Person:
Jiménez Aparicio, Reyes

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First Name
Reyes
Last Name
Jiménez Aparicio
Affiliation
Universidad Complutense de Madrid
Faculty / Institute
Ciencias Químicas
Department
Química Inorgánica
Area
Química Inorgánica
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Now showing 1 - 10 of 14
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    Tetracarbonatodiruthenium Fragments and Lanthanide(III) Ions as Building Blocks to Construct 2D Coordination Polymers
    (Polymers, 2019) Gutiérrez Martín, Daniel; Cortijo Montes, Miguel; Martín Humanes, Álvaro; González Prieto, Rodrigo; Delgado Martínez, Patricia; Herrero Domínguez, Santiago; Priego Bermejo, José Luis; Jiménez Aparicio, Reyes
    Two-dimensional coordination polymers of [Pr(DMSO)2(OH2)3][Ru2(CO3)4(DMSO)(OH2)]·5H2O (Prα) and [Ln(OH2)5][Ru2(CO3)4(DMSO)]·xH2O (Ln = Sm (Smβ), Gd (Gdβ)) formulae have been obtained by reaction of the corresponding Ln(NO3)3·6H2O dissolved in dimethyl sulphoxide (DMSO) and K3[Ru2(CO3)4]·4H2O dissolved in water. Some DMSO molecules are coordinated to the metal atoms reducing the possibilities of connection between the [Ru2(CO3)4]3− and Ln3+ building blocks giving rise to the formation of two-dimensional networks. The size of the Ln3+ ion and the synthetic method seem to have an important influence in the type of two-dimensional structure obtained. Slow diffusion of the reagents gives rise to Prα that forms a 2D net that is built by Ln3+ ions as triconnected nodes and two types of Ru25+ units as bi- and tetraconnected nodes with (2-c)(3-c)2(4-c) stoichiometry (α structure). An analogous synthetic procedure gives Smβ and Gdβ that display a grid-like structure, (2-c)2(4-c)2, formed by biconnected Ln3+ ions and two types of tetraconnected Ru25+ fragments (β structure). The magnetic properties of these compounds are basically explained as the sum of the individual contributions of diruthenium and lanthanide species, although canted ferrimagnetism or weak ferromagnetism are observed at low temperature.
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    Microwave and solvothermal methods for the synthesis of nickel and ruthenium complexes with 9-anthracene carboxylate ligand
    (Inorganica Chimica Acta, 2015) Cortijo Montes, Miguel; Delgado-Martínez, Patricia; González Prieto, Rodrigo; Herrero Domínguez, Santiago; Jiménez Aparicio, Reyes; Perles Hernáez, Josefina; Priego Bermejo, José Luis; M.R. Torres
    Microwave and solvothermal activation processes have been explored as tools for the preparation of various nickel and ruthenium complexes. Different reaction conditions are tested using ethanol or water as solvents. Three nickel derivatives, [Ni(9-atc)2(OH2)2(py)2]·2EtOH (1), [Ni2(9-atc)4(OH2)(py)4]·2H2O (2·2H2O), and [Ni2(9-atc)4(py)2] (3), and two diruthenium compounds, {[Ru2Cl(9-atc)4]·2H2O}n (4) and [Ru2(9-atc)4(EtOH)2]·2EtOH (5), are obtained. The crystal structure determination of complexes 1-3 and 5 is also described. Compound 1 displays a 1D extended supramolecular structure with hydrogen bonds involving crystallization solvent molecules. Compound 2 is dimetallic, and both nickel centers show an octahedral coordination environment, whereas complexes 3 and 5 display a typical carboxylate-bridged paddlewheel-type structure with two metal atoms connected by four bridging carboxylate ligands. All compounds show weak antiferromagnetic interactions except 3, where a strong intra-dimer antiferromagnetic coupling is observed. Compound 4 also shows a strong zero field splitting.
