Interested

• general chemistry
• 15
• porphyrin
• catalysis
• macrocycles
• aromaticity
• organometallic chemistry
• macrocycle
• carbaporphyrinoid
• porphyrinoids

Scientific discipline

• chemical sciences

Latest publications

• 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.
• Kinetic versus thermodynamic control over multiple conformations of di‐2,7‐naphthihexaphyrin(1.1.1.1.1.1)
• Expanded carbaporphyrinoids
• A meso-tetraaryl-21-carbaporphyrin: incorporation of a cyclopentadiene unit into a porphyrin architecture.
• 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
• 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.
• Three-stage aromaticity switching in boron(III) and phosphorus(V) N-fused p-benziporphyrin.
• Dicarba[26]hexaporphyrinoids(1.1.1.1.1.1) with an embedded cyclopentene moiety—conformational switching.
• Organocopper(III) phenanthriporphyrin—exocyclic transformations.
• Chemistry inside a porphyrin skeleton: platinacyclopentadiene from tellurophene.
• 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.
• 28-Hetero-2,7-naphthiporphyrins: horizontal expansion of the m-benziporphyrin macrocycle.
• Shaping a porphyrinoid frame by heteroatoms extrusion: formation of an expanded [22]triphyrin(6.6.0).
• Expanded porphyrin contraction: from [22]triphyrin(6.6.0) to [22]triphyrin(6.5.0).
• Phenanthrene cyclocarbonylation – core post-synthetic modification of phenanthriporphyrin