Head of the group
Prof. Witold Danikiewicz
Publications
A. Lipko, C. Pączkowski, L. Perez-Fons, P. D Fraser, M. Kania, M. Hoffman-Sommer, W. Danikiewicz, M. Rohmer, J. Poznanski, E. Swiezewska, „Divergent contribution of the MVA and MEP pathways to the formation of polyprenols and dolichols in Arabidopsis”, Biochem J.
G. Sanil, M. Krzeszewski, W. Chaładaj, W. Danikiewicz, I. Knysh, Ł. Dobrzycki, O. Staszewska-Krajewska, M. Cyrański, D. Jacquemin, D. T. Gryko, „Gold-Catalyzed 1,2-Aryl Shift and Double Alkyne Benzannulation”, Angew. Chem. Int. Ed.
V. Ayerdurai, A. Garcia-Cruz, J. Piechowska, M. Cieplak, P. Borowicz, K. R. Noworyta, G. Spólnik, W. Danikiewicz, W. Lisowski, A. Pietrzyk-Le, F. D’Souza, W. Kutner, P. S. Sharma, „Selective Impedimetric Chemosensing of Carcinogenic Heterocyclic Aromatic Amine in Pork by dsDNA-Mimicking Molecularly Imprinted Polymer Film-Coated Electrodes”, J. Agric. Food Chem.
M. Zimnicka, E. Kalenius, J. Jurczak, W. Danikiewicz, „Ion mobility mass spectrometry – an efficient tool for the analysis of conformational switch of macrocyclic receptors upon anion binding”, Analyst
M. Mąkosza, M. Bechcicka, K. Wojciechowski, „Simple Synthesis of Dimethyl Nitrobenzhydrylphosphonates and Heteroarylnitroarylacetonitriles via Vicarious Nucleophilic Substitution (VNS) Reaction”, Synthesis
R. Loska, M. Mąkosza, „Introduction of Carbon Substituents into Nitroarenes via Nucleophilic Substitution of Hydrogen: New Developments”, Synthesis
M. Mąkosza, „Electrophilic and Nucleophilic Aromatic Substitutions are Mechanistically Similar with Opposite Polarity”, Chem. Eur. J.
M. Mąkosza, M. Fedoryński, „Interfacial Processes—The Key Steps of Phase Transfer Catalyzed Reactions”, Catalysts
A. Kurpanik, M. Matussek, G Szafraniec‐Gorol, M. Filapek, P. Lodowski, B. Marcol‐Szumilas, W. Ignasiak, J. G. Małecki, B. Machura, M. Małecka, W. Danikiewicz, S. Pawlus, S. Krompiec, „APEX Strategy Represented by Diels–Alder Cycloadditions—New Opportunities for the Syntheses of Functionalised PAHs”, Chem. Eur. J.
K. Błaziak, W. Danikiewicz, M. Mąkosza, „How Do Aromatic Nitro Compounds React with Nucleophiles? Theoretical Description Using Aromaticity, Nucleophilicity and Electrophilicity Indices”, Nucleophiles
A. Wołos, R. Roszak, A. Żądło-Dobrowolska, W. Beker, B. Mikulak-Klucznik, G. Spólnik, M. Dygas, S. Szymkuć, B. A. Grzybowski, „Synthetic connectivity, emergence, and self-regeneration in the network of prebiotic chemistry”, Science
A. Kurpanik, M. Matussek, G. Szafraniec-Gorol, M. Filapek, P. Lodowski, B. Marcol-Szumilas, W. Ignasiak, J.G. Malecki, B. Machura, M. Malecka, W. Danikiewicz, S. Pawlus, S. Krompiec, „APEX Strategy Represented by Diels-Alder Cycloadditions-New Opportunities for the Syntheses of Functionalised PAHs”, Chem. Eur. J.
S. R. Rao, L. A. Skelton, F. Wu, A. Onysk, G. Spolnik, W. Danikiewicz, M. C. Butler, D. A. Stacks, L. Surmacz, X. Mu, E. Swieżewska, S. J. Pittler, S. J. Fliesler, „Retinal Degeneration Caused by Rod-Specific Dhdds Ablation Occurs without Concomitant Inhibition of Protein N-Glycosylation”, iScience
G. Spólnik, P. Wach, Z. Wróbel, W. Danikiewicz, „2-Iodomalondialdehyde is an abundant component of soluble organic iodine in atmospheric wet precipitation”, Sci. Total Environ.
