
ul. F. Joliot-Curie 14
michal.bialek@uwr.edu.pl
tel. +48 71 375 70 07, +48 71 375 72 56
Interested
- general chemistry
- coordination chemistry
- catalysis
- macrocycles
- porphyrinoids
- azulene
- carbaporphyrinoid
- chirality
- palladium
- molecular switches
Scientific discipline
- chemical sciences
Latest publications
- 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.