Dr. Michał Białek
Department of Chemistry, University of Wrocław,
14 F. Joliot-Curie St.
50-383 Wrocław, POLAND
Phone:
(48)(71)3757007 (room 1065, office)
(48)(71)3757629 (room 1072, lab)
michal.bialek[at]chem.uni.wroc.pl
Carbaporphyrin (mainly azuliporphyrinoid systems) coordination chemistry with catalytically active metal ions. Supramolecular and coordination assemblies (molecular cages, switches) and intermolecular interactions. Currently doing his postdoc at Rafal Klajn Lab.
Profiles: ResearchGate, Google Scholar
Białek, M. J.; Latos-Grażyński, L.; Aromaticity switching via azulene transformations in azulene-bridged A,D-dithiahexaphyrin. Chem. Commun. 2018, 54, 1837.
Szyszko, B.; Białek, M. J.; Dudziak, E.; Latos-Grażyński, L.; Flexible Porphyrinoids. Chem. Rev. 2017, 117, 2839.
Białek, M. J.; Sprutta, N.; Latos-Grażyński, L. Coordination-Induced Molecular Tweezing – Ruthenium Clusters Docked at Azuliporphyrinogens. Inorg. Chem. 2016, 55, 12061.
Białek, M. J.; Latos-Grażyński, L. Palladium(II), Ruthenium(II) and Ruthenium(III) Complexes of 23-thiaazuliporphyrin. The Case of Coordination-induced Contraction. Inorg. Chem. 2016, 55, 1758.
Białek, M. J.; Białońska, A.; Latos-Grażyński, L. Oxidation and Oxygenation of Carbonyl Ruthenium(II) Azuliporphyrin. Inorg. Chem. 2015, 54, 6184.
Zaręba, J. K.; Białek, M. J.; Janczak, J.; Zoń, J.; Dobosz, A. Extending the Family of Tetrahedral Tectons: Phenyl Embraces in Supramolecular Polymers of Tetraphenylmethane-based Tetraphosphonic Acid Templated by Organic Bases Cryst. Growth Des. 2014, 14, 6143.
Białek, M. J.; Latos-Grażyński, L. Merging of inner and outer ruthenium organometallic coordination motifs within an azuliporphyrin framework Chem. Commun. 2014, 50, 9270.
Białek, M. J.; Zaręba, J. K.; Janczak, J.; Zoń, J. Chains, Layers, Channels, and More: Supramolecular Chemistry of Potent Diphosphonic Tectons with Tuned Flexibility. The Generation of Pseudopolymorphs, Polymorphs, and Adducts Cryst. Growth Des. 2013, 13, 4039.
Białek, M.; Janczak, J.; Zoń, J. Naphthalene-based linkers for metal phosphonates. Synthesis, structure, and interesting conformational flexibility influence on final lanthanum hybrids CrystEngComm 2013, 15, 390.
Zoń, J.; Garczarek, P.; Białek, M. Synthesis of Phosphonic Acids and Their Esters as Possible Substrates for Reticular Chemistry In Metal Phosphonate Chemistry. From Synthesis to Applications, Clearfield, A.; Demadis, K., eds. RSC Publishing, Cambridge, 2012, pp. 170-191.
(See the complete publication list of our group.)