinativ kreuzverlinkten, stark viskosen Gelen führt. / One approach to develop novel functional materials is based on the synthesis of macromolecules with characteristic properties, in particular foldamers. However, preparation and structural variation of macromolecules of controllable size and specific shape are often cumbersome and versatile synthetic routes are still needed. In this dissertation, the high efficiency of the so called “click”-reaction, i.e. the Cu(I)-catalyzed Huisgen-type 1,3-dipolar cycloaddition, has been used to design a novel class of heteroaromatic (macromolecular) scaffolds. In these structures the formed triazole moieties constitute an essential integral part rather than a mere connecting unit. In a first step, structurally varying 2,6-Bis(1-aryl-1,2,3-triazolyl-4-yl)pyridines (BTPs) have been generated in an easy and modular way. The BTP scaffold adopts a kinked conformation and therefore functions as helicogenic building block for the construction of helical foldamers. Additionally, the BTP framework is responsive towards protonation and transition metal ion complexation, thereby undergoing a significant structural change from the kinked anti-anti into the extended syn-syn conformation. The conformational switching has been investigated in solution and in the solid state but can also be visualized at the liquid-solid interface on graphite by STM imaging. The BTPs represent a novel class of pyridine-centered, tridentate ligands, which form complexes with interesting magnetic and luminescent properties by the coordination to numerous transition metal ions. Varying heteroaromatic oligomeric and polymeric foldamers with remarkable properties have been generated using the “click”-reaction as synthesis tool. The BTP building blocks, which have (partly) been integrated into the backbones, support the stability of the helical conformation and provide responsiveness towards external stimuli. Three oligomer series of different length have been synthesized and analyzed. Oligomers consisting of 17 aromatic rings, termed clickamers, fold into a helical conformation in polar solvents. One of the three clickamers shows an unexpected phenomenon of helix inversion upon interaction with chloride ions as an achiral stimulus. The corresponding polymeric strands fold into an even more stable helical conformation, which breaks up upon exposure to transition metal ions leading to coordinatively crosslinked, highly viscous gels.