Articles in journals
1. P. Latos, J. Gabzdyl, S. Jurczyk, A. Chrobok, Ind. Eng. Chem. Res. 2024, 63, 8102–8110. IF = 4.2
Synergistic Effect of Deep Eutectic Solvent and Zinc Oxide in Transesterification of Dimethyl Terephthalate for the Synthesis of Alkyl Terephthalate Esters
2. P. Latos, J. Gabzdyl, K. Erfurt, D. Łukowiec, A. Maximenko, S. Jurczyk, A. Chrobok, Catal. Today, 2024, 114806. IF = 5.3 Incorporation of zinc into the protic imidazolium-based ionic liquid: A novel catalytic route to esters plasticizers
3. B. Podlesny, B. Gaida, A. Brzęczek-Szafran, A. Chrobok, D. Janas, Separation and Purification Technology, 343, 127120, 2024, IF=8.6
Partitioning of SWCNT mixtures using amphiphilic carbohydrate-based surfactants
2. A. Wolny, P. Latos, K. Szymańska, S. Jurczyk, A. Jakóbik-Kolon, A. Chrobok, Appl. Catal. A: Gen. 676, 119676, 2024, IF= 5.5
Construction of trifloaluminate ionic liquid catalyst on the silica surface dedicated for continuous flow Diels-Alder synthesis
3. K. Matuszek, S. L. Piper, A. Brzęczek-Szafran, B. Roy, S. Saher, J.M. Pringle, D. R. MacFarlane, Adv. Mater., 2024 IF=29 https://doi.org/10.1002/adma.202313023 Unexpected Energy Applications of Ionic Liquids
4. B. Gaida, J. Kondratowicz, S. L.Piper, C. M. Forsyth, A. Chrobok, D. R. Macfarlane, K. Matuszek, A. Brzęczek-Szafran, ACS Sustain. Chem. Eng. 2024, 12(1), 623-632. IF=8.4
Transforming Sugars into Salts─A Novel Strategy to Reduce Supercooling in Polyol Phase-Change Materials
1. A. Brzęczek-Szafran, A. Siewniak, A. Chrobok, ACS Sustain. Chem. Eng. 2023, 11(31), 11415-11423. IF=9.224
Assessment of green chemistry metrics for carbon dioxide fixation into cyclic carbonates using eutectic mixtures as catalyst: comprehensive evaluation on the example of a tannic acid-derived system
2. P. Latos, A. Wolny, J. Zdarta, F. Ciesielczyk, S. Jurczyk, T. Jesionowski, A. Chrobok, Environ. Technol. Innov. 2023, 31, 103164. IF=7.758
Highly stable Lewis acidic trifloaluminate ionic liquid supported on silica and metallosilicates as an efficient catalyst for continuous flow aminolysis of epoxides
3. N. Barteczko, M. Grymel, K. Erfurt, A. Jakóbik-Kolon, A. Brzęczek-Szafran, A. Chrobok, J. Mol. Liq. 2023, 386, 1-11. IF=6.633
Aqueous olefin metathesis with D-glucose-based bromides giving more efficient catalysis
4. K. Krukiewicz, D. Czerwińska-Główka, R. Turczyn, A. Blacha-Grzechnik, C. Vallejo-Giraldo, K. Erfurt, A. Chrobok, J. Faure-Vincent, S. Pouget, D. Djurado, M.J.P. Biggs, ACS Appl. Mater Interfaces 2023, 15(39), 45701-45712. IF=10.383
Flexible, transparent, and cytocompatible nanostructured indium tin oxide thin films for bio-optoelectronic applications.
5. I. Klapiszewska, P. Latos, A. Parus, S. Balicki, P. Lodowski, K.A. Wilk, T. Jesionowski, A. Chrobok, Ł. Klapiszewski, A. Ślosarczyk, J. Mater. Res. Technol. 2023, 27, 542-563. IF=6.4
New insights into sustainable cementitious composites doped with a hybrid system based on zinc oxide and a designable deep eutectic solvent
6. P. Latos, A. Brzęczek-Szafran, M. Krzywiecki, M. Pawlyta, A. Jakóbik-Kolon, A. Kolanowska, A. Chrobok, Appl. Catal. A: Gen. 2023, 651, 119027. IF=5.723
Highly active and stable catalysts for Bayer-Villiger oxidation – traditionaal postloading vs in situ synthesis of Fe/N/C nanoparticles
7. N. Barteczko, A. Brzęczek-Szafran, A. Wolny, S. Jurczyk, A. Jakóbik-Kolon, A. Chrobok, Appl. Catal. A: Gen. 2023, 661, 119226. IF=5.723
Supported ionic liquids for effective ruthenium olefin metathesis
8. J. Więcławik, A. Chrobok, Molecules 2023, 28(4), 1-18. IF=4.927
Gallium(III)- and Indium(III)-containing ionic liquids as highly active catalysts in organic synthesis
9. A. McGrogan, E.L. Byrne, R. Guiney, T.F. Headen, T.G.A. Youngs, A. Chrobok, J.D. Holbrey, M. Swadźba-Kwaśny, Phys. Chem. Chem. Phys. 2023, 25(14), 9785-9795, IF=3.676
The structure of protic ionic liquids based on sulfuric acid, doped with excess of sulfuric acid or with water
10. P. Latos, A. Wolny, A. Chrobok, Materials 2023, 16(5), 1-18. IF=3.748
Supported ionic liquid phase catalysts dedicated for continuous flow synthesis
11. N. Barteczko, M. Grymel, A. Chrobok, Catal. Commun. 2023, 177, 1-19. IF=3.7
Heterogeneous catalysts for olefin metathesis
12. A. Wolny, A. Chrobok, Curr. Org. Chem. 2023, 1-4. IF=2.226
Supported ionic liquid phase for biocatalysis: the current applications, synthesis and prospects
1. A. Brzęczek-Szafran, K. Erfurt, M. Swadźba-Kwaśny, T. Piotrowski, A. Chrobok, ACS Sustain. Chem. Eng. 2022, 10(41), 13568-13575. IF=9.224
