Persona: Pérez Mayoral, María Elena
Cargando...
Dirección de correo electrónico
eperez@ccia.uned.es
ORCID
0000-0003-4554-141X
Fecha de nacimiento
Proyectos de investigación
Unidades organizativas
Puesto de trabajo
Apellidos
Pérez Mayoral
Nombre de pila
María Elena
Nombre
20 resultados
Resultados de la búsqueda
Mostrando 1 - 10 de 20
Publicación Developing strategies for the preparation of Co-carbon catalysts involved in the free solvent selective synthesis of aza-heterocycles(Elsevier, 2018-02) Godino Ojer, Marina; Pérez Cadenas, Agustín Francisco; Pérez Mayoral, María Elena; Martín Aranda, Rosa MaríaWe report herein different series of new zero valent Cobalt nanocarbons, as doped and supported aerogels, able to efficiently catalyze the reaction of 2-amino-5-chlorobenzaldehyde and -ketoesters, via Friedländer reaction. The reaction works under solvent-free and mild conditions affording yields over 80% in only 30 min of reaction time. The catalysts could be reused almost during two consecutive cycles without almost any activity loss. A comparative study between supported and doped-carbon aerogels, as catalysts highly efficient in the reaction, has allowed to stablish the relationship between the catalyst structure and the catalytic performance. At this regard, different parameters such as carbonization temperature and surface chemistry on the aerogels under study have been also explored. As a result, although the carbon matrix is involved in the reaction, the Co(0) nanoparticles on the carbon surface are the predominant active catalytic species. Oxygen functionalities on the oxidized samples in the surroundings of Co(0) nanoparticles probably prevent the access of the reagents, notably decreasing their catalytic performance.Publicación Efemérides: 250 años del descubrimiento del hidrógeno por Henry Cavendish: Experiments on Factitious Air(Universidad Nacional de Educación a Distancia (España). Facultad de Ciencias, 2016-01-01) Godino Ojer, Marina; González Rodal, Daniel; Milla Díez, Leticia; Pérez Mayoral, María ElenaPublicación Basolites: A type of Metal Organic Frameworks highly efficient in the one-pot synthesis of quinoxalines from α-hydroxy ketones under aerobic conditions(Elsevier, 2020-04-01) Godino Ojer, Marina; Shamzhy, Mariya; Čejka, Jiři; Pérez Mayoral, María ElenaWe report here efficient synthesis of quinoxalines from o-phenylendiamine and α-hydroxy ketones over commercial Basolites. The concentration and type of acid centres, as CUS sites, together with the porosity of the samples strongly influence the resulting conversion and selectivity. Our results indicate that the formation of quinoxalines preferentially follows a new route, in which tautomerization reactions are also involved.Publicación Tantalum vs Niobium MCF nanocatalysts in the green synthesis of chromene derivatives(Elsevier, 2019-03-15) Smuszkiewicz, Agata; López Sanz, Jesús; Sobczakb, Izabela; Ziolek, María; Martín Aranda, Rosa María; Pérez Mayoral, María ElenaTaMCF silicas modified with alkaline metals can be considered a novel family of highly efficient bifunctional catalysts involved in the synthesis of chromene derivatives, from salicylaldehyde 2 and acetonitrile compounds, under mild conditions, showing enhanced catalytic performance than their NbMCF analogues. The observed reactivity was mainly attributed to the higher basicity of the Me/TaMCF but also the texture of the samples. The Me/TaMCF silicas showed higher Brønsted basicity than the Nb ones as indicated by the stronger interaction between alkali metals and Ta in the UV–vis and the test reaction experiments. On the other hand, the basicity of Me/TaMCF together the reactivity degree and steric hindrance of the starting acetonitriles are key factors influencing the reaction selectivity. In conclusion, the basicity of the samples plays an important role initiating the reaction by activation of nucleophile but also a compromise between alkaline cation size and basicity is required.Publicación Cobalt oxide-Carbon nanocatalysts with highly enhanced catalytic performance for the green synthesis of nitrogen heterocycles through Friedländer condensation(Royal Society of Chemistry, 2019-03-19) Godino Ojer, Marina; López Peinado, Antonio José; Maldonado Hódar, Francisco J.; Bailón García, Esther; Pérez Mayoral, María ElenaA novel series of eco-sustainable catalysts developed by supporting CoO nanoparticles on different carbon supports, highly efficient in the synthesis of quinolines and naphthyridines, through the Friedländer condensation, are reported for the first time. Textural properties, dispersion and location of the Co-phase are influenced by the nature of the carbon support, Co-precursor salt and metal loading, having a significant impact on the catalytic performance. Thus, the presence of the mesopores and macropores in carbon aerogels together with the homogeneous distribution of the active phase favours the formation of product 3a as a function of the metal loading. However, an increase in the metal content when using CNTs indicates the formation of CoO aggregates and an optimal concentration of 3 wt% CoO was observed, providing the highest conversion values. The carbon-based catalysts herein reported can be considered to be a sustainable alternative having advantages such as easy preparation, superior stability and notably enhanced catalytic performance, operating at lower temperature and under solvent-free conditions.Publicación Porous carbons-derived from vegetal biomass in the synthesis of quinoxalines. Mechanistic insights(Elsevier, 2020-09-01) Godino Ojer, Marina; Blazquez García, R.; Matos, Ines; Bernardo, M.; Fonseca I.M.; Pérez Mayoral, María ElenaWe report herein for the first-time acid biomass-derived