M. Zimnicka, K. Kozłowska, W. Danikiewicz, „Beyond Size Complementary Factors in Anion–Tetralactam Macrocycle Complexes: From Intrinsic Gas-Phase to Solvent-Predicted Stabilities”, J. Org. Chem.
P. Wach, G. Spólnik, J. Surratt, K. Blaziak, K. Rudzinski, Y.-H. Lin, W. Maenhaut, W. Danikiewicz, M. Claeys, R. Szmigielski, „Structural Characterization of Lactone-Containing MW 212 Organosulfates Originating from Isoprene Oxidation in Ambient Fine Aerosol”, Environ. Sci. Technol.
G. Spólnik, P. Wach-Panfiłow, K. Rudziński, R. Szmigielski, W. Danikiewicz, „Tracing the biogenic secondary organic aerosol markers in rain, snow and hail”, Chemosphere
P. Wach, G. Spólnik, K. J. Rudzinski, K. Skotak, M. Claeys, W. Danikiewicz, R. Szmigielski, „Radical oxidation of methyl vinyl ketone and methacrolein in aqueous droplets: Characterization of organosulfates and atmospheric implications”, Chemosphere
A. Slodek, A. Maron, M. Pajak, M. Matussek, I. Grudzka-Flak, J.G. Malecki, A. Switlicka, S. Krompiec, W. Danikiewicz, M. Grela, I. Gryca, M. Penkala, „Luminescent-Substituted Fluoranthenes-Synthesis, Structure, Electrochemistry, and Optical Properties”, Chem. Eur. J.
G. Spólnik, P. Wach, K.J. Rudzinski, K. Skotak, W. Danikiewicz, R. Szmigielski, „Improved UHPLC-MS/MS Methods for Analysis of Isoprene-Derived Organosulfates”, Anal. Chem.
B. Franczuk, W. Danikiewicz, „Gas-Phase Reactions of Dimethyl Disulfide with Aliphatic Carbanions – A Mass Spectrometry and Computational Study”, J. Am. Soc. Mass Spectrom.
M. Ogrodowczyk, K. Dettlaff, W. Bednarski, B. Cwiertnia, M. Stawny, G. Spólnik, J. Adamski, W. Danikiewicz, „Radiodegradation of nadolol in the solid state and identification of its radiolysis products by UHPLC-MS method”, Chem. Papers
J. Sniechowska, P. Paluch, T. Pawlak, G.D. Bujacz, W. Danikiewicz, M.J. Potrzebowski, „New synthetic pathway leading to oxospirochlorins”, RSC Adv.
J. Brześkiewicz, R. Loska, M. Mąkosza, „alpha-Chlorobenzylation of Nitroarenes via Vicarious Nucleophilic Substitution with Benzylidene Dichloride: Umpolung of the Friedel-Crafts Reaction”, J. Org. Chem.
M. Hamkalo, P. Fita, M. Fedoryński, M. Mąkosza, „Interfacial Generation of a Carbanion: The Key Step of PTC Reaction Directly Observed by Second Harmonic Generation”, Chem. Eur. J.
R. Nazar, M. Mąkosza, „Simple Synthesis of Aryl p-Nitroarylacetonitriles by Vicarious Nucleophilic Substitution with Carbanions of Protected Cyanohydrins”, Eur. J. Org. Chem.
M. Nowacki, K. Wojciechowski, „Transition-metal-free [3+3] annulation of indol-2-ylmethyl carbanions to nitroarenes. A novel synthesis of indolo[3,2-b] quinolines (quindolines)”, Beilstein J. Org. Chem.
Research topics
- Studies of mechanisms of the reactions of ions with neutral molecules in the gas phase and in solution with the use of mass spectrometry and computational methods.
- Studies on the mechanisms of fragmentation of biomolecules.
- Application of the ion mobility technique coupled with mass spectrometry (IM-MS) to study the structure of ions and the non-covalent interactions of ions with neutral molecules in the gas phase.
- Developing applications of mass spectrometry in the analysis of contamination of drugs and other products available on the market and in the study of organic compounds present in the atmosphere.
- Studies on the reactions of nitro compounds and other electrophilic aromatic compounds with nucleophiles.