Beckmann rearrangement with improved atom economy, catalyzed by inexpensive, reusable, Bronsted acidic ionic liquid
2. A. Wolny, A. Siewniak, J. Zdarta, F. Ciesielczyk, P. Latos, S. Jurczyk, L.D. Nghiem, T. Jesionowski, A. Chrobok, Environ. Technol. Innov. 2022, 28, 1-12. IF=7.758
Supported ionic liquid phase facilitated catalysis with lipase from Aspergillus oryzae for enhace enantiomeric resolution of racemic ibuprofen
3. A. Wolny, A. Chrobok, Molecules 2022, 27(18), 1-31. IF=4.927
Silica-based supported ionic liquid-like phases as heterogeneous catalysts
4. A. Siewniak, E. Monasterska, E. Pankalla, A. Chrobok, Molecules 2022, 27(19), 1-9, IF=4.927
Polymer-supportted poly(ethylene glycol) as a phase-transfer catalyst for cross-aldol condensation of isobutyroaldehyde and formaldehyde
5. J. Chrobak, J. Iłłowska, A. Chrobok, Molecules 2022, 27(15), 1-16. IF=4.927
Formaldehyde-free resins for the wood-based panel industry: alternatives to formaldehyde and novel hardeners
6. Ł. Kotyrba, A. Chrobok, A. Siewniak, Catalysts 2022, 12(3), 1-18. IF=4.501
Synthesis of propylene carbonate by urea alcoholysis – recent advances
7. M. Heba, A. Wolny, A. Kastelik-Hryniewiecka, D. Stradomska, S. Jurczyk, A. Chrobok, N. Kuźnik, Catalysts 2022, 12(11), 1-10. IF=4.501
Green dynamic kinetic resolution – stereoselective acylation of secondary alcohols by enzyme-assisted ruthenium complexes
8. R. Bielas, P. Maksym, K. Erfurt, B. Hachuła, R. Gawecki, M. Tarnacka, S. Waśkiewicz, Ł. Mielańczyk, A. Mrozek-Wilczkiewicz, A. Chrobok, M. Paluch, K. Kamiński, J. Mat. Sci. 2022, 57(3), 2257-2276. IF=4.5
Sugar decarated star-shaped (co)polymers with resveratrol-based core-physicochemical and biological properties
9. J. Bińczak, A. Szelwicka, A. Siewniak, K. Dziuba, A. Chrobok, Materials 2022, 15(19), 1-16. IF=3.748
Oxidation of cyclohexanone with peracids – a straight path to the synthesis of ε-caprolactone oligomers
10. A. Tracz, E. Pankalla, S. Boncel, A. Chrobok, Przem. Chem. 2022, 101(10), 815-821. IF=0.5
Succinic acid and sebacic acid in the production pathway of plasticizers.
11. Ł. Kotyrba, A. Siewniak, P. Woszczyński, E. Nowakowska-Bogdan, A. Chrobok, Przem. Chem. 2022, 101(12), 1112-117. IF=0.5
Urea alcoholysis as a potential method of obtaining propylene carbonate on a technical scale
12. M. Gwóźdź, A. Brzęczek-Szafran, International Journal of Molecular Sciences 2022, 23(19), 11282. IF=5.6
Carbon-based electrocatalyst design with phytic acid- a versatile biomass-derived modifier of functional materials
1. A. Brzęczek-Szafran, J. Więcławik, N. Barteczko, A. Szelwicka, E. Byrne, A. Kolanowska, M. Swadźba-Kwaśny, A. Chrobok, Green Chem. 2021,23, 4421-4429. IF=10.182
Protic ionic liquids from di- or triamines: even cheaper Bronsted acidic catalysts
2. N. Barteczko, J. Więcławik, A. Tracz, E. Pankalla, K. Erfurt, P. Latos, S. Boncel, K. Matuszek, A. Chrobok, Materials 2021, 14(20), 6219. IF=3.623
Dialkyl succinates and adipates as alternative plasticizers-even more efficient synthesis
3. A. Wolny, A. Chrobok, Nanomaterials 2021, 11, 2030. IF = 5.346
Ionic Liquids for Development of Heterogeneous Catalysts Based on Nanomaterials for Biocatalysis
4. A. Brzęczek-Szafran, B. Gaida, A. Blacha-Grzechnik, K. Matuszek, A. Chrobok, Int. J. Mol. Sci. 2021, 22(19), 10426. IF = 5.923
Bioderived Ionic Liquids and Salts with Varius Cyano Anions as Precursors for Doped Carbon Materials
5. J. Binczak, K. Dziuba, A. Chrobok, Materials, 2021, 14(11), 2881. IF=3.623
Recent developments in lactone monomers and polymers synthesis and application
6. S. Kula, A. Szlapa-Kula, S. Krompiec, E. Schab-Balcerzak, A. Chrobok, P. Gancarz, M. Filapek, Mater. Sci. Eng. B Solid State Mater. Adv. Technol. 2021, 263, 114820. IF= 4.051
New possibilities of 2-pyranone derivatives – thermal, optical and electrochemical properties
7. E. Monasterska, E. Pankalla, A. Siewniak, A. Chrobok, Molecules 2021, 26(19). IF=4.412
Development of methods for the synthesis of neopentylglycol by hydrogenation of hydroxypivaldehyde
8. P. Maksym, M. Tarnacka, R. Bernat, A. Dzienia, A. Szelwicka, B. Hachula, A. Chrobok, M. Paluch, K. Kamiński, Polym. Chem. 2021, 12(30), 4418-4427. IF=5.582
Light-mediated controlled and classical polymerizations of less-activated monmers under high-pressure conditions
9. A. Szelwicka, A. Wolny, S. Jurczyk, M. Grymel, S. Boncel, A. Chrobok, Materials 2021, 14, 3443. IF= 3.623
Chemi-Enzymatic Baeyer-Villger Oxidation Facilitated with Lipases Immobilized in Supported Ionic Liquid Phase
