Jarosław Zaklika, MSc
Graduate Students, Komorowski Group
Email: jaroslaw.zaklika@pwr.edu.pl
Office:A3 / 220a
Phone:+48 71 320 3209

Computational chemist with research interests in molecular modelling. Jaroslaw Zaklika graduated from Wroclaw University of Science and Technology (WUST) where he obtained M.Sc. degree in Biotechnology in 2011. Since 2012 he is Ph.D. student at the WUST Faculty of Chemistry. His scientific advisors are Prof. Ludwik Komorowski and Dr. Robert W. Góra.

Papers

2699861 Z7SI4AU4 1 american-chemical-society-with-titles-doi-no-et-al 50 date desc title 1 550 https://fermi.pwr.edu.pl/wp-content/plugins/zotpress/
%7B%22status%22%3A%22success%22%2C%22updateneeded%22%3Afalse%2C%22instance%22%3Afalse%2C%22meta%22%3A%7B%22request_last%22%3A0%2C%22request_next%22%3A0%2C%22used_cache%22%3Atrue%7D%2C%22data%22%3A%5B%7B%22key%22%3A%22TARXZSNG%22%2C%22library%22%3A%7B%22id%22%3A2699861%7D%2C%22meta%22%3A%7B%22creatorSummary%22%3A%22Beker%20et%20al.%22%2C%22parsedDate%22%3A%222015%22%2C%22numChildren%22%3A1%7D%2C%22bib%22%3A%22%26lt%3Bdiv%20class%3D%26quot%3Bcsl-bib-body%26quot%3B%20style%3D%26quot%3Bline-height%3A%201.35%3B%20%26quot%3B%26gt%3B%5Cn%20%26lt%3Bdiv%20class%3D%26quot%3Bcsl-entry%26quot%3B%20style%3D%26quot%3Bclear%3A%20left%3B%20%26quot%3B%26gt%3B%5Cn%20%26lt%3Bdiv%20class%3D%26quot%3Bcsl-left-margin%26quot%3B%20style%3D%26quot%3Bfloat%3A%20left%3B%20padding-right%3A%200.5em%3B%20text-align%3A%20right%3B%20width%3A%201em%3B%26quot%3B%26gt%3B%281%29%26lt%3B%5C%2Fdiv%26gt%3B%26lt%3Bdiv%20class%3D%26quot%3Bcsl-right-inline%26quot%3B%20style%3D%26quot%3Bmargin%3A%200%20.4em%200%201.5em%3B%26quot%3B%26gt%3BBeker%2C%20W.%3B%20Stachowicz-Ku%5Cu015bnierz%2C%20A.%3B%20Zaklika%2C%20J.%3B%20Ziobro%2C%20A.%3B%20Ordon%2C%20P.%3B%20Komorowski%2C%20L.%20%26lt%3Ba%20class%3D%26%23039%3Bzp-ItemURL%26%23039%3B%20href%3D%26%23039%3Bhttp%3A%5C%2F%5C%2Fwww.sciencedirect.com%5C%2Fscience%5C%2Farticle%5C%2Fpii%5C%2FS2210271X15001802%26%23039%3B%26gt%3BAtomic%20polarization%20justified%20Fukui%20indices%20and%20the%20affinity%20indicators%20in%20aromatic%20heterocycles%20and%20nucleobases%26lt%3B%5C%2Fa%26gt%3B.%20%26lt%3Bi%26gt%3BComp.%20Theo.%20Chem.%26lt%3B%5C%2Fi%26gt%3B%20%26lt%3Bb%26gt%3B2015%26lt%3B%5C%2Fb%26gt%3B%2C%20%26lt%3Bi%26gt%3B1065%26lt%3B%5C%2Fi%26gt%3B%2C%2042%5Cu201349.%20https%3A%5C%2F%5C%2Fdoi.org%5C%2F10.1016%5C%2Fj.comptc.2015.04.023.%26lt%3B%5C%2Fdiv%26gt%3B%5Cn%20%26lt%3B%5C%2Fdiv%26gt%3B%5Cn%26lt%3B%5C%2Fdiv%26gt%3B%22%2C%22data%22%3A%7B%22itemType%22%3A%22journalArticle%22%2C%22title%22%3A%22Atomic%20polarization%20justified%20Fukui%20indices%20and%20the%20affinity%20indicators%20in%20aromatic%20heterocycles%20and%20nucleobases%22%2C%22creators%22%3A%5B%7B%22creatorType%22%3A%22author%22%2C%22firstName%22%3A%22Wiktor%22%2C%22lastName%22%3A%22Beker%22%7D%2C%7B%22creatorType%22%3A%22author%22%2C%22firstName%22%3A%22Anna%22%2C%22lastName%22%3A%22Stachowicz-Ku%5Cu015bnierz%22%7D%2C%7B%22creatorType