Zainteresowania

• general chemistry
• coordination chemistry
• catalysis
• macrocycles
• porphyrinoids
• azulene
• carbaporphyrinoid
• chirality
• palladium
• molecular switches

Dyscyplina naukowa

• nauki chemiczne

Najnowsze publikacje

• Altering the Properties of Spiropyran Switches Using Coordination Cages with Different Symmetries
• Organometallic chemistry confined within a porphyrin-like framework
• Diphenanthrioctaphyrin(1.1.1.0.1.1.1.0): conformational switching controls the stereochemical dynamics of the topologically chiral system.
• Diamond grows up.
• Complexes of N-Confused Porphyrin Derivatives as Ortho-Metallating Ligands. Synthesis, Structure, Redox Properties, and Chirality
• Guest Encapsulation Alters the Thermodynamic Landscape of a Coordination Host
• Ternary host-guest complexes with rapid exchange kinetics and photoswitchable fluorescence
• Bispalladium(II) Complexes of di‐p‐Pyrirubyrin Derivatives as Promising Near‐Infrared Photoacoustic Dyes
• 21‐Carba‐23‐selenaporphyrinoid Dyads ‐ An Azepine Unit as a Merging Motif
• Disequilibrating azobenzenes by visible-light sensitization under confinement
• C−H and C−M activation, aromaticity tuning, and Co⋅⋅⋅Ru interactions confined in the azuliporphyrin framework.
• 21-Carba-23-oxaporphyrinoids and 21-oxo-21-carba-23-oxaporphyrinoids: macrocyclic π-conjugation involving the carbonyl moiety
• Oxygenation of phenanthriporphyrin and copper(III) phenanthriporphyrin : an efficient route to phenanthribilinones.
• Dicarba[26]hexaporphyrinoids(1.1.1.1.1.1) with an embedded cyclopentene moiety—conformational switching.
• Organocopper(III) phenanthriporphyrin—exocyclic transformations.
• An exocyclic π-system extension of the phenanthriporphyrin framework : towards azaaceneporphyrinoids.
• Conformation‐dependent response to the protonation of diphenanthrioctaphyrin(1.1.1.0.1.1.1.0): a route to pseudorotaxane‐like structures.
• Functionalization of 10-azacorroles: nitration, bromination and acylation
• Phenanthrene cyclocarbonylation – core post-synthetic modification of phenanthriporphyrin
• Reversible switching of arylazopyrazole within a metal–organic cage.