10. A. Szelwicka, K. Erfurt, S. Jurczyk, S. Boncel, A. Chrobok, Materials 2021, 14, 3090. IF= 3.623
Autperformance in Acrylation: Supported D-glucose-based ionic liquid phase on MWCNTs for Immobilized Lipase B from Candida Antarctica as catalytic system
11. E. Monasterska, A. Siewniak, E. Pankalla, A. Chrobok, Przem. Chem. 2021, 100(1), 62-66. IF=0.464
Synthesis and application of hydroxypivaldehyde
12. M. Gwóźdź, A. Brzęczek-Szafran, A. Chrobok, Przem. Chem. 2021, 100(4), 386-392. IF=0.464
Task-specific ionic liquids functionalized with sulfonic groups. Environmetally friendly catalysts
13. A. Brzęczek-Szafran, M. Gwóźdź, A. Kolanowska, M. Krzywiecki, P. Latos, A. Chrobok, React. Chem. Eng. 2021, 6, 1246-1253. IF=4.239
N-doped carbon as a solid base catalyst for continuous flow Knoevenagel condensation
14. A. Szelwicka, A. Siewniak, A. Kolanowska, S. Boncel, A. Chrobok, Materials 14, 6, 1518. IF=3.623
PTFE-Carbon Nanotubes and Lipase B from Candida antarctica-Long-Lasting Marriage for Ultra-Fast and Fully Selective Synthesis of Levulinate Esters
15. R. Bernat, P. Maksym, M. Tarnacka, A. Szelwicka, R. Bielas, M. Wojtyniak, K. Balin, B. Hachuła, A. Chrobok, M. Paluch, K. Kamiński, Polym. Chem. 2021, 12, 1105-1113. IF=5.582
Hard confinement systems as effective nanoreactors for in situ photo-RAFT: towards control over molecular weight distribution and morphology
16. K. Duale, P. Latos, A. Chrobok, A. Domiński, M. M. Maksymiak, G. Adamus, M. Kowalczuk, Molecules 2021, 26(16), 1-14. IF = 4.411
Towards advances in molecular understanding of boric acid biocatalyzed ring-opening (co)polymerization of valerolactone in the presence of ethylene glycol as an initiator
1. K. Erfurt, M. Markiewicz, A. Siewniak, D. Lisicki, M. Zalewski, S. Stolte, A. Chrobok, ACS Sustainable Chem. Eng. 2020, 8, 29, 10911. IF=6.97
Biodegradable Surface Active D-Glucose based Quaternary Ammonium Ionic Liquids in the Solventless Synthesis of Chloroprene
2. B. Gaida, A. Brzeczek-Szafran, Molecules 2020, 25, 3285. IF=3.267
Insights into the properties and potential applications of renewable carbohydrate-based ionic liquids: a review
3. N. Barteczko, M. Grymel, A. Chrobok, Przemysł Chemiczny 2020, 99/6, 927. IF=0.428
Ionic liquids in olefin metathesis. Challenges and barriers
(Ciecze jonowe w metatezie olefin. Wyzwania i bariery)
4. P. Latos, A. Siewniak, M. Sitko, A. Chrobok, RSC Adv., 2020, 10, 21382. IF= 3.049
The Baeyer–Villiger rearrangement with metal triflates: new developments toward mechanism
5. J. Więcławik, A. Chrobok, Przemysł Chemiczny 2020, 99/5, 795. IF=0.428
Perspective electrolytes for Li-ion batteries
(Perspektywiczne elektrolity do baterii litowo-jonowych)
6. A. Brzeczek-Szafran, P. Wiecek, M. Guzik, A. Chrobok, RSC Adv., 2020, 10, 18355-18359. IF= 3.049
Combining amino acids and carbohydrates into readily biodegradable, task specific ionic liquids
7. M. Przypis, K. Matuszek, A. Chrobok, M. Swadzba-Kwasny, D. Gillner, Journal of Molecular Liquids 2020, 308, 113166. IF= 4.561
Inexpensive and tuneable protic ionic liquids based on sulfuric acid for the biphasic synthesis of alkyl levulinates
8. K. Krukiewicz, D. Kobus, R. Turczyn, K. Erfurt, A. Chrobok, M. J. P. Biggs, Electrochemistry Communications 2020, 110, 106616. IF= 4.197
Low resistance, highly corrugated structures based on poly(3,4-ethylenedioxythiophene) doped with a D-glucopyranoside-derived ionic liquid
9. U. Dorosz, N. Barteczko, P. Latos, K. Erfurt, E. Pankalla, A. Chrobok, Catalysts 2020, 10(1), 37. IF= 3.444
Highly efficient biphasic system for the synthesis of alkyl lactates in the presence of acidic ionic liquids
10. A. Szelwicka, A. Kolanowska, P. Latos, S. Jurczyk, S. Boncel, A. Chrobok, Catalysis Science and Technology, IF=5.726 Carbon nanotube/PTFE as a hybrid platform for lipase-assisted transformation of α-angelica lactone to alkyl levulinates
11. D. Kopeć, S. Baj, A. Siewniak, Molecules 2020, 25, 118. IF=3.06
Ultrasound-Assisted Green Synthesis of Dialkyl Peroxides under Phase-Transfer Catalysis Conditions
12. P. Latos, A. Siewniak, N. Barteczko, S. Jurczyk, S. Boncel, A. Chrobok, Catalysts 2020, 10, 1469-1479. IF=3.520
Highly Active Trifloaluminate Ionic Liquids as Recyclable Catalysts for Green Oxidation of 2,3,6-Trimethylphenol to Trimethyl-1,4-Benzoquinone
13. S. Bajkacz, K. Rusin, A. Wolny, J. Adamek, K. Erfurt, A. Chrobok, Molecules 2020, 25(20), 1-14. IF = 4.411
Highly efficient extraction procedures based on natural deep eutectic solvents or ionic liquids for determination of 20-hydroxyecdycone in spinach