%22%3A%22author%22%2C%22firstName%22%3A%22Jaros%5Cu0142aw%22%2C%22lastName%22%3A%22Zaklika%22%7D%2C%7B%22creatorType%22%3A%22author%22%2C%22firstName%22%3A%22Aleksandra%22%2C%22lastName%22%3A%22Ziobro%22%7D%2C%7B%22creatorType%22%3A%22author%22%2C%22firstName%22%3A%22Piotr%22%2C%22lastName%22%3A%22Ordon%22%7D%2C%7B%22creatorType%22%3A%22author%22%2C%22firstName%22%3A%22Ludwik%22%2C%22lastName%22%3A%22Komorowski%22%7D%5D%2C%22abstractNote%22%3A%22Atomic%20Fukui%20indices%20have%20been%20calculated%20by%20integration%20of%20the%20polarization%20justified%20Fukui%20functions%20over%20the%20atomic%20basins.%20Resulting%20indices%20have%20been%20explored%20in%20the%20definition%20of%20the%20atomic%20and%20group%20affinity%20indicator%20and%20softnesses%20on%20the%20ground%20of%20the%20formal%20analysis%20of%20the%20polarization%20effect.%20These%20indicators%20combine%20the%20effect%20of%20the%20atomic%20charge%20and%20atomic%20Fukui%20index.%20They%20are%20potentially%20applicable%20in%20testing%20a%20sensing%20effect%20on%20a%20molecule%20induced%20by%20an%20approaching%20point%20agent%2C%20nucleophilic%20%28%5Cu2212%29%20or%20electrophilic%20%28%2B%29%2C%20at%20a%20distance%20in%20the%20order%20of%20v.d.%20Waals%20radii.%20Calculated%20atomic%20and%20group%20affinity%20and%20softness%20indicators%20have%20been%20proved%20to%20be%20consistent%20with%20the%20well%20established%20trends%20of%20reactivity%20for%20a%20control%20group%20of%20the%20five-atom-ring%20heterocycles%20%28imidazole%2C%20oxazole%2C%20thiazole%29.%20The%20indices%20have%20been%20applied%20to%20the%20set%20of%205%20nucleobases%20%28adenine%2C%20guanine%2C%20cytosine%2C%20thymine%2C%20uracyl%29%2C%20whose%20diverse%20reactivity%20towards%20electrophiles%20has%20been%20recognized%20as%20a%20key%20factor%20determining%20the%20sensitivity%20of%20DNA%20to%20cytotoxic%20agents.%20The%20pairing%20effect%20of%20the%20nucleobases%20bases%20in%20the%20DNA%20chain%20and%20the%20experimental%20trends%20of%20the%20site%20reactivity%20of%20these%20molecules%20have%20been%20properly%20accounted%20for%20by%20the%20calculated%20indicators.%22%2C%22date%22%3A%22Sierpie%5Cu0144%201%2C%202015%22%2C%22language%22%3A%22%22%2C%22DOI%22%3A%2210.1016%5C%2Fj.comptc.2015.04.023%22%2C%22ISSN%22%3A%222210-271X%22%2C%22url%22%3A%22http%3A%5C%2F%5C%2Fwww.sciencedirect.com%5C%2Fscience%5C%2Farticle%5C%2Fpii%5C%2FS2210271X15001802%22%2C%22collections%22%3A%5B%225VJ6AZ6M%22%2C%22SZ6CRKMA%22%2C%22CITXSV2X%22%2C%22Z7SI4AU4%22%5D%2C%22dateModified%22%3A%222015-10-29T10%3A54%3A38Z%22%7D%7D%5D%7D
(1)
Beker, W.; Stachowicz-Kuśnierz, A.; Zaklika, J.; Ziobro, A.; Ordon, P.; Komorowski, L. Atomic polarization justified Fukui indices and the affinity indicators in aromatic heterocycles and nucleobases. Comp. Theo. Chem. 2015, 1065, 42–49. https://doi.org/10.1016/j.comptc.2015.04.023.

Your name: *
Your phone: *
Your e-mail: *
Contact Preference:
Title of Message: *
Text: *
Please, Enter the Code