Porphyrin Chemistry Research - P. J. Chmielewski
Print view Sitemap
Zespół chemii porfiryn i metaloporfiryn

You are here: Members > Staff > P. J. Chmielewski

Prof. Piotr J. Chmielewski

Contact information

Address:

Department of Chemistry, University of Wrocław,
14 F. Joliot-Curie St.
50-383 Wrocław, POLAND

Phone:

(48)(71)3757277 (room 1068, office)
(48)(71)3757629 (room 1072, lab)

E-mail:

piotr.chmielewski[at]chem.uni.wroc.pl

Research Interests

Professor Chmielewski was one of the main contributors to the investigations of coordination chemistry of mono- and diheteroporphyrins, especially with nickel. He also worked on the coordination chemistry of N-alkylporphyrins and reactivity of porphyrin cation radicals.

His major achievement is the synthesis of inverted porphyrin (published 1994) which subsequently yielded a series of papers describing its reactivity and coordinating properties.

At present prof. Chmielewski continues his research independently. He uses inverted porphyrin to construct supramolecular assemblies.

Selected Papers

Chmielewski, P. J.; Latos-Grażyński, L.; Rachlewicz, K.; Głowiak, T.Tetra-p-Tolylporphyrin With an Inverted Pyrrole Ring: A Novel Isomer of Porphyrin.Angew. Chem., Int. Ed. Engl. 1994, 33, 779.

Chmielewski, P. J.; Latos-Grażyński, L.; Olmstead, M. M.; Balch, A. L.Nickel Complexes of 21-Oxaporphyrin and 21,23-Dioxadioxaporphyrin: Synthesis and Characterization.Chem. Eur. J. 1997, 3, 268.

I. Schmidt, P. J. Chmielewski, An inverted porphyrin with a pendant pyrrole - identification of a tetraphenylsapphyrin isomer in the Rothemund synthesis. Tetrahedron Lett., 2001, 42, 1151.

I. Schmidt, P. J. Chmielewski, Application of 2-ethylpyrrole for a direct synthesis of 3-substituted inverted porphyrin. Tetrahedron Lett., 2001, 42, 6389.

I. Schmidt, P. J. Chmielewski, First example of a covalently bound dimeric inverted porphyrin. Chem. Commun., 2002, 92.

I. Schmidt, P. J. Chmielewski, Z. Ciunik, Alkylation of the Inverted Porphyrin Nickel(II) Complex by Dihalogenalkanes: Formation of Monomeric and Dimeric Derivatives. J. Org. Chem., 2002, 67, 8917

I. Schmidt, P. J. Chmielewski, Nickel(II) Complexes of 21-C Alkylated Inverted Porphyrins: Synthesis, Protonation and Redox Properties. Inorg. Chem. 2003, 42, 5579

P. J. Chmielewski, I. Schmidt, Diastereoselective Assembling of 21-C-alkylated Nickel(II) Complexes of Inverted Porphyrin in a Platinum(II) Template. Inorg. Chem. 2004, 43, 1885

P. J. Chmielewski, Synthesis and Characterization of a Directly Linked N-Confused Porphyrin Dimer. Angew. Chem. Int. Ed. 2004, 43, 5655

P. J. Chmielewski, Extension of N-Confused Porphyrin by an o-Xylene Fragment. Org. Lett. 2005, 7, 1789

P. J. Chmielewski, Synthesis and Characterization of a Cyclic Bis-silver(I) Assembly Consisting of Four 2-Aza-21-carba-porphyrinatosilver(III) Subunits. Angew. Chem. Int. Ed. 2005, 44, 6417

Chmielewski, P. J.; Latos-Grażyński L., Core modified porphyrins-a macrocyclic platform for organometallic chemistry. Coord. Chem. Rev. 2005249, 2510.

Siczek, M.; Chmielewski, P. J., Synthesis, characterization, and chirality of dimeric N-confused porphyrin-zinc complexes: toward the enantioselective synthesis of bis(porphyrinoid) systems. Angew. Chem. Int. Ed., 200746, 7432.