14. K. Krukiewicz, D. Kobus, R. Turczyn, K. Erfurt, A. Chrobok, M. J. P. Biggs, Electrochem. Commun. 2020, 110, 1-5. IF = 4.724
Low resistance, highly corugated structures based on poly(3,4-ethylenedioxythiophene) doped with a d-glucopyranoside -derived ionic liquid
1. K. Matuszek, E. Pankalla, A. Grymel, P. Latos, A. Chrobok, Molecules 2019, 25(1), 80. IF= 3.06
Studies on the solubility of terephthalic acid in ionic liquids
2. A. Brzeczek-Szafran, K. Erfurt, A. Blacha-Grzechnik, M. Krzywiecki, S. Boncel, A. Chrobok, ACS Sustainable Chem. Eng. 2019, 7, 24, 19880–19888. IF=6.97
Carbohydrate Ionic Liquids and Salts as All-in-One Precursors for N-Doped Carbon
3. M. Sitko, A. Szelwicka, M. Szmatoła, A. Skwarek, L. Schimmelpfennig, K. Dziuba, M. Morawiec-Witczak, J. Iłowska, A. Chrobok, Przemysł Chemiczny 2019, 98(10), 1587-1593. IF=0.339
Method of ε-caprolactone synthesis by chemo-enzymatic oxidation of cyclohexanone in emulsion
4. M. Socka, M. Sitko, S. Boncel, B. Kost, A. Chrobok, M. Brzezinski, Polymer Degradation and Stability 2019, 170, 10900. IF=3.780
Nanobiocatalyst from lipase non-covalently immobilized on multiwalled carbon nanotubes for copolymerization of ε-caprolactone and trimethylene carbonate
5. M. Sitko, A. Szelwicka, A. Wojewódka, A. Skwarek, D. Tadasiewicz, L. Schimmelpfennig, K. Dziuba, M. Morawiec-Witczak, A. Chrobok, RSC Adv. 2019, 9, 30012-30018. IF=3.049
Perdecanoic acid as a safe and stable medium-chain peracid for Baeyer–Villiger oxidation of cyclic ketones to lactones
6. A. Szelwicka, P. Zawadzki, M. Sitko, S. Boncel, W. Czardybon, A. Chrobok, Org. Proc. Res. Dev. 2019, 23, 7, 1386–1395. IF=3.327
Continuous Flow Chemo-Enzymatic Baeyer-Villiger Oxidation with Superactive and Extra-Stable Enzyme/Carbon Nanotube Catalyst: An Efficient Upgrade from Batch to Flow
7. Szafraniec-Gorol, A. Slodek, D. Zych, M. Filapek, W. Ignasiak, A. Maron, K. Leszczynska-Sejda, A. Chrobok, S. Krompiec, J. Luminescence 2019, 211, 446. IF=2.961
Luminescent NˆCˆN cyclometalated iridium(III) acetylide complexes with fluorene and carbazole motifs
8. P. Latos, A. Szelwicka, S. Boncel, S. Jurczyk, M. Swadzba-Kwasny, A. Chrobok, ACS Sus. Chem. Eng. 2019, 7,5184. IF=5.951
Highly Efficient Synthesis of Alkyl Levulinates from α-Angelica Lactone, Catalyzed with Lewis Acidic Trifloaluminate Ionic Liquids Supported on Carbon Nanotubes
9. A. Szelwicka, S. Boncel, S. Jurczyk, A. Chrobok, Appl. Catal., A: Gen. 2019, 574, 41. IF=4.521
Exceptionally active and reusable nanobiocatalyst comprising lipase non-covalently immobilized on multi-wall carbon nanotubes for the synthesis of diester plasticizers
10. K. Matuszek, A. Brzeczek-Szafran, D. Kobus, D. MacFarlane, M. Swadzba-Kwasny, A. Chrobok, Aust. J. Chem. 2019, 72, 130. IF=1.427
Protic Ionic Liquids Based on Oligomeric Anions [(HSO4)(H2SO4)x]- (x=0, 1, or 2) for a Clean ε-Caprolactam Synthesis
11. P. Maksym, M. Tarnacka, A. Dzienia, K. Wolnica, M. Dulski, K. Erfurt, A. Chrobok. Zieba, A. Brzozka, G. Sulka, R. Bielas, K. Kaminski, M. Paluch, RSC Adv. 2019, 9, 6396. IF=2.936
Efficient metal-free strategies for polymerization of a sterically hindered ionic monomer through the application of hard confinement and high pressure
1. P. Latos, N. Barteczko ,A. Chrobok, A. Culkin, L. Brown, P. Nockemann, M. Swadzba-Kwasny, S. Boncel, S. Jurczyk, Front. Chem. 2018, 6, 535. IF=4.155
Water-Tolerant Trifloaluminate Ionic Liquids: New and Unique Lewis Acidic Catalysts for the Synthesis of Chromane
2. M. Markiton, A. Szelwicka, S. Boncel, S. Jurczyk, A. Chrobok, Appl. Catal., A: Gen. 2018, 556, 81. IF=4.521
Superactive tin(II) triflate/carbon nanotube catalyst for the Baeyer-Villiger oxidation
3. M. Markiton, A. Ciemiega, K. Maresz, A. Szelwicka, J. Mrowiec-Bialon, A. Chrobok, New J. Chem. 2018, 42, 13602. IF=3.201
Water-tolerant solid Lewis-acid sites: Baeyer-Villiger oxidation with hydrogen peroxide in the presence of gallium-based silica catalysts
4. T. Klemes, A. Switlicka, A. Szlapa-Kula, S. Krompiec, P. Lodowski, A. Chrobok, M. Godlewska, S. Kotowicz, M. Siwy, K. Bednarczyk, M. Libera, S. Maćkowski, T. Pedzinski, E. Schab-Balcerzak, B. Machura, Appl. Organomet. Chem. 2018, 2018, e4611. IF=3.581
Experimental and computational exploration of photophysical and electroluminescent properties of modified 2,2′:6′,2′′-terpyridine, 2,6-di(thiazol-2-yl)pyridine and 2,6-di(pyrazin-2-yl)pyridine ligands and their Re(I) complexes. Effect of donor–acceptor ligand.