carbons from vegetal biomass, with high developed porosity, prepared through integrating method comprising pyrolysis and surface phosphonation, able to efficiently catalyze the synthesis of quinoxalines from 1,2-diamines and α-hydroxi ketones, under aerobic conditions. The obtained results indicate that the reaction is mainly driven by a combination of acid function strength and textural properties in terms of conversion and selectivity. Furthermore, our experimental and theoretical observations suggest that the preferred reaction pathway for this transformation, in the presence of the investigated acid carbon catalysts, involves cascade reactions including imination reaction between reactants, successive imine-enamine and keto-enol tautomerisms, heterocyclization followed by dehydration, and aromatization. While the acid sites seem to be a relevant role in each reaction step, the system formed by activated carbon and molecular oxygen could be behind the last oxidative reaction to give the corresponding nitrogen heterocycles.Publicación Amino-grafted basic mesoporous silicas: a type of highly performant catalysts for the green synthesis of 2-amino-4H-chromenes(Elsevier, 2024-03-15) González Rodal, Daniel; Godino Ojer, Marina; Palomino Cabello, Carlos; Turnes Palomino, Gemma; López Peinado, Antonio José; Pérez Mayoral, María ElenaNovel series of amino-grafted mesoporous silica materials applied to the green and efficient synthesis of 2-amino-4H-chromenes, from salicylaldehydes and ethyl cyanoacetate, under mild and free-solvent conditions, is herein reported for the first time. These catalysts are easily prepared by using the post-synthetic method, by functionalizing the SBA-15 silica with the corresponding amino silanes. The observed catalytic performance is mainly controlled by the type and concentration of basic sites. The methodology herein reported could be considered as an environmentally friendly alternative for the selective chromene synthesis, which allows to achieve high yields in short reaction times using notably small amounts of the catalysts. The experimental results are also supported with theoretical calculations, which suggest that the amine groups at the silica surface are behind the observed catalytic performance with the assistance of the silica matrix.Publicación Premio Nobel de Química 2008(Universidad Nacional de Educación a Distancia (España). Facultad de Ciencias, 2009-01-01) López Sanz, Jesús; Martín Aranda, Rosa Mª; Pérez Mayoral, María Elena; López Peinado, Antonio JoséPublicación Metal-free synthesis of quinolines catalyzed by carbon aerogels: Influence of the porous texture and surface chemistry(Elsevier, 2017-04-17) Godino Ojer, Marina; Soriano, Elena; Calvino Casilda, Vanesa; Maldonado-Hódar, Francisco J.; Pérez Mayoral, María ElenaWe report herein an experimental and theoretical study of the Friedländer reaction, from 2-amino-5-chlorobenzaldehyde and ethyl acetoacetate, catalyzed by free-metal nanocatalysts based on carbon aerogels, to afford quinoline 3a. The developed methodology implies the combined use of carbon aerogels with solvent-free technologies under MW irradiation yielding the corresponding quinoline with moderated yield (66%) in only 5 min of reaction time. Our results demonstrated that the reactivity of the samples upon MW irradiation is strongly dependent on the porosity and surface chemistry of the carbon aerogels, the most active catalytic species being the most acidic oxygenated functional groups, –CO2H groups originated by oxidant treatment, or even in situ by hydrolysis of –CO–O–CO–, over the carbon surface. The theoretical investigation of the reaction mechanism, by using computational methods, demonstrated that the synthesis of quinoline 3a in the absence or in the presence of carbon aerogels takes place by aldolization, subsequent heterocyclization and finally double dehydration. Relatively strong π-π stacking interactions between carbon support and reagents could be behind of the observed catalytic performance also extended for the oxygenated models. Furthermore, the concentration of –CO2H groups over the carbon surface is a key factor favoring each step of the reaction but acting as individual catalytic sites.Publicación Enhanced Catalytic Performance of ZnO/Carbon Materials with Highly Dense Active Sites in the Green Synthesis of Poly-substituted Quinolines(Elsevier, 2022-02) Godino Ojer, Marina; Morales Torres, Sergio; Pérez Mayoral, María Elena; Maldonado Hódar, Francisco J.A highly efficient methodology for the selective synthesis of nitrogen heterocycles via Friedländer reaction using carbon materials supported ZnO catalysts under the green chemistry domain is presented. The influence of the physicochemical properties of different carbon supports, in particular an activated carbon (AC), multi-walled carbon nanotubes (MWCNT) and a carbon aerogel (CA), on the catalytic performance is discussed. The developed catalysts are easily prepared by simple incipient wetness impregnation and a subsequent thermal treatment. These ZnO/carbon catalysts showed a great performance in the Friedländer condensation of 2-amino-5-chlorobenzaldehyde and carbonylic compounds with enolizable hydrogens, under solvent-free and mild conditions, affording in all cases selectively a total conversion to the corresponding quinoline. Both the Zn loading in combination with the developed microporosity of the selected carbon supports seem to be the key factors determining the catalytic performance. Yields obtained with ZnO/carbon composites catalysts are superior to those obtained by others widely used in fine chemistry such as, Zn-catalysts supported on mesoporous silica (SBA-15) and Zn-metal-organic-frameworks (MOF).