Wybrane publikacje

E. R. Abdurakhmanova, D. Mondal, H. Jędrzejewska, P. Cmoch, O. Danylyuk, M. J. Chmielewski, A. Szumna “Supramolecular umpolung: Converting electron-rich resorcin[4]arenes into potent CH-bonding anion receptors and transporters” Chem (Cell Press), 2024, 10, 1910-1924; DOI: 10.1016/j.chempr.2024.03.003

K. M. Bąk, B. Trzaskowski, M. J. Chmielewski „Anion-templated synthesis of a switchable fluorescent [2]catenane with sulfate sensing capability” Chem. Sci., 2024, 15, 1796-1809; DOI: 10.1039/D3SC05086F

Graphical abstract: Anion-templated synthesis of a switchable fluorescent [2]catenane with sulfate sensing capability

K. Dworakowski, A. Chołuj, M. J. Chmielewski, D. Gryko „Vitamin B12 and a metal-organic framework enable the photocatalytic generation of alkyl radicals” Chem. Commun., 2023, 59, 11236-11239; DOI: 10.1039/D3CC02941G

Graphical abstract: Vitamin B12 and a metal–organic framework enable the photocatalytic generation of alkyl radicals
Graphical abstract: Front cover

 K. Maslowska-Jarzyna, K. M. Bąk, B. Zawada, M. J. Chmielewski, „pH-Dependent Transport of Amino Acids across Lipid Bilayers by Simple Monotopic Anion Carriers” Chem. Sci., 2022, 13, 12374-12381.

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 L. Xie, S. S. Park, M. J. Chmielewski, H. Li, R. A. Kharod, M. G. Campbell, M. Dincă, „Isoreticular Linker Substitution in Conductive Metal‐Organic Frameworks with Through‐Space Transport Pathways” Angew. Chem. Int. Ed. 2020, 132, 19791-19794.

Graphical abstract: Front cover

K. M. Bąk, B. van Kolck, K. Maslowska-Jarzyna, P. Papadopoulou, A. Kros, M. J. Chmielewski „Oxyanion transport across lipid bilayers: direct measurements in large and giant unilamellar vesicles” Chem. Commun. 2020, 56, 4910-4913.

Graphical abstract: Oxyanion transport across lipid bilayers: direct measurements in large and giant unilamellar vesicles
ACS AMI

Z. Kokan, M. J. Chmielewski, „A Photoswitchable Heteroditopic Ion-Pair Receptor” J. Am. Chem. Soc. 2018, 140, 16010-16014.

Graphical Abstract - OBC 2018
ACS AMI

K. M. Bąk, K. Chabuda, H. Montes, R. Quesada, M. J. Chmielewski, „1,8-Diamidocarbazoles: an easily tuneable family of fluorescent anion sensors and transporters” Org. Biomol. Chem. 2018, 16, 5188–5196.

Graphical Abstract - OBC 2018
ACS AMI

K. Zwoliński, M. J. Chmielewski, „TEMPO-Appended Metal–Organic Frameworks as Highly Active, Selective, and Reusable Catalysts for Mild Aerobic Oxidation of Alcohols” ACS Appl. Mater. Interfaces 2017, 9, 33956–33967.

Graphical Abstract - ACS AMI 2017
Chem. Commun.

A. Chołuj, N. Nikishkin, M. J. Chmielewski, „Facile post-synthetic deamination of MOFs and the synthesis of the missing parent compound of the MIL-101 family” Chem. Commun. 2017, 53, 10196-10199.

Graphical Abstract - ChemComm 2017
ACS Catalysis

A. Chołuj, A. Zieliński, K. Grela, M. J. Chmielewski, „Metathesis@MOF: Simple and Robust Immobilization of Olefin Metathesis Catalysts inside (Al)MIL-101-NH2” ACS Catal. 2016, 6, 6343-6349.

Graphical Abstract - ACS Catal 2016
ChemEurJ

K. M. Zwoliński, P. Nowak, M. J. Chmielewski, „Towards multifunctional MOFs – transforming a side reaction into a post-synthetic protection/deprotection method” Chem. Commun. 2015, 51, 10030-10033.