5. I. Gryca, K. Czerwińska, B. Machura, A. Chrobok, L. S. Shul’pina, M. L. Kuznetsov, D. S. Nesterov∥, Y. N. Kozlov, A. J. L. Pombeiro, I. A. Varyan, G. B. Shul’pin, Inorg. Chem. 2018, 57, 1824. IF=4.700
High Catalytic Activity of Vanadium Complexes in Alkane Oxidations with Hydrogen Peroxide: An Effect of 8-Hydroxyquinoline Derivatives as Noninnocent Ligands
6. P. Maksym, M. Tarnacka, A. Dzienia, K. Erfurt, A. Brzeczek-Szafran, A. Chrobok, A. Zieba, K. Kaminski, M. Paluch, Polymer, 2018, 140, 158. IF=3.483
High pressure RAFT of sterically hindered ionic monomers. Studying relationship between rigidity of the polymer backbone and conductivity
7. A. Szelwicka, A. Chrobok, Przem. Chem. 2018, 97, 89. IF=0.399
Methods for increasing activity and stability of enzymes in processes carried out in presence of ionic liquids.
8. P. Maksym, M. Tarnacka, K. Wolnica, A. Dzienia, K. Erfurt, A. Chrobok, A. Zieba, Andrzej, R. Bielas, K. Kaminski, M. Paluch, Polym. Chem. 2018, 9, 335. IF=4.927
Studies on the hard confinement effect on the RAFT polymerization of a monomeric ionic liquid. Unexpected triggering of RAFT polymerization at 30 °C
9. M. Matussek, M. Filapek, P. Gancarz, S. Krompiec, J. G. Małecki, S. Kotowicz, M. Siwy, S. Maćkowski, A. Chrobok, E. Schab-Balcerzak, A. Słodek, Dyes Pigm. 2018, 159, 590, IF=3.767
Synthesis and photophysical properties of new perylene bisimide derivatives for application as emitting materials in OLEDs
10. A. Brzęczek-Szafran, C. Richardson, V. Lopez, P. Wagner, A. Nattestad, Phys. Status Solidi A 2018, 215, 1800551. IF= 1.795
Aesthetically Pleasing, Visible Light Transmissive, Luminescent Solar Concentrators Using a BODIPY Derivative
11. A. Kurowska, A.Brzeczek-Szafran, P. Zassowski, M. Lapkowski, W. Domagala, P. Wagner, K.K. Wagner, Electrochim. Acta 2018, 271, 685. IF= 5.116
Mono and di-substituted BODIPY with electron donating carbazole, thiophene, and 3,4-ethylenedioxythiophene units
1. J. Hogg, L. Christobel, K. Matuszek, P. Latos, A. Chrobok, M. Swadźba-Kwasny, Dalton Trans. 2017, 46, 11561. IF=4.029
Liquid coordination complexes of Lewis acidic metal chlorides: Lewis acidity and insights into speciation
2. P. Maksym, M. Tarnacka, A. Dzienia, K. Erfurt, A. Chrobok, A. Zieba, K. Wolnica, K. Kaminski, M. Paluch, Polym. Chem. 2017, 8, 5433. IF=5.375
Facile route to well-defined imidazolium-based poly(ionic liquid)s of enhanced conductivity via RAFT
3. M. Markiton, S. Boncel, D. Janas, A. Chrobok, ACS Sus. Chem. Eng. 2017, 5, 1685. IF=5.951
Highly active nanobiocatalyst from lipase noncovalently immobilized on multiwalled carbon nanotubes for Baeyer-Villiger synthesis of lactones
4. K. Matuszek, S. Coffie, A. Chrobok, M. Swadźba-Kwasny, Catal. Sci. Technol. 2017, 7, 1045. IF=5.773
Borenium ionic liquids as catalysts for Diels-Alder reaction: tuneable Lewis superacids for catalytic applications
5. A. Maron, S. Kula, A. Szlapa-Kula, A. Świtlicka, B. Machura, S. Krompiec, J. Malecki, R. Kruszyński, A. Chrobok, E. Schab-Balcerzak, S. Kotowicz, M. Siwy, K. Smolarek, S. Maćkowski, H. Janeczek, M. Libera, Eur. J. Org. Chem. 2017, 2730. IF=2.834
2,2′:6′,2”-Terpyridine analogues: structural, electrochemical, and photophysical properties of 2,6-di(thiazol-2-yl)pyridine derivatives
6. P. Maksym, M. Tarnacka, A. Dzienia, K. Matuszek, A. Chrobok, K. Kaminski, M. Paluch, Macromolecules 2017, 50, 3262. IF=5.835
Enhanced polymerization rate and conductivity of ionic liquid-based epoxy resin
1. A. Drożdż, U. Hanefeld, K. Szymańska, A. Jarzębski, A. Chrobok, Catal. Commun. 2016, 81, 37. IF=3.330
A robust chemo-enzymatic lactone synthesis using acyltransferase from Mycobacterium smegmatis
2. M. Markiton, A. Chrobok, K. Matuszek, K. Seddon, M. Swadźba-Kwasny, RSC Adv. 2016, 6, 30460. IF=3.108
Exceptional activity of gallium(III) chloride and chlorogallate(III) ionic liquids for Baeyer-Villiger oxidation
3. K. Matuszek, A. Chrobok, P. Latos, M. Markiton, K. Szymańska, A. Jarzębski, M. Swadźba-Kwasny, Catal. Sci. Technol. 2016, 622, 8129. IF=5.773
Silica-supported chlorometallate (III) ionic liquids as recyclable catalysts for Diels-Alder reaction under solventless conditions