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    Heteronuclear Dirhodium-Gold Anionic Complexes: Polymeric Chains and Discrete Units
    (Polymers, 2020) Fernández Bartolomé, Estefanía; Paula Cruz; Abad Galán, Laura; Cortijo Montes, Miguel; Patricia Delgado-Martínez; González Prieto, Rodrigo; Priego Bermejo, José Luis; Jiménez Aparicio, Reyes
    In this article, we report on the synthesis and characterization of the tetracarboxylatodirhodium(II) complexes [Rh2(μ–O2CCH2OMe)4(THF)2] (1) and [Rh2(μ–O2CC6H4–p–CMe3)4(OH2)2] (2) by metathesis reaction of [Rh2(μ–O2CMe)4] with the corresponding ligand acting also as the reaction solvent. The reaction of the corresponding tetracarboxylato precursor, [Rh2(μ–O2CR)4], with PPh4[Au(CN)2] at room temperature, yielded the one-dimensional polymers (PPh4)n[Rh2(μ–O2CR)4Au(CN)2]n (R = Me (3), CH2OMe (4), CH2OEt (5)) and the non-polymeric compounds (PPh4)2{Rh2(μ–O2CR)4[Au(CN)2]2} (R = CMe3 (6), C6H4–p–CMe3 (7)). The structural characterization of 1, 3·2CH2Cl2, 4·3CH2Cl2, 5, 6, and 7·2OCMe2 is also provided with a detailed description of their crystal structures and intermolecular interactions. The polymeric compounds 3·2CH2Cl2, 4·3CH2Cl2, and 5 show wavy chains with Rh–Au–Rh and Rh–N–C angles in the ranges 177.18°–178.69° and 163.0°–170.4°, respectively. A comparative study with related rhodium-silver complexes previously reported indicates no significant influence of the gold or silver atoms in the solid-state arrangement of these kinds of complexes.
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    Project number: 52
    I.amAble: El aprendizaje en ciencias al servicio de la inclusión educativa
    (2019) Herrero Domínguez, Santiago; Corrales Castellanos, María Eugenia; Sobrino Díaz, María Lourdes; Cilleros Prados, Olga; Barba Fernández, Carmen; Azor Lafarga, Alberto Eduardo; Hernández Díaz, María Yolanda; Martínez del Pozo, Álvaro; Ranchal Sánchez, Rocío; Maestre Varea, David; Méndez Pozo, Gonzalo Rubén; Gervás Gómez-Navarro, Pablo; Pastor Gil, Lorena; Taravillo Corralo, Mercedes; Guerrero Martínez, Andrés; Sánchez Benítez, Francisco Javier; Martín Conde, María; Priego Bermejo, José Luis; González Prieto, Rodrigo; Jiménez Aparicio, Reyes; Álvarez Serrano, Inmaculada; Cortés Gil, Raquel; Osío Barcina, José de Jesús; Mancheño Real, María José; Arribas Fernández, Paula; Lobato Fernández, Álvaro; Sánchez Arroyo, Antonio José; Torrecilla Manresa, Sofía; Cárdenas Bonett, Marlón Félix; Desvoyes, Benedicte; Bárcena Espelleta, Araceli; Nacenta Torres, Pablo; Rubio Lago, Luis; Bautista Blasco, Susana; Julián Cortés, Alvaro; Arancibia Llaneza, Julieta Noelia; Lombraña Pascual, Rodrigo; Catalán Torrecilla, Cristina; Gutiérrez Franco, Yanna María; Mártínez Ruiz, María Paloma
    I.amAble es un proyecto que nació con una filosofía centrada en la utilización de acciones de solidaridad como método de aprendizaje. Se diseñan y organizan talleres científicos inclusivos para realizarlos en parejas formadas por personas con discapacidad cognitiva y de educación secundaria ordinaria. Se pretende aprender a la vez que se da un servicio a la universidad y a la sociedad, y ese es el espíritu que se ha seguido manteniendo durante esta tercera edición del curso 2018-2019.
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    Linear One-Dimensional Coordination Polymers Constructed by Dirhodium Paddlewheel and Tetracyanido-Metallate Building Blocks
    (Crystals, 2019) Prior, David; Cortijo Montes, Miguel; González Prieto, Rodrigo; Herrero Domínguez, Santiago; Jiménez Aparicio, Reyes; Perles Hernáez, Josefina; Priego Bermejo, José Luis
    In this article, we describe the preparation of anionic heteronuclear one-dimensional coordination polymers made by dirhodium paddlewheels and tetracyanido-metallatate building blocks. A series of complexes of (PPh4)2n[{Rh2(µ-O2CCH3)4}{M(CN)4}]n (M = Ni (1), Pd (2), Pt (3)) formulae were obtained by reaction of [Rh2(μ-O2CCH3)4] with (PPh4)2[M(CN)4] in a 1:1 or 2:1 ratio. Crystals of 1−3 suitable for single crystal X-ray diffraction were grown by slow diffusion of a dichloromethane solution of the dirhodium complex into a chloroform solution of the corresponding tetracyanido–metallatate salt. Compounds 1 and 2 are isostructural and crystallize in the triclinic P-1 space group, while compound 3 crystallizes in the monoclinic P21/n space group. A detailed description of the structures is presented, including the analysis of the packing of anionic chains and PPh4+ cations.
