Browsing by Author "Gomez, Germán E."
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Item Chain-like uranyl-coordination polymer as a bright green light emitter for sensing and sunlight driven photocatalysis(Royal Society of Chemistry, 2020-07-02) Gomez, Germán E.; Onna, Diego; D'Vries, Richard Fernando; Barja, Beatriz C.; Alcides Ellena, Javier; Narda, Griselda Edith; Soler-Illia, G. J.A.A.A new uranyl-coordination polymer (UCP) has been solvothermally synthesized employing succinic acid and 1,10-phenanthroline (phen) as ligands. The obtained compound with the formula [(UO2)2(phen)(succ)0.5(OH)(O)4(μ3-O)(H2O)]·H2O (UNSL-1) is classified as 1D chains showing I0O1 connectivity. Also, the asymmetric unit is composed of two hepta-coordinated uranyl centers: U1 is surrounded by five oxygen atoms from succinate, while U2 is surrounded by two nitrogen atoms from phen and three oxygen atoms from succinate ([U1O7] and [U2N2O5]). The secondary-building unit (SBU) is composed of a sharing edge tetrameric cluster linked with a succinate ligand in the [−1 0 1] direction. Besides, the chains are reinforced by π–π stacking interactions between the aromatic rings of the phen molecules to conform a 2D supramolecular arrangement. Moreover, photoluminescence experiments show strong green emission consistent with uranyl crystalline materials. Photophysical characterization was completed via low-temperature measurements (77 K) and recording the decay emission for calculating the lifetime (τobs) value. Regarding its multifunctional properties, a cation-sensing performance was achieved showing selective quenching toward iron ions in aqueous media. Finally, UNSL-1 was tested as an efficient water photocatalyst for dye degradation under simulated sunlight irradiation, exhibiting promising results for organic-pollutant water remediation.Item Highlighting Recent Crystalline Engineering Aspects of Luminescent Coordination Polymers Based on F-Elements and Ditopic Aliphatic Ligands(MDPI, 2022-06-02) D’Vries, Richard F.; Gomez, Germán E.; Aguilera, Lorgio RudyThree principal factors may influence the final structure of coordination polymers (CPs): (i) the nature of the ligand, (ii) the type and coordination number of the metal center, and (iii) the reaction conditions. Further, flexible carboxylate aliphatic ligands have been widely employed as building blocks for designing and synthesizing CPs, resulting in a diverse array of materials with exciting architectures, porosities, dimensionalities, and topologies as well as an increasing number of properties and applications. These ligands show different structural features, such as torsion angles, carbon backbone number, and coordination modes, which affect the desired products and so enable the generation of polymorphs or crystalline phases. Additionally, due to their large coordination numbers, using 4f and 5f metals as coordination centers combined with aliphatic ligands increases the possibility of obtaining different crystal phases. Additionally, by varying the synthetic conditions, we may control the production of a specific solid phase by understanding the thermodynamic and kinetic factors that influence the self-assembly process. This revision highlights the relationship between the structural variety of CPs based on flexible carboxylate aliphatic ligands and f-elements (lanthanide and actinides) and their outstanding luminescent properties such as solid-state emissions, sensing, and photocatalysis. In this sense, we present a structural analysis of the CPs reported with the oxalate ligand, as the one rigid ligand of the family, and other flexible dicarboxylate linkers with –CH2– spacers. Additionally, the nature of the luminescence properties of the 4f or 5f-CPs is analyzed, and finally, we present a novel set of CPs using a glutarate-derived ligand and samarium, with the formula [2,2′-bipyH][Sm(HFG)2 (2,2′-bipy) (H2O)2]•(2,2′-bipy) (α-Sm) and [2,2′-bipyH][Sm(HFG)2 (2,2′-bipy) (H2O)2] (β-Sm).Item Microfluidic amperometric immunosensor based on porous nanomaterial towards claudin7 determination for colorectal cancer diagnosis(Elsevier B.V., 2023-01-01) Ortega, Francisco G.; Gomez, Germán E.; Boni, Chiara; García, Inés Cañas; Navas, Carmen Garrido; D'vries, Richard F.; Molina Vallejos, María Pilar; Serrano, María José; Messina, Germán A.; Hernández, José Expósito; Fernández-Baldo, Martín A.In this work, we present a microfluidic amperometric immunosensor for cancer biomarker claudin7 (CLD7) determination in circulating extracellular vesicles (EVs) as well as its validation in colorectal cancer (CC) patients. The device is based on synthetized nanosized MIL-125-NH2 particles, covalently anchored to the central channel of the microfluidic immunosensor. This nanomaterial was employed as efficient platform for anti-CLD7 monoclonal antibodies immobilization for specifically recognize and capture CLD7 in EVs samples. Afterwards, the amount of this trapped CLD7 was quantified by HRP-conjugated anti-CLD7-antibody. HRP reacted with its enzymatic substrate in a redox process which resulted in the appearance of a current whose magnitude was directly proportional to the level of CLD7 in the sample. This immunosensor, under optimum conditions, gave the limit of detection for CLD7 of 0.1 pg mL− 1 , with a wide linear range from 2 to 1000 pg mL− 1 . The results reported herein open up the use of porous open framework platforms for sensing applications for biomedicine and diagnosis