4. A. Drożdż, A. Chrobok, Chem. Commun. 2016, 52, 1230, IF=6.319.
Chemo-enzymatic Baeyer-Villiger oxidation of 4-methylcyclohexanone via kinetic resolution of racemic carboxylic acids: direct access to enantioenriched lactone
5. J. Pernak, K. Czerniak, A. Biedziak, K. Marcinkowska, T. Praczyk, K. Erfurt, A. Chrobok, RSC Adv. 2016, 6, 52781. IF=3.108
Herbicidal ionic liquids derived from renewable sources
5. K. Jasiak, A. Siewniak, K. Kopczynska, A. Chrobok, S. Baj, J. Chem. Technol, Biotechnol. 2016, 91, 2827. IF=3.135
Hydrogensulphate ionic liquids as an efficient catalyst for the synthesis of cyclic carbonates from carbon dioxide and epoxides
6. K. Matuszek, A. Chrobok, Przem. Chem. 2016, 95, 1215. IF=0.385
Acidic ionic liquids as catalysts in the industrial organic synthesis
(Kwasowe ciecze jonowe jako katalizatory w przemysłowej syntezie organicznej)
7. P. Latos, S. Boncel, A. Chrobok, Przem. Chem. 2016, 95, 1310. IF=0.385
Heterogeneous catalysts based on carbon nanostructures in model chemical processes
(Katalizatory heterogeniczne na bazie nanostruktur węglowych w modelowych procesach chemicznych)
8. G. Szafraniec-Gorol, A. Slodek, E. Schab-Balcerzak, M. Grucela, M. Siwy, M. Filapek, M. Matussek, D. Zych, S. Mackowski, D. Buczynska, J. Grzelak, K. Erfurt, A. Chrobok, S. Krompiec, Opt. Mater. 2016, 62, 543. IF=2.238
Cyclometalated NCN platinum(II) acetylide complexes – Synthesis, photophysics and OLEDs fabrication
9. A. Slodek, M. Filapek, E. Schab-Balcerzak, M. Grucela, S. Kotowicz, H. Janeczek, K. Smolarek, S. Mackowski, J. Malecki, A. Jędrzejowska, G. Szafraniec-Gorol, A. Chrobok, B. Marcol, S. Krompiec, M. Matussek, Eur. J. Org. Chem. 2016, 4020. IF=2.834
Highly luminescence anthracene derivatives as promising materials for OLED applications,
10. T. Klemens, A. Switlicka-Olszewska, B. Machura, M. Grucela, E. Schab-Balcerzak, K. Smolarek, S. Mackowski, A. Szlapa, S. Kula, S. Krompiec, P. Lodowski, A. Chrobok, Dalton Trans. 2016, 45, 1746. IF=4.029
Rhenium(I) terpyridine complexes – synthesis, photophysical properties and application in organic light emitting devices,
11. A. Maron, A. Szlapa, T. Klemens, S. Kula, B. Machura, S. Krompiec, J. Malecki, A. Świtlicka-Olszewska, K. Erfurt, A. Chrobok, Org. Biomol. Chem. 2016, 14, 3793. IF=3.564
Tuning the photophysical properties of 4′-substituted terpyridines – an experimental and theoretical study
12. E. Kaminska, M. Tarnacka, O. Madejczyk, A. Chrobok, K. Kaminski, M. Paluch, Phys. Chem. Chem. Phys. 2016, 18, 8901. IF=4.123
Observation of the nearly constant loss in super rigid saccharides: in search of a hidden crossover in dynamics deep in the glassy state
13. M. Tarnacka, A. Chrobok, K. Matuszek, S. Golba, P. Maksym, K. Kaminski, M. Paluch, ACS Appl. Mater. Inter. 2016, 8, 29779. IF=7.504
Polymerization of monomeric ionic liquid confined within uniaxial alumina pores as a new way of obtaining materials with enhanced conductivity
14. M. Tarnacka, A. Chrobok, K. Matuszek, D. Neugebauer, R. Bielas, S. Golba, K. Wolnica, M. Dulski, K. Kaminski, M. Paluch, Polym. Chem. 2016, 7, 6363. IF=5.375
Studies on the radical polymerization of monomeric ionic liquids: nanostructure ordering as a key factor controlling the reaction and properties of nascent polymers
1. A. Drożdż, K. Erfurt, R. Bielas, A. Chrobok, New J. Chem. 2015, 39, 1315. IF=3.277
Chemo-enzymatic Baeyer-Villiger oxidation in the presence of Candida antarctica lipase B and ionic liquids
2. K. Matuszek, A. Chrobok, J. Hogg, F. Coleman, M. Swadźba-Kwasny, Green Chem. 2015, 17, 4255. IF=8.506
Friedel-Crafts alkylation catalysed by GaCl3-based liquid coordination complexes
3. P. Zawadzki, K. Matuszek, W. Czardybon, A. Chrobok, New J. Chem. 2015, 39, 5282. IF=3.277
A versatile method of epoxide formation with the support of peroxy ionic liquids
4. D. Nieszporek, W. Simka, K. Matuszek, A. Chrobok, A. Maciej, Solid State Phenomena 2015, 227, 143. IF=0.23
