Michał Białek

Assistant professor

University of Wrocław

Poland

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About

Dr. Michał Białek is an Assistant Professor at the University of Wrocław, Poland. His research focuses on the synthesis and application of advanced porphyrinoid derivatives and coordination chemistry, as evidenced by his recent articles on topics such as cobalt-assisted activation of ketones and complexes of N-confused porphyrin derivatives. He is particularly interested in the structural and redox properties of these compounds, as well as their interactions in confined environments.

Articles (20)

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2025

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2025

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2025

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2024

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2024

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2024

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2024

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2023

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2023

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2022

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2022

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2022

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2020

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2020

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2020

Collaborators (10)

Nikita A. Durandin

University of Tampere

FINLAND

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Piotr Chmielewski

professor

University of Wrocław

POLAND

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POLAND

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Bartosz Szyszko

POLAND

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Angela Grommet

Assistant Professor at Chalmers University of Technology

Chalmers University of Technology

SWEDEN

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Michał Białek

Research Interests

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About

Articles (20)

Bis(10‐oxacorrole) with Fused Pyridine as a Linker: Synthesis, Structure, and Interaction between the Subunits in the Neutral, Mono‐, and Dicationic States

Cobalt‐Assisted α‐Activation of Ketones, Their Arylation and Keto‐Enol Equilibrium Confined into a Macrocycle

Ruthenocenoporphyrinoids─π-Conjugation Transmitted across 1,3-Substituted Ruthenocene

Complexes of N‐Confused Porphyrin Derivatives as Ortho‐Metallating Ligands. Synthesis, Structure, Redox Properties, and Chirality

21‐Carba‐23‐selenaporphyrinoid Dyads—An Azepine Unit as a Merging Motif

21‐Carba‐23‐selenaporphyrinoid Dyads—An Azepine Unit as a Merging Motif

Inside Cover: 21‐Carba‐23‐selenaporphyrinoid Dyads—An Azepine Unit as a Merging Motif (Angew. Chem. Int. Ed. 3/2024)

Bispalladium(II) Complexes of di‐p‐Pyrirubyrin Derivatives as Promising Near‐Infrared Photoacoustic Dyes

Bispalladium(II) Complexes of di‐p‐Pyrirubyrin Derivatives as Promising Near‐Infrared Photoacoustic Dyes

Functionalization of 10-azacorroles: nitration, bromination and acylation

Organometallic chemistry confined within a porphyrin-like framework

Innentitelbild: 21‐Carba‐23‐selenaporphyrinoid Dyads—An Azepine Unit as a Merging Motif (Angew. Chem. 3/2024)

Guest Encapsulation Alters the Thermodynamic Landscape of a Coordination Host

Disequilibrating azobenzenes by visible-light sensitization under confinement

21-Carba-23-oxaporphyrinoids and 21-oxo-21-carba-23-oxaporphyrinoids: macrocyclic π-conjugation involving the carbonyl moiety

Encapsulation within a coordination cage modulates the reactivity of redox-active dyes

Phenanthrene cyclocarbonylation – core post-synthetic modification of phenanthriporphyrin

Dicarba[26]hexaporphyrinoids(1.1.1.1.1.1) with an Embedded Cyclopentene Moiety—Conformational Switching

Front Cover: Dicarba[26]hexaporphyrinoids(1.1.1.1.1.1) with an Embedded Cyclopentene Moiety—Conformational Switching (Chem. Eur. J. 54/2020)

Dicarba[26]hexaporphyrinoids(1.1.1.1.1.1) with an embedded cyclopentene moiety—conformational switching.

Collaborators (10)

Nikita A. Durandin

Piotr Chmielewski

Anna Berlicka

Milosz Pawlicki

Karolina Hurej

Szymon Zelewski

Hiroyuki Furuta

Lechosław Latos‐Grażyński

Bartosz Szyszko

Angela Grommet

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