Miguel A. Revuelta‐Maza

Self‐Assembled Binaphthyl‐Bridged Amphiphilic AABB Phthalocyanines: Nanostructures for Efficient Antimicrobial Photodynamic Therapy

Miguel A. Revuelta‐Maza, Elena de las Heras, Montserrat Agut, Santi Nonell et autres

Pcs (PS-1 and PS-2), with an AABB geometry (where A and B refer to differently substituted isoindole constituents). They contain differently functionalized, chiral binaphthyloxy-linked A isoindole units, which determine the hydrophobicity of the system, and cationic methyl pyridinium moieties in the other …

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Assessing Amphiphilic ABAB Zn(II) Phthalocyanines with Enhanced Photosensitization Abilities in In Vitro Photodynamic Therapy Studies Against Cancer

Miguel A. Revuelta‐Maza, Marta Mascaraque, Patricia González-Jiménez, Arturo González‐Camuñas et autres

We have previously demonstrated that singlet oxygen photosensitization abilities of Zn(II) phthalocyanines (Zn(II)Pcs) are enhanced through α-functionalization with bulky fluorinated substituents (i.e., bis(trifluoromethyl)phenyl units) at facing positions of ABAB Zn(II)Pcs, where A and B refer to differently functionalized isoindoles. In this work, …

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Fluorine-substituted tetracationic ABAB-phthalocyanines for efficient photodynamic inactivation of Gram-positive and Gram-negative bacteria

Miguel A. Revuelta‐Maza, Patricia González-Jiménez, Cormac Hally, Montserrat Agut et autres

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Synthesis and Aggregation Studies of Functional Binaphthyl-Bridged Chiral Phthalocyanines

Miguel A. Revuelta‐Maza, Tomás Torres⊗, Gema de la Torre

We describe the preparation of a battery of chiral Zn(II) phthalocyanines with an AABB substitution pattern through cross-condensation of different chiral, binaphthyloxy-linked bisphthalonitriles and (non)functionalized single phthalonitriles. All the compounds are endowed with reactive groups (halogen and/or ethynyl moieties) that will allow …

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Crosswise Phthalocyanines with Collinear Functionalization: New Paradigmatic Derivatives for Efficient Singlet Oxygen Photosensitization

Miguel A. Revuelta‐Maza, Cormac Hally, Santi Nonell, Gema de la Torre et autres

Abstract We describe here the preparation of a series of trans‐ABAB Zn(II) phthalocyanines (ZnPcs, which combine several interesting features. First, these compounds present high solubility and hindered aggregation, due to the functionalization of two facing isoindole constituents (B) of the ZnPc with …

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Boosting the singlet oxygen photosensitization abilities of Zn( ii ) phthalocyanines through functionalization with bulky fluorinated substituents

Miguel A. Revuelta‐Maza, Santi Nonell, Gema de la Torre, Tomás Torres⊗

Non-aggregated, crosswise ZnPcs functionalized with bis(trifluoromethyl)phenyl groups in facing isoindoles have proved efficient photosensitizers for singlet oxygen generation.

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Metallo-organic ensembles of tritopic subphthalocyanine ligands

Miguel A. Revuelta‐Maza, Ettore Fazio, Gema de la Torre, Tomás Torres⊗

Organic building blocks containing amines and aldehydes can be used for the preparation of complex metallo-organic structures, such as M[Formula: see text]L[Formula: see text] triple helicates or face-capped M[Formula: see text]L[Formula: see text] tetrahedral cages, through the formation of both dynamic covalent …

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