Electrodeposition of zinc coatings from ionic liquid
1. K. Matuszek, A. Chrobok, F. Coleman, K. Seddon, M. Swadźba-Kwasny, Green Chem. 2014, 16, 3463. IF=8.020
Tailoring ionic liquid catalysts: structure, acidity and catalytic activity of protonic ionic liquids based on anionic clusters, [(HSO4)(H2SO4)x]- (x = 0, 1, or 2)
2. A. Drożdż, M. Foreiter, A. Chrobok, Synlett 2014, 25, 559. IF=2.419
Stable chiral complexes of ionic liquids with aluminum and biaryl ligands as efficient catalysts for the synthesis of chiral lactones
3. K. Matuszek, P. Zawadzki, W. Czardybon, A. Chrobok, New J. Chem. 2014, 38, 237. IF=3.942
New strategies for the synthesis of lactones using peroxymonosulphate salts, ionic liquids and microwave or ultrasound irradiation
4. K. Erfurt, I. Wandzik, K. Walczak, K. Matuszek, A. Chrobok, Green Chem. 2014, 16, 3508. IF=8.020
Hydrogen-bond-rich ionic liquids as effective organocatalysts for Diels-Alder reactions
5. K. Matuszek, B. Guszta, A. Kutela, A. Maciej, A. Chrobok, Przem. Chem. 2014, 93, 737. IF=0.399
Use of ionic liquids in separation of azeotropic systems
(Zastosowanie cieczy jonowych w procesie rozdziału mieszanin azeotropowych)
6. M. Sitko, W. Oleksy, A. Chrobok, Przem. Chem. 2014, 93, 722. IF=0.399
Heterogeneous catalysis in oxidation processes of cyclic ketones to lactones
(Kataliza heterogeniczna w procesach utleniania cyklicznych ketonów do laktonów)
7. A. Drożdż, A. Chrobok, Current Top. Catal. 2014, 11, 25. IF=6.562
Cyclohexanone monooxygenase mediated Baeyer-Villiger oxidation of cyclic ketones to lactones in the presence of ionic liqu
Patents
1. Method of obtaining flexible carbon composites, A. Chrobok, D. Janas, A. Brzęczek-Szafran, M. Gwóźdź
PL 444443A1
2. Method for the preparation of Knoevenagel reaction products, A. Brzęczek-Szafran, A. Chrobok, M. Gwóźdź
PL 242389B1 (PL 433112A1)
3. Method for preparing amides in the environment of polycationic protic ionic liquids, A. Brzęczek-Szafran, A. Chrobok, K. Erfurt, T. Piotrowski
PL 440344A1
4. Method for preparing of hydroxypivalaldehyde, A. Chrobok, A. Siewniak, P. Latos, J. Więcławik, E. Pankalla, U. Dorosz, R. Michalik, E. Monasterska
PL 244139B1 (PL 439786A1)
5. Method of obtaining hydroxypivalaldehyde, A. Chrobok, P. Latos, A. Siewniak, J. Więcławik, E. Monasterska, E. Pankalla
PL 242802B1 (PL 437886A1)
6. Method of preparing di-, tri-, tetra-, penta- and hexacationic protic ionic liquids, A. Brzęczek-Szafran, A. Chrobok, N. Barteczko, A. Szelwicka, J. Więcławik
EP 3998250A2 (EP 3998250A3) / PL 243578B1 (PL 436443A1)
7. Method of preparing esters of higher fatty acids, A. Brzęczek-Szafran, A. Chrobok, J. Więcławik
EP 4011860A2 (EP 4011860A3) / PL 436442A1
8. Method of preparing solvate ionic liquids, A. Chrobok, J. Więcławik
PL 242687B1 (PL 436499A1)
9. Method of conducting ring closing metathesis, A. Chrobok, N. Barteczko, M. Grymel, K. Erfurt
PL 241663B1 (PL 436391A1)
10. Method of obtaining levulinic acid esters, A. Chrobok, A. Szelwicka
PL 239702B1 (PL 432571A1)
11. Method of synthesizing a hybrid material based on multi-wall carbon nanotubes, A. Chrobok, A. Szelwicka, S. Boncel, A. Kolanowska
PL 432570A1
12. Method of purifying a polymer solution from ionic liquid, D. Babilas, A. Milewski, A. Mielańczyk, K. Goc, P. Dydo, A. Chrobok
PL 242326B1 (PL 430102A1)
13. Method of preparing n-decanoic peracid, A. Chrobok, M. Sitko, A. Szelwicka, L. Schimmelpfennig, K. Dziuba, D. Tadasiewicz, M. Morawiec-Witczak, A. Skwarek, J. Iłowska, M. Szmatoła, R. Grabowski, W. Haas, J. Bubicz
PL 239875B1 (PL 429462A1)
14. Method of preparing n-decanoic peracid, A. Chrobok, M. Sitko, A. Szelwicka, L. Schimmelpfennig, K. Dziuba, D. Tadasiewicz, M. Morawiec-Witczak, A. Skwarek, J. Iłowska, M. Szmatoła, R. Grabowski, W. Haas, J. Bubicz
PL 239874B1 (PL 429461A1)
15. Method of preparing n-decanoic peracid, A. Chrobok, M. Sitko, A. Szelwicka, L. Schimmelpfennig, K. Dziuba, D. Tadasiewicz, M. Morawiec-Witczak, A. Skwarek, J. Iłowska, M. Szmatoła, R. Grabowski, W. Haas, J. Bubicz
