Resultados totales (Incluyendo duplicados): 4
Encontrada(s) 1 página(s)
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/IIQ183
Dataset. 2024

SUPRAMOLECULAR SUBPHTHALOCYANINE CAGE AS CATALYTIC CONTAINER FOR THE FUNCTIONALIZATION OF FULLERENES IN WATER [DATASET]

  • Salazar, Ainhoa
  • Moreno Simoni, Marta
  • Kumar, Sumit
  • Labella, Jorge
  • Torres, Tomás
  • De la Torre, Gema
It is reported the first example of a supramolecular cage that works as a catalytic molecular reactor to perform transformations over fullerenes in aqueous medium.Taking advantage of the ability of metallo–organic Pd(II)-subphthalocyanine (SubPc) capsules to form stable host:guest complexes with C60, we have prepared a water-soluble cage that provides a hydrophobic environment for conducting cycloadditions over encapsulated C60, namely, Diels–Alder reactions with anthracene. Indeed,the presence of catalytic amounts of SubPc cage dissolved in water promotes coencapsulation of insoluble C60 and anthracene substrates, allowing the reaction to occur inside the cavity under mild conditions. The lower stability of the host:guest complex with the resulting C60 cycloadduct facilitates its displacement by pristine C60, which grants catalytic turnover. Moreover, bis-addition compounds are regioselectively formed inside the cage when using excess anthracene.

DOI: https://doi.org/10.21950/IIQ183
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/IIQ183
HANDLE: https://doi.org/10.21950/IIQ183
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/IIQ183
PMID: https://doi.org/10.21950/IIQ183
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/IIQ183
Ver en: https://doi.org/10.21950/IIQ183
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/IIQ183

e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/PPAP6T
Dataset. 2024

GLYCOSYLATED BODIPY- INCORPORATED PT(II) METALLACYCLES FOR TARGETED AND SYNERGISTIC CHEMO-PHOTODYNAMIC THERAPY [DATASET]

  • Durán-Sampedro, Gonzalo
  • Xue, Evelyn Y.
  • Moreno Simoni, Marta
  • Paramio, Celia
  • Torres, Tomás
  • Dennis K. P. Ng
  • De la Torre, Gema
Pt(II)-BODIPY complexes combine the chemotherapeutic activity of Pt(II) with the photocytotoxicity of BODIPYs. Additional conjugation with targeting ligands can boost the uptake by cancer cells that overexpress the corresponding receptors. We describe two Pt(II) triangles, 1 and 2, built with pyridyl BODIPYs functionalized with glucose (3) or triethylene glycol methyl ether (4), respectively. Both 1 and 2 showed higher singlet oxygen quantum yields than 3 and 4, due to the enhanced singlet-to-triplet intersystem crossing. To evaluate the targeting effect of the glycosylated derivative, in vitro experiments were performed using glucose transporter 1 (GLUT1)-positive HT29 and A549 cancer cells, and noncancerous HEK293 cells as control. Both 1 and 2 showed higher cellular uptake than 3 and 4. Specifically, 1 was selective and highly cytotoxic toward HT29 and A549 cells. The synergistic chemo- and photodynamic behavior of the metallacycles was also confirmed. Notably, 1 exhibited superior efficacy toward the cisplatin-resistant R-HepG2 cells.

DOI: https://doi.org/10.21950/PPAP6T
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/PPAP6T
HANDLE: https://doi.org/10.21950/PPAP6T
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/PPAP6T
PMID: https://doi.org/10.21950/PPAP6T
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/PPAP6T
Ver en: https://doi.org/10.21950/PPAP6T
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/PPAP6T

e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/T22OXY
Dataset. 2024

CONTROLLING THE REACTIVITY OF PHTHALONITRILES FOR THE EFFICIENT SYNTHESIS OF CHIRAL PHTHALOCYANINES WITH SELF-ASSEMBLY ABILITIES [DATASET]

  • De la Torre, Gema
  • Paramio, Irene
  • Torres, Tomás
Binaphthol-bridged phthalonitriles are common precursors for the preparation of chiral phthalocyanines (Pcs). However, self-condensation of these phthalonitriles usually leads to the target Pcs in extremely low yields. In this work, we report a smart approach to enhance the reactivity towards self-condensation of binaphthol-bridged phthalonitriles, which relies on the addition of another highly reactive phthalonitrile that initiates the macrocyclization process, but it is eventually released. After optimization of the reaction conditions, ethynyl-containing binaphthyloxy-bridged Zn(II)Pc (AA)2-2 has been obtained in remarkable yields. This Pc synthon has been further endowed with hydrophilic cationic tails, giving the strongly amphiphilic Zn(II)Pc 1, which has shown the ability to form nanostructures in aqueous solutions.

DOI: https://doi.org/10.21950/T22OXY
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/T22OXY
HANDLE: https://doi.org/10.21950/T22OXY
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/T22OXY
PMID: https://doi.org/10.21950/T22OXY
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/T22OXY
Ver en: https://doi.org/10.21950/T22OXY
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/T22OXY

e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/VPQUHK
Dataset. 2024

NANOSTRUCTURED AABB ZN (II) PHTHALOCYANINES AS PHOTODYNAMIC AGENTS FOR BACTERIAL INACTIVATION [DATASET]

  • Paramio, Irene
  • Salazar, Ainhoa
  • Jordà-Redondo, Mireia
  • Nonell, Santi
  • Torres, Tomás
  • De la Torre, Gema

The ability of amphiphilic Phthalocyanine (Pc) photosensitizers (PS) (Zn(II)Pcs PS1, PS2, and PS3) to assemble into cationic nanoparticles in water and to photo-inactivate bacterial strains is demonstrated. All the synthesized Zn(II)Pcs exhibit an AABB functionalization pattern, having a binaphthyloxy-linked bisisoindole (AA) functionalized at the chiral binaphthol core with branched (PS1) or linear (PS2 and PS3) poly-ammonium chains, and two non-functionalized isoindole rings (BB). The aggregation behavior and the stability of the nanoparticles formed by the three PS in water is studied by UV–vis, fluorescence and circular dichroism (CD) spectroscopies, and their shape and size is determined by transmission electron microscopy (TEM) and dynamic light scattering (DLS). The PS nanoparticles prove efficient in the photoinactivation of S. aureus and E. coli. Although PS2 and PS3 present better photophysical features in their monomeric form (i.e., improved singlet oxygen quantum yield), PS1 is more effective in killing both types of strains, especially the gram-negative E. coli. This observation may derive from the low stability found for PS1 nanoparticles, which easily disassemble after binding to the bacteria surface, recovering the photophysical properties of the non-aggregated species.

Structural and photophysical characterization of compounds (Raw data).


DOI: https://doi.org/10.21950/VPQUHK
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/VPQUHK
HANDLE: https://doi.org/10.21950/VPQUHK
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/VPQUHK
PMID: https://doi.org/10.21950/VPQUHK
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/VPQUHK
Ver en: https://doi.org/10.21950/VPQUHK
e-cienciaDatos, Repositorio de Datos del Consorcio Madroño
doi:10.21950/VPQUHK

Buscador avanzado