Chmielewski, P. J.; Durlej, B.; Siczek, M.; Szterenberg, L., Helical bis(N-confused porphyrins) with subunits fused by double orthometalation with platinum: adaptability of an apparently rigid system. Angew. Chem. Int. Ed., 200948, 8736.

Chmielewski, P. J., Lucky seven: characterization of stable T-shaped copper(II) complexes of [32]heptaphyrins. Angew. Chem. Int. Ed., 201049, 1359.

Chmielewski, P. J.; Siczek, M.; Szterenberg, L., Protonated N-confused porphyrin dimer: formation, structure, and guest binding. Inorg. Chem., 201150, 6719.

Chmielewski, P. J.; Maciołek, J., Diastereoselective methylation of bis(N-confused porphyrinatonickel(II): access to configurationally stable chiral bis(porphyrinoid) and non-symmetric dimers. Chem. Commun., 201248, 428.

Liu, B.; Li X.; Xu, X.; Stępień, M.; Chmielewski, P. J., 3-(dialkoxyphosphoryl)-N-confused phlorin and porphyrin. Synthesis, stereochemistry and coordination properties. J. Org. Chem., 201378, 1354

Chmielewski, P. J.; Siczek, M.; Stępień, M., Bis(N-confused porphyrin) as a semirigid receptor with a chirality memory: a two-way host enantiomerization through point-to-axial chirality transfer. Chem. Eur. J., 201521, 2547.

Myśliwiec, D.; Kondratowicz, M.; Lis, T.; Chmielewski, P. J.; Stępień, M., Highly Strained Nonclassical Nanotube Endcaps. A Single-Step Solution Synthesis from Strain-Free, Non-Macrocyclic PrecursorsJ. Am. Chem. Soc. 2015, 137, 1643.

Liu, B.; Li, X.; Stępień, M.; Chmielewski, P. J., Towards Norcorrin: Hydrogenation Chemistry and the Heterodimerization of Nickel(II) NorcorroleChem. Eur. J. 2015, 21, 7790.

Żyła, M.; Gońka, E.; Chmielewski, P. J.; Cybińska, J.; Stępień, M., Synthesis of a Peripherally Conjugated5-6-7Nanographene. Chem. Sci. 2016, 7, 286.

Deng, Z.; Li, X.; Stępień, M.; Chmielewski, P. J., Nitration of Norcorrolatonickel(II): First Observation of a Diatropic Current in a System Comprising Norcorrole RingChem. Eur. J. 2016, 22, 4231.

Zhylitskaya, H.; Cybińska, J.; Chmielewski, P. J.; Lis, T.; Stępień, M., Bandgap Engineering in π-Extended Pyrroles. A Modular Approach to Electron-Deficient Chromophores with Multi-Redox ActivityJ. Am. Chem. Soc. 2016, 138, 11390.

Liu, B.; Yoshida, T.; Li, X.; Stępień, M.; Shinokubo, H.; Chmielewski, P. J., Reversible C-C Bond Breaking and Spin Equilibria in Bis(Pyrimidinenorcorrole)Angew. Chem. Int. Ed. 2016, 55, 13142.

Majewski, M. A.; Hong, Y.; Lis, T.; Gregoliński, J.; Chmielewski, P. J.; Cybińska, J.; Kim, D.; Stępień M., Octulene. A Hyperbolic Molecular Belt that Binds Chloride AnionsAngew. Chem. Int. Ed. 2016, DOI: 10.1002/anie.201608384.

Żyła-Karwowska, M.; Zhylitskaya, H.; Cybińska, J.; Lis, T.; Chmielewski, P. J.; Stępień, M., An Electron-Deficient Azacoronene via Radial π-ExtensionAngew. Chem. Int. Ed. 2016, DOI: 10.1002/anie.201608400

(Also see the complete publication list of our group.)