Graphical Abstract - ChemComm 2015
ChemEurJ

M. J.Chmielewski, E. Buhler, J. Candau and J.-M. Lehn, „Multivalency by Self-Assembly – Binding of Concanavalin A to Metallosupramolecular Architectures Decorated with Multiple Carbohydrate Groups” Chem. Eur. J. 2014, 20, 6960–6977.

Graphical Abstract - Chem. Eur. J. 2014
ChemComm

K. M. Bąk, M. J. Chmielewski “Sulfate templated assembly of neutral receptors in aqueous DMSO – orthogonal versus biplane structures”, Chem. Commun. 2014, 50, 1305-1308.

Graphical Abstract - Chem. Commun. 2014
Fig 5a_JACS2009_Cover_180

A. Brown, K. Mullen, J. Ryu, M. Chmielewski, S. Santos, V. Felix, A. Thompson, J. Warren, S. Pascu, P. D. Beer “Interlocked Host Anion Recognition by an Indolocarbazole-Containing [2]Rotaxane”, J. Am. Chem. Soc. 2009, 131, 4937–4952.

Fig 5b_JACS2009_TOC
Fig 6a_OBC_Cover_180

M. J. Chmielewski, J. J. Davis, P. D. Beer “Interlocked host rotaxane and catenane structures for sensing charged guest species via optical and electrochemical methodologies”Org. Biomol. Chem. 2009, 7, 415-424.

Fig 6b_OBC_TOC
Fig 7a_Organic Nanostructures_Cover

M. J. Chmielewski, P. D. Beer “Strategic anion templation for the assembly of interlocked structures” in: Organic Nanostructures, J. L. Atwood and J. W. Steed (eds.), Wiley-VCH, 2008.http://onlinelibrary.wiley.com/doi/10.1002/9783527622504.ch3/summary

Fig 8a_ChemCommun2008_Cover

M. J. Chmielewski, L. Zhao, A. Brown, D. Curiel, M. R. Sambrook, A. L. Thompson, S. M. Santos, V. Felix, J. J. Davis, P. D. Beer “Sulfate anion templation of a neutral pseudorotaxane assembly using an indolocarbazole threading component”Chem. Comm. 2008, 3154–3156.

Fig 8b_ChemCommun_TOC_Sulfate anion templation of a neutral pseudorotaxane assembly
Fig 9a_ChemCommun2007_Cover

S. R. Bayly, T. M. Gray, M. J. Chmielewski, J. J. Davis, P. D. Beer “Anion templated surface assembly of a redox-active sensory rotaxane” Chem. Comm. 2007, 2234–2236.

Fig 9b_ChemCommun_TOC_Anion Templated Surface Assembly
Fig 10a_Inorganic Chemistry_Cover

M. J. Chmielewski, M. Pawlicki, N. Sprutta, L. Szterenberg, L. Latos-Grażyński “Cadmium(II) and Zinc(II) Complexes of S-Confused Thiaporphyrin” Inorg. Chem. 2006, 45, 8664-8671.

Fig 10b_Inorganic Chemistry_TOC
Fig 11a_ChemEurJ 2006_Cover_Anion Binding vs Intramolecular hydrogen bonding

M. J. Chmielewski, J. Jurczak “Anion Binding versus Intramolecular Hydrogen Bonding in Neutral Macrocyclic Amides” Chem. Eur. J. 2006, 12, 7652-7667.

Fig 11b_ChemEurJ 2006_TOC_Anion Binding vs Intramolecular hydrogen bonding
Fig 12a_ChemEurJ2005_Cover_Anion Recognition by Neutral Macrocyclic Amides

M. J. Chmielewski, J. Jurczak “Anion Recognition by Neutral Macrocyclic Amides” Chem. Eur. J. 2005, 11, 6080-6094.

Fig 12b_ChemEurJ2005_TOC_Anion Recognition by Neutral Macrocyclic Amides
Unknown

M. J. Chmielewski, M. Charon, J. Jurczak “1,8-Diamino-3,6-dichlorocarbazole – a promising building block for anion receptors” Org. Lett. 2004, 6, 3501-3504.

Fig 16b_OL2004_TOC_1,8-Diamino-3,6-dichlorocarbazole