Chemical and Biological Systems Simulation Laboratory

Magdalena Jawiczuk

m.jawiczuk@cent.uw.edu.pl

19. M. Jawiczuk, N. Kuźmierkiewicz, A.M. Nowacka, M. Moreń, B. Trzaskowski, "A mechanistic, computational study of alkene-diazene heterofunctional cross metathesis catalyzed by ruthenium complexes", Organometallics, 42, 146-156 (2023).

18. M. Jawiczuk, A. Marczyk, B. Trzaskowski, "Decomposition of ruthenium olefin metathesis catalyst; a review", Catalysts, 10, 887 (2020).

17. M. Jawiczuk, A. Marczyk, K. Młodzikowska-Pieńko, B. Trzaskowski, "Impact of the Carbene Derivative Charge on the Decomposition Rates of Hoveyda-Grubbs-Like Metathesis Catalysts", J. Phys. Chem. A, 124, 6158-6167 (2020).

16. M. Jawiczuk, K. Młodzikowska-Pieńko, B. Trzaskowski, "Impact of the olefin structure on the catalytic cycle and decomposition rates of Hoveyda-Grubbs metathesis catalyst", Phys. Chem. Chem. Phys., 22, 13062-13069 (2020).

15. M. Jawiczuk, K. Młodzikowska-Pieńko, S. Osella, B. Trzaskowski, "Molecular modelling of mechanisms of decomposition of ruthenium metathesis catalysts by acrylonitrile", Organometallics, 39, 239-246 (2020).

14. D.J. Walaszek, M. Jawiczuk, J. Durka, O. Drapała, D. Gryko, "alpha-Photooxygenation of chiral aldehydes with singlet oxygen", Beilstein J. Org. Chem., 15, 2076-2084 (2019).

13. J.E. Rode, D. Kaczorek, A. Wasiewicz, R. Kawęcki, M. Jawiczuk, J.C. Dobrowolski, "Vibrational and electronic circular dichroism of a chiral terthiophene sulfonamide", J. Mol. Spectrosc., 354, 37-44 (2018).

12. M. Jawiczuk, A. Janaszkiewicz, B. Trzaskowski, "The influence of the cationic carbenes on the initiation kinetics of ruthenium-based metathesis catalysts; a DFT study", Beilstein J. Org. Chem., 14, 2872-2880 (2018).

11. J.E. Rode, K. Lyczko, M. Jawiczuk, R. Kawęcki, W. Stańczyk, A. Jaglińska, J.C. Dobrowolski, "The Vibrational Circular Dichroism Pattern of the ν(C=O) Bands in Isoindolinones", ChemPhysChem, 19, 2411-2422 (2018).

10. M. Jawiczuk, "A theoretical study on the hydrogen bond and stability of cytosine and thymine dimers", Comput. Theor. Chem., 1123, 26-34 (2018).

9. M. Jawiczuk, M. Górecki, M. Masnyk, J. Frelek, "Complementarity of electronic and vibrational circular dichroism based on stereochemical studies of vic-diols" Trac-Trend. Anal. Chem., 73, 119-128 (2015).

8. M. Jawiczuk, M. Górecki, J. Jaźwiński, M. Karchier, A. Suszczyńska, P. Ruskowska, B. Słomińska, P. Kalicki, M. Masnyk, J. Frelek, "Structural, spectroscopic, and computational characterization of the cleavage product of dimolybdenum(II) core under aerobic conditions" Tetrahedron Asym., 25, 1431-1442 (2014).

7. O. Popik, M. Pasternak-Suder, K. Leśniak, M. Jawiczuk, M. Górecki, J. Frelek, J. Młynarski, "Amine-catalyzed direct aldol reactions of hydroxy- and dihydroxyacetone: Biomimetic synthesis of carbohydrates" J. Org. Chem., 79, 5728-5739 (2014).

6. K. Pakulski, N. Gajda, M. Jawiczuk, J. Frelek, P. Cmoch, S. Jarosz, "Synthesis of a sucrose dimer with enone tether; A study on its functionalization" Beilstein J. Org. Chem., 10, 1246-1254 (2014).

5. M. Jawiczuk, J.E. Rode, A. Suszczyńska, A. Szugajew, J. Frelek, "The utility of dimolybdenum tetrakis(μ-isovalerate) and tetrakis(μ-pivalate) in the stereochemical studies of various transparent compounds" RSC Adv., 4, 43691-43707 (2014).

4. M. Jawiczuk, M. Górecki, A. Suszczyńska, M. Karchier, J. Jaźwiński, J. Frelek, "Dimolybdenum tetracarboxylates as auxiliary chromophores in chiroptical studies of vic-diols" Inorg. Chem., 52, 8250-8263 (2013).

3. T. Wdowik, C. Samojłowicz, M. Jawiczuk, M. Malińska, K. Woźniak, K. Grela, "Ruthenium nitronate complexes as tunable catalysts for olefin metathesis and other transformations" Chem. Commun., 49, 674-676 (2013).

2. T. Wdowik, C. Samojłowicz, M. Jawiczuk, A. Zarecki, K. Grela, "Olefin cross-metathesis with 3-nitropropene" Synlett., 19, 2931-2935 (2010).

1. E. Rozniecka, I. Zawisza, M. Jawiczuk, M. Branowska, M. Opallo, "Electrochemical and IR spectroscopic detection of oxidation products of the monomer and dimer of vanillyl alcohol in a sol-gel processed silicate matrix", J. Electroanal. Chem., 645, 123-134 (2010).