PL 239873B1 (PL 429460A1)
16. Method of preparing n-decanoic peracid, A. Chrobok, M. Sitko, A. Szelwicka, L. Schimmelpfennig, K. Dziuba, D. Tadasiewicz, M. Morawiec-Witczak, A. Skwarek, J. Iłowska, M. Szmatoła, R. Grabowski, W. Haas, J. Bubicz
PL 239872B1 (PL 429458A1)
17. Method of preparing ɛ-caprolactone, A. Chrobok, M. Sitko, A. Szelwicka, L. Schimmelpfennig, K. Dziuba, D. Tadasiewicz, M. Morawiec-Witczak, A. Skwarek, J. Iłowska, M. Szmatoła, R. Grabowski, W. Haas, J. Bubicz
PL 239587B1 (PL 429459A1)
18. Method of obtaining alkyl lactate, A. Chrobok, K. Erfurt, P. Latos, N. Barteczko, E. Pankalla, U. Dorosz, A. Iwachów, E. Monasterska
PL 239507B1 (PL 431940A1)
19. Method of preparing oligo(ε-caprolactone), A. Chrobok, A. Szelwicka, M. Sitko, D. Tadasiewicz, L. Schimmelpfennig, K. Dziuba, M. Morawiec-Witczak, A. Skwarek
PL 239463B1 (PL 429811A1)
20. Method of preparing lactams in an ionic liquid environment, A. Chrobok, A. Brzęczek-Szafran, A. Szelwicka, N. Barteczko, K. Matuszek, D. Tadasiewicz, L. Schimmelpfennig, K. Dziuba, T. Martyniuk, A. Pieńczakowska
PL 238346B1 (PL 430900A1)
21. Method of preparing levulinic acid esters, A. Chrobok, P. Latos
PL 238383B1 (PL 427293A1)
22. Method of preparing dialkyl phthalates, A. Chrobok, K. Erfurt, P. Latos, K. Matuszek, B. Siwik, A. Grymel, K. Potajczuk-Czajka, R. Grzybek, PL 237885B1 (PL 428213A1)
23. Method for obtaining acid ionic liquids, A. Chrobok, P. Latos
PL 237957B1 (PL 422645A1)
24. Method for obtaining the Diels-Adler cycloadducts, A. Chrobok, K. Matuszek
PL 237883B1 (PL 421003A1)
25. Method for obtaining dialkyl terephthalates, A. Chrobok, K. Erfurt, P. Latos, K. Matuszek, A. Grymel, B. Siwik, R. Grzybek, K. Potajczuk-Czajka
PL 234516B1 (PL 423579A1)
26. Method for obtaining dialkyl succinates, A. Chrobok, K. Erfurt, P. Latos, N. Serwata, A. Grymel, B. Siwik, K. Potajczuk-Czajka, R. Grzybek
PL 234515B1 (PL 423578A1)
27. Method for obtaining dicarboxylic acid esters, A. Chrobok, A. Szelwicka, M. Markiton, S. Boncel
PL 233979B1 (PL 423446A1)
28. Method for obtaining Ɛ-caprolactone, A. Chrobok, M. Markiton, K. Dziuba, L. Schimmelpfennig, A. Szewlicka, D. Tadasiewicz, M. Morawiec-Witczak
PL 233370B1 (PL 422994A1)
29. Method for obtaining liquid triflan complexes and their application, A. Chrobok, K. Matuszek
PL 231866B1 (PL 421005A1)
30. Sposób otrzymywania estrów kwasu lewulinowego, M. Musioł, D. Gillner, K. Matuszek, A. Chrobok
PL 232790B1 (PL 419458A1)
31. Method for obtaining amides, A. Chrobok, K. Matuszek
PL 231053B1 (PL 418416A1)
32. Ionic liquids with N-[2-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)ethyl]-N,N,N alkyl dimethylammonium cation and (4-chloro-2-methylphenoxy)acetate anion and method for obtaining them, J. Pernak, A. Chrobok, K. Erfurt, K. Czerniak, K. Marcinkowska, T. Praczyk
PL 228038B1 (PL 413284A1)
33. Ionic liquids with cation N-[2-(2,3,4,6-tetra-O-acetyl β-D-glucopyranosyloxy)ethyl]-N,N,N-alkyl dimethyloammonium cation and (2,4-dichlorophfenoxy)acetate anion and method for obtaining them, A. Chrobok, K. Erfurt, K. Czerniak, K. Marcinkowska, T. Praczyk, J. Pernak
PL 227335B1 (PL 413612A1)
34. Method for obtaining lactones, A. Chrobok, A. Jarzębski, K. Szymańska, A. Drożdż, U. Hanefeld
PL 414642A1
35. Method for obtaining chiral lactones, A. Chrobok, A. Drożdż, K. Erfurt
PL 412035A1
36. Method for obtaining lactones, A. Chrobok, S. Boncel, M. Sitko
PL 411711A1
37. Method for obtaining the Diels-Adler cycloadducts, A. Chrobok, A. Jarzębski, K. Matuszek, M. Sitko, K. Szymańska
PL 411332A1
38. Method for obtaining lactones in the Baeyer-Villiger oxidizing reaction, A. Chrobok, K. Matuszek, M. Sitko
PL 224672B1 (PL 409547A1)
39. Method for preparing ionic liquids, particularly applicable to the preparation of ε-caprolactone, A. Chrobok, K. Matuszek
PL 402724A