Marek Κ. Kalinowski

ORCID: 0009-0001-0376-2639
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About
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Research Areas
  • Electrochemical Analysis and Applications
  • Photochemistry and Electron Transfer Studies
  • Inorganic and Organometallic Chemistry
  • Analytical Chemistry and Chromatography
  • Analytical Chemistry and Sensors
  • Radical Photochemical Reactions
  • Electrochemical sensors and biosensors
  • Spectroscopy and Quantum Chemical Studies
  • Molecular Junctions and Nanostructures
  • Ionic liquids properties and applications
  • Molecular Sensors and Ion Detection
  • Free Radicals and Antioxidants
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Various Chemistry Research Topics
  • Lanthanide and Transition Metal Complexes
  • Adsorption, diffusion, and thermodynamic properties of materials
  • Mass Spectrometry Techniques and Applications
  • Chemical Thermodynamics and Molecular Structure
  • Chemical and Physical Properties in Aqueous Solutions
  • Molecular spectroscopy and chirality
  • History and advancements in chemistry
  • Conducting polymers and applications
  • Crystallography and molecular interactions
  • Electrocatalysts for Energy Conversion
  • Radioactive element chemistry and processing

University of Warsaw
1992-2009

Institute of Fundamental Technological Research
1976

Institute of Physics
1973

Polish Academy of Sciences
1973

10.1016/s0022-0728(74)80127-0 article EN Journal of Electroanalytical Chemistry 1974-09-01

Acid-base equilibria of aromatic ketyl radicals and their dimers (pinacols) were studied by flash photolysis ketones electrochemical methods. pK values the ketyls found: fluorenone, 9.5; xanthone, 9.8; benzophenone, 9.15; 4-chlorobenzophenone, 9.2. The corresponding pinacols are 13.7, 13.5, 12.6 13.6, respectively. difference in acidity between free is due to different hybridization C atom bonded OH group. Some new data reported on normal red-ox potentials ketone-ketyl anion systems,...

10.1039/tf9666200918 article EN Transactions of the Faraday Society 1966-01-01

Dimerization equilibria and dismutation kinetics of fluorenone xanthone ketyl radicals were studied by electrochemical methods at various pH. The dimerization equilibrium constant in aqueous-ethanolic solution is 7.1×1011 1.3×1013 M–1 for neutral ketyl, respectively. constants the RH (neutral radical)+R–(radical anion) systems are much lower; those R–+R– negligible. Dismutation resolved into component reactions. Rate RH+R– higher than found RH+RH or support electron-transfer mechanism ketyls.

10.1039/tf9666200926 article EN Transactions of the Faraday Society 1966-01-01

Abstract The formation of alkali metal cation complexes with 15-crown-5 and benzo-15-crown-5 in ten organic solvents has been investigated by cyclic voltammetry at 25°C. Stability constants the resulting 1 : have determined monitoring shift reduction potentials cations against ligand concentration. Based on results obtained dependences stabilities Gutmann donicity standard Gibbs transfer energies ion from water to a given solvent analyzed discussed.

10.1080/00958979908048471 article EN Journal of Coordination Chemistry 1999-01-01

Abstract Solvent effects on the Hammett ρ value for cathodic reduction of substituted benzophenones were determined. The electrochemistry a series 11 compounds was studied in acetonitrile, acetone, dimethyl sulphoxide, propylene carbonate, N , ‐dimethylformamide, ‐dimethylacetamide, ‐diethylformamide and hexamethylphosphoric triamide. values reversible one‐electron transfer are described by Lewis acid‐base model = − 0.006 AN + 0.003 DN 0.391, where solvent acceptor number donor number.

10.1002/poc.610050906 article EN Journal of Physical Organic Chemistry 1992-09-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTDo aromatic pinacols oxidize at a mercury electrodeWiktor Kemula, Zbigniew R. Grabowski, and Marek K. KalinowskiCite this: J. Am. Chem. Soc. 1969, 91, 24, 6863–6864Publication Date (Print):November 1, 1969Publication History Published online1 May 2002Published inissue 1 November 1969https://pubs.acs.org/doi/10.1021/ja01052a062https://doi.org/10.1021/ja01052a062research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/ja01052a062 article EN Journal of the American Chemical Society 1969-11-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTDisproportionation of (azobenzene)-.cntdot....lithium(1+) ion pairs in dimethylformamideAndrzej Kapturkiewicz and Marek K. KalinowskiCite this: J. Phys. Chem. 1978, 82, 10, 1141–1144Publication Date (Print):May 1, 1978Publication History Published online1 May 2002Published inissue 1 1978https://pubs.acs.org/doi/10.1021/j100499a011https://doi.org/10.1021/j100499a011research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/j100499a011 article EN The Journal of Physical Chemistry 1978-05-01
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