Silvia Simón‐Fuente

ORCID: 0000-0002-3202-9196
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About
Contact & Profiles
Research Areas
  • Nanoplatforms for cancer theranostics
  • Electrochemical sensors and biosensors
  • Photodynamic Therapy Research Studies
  • Photoreceptor and optogenetics research
  • Synthesis and Properties of Aromatic Compounds
  • Advanced Chemical Sensor Technologies
  • Supramolecular Self-Assembly in Materials
  • Supramolecular Chemistry and Complexes
  • Photochromic and Fluorescence Chemistry
  • Oxidative Organic Chemistry Reactions
  • Analytical Chemistry and Sensors
  • Radical Photochemical Reactions
  • Luminescence and Fluorescent Materials
  • Advanced biosensing and bioanalysis techniques
  • Catalytic C–H Functionalization Methods
  • Photoacoustic and Ultrasonic Imaging
  • Porphyrin and Phthalocyanine Chemistry

Universidad Autónoma de Madrid
2021-2024

We present the synthesis, photophysical properties, and biological application of nontoxic 3-azo-conjugated BODIPY dyes as masked fluorescent biosensors hypoxia-like conditions. The synthetic methodology is based on an operationally simple N═N bond-forming protocol, followed by a Suzuki coupling, that allows for direct access to underexplored 3-azo-substituted BODIPY. These can turn their emission properties under both chemical reductive conditions, including bacterial human azoreductases,...

10.1021/jacs.2c01197 article EN cc-by Journal of the American Chemical Society 2022-04-29

Chiral metallo-supramolecular fibres can be easily obtained by mixing a chloroform solution of phenylacetylene monomer (PA) that bears chiral sulfoxide group as pendant, with different equivalents methanolic AgClO

10.1002/anie.202318454 article EN Angewandte Chemie International Edition 2024-01-08

A straightforward methodology for the regioselective synthesis of pyrazoles has been developed by a domino sequence based on photoclick cycloaddition followed photocatalyzed oxidative deformylation reaction. Distinguishing features this protocol include an unprecedented photoredox-catalyzed Norrish type fragmentation under green-light irradiation and use α,β-unsaturated aldehydes as synthetic equivalents alkynes, where aldehyde is acting novel photoremovable directing group.

10.1021/acs.orglett.1c01665 article EN cc-by Organic Letters 2021-06-07

Abstract Chiral metallo‐supramolecular fibres can be easily obtained by mixing a chloroform solution of phenylacetylene monomer (PA) that bears chiral sulfoxide group as pendant, with different equivalents methanolic AgClO 4 . Thus, while the PA is found molecularly dissolved in chloroform, addition Ag + ions induce its aggregation through formation an axially aggregate high thermal stable properties. In this case, ability metal ion to coordinate triple bond, combined argentophilicity and...

10.1002/ange.202318454 article EN Angewandte Chemie 2024-01-09

Herein we report the synthesis and biological properties of sugar-conjugated oligophenylene ethynylene (OPE) dyes, used as novel photosensitizers (PSs) for photodynamic treatment (PDT) under blue light. The OPE-bearing glycosides at both ends are successfully prepared by a Pd-catalyzed Sonogashira cross-coupling reaction. live-cell imaging studies have shown that these OPE (including glucose, mannose maltose derivatives) efficiently penetrate cytoplasm cultured HeLa cancer cells. No dark...

10.1039/d2ob01742c article EN Organic & Biomolecular Chemistry 2022-12-12

Functionalized upconverting nanoparticles (UCNPs) are promising theragnostic nanomaterials for simultaneous therapeutic and diagnostic purposes. We present two types of non-toxic eosin Y (EY) nanoconjugates derived from UCNPs as novel nanophotosensitizers (nano-PS) deep-tissue bioimaging agents employing light at 800 nm. This excitation wavelength ensures minimum cell damage, since the absorption water is negligible, increases tissue penetration, enhancing specificity photodynamic treatment...

10.3390/cancers15010102 article EN Cancers 2022-12-23
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