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    Synthesis of Ru2Br(μ-O2CC6H4–R)4 (R = o-Me, m-Me, p-Me) Using Microwave Activation: Structural and Magnetic Properties
    (Inorganics, 2014) Delgado Martínez, Patricia; Elvira Bravo, Alejandra; González Prieto, Rodrigo; Priego Bermejo, José Luis; Jiménez Aparicio, Reyes; Torres, María Rosario
    New bromidotetracarboxylatodiruthenium(II,III) compounds of the type [Ru2Br(μ-O2CC6H4–R)4]n [R = o-Me (1), m-Me (2), p-Me (3)] have been prepared using microwave-assisted methods. Syntheses by means of solvothermal and conventional activations have also been carried out to compare different preparation methods. The crystal structure determination of complexes 1–3 is also described. All compounds display a typical carboxylate-bridged paddlewheel-type structure with the metal atoms connected by four bridging carboxylate ligands. The axial bromide ligands connect the dimetallic units giving one-dimensional zigzag chains. The magnetic properties of all compounds have also been analyzed. Weak antiferromagnetic intermolecular interactions mediated by the bromide ligands and an appreciable zero field splitting are calculated in the fits of the magnetic data of these complexes.
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    The use of amidinate ligands in paddlewheel diruthenium chemistry
    (Coordination Chemistry Reviews, 2019) Cortijo Montes, Miguel; González Prieto, Rodrigo; Herrero Domínguez, Santiago; Priego Bermejo, José Luis; Jiménez Aparicio, Reyes
    The amidinate anions have been widely used in the formation of dinuclear complexes with paddlewheel structure. The higher donor character of this type of ligands, compared to carboxylate ligands, increases the electronic density of the dimetallic units giving, in the case of ruthenium, stable complexes with a large variety of oxidation states containing Ru24+, Ru25+ and Ru26+ units. Even complexes with Ru22+, Ru23+ and Ru27+ cores have been detected in electrochemical measurements and isolated in some cases. The influence of formamidinate and benzamidinate ligands in the synthesis, characterization, properties and reactivity of metal-metal bonded diruthenium complexes with paddlewheel structure in several oxidation states is considered. A revision of the electronic and magnetic properties of diruthenium complexes and their relationship with the different electronic configurations found in this type of complexes is broadly documented. Additionally, the switching between oxidation states is considered through the discussion of the results obtained by electrochemical measurements. Finally, the most relevant applications of the amidinatodiruthenium complexes are also reviewed.
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    Steric, Activation Method and Solvent Effects on the Structure of Paddlewheel Diruthenium Complexes
    (Applied Sciences, 2022) Delgado Martínez, Patricia; Moreno Martínez, Luis; González Prieto, Rodrigo; Herrero, Santiago; Priego Bermejo, José Luis; Jiménez Aparicio, Reyes
    Conventional heating and solvothermal synthetic methods (with or without microwave activation) have been used to study the reaction of o-, m- and p-methoxybenzoic acid with [Ru2Cl(μ-O2CMe)4]. The tetrasubstituted series [Ru2Cl(µ-O2CC6H4-R)4], with R = o-OMe, m-OMe and p-OMe, has been prepared by the three procedures. Depending on the synthetic method and the experimental conditions, three compounds have been isolated (1a, 1b, 1c) with the o-methoxybenzoate ligand. However, with the m- and p-methoxybenzoate ligands, only the complexes 2 and 3 have been obtained, respectively. Compound 1a, with stoichiometry [Ru2Cl(µ-O2CC6H4-o-OMe)4]n, shows a polymeric structure with the chloride ions bridging the diruthenium units to form linear chains. Compounds 2 and 3, with the same stoichiometry, predictably form zig-zag chains in accordance with their insolubility and their magnetic measurements. Compound 1b, [Ru2Cl(µ-O2CC6H4-o-OMe)4(EtOH)], is a discrete molecular species with a chloride ion and one ethanol molecule occupying the axial positions of the dimetallic unit. Compound 1c is a cation-anion complex, [Ru2(µ-O2CC6H4-o-OMe)4(MeOH)2][Ru2Cl2(µ-O2CC6H4-o-OMe)4]. The cationic complex has two solvent molecules at the axial positions whereas the anionic complex has two chloride ligands at these positions. Complexes have been characterized by elemental analyses, mass spectrometry and IR and UV-vis-NIR spectroscopies. A magnetic study of complexes 1a, 1b, 2 and 3 have also been carried out. The crystal structure of compounds 1b and 1c have been solved by single X-ray crystal methods.
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    Project number: 73
    I.amAble: la ciencia (química) al alcance de toda la sociedad
    (2017) Herrero Domínguez, Santiago; Herrero Ansorregui, Irene; Martín Rodríguez, Pablo; Merí Bofí, Laura; Sobrino Gómez-Escalonilla, Inés; Valentín Pérez, Ángela; Azor Lafarga, Alberto; Calderón Saturio, Delia; Cilleros Prados, Olga; Hernández Díaz, Yolanda; Molero García, Julián; Sobrino Díaz, Lourdes; González Cortés, Araceli; Mena Fernández, María Luz; Muñoz Olivas, Riansares; Martínez del Pozo, Álvaro; González Prieto, Rodrigo; Jiménez Aparicio, Reyes; Priego Bermejo, José Luis; Varela Losada, Áurea; Mancheño Real, María José; Osío Barcina, José; Guerrero Martínez, Andrés; Cabañas Poveda, Albertina; Bautista Blasco, Susana; Gervás Gómez-Navarro, Pablo; González Acebrón, Laura; Méndez Pozo, Gonzalo; Pavón Mestras, Juan; Desvoyes, Bénédicte; Landa Cánovas, Ángel; Fernández Rodríguez, Juan Miguel; Perles Hernáez, Josefina
    En este proyecto de innovación, que nace con vocación de continuar en años sucesivos, se persigue mejorar la calidad de la formación de los estudiantes de la Facultad de Ciencias Químicas (F. CC.QQ.) en el ámbito de la docencia teórico-práctica y de la divulgación científica. El trabajo ha consistido en la preparación de unos experimentos prácticos para llevarlos a cabo en centros educativos no universitarios en los que se ha tenido en cuenta la participación conjunta de personas con y sin diversidad funcional, desde una perspectiva inclusiva colaborativa. Estas actividades las han realizado los estudiantes bajo la supervisión de profesores (PDI) y personal de administración y servicios (PAS). Los experimentos se han recogido en fichas didácticas para facilitar su desarrollo y aplicación por parte de otros usuarios. En estas fichas se explica detalladamente cómo realizar las experiencias en formato de taller. Las fichas de los talleres realizados están disponibles en una página web vinculada a la Universidad Complutense bajo el título I.amAble (iamable.ucm.es). Está página ha sido construida por un estudiante de la Facultad de Informática , bajo la supervisión de profesionales, tanto de esa facultad como del Instituto de Tecnología del Conocimiento, y está abierta a contribuciones similares de otras facultades y otras instituciones. La página web está diseñada de manera que resulte lo más intuitiva y accesible posible para todo tipo de público. Entre todos los experimentos se han elegido cuatro para llevarlos a la práctica en centros educativos como actividades inclusivas en las que han participado conjuntamente personas con y sin discapacidad. Con este proyecto se pretende mejorar la calidad docente al ofrecer a los estudiantes la posibilidad de aprender enseñando mediante una actividad semipresencial. El desarrollo por parte de los estudiantes de competencias transversales en educación y en divulgación de la ciencia facilitarán algunas salidas profesionales en el ámbito educativo formal (centros de enseñanza) o informal (museos, animación sociocultural). Otro aspecto importante a resaltar es la potenciación de la colaboración entre todos los miembros de la institución universitaria. Este proyecto pretende contribuir a la mejora de la cultura científica, así como al establecimiento de puentes entre la UCM y la sociedad a la que debe servir. Finalmente, es importante subrayar que incidirá en la inclusión de las personas con discapacidad como parte de la sociedad, a través del acercamiento compartido a la ciencia (Dimensiones de inclusión social y derechos de Schalock; NAVAS MACHO, P. y otros, 2012. Derechos de las personas con discapacidad intelectual: implicaciones de la Convención de Naciones Unidas. Siglo Cero. 43 (243): 7-28.).
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    Synthesis, Crystal Structure, and Magnetic Properties of Amidate and Carboxylate Dimers of Ruthenium
    (Crystals, 2017) Delgado Martínez, Patricia; Freire, Carlos; González Prieto, Rodrigo; Jiménez Aparicio, Reyes; Priego Bermejo, José Luis; Torres, M. Rosario
    Solvothermal and microwave-assisted methods have been used to prepare several amidate and carboxylate complexes of the type [Ru2X(µ-NHOCC6H3-3,5-(OMe)2)4]n [X = Cl (1), Br (2), I (3)] and [Ru2X(µ-O2CC6H3-3,5-(OMe)2)4]n [X = Cl (4), Br (5), I (6)]. Complexes 4–6 have also been obtained by conventional synthesis which is ineffective to prepare the amidate compounds. However, single crystals of complexes 1–5 were obtained using the solvothermal method. The single crystal X-ray structure determination of compounds 1–5 have been carried out. All complexes display a paddlewheel-type structure with the metal atoms connected by four bridging amidate or carboxylate ligands. Chloride, bromide, or iodide anions connect the dimetallic units, producing one-dimensional zigzag chains. The magnetic properties of all compounds were studied. The magnetic moment at room temperature are in accordance with an electronic configuration with three unpaired electrons σ2π4δ2(π*δ*)3 per dimer unit. The fit of the magnetic data suggests the existence, in these complexes, of a weak antiferromagnetic intermolecular interaction between the diruthenium units mediated by the halide ligand and an appreciable zero-field splitting in the diruthenium moieties.