Ángela Sastre‐Santos

ORCID: 0000-0002-8835-2486
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About
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Research Areas
  • Porphyrin and Phthalocyanine Chemistry
  • Organic Electronics and Photovoltaics
  • Fullerene Chemistry and Applications
  • Conducting polymers and applications
  • Perovskite Materials and Applications
  • Molecular Junctions and Nanostructures
  • Luminescence and Fluorescent Materials
  • Photochemistry and Electron Transfer Studies
  • TiO2 Photocatalysis and Solar Cells
  • Photorefractive and Nonlinear Optics
  • Graphene research and applications
  • Photonic and Optical Devices
  • Carbon Nanotubes in Composites
  • Organic Chemistry Cycloaddition Reactions
  • Organic Light-Emitting Diodes Research
  • Advanced Photocatalysis Techniques
  • Nonlinear Optical Materials Research
  • Photochromic and Fluorescence Chemistry
  • Molecular Sensors and Ion Detection
  • Photosynthetic Processes and Mechanisms
  • Advanced Fiber Laser Technologies
  • Quantum Dots Synthesis And Properties
  • Nonlinear Optical Materials Studies
  • Photodynamic Therapy Research Studies
  • 2D Materials and Applications

Universitat de Miguel Hernández d'Elx
2016-2025

Hospital General Universitario de Elche
2014-2020

Instituto de Química Orgánica General
2014-2020

Universidad Univer
2019

Osaka University
2007-2014

Universitat Jaume I
2014

Japan Science and Technology Agency
2007-2011

Universidad Autónoma de Madrid
1995-2009

Universitat de València
2009

IMDEA Nanoscience
2009

Perylenediimides are ideal candidates for the substitution of fullerene derivatives as electron acceptors in bulk heterojunction organic solar cells due to their extremely intense light absorbance, high mobility and excellent photochemical stability.

10.1039/c6ta02045c article EN Journal of Materials Chemistry A 2016-01-01

Phthalocyanines (Pcs) are promising candidates for photon collectors the near-infrared region of solar spectrum in dye cells (DSC). Using two new Pc sensitizers, differing only their Zn or metal-free center, we discuss behaviour dyes as sensitizers DSC, and influence on cell performance, comparison with standard N719 dye, at identical electrolyte conditions. Based separate identification recombination resistance energy levels titania by impedance spectroscopy, determine rates also map...

10.1039/c0ee00185f article EN Energy & Environmental Science 2010-01-01

Phthalocyanines are among the most promising of efficient molecules for commercial application in dye sensitized solar cells due to their extremely intense red absorbance and excellent photochemical stability.

10.1039/c4ta01894j article EN Journal of Materials Chemistry A 2014-01-01

Graphene exfoliation upon tip sonication in o-dichlorobenzene (o-DCB) was accomplished. Covalent grafting of (2-aminoethoxy)(tri-tert-butyl) zinc phthalocyanine (ZnPc) to exfoliated graphene sheets then achieved. The newly formed ZnPc–graphene hybrid material found be soluble common organic solvents without any precipitation for several weeks. Application diverse spectroscopic techniques verified the successful formation material, while thermogravimetric analysis revealed amount ZnPc loading...

10.1021/jp305783v article EN The Journal of Physical Chemistry C 2012-09-04

This review highlights the most relevant works on phthalocyanines, porphyrins and other porphyrinoids as components of perovskite solar cells from last four years acting hole transporting materials, additives, interlayers.

10.1039/d2tc04441b article EN Journal of Materials Chemistry C 2023-01-01

Despite the potential of photodynamic therapy (PDT) in cancer treatment, development efficient and photostable photosensitizing molecules that operate at long wavelengths light has become a major hurdle. Here, we report for first time an Ir(III)-phthalocyanine conjugate (

10.1021/acsami.4c05181 article EN cc-by ACS Applied Materials & Interfaces 2024-07-23

The synthesis and characterization of a variety subphthalocyanines subnaphthalocyanines are reported. isomers several trisubstituted were separated by HPLC. physical properties investigated their use as novel targets for NLO applications is discussed.

10.1055/s-1996-4349 article EN Synthesis 1996-09-01

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTSubphthalocyanines: Novel Targets for Remarkable Second-Order Optical NonlinearitiesA. Sastre, T. Torres, M. A. Díaz-García, F. Agulló-López, C. Dhenaut, S. Brasselet, I. Ledoux, and J. ZyssView Author Information Departments of Organic Chemistry C-I Physics Materials C-IV Universidad Autónoma de Madrid Cantoblanco, 28049, Spain France Telecom, CNET Paris-B Dep. d'Electronique Quantique et Moléculaire 196, Av. Henri Ravera, 92225 Bagneux,...

10.1021/ja9533050 article EN Journal of the American Chemical Society 1996-01-01

A two-layer light-emitting electrochemical cell device based on a new perylenediimide-iridium-complex dyad is presented emitting in the deep-red region with high external quantum efficiencies (3.27%).

10.1039/b905367k article EN Chemical Communications 2009-01-01

Photoexcitation of a zinc phthalocyanine−perylenediimide (ZnPc−PDI) dyad and bis(zinc phthalocyanine)−perylenediimide [(ZnPc)2−PDI] triad results in formation the triplet excited state PDI moiety without fluorescence emission, whereas addition Mg2+ ions to long-lived charge-separated (CS) states (ZnPc•+−PDI•−/Mg2+ (ZnPc)2•+−PDI•−/Mg2+) which PDI•− forms complex with Mg2+. Formation CS presence was confirmed by appearance absorption bands due ZnPc•+ PDI•−/Mg2+ time-resolved transient spectra...

10.1021/jp805464e article EN The Journal of Physical Chemistry A 2008-10-04

Abstract The functionalization of MoS 2 is paramount importance for tailoring its properties towards optoelectronic applications and unlocking full potential. Zinc phthalocyanine (ZnPc) carrying an 1,2‐dithiolane oxide linker was used to functionalize at defect sites located the edges. structure ZnPc‐MoS fully assessed by complementary spectroscopic, thermal, microscopy imaging techniques. An energy‐level diagram visualizing different photochemical events in established revealed a...

10.1002/anie.201900101 article EN Angewandte Chemie International Edition 2019-02-21

Abstract Three diketopyrrolopyrrole (DPP) dimers, linked via different dithienylphenylene spacers, ortho ‐DPP ( o ‐DPP), meta m and para p are synthesized, characterized, probed in light of intramolecular singlet fission i ‐SF). Importantly, the corresponding DPP reference (DPP‐Ref) triplet excited state energies 2.22 1.04 eV, respectively, suggest that ‐SF is thermodynamically feasible. The investigations focus on impact relative positioning DPPs, give compelling evidence solvent polarity...

10.1002/aenm.202001496 article EN cc-by Advanced Energy Materials 2020-10-02

Phthalocyanines linked to C60 have been synthesized by two general strategies. One of them involves the addition an azomethine ylide prepared in situ from a formyl phthalocyanine C60, and other one statistical condensation substituted phthalonitriles, bearing moiety covalently attached. These new phthalocyanine-fullerene dyads studied cyclic voltammetry Osteryoung square wave voltammetry, inter- intramolecular electronic interactions between electroactive subunits demonstrated.

10.1002/1521-3765(20001002)6:19<3600::aid-chem3600>3.3.co;2-s article EN Chemistry - A European Journal 2000-10-02

The synthesis and characterization of novel non-centrosymmetrically push-pull substituted metal-free phthalocyanines 3−9 are described. compounds have different donor (dialkoxy, tert-butyl, methyl, p-tolylthio) and/or attractor (p-tolylsulfinyl, p-tolylsulfonyl, nitro) functional groups, soluble in organic solvents, especially designed to study their second- third-order nonlinear optical properties. Compounds 7−9 mixtures the four corresponding regioisomers. For preparing unsymmetrical 7−9,...

10.1021/jo961018o article EN The Journal of Organic Chemistry 1996-01-01

Photoexcitation of a zinc phthalocyanine–perylenediimide (ZnPc–PDI) dyad affords the triplet excited state without fluorescence emission, whereas addition Mg2+ to photoexcited ZnPc–PDI results in formation long-lived charge-separated (ZnPc˙+–PDI˙−/Mg2+) which PDI˙− forms complex with Mg2+.

10.1039/b506412k article EN Chemical Communications 2005-01-01

Two Zn−Pc−peptide conjugates bearing either a short linker or long PEG−linker between the macrocycle and bifunctional peptide containing nucleoplasmin HIV-1 Tat 48−60 sequences have been synthesized in order to increase Pc cell-targeting ability evaluate effect of linker. The presence chain increased water solubility and, consequently, its fluorescence aqueous solutions. highest quantum yields were observed at low pH (5.0) for both always higher conjugate Both found dark cytotoxicity toward...

10.1021/bc060297b article EN Bioconjugate Chemistry 2007-02-06

Efficient ASE at wavelengths >620 nm from PS films doped with a bay-substituted perylenediimide (PDI) derivative is reported. The maximum PDI content around 40 times larger than in prior studies. ability to introduce large dye amounts into the film without photoluminescence (PL) quenching allows very high PL and efficiencies low thresholds. A distributed feedback (DFB) laser device using one of best-performing fabricated characterized. As service our authors readers, this journal provides...

10.1002/adom.201300301 article EN Advanced Optical Materials 2013-11-11

We have successfully been able to synthesise a specific estrogen receptor-directed biolabel based on fluorescent water-soluble perylenebisimide, thus offering great potential for determining the presence of receptors in any kind cell. Moreover, this synthetic strategy allows preparation other conjugates involved study receptor, simply by selecting appropriate agonist or antagonist.

10.1039/c1cc10966a article EN Chemical Communications 2011-01-01

A new ZnPc–PDI dyad presenting for the first time a charge-separated state lower in energy than triplet excited of ZnPc and PDI has been synthesized. The rational design implies substitution with phenoxy groups bay sulfonyl substituents. lifetime was 72 μs.

10.1039/c2cc31087b article EN Chemical Communications 2012-01-01

A fully electronically conjugated phthalocyanine–perylenemonoimidebenzimidazole system has been synthesized, in which the conjugation goes through imide position of perylene.

10.1039/c4sc01579g article EN Chemical Science 2014-01-01

Orientation and distance‐dependent intervalence charge transfer phenomenon is demonstrated in far‐red capturing zinc phthalocyanine dimers connected by a bis‐acetylene‐phenyl π‐spacer (ortho, meta, or para positions) upon oxidizing one of the rings, resulting split oxidation waves new optical transition near‐infrared region. Optical studies initially probed symmetry‐breaking separation events these wherein solvent polarity‐dependent quenching was witnessed. Interestingly, efficient nonpolar...

10.1002/ange.202502516 article EN Angewandte Chemie 2025-03-18

Orientation and distance‐dependent intervalence charge transfer phenomenon is demonstrated in far‐red capturing zinc phthalocyanine dimers connected by a bis‐acetylene‐phenyl π‐spacer (ortho, meta, or para positions) upon oxidizing one of the rings, resulting split oxidation waves new optical transition near‐infrared region. Optical studies initially probed symmetry‐breaking separation events these wherein solvent polarity‐dependent quenching was witnessed. Interestingly, efficient nonpolar...

10.1002/anie.202502516 article EN Angewandte Chemie International Edition 2025-03-18

10.1142/s1088424625020018 article Journal of Porphyrins and Phthalocyanines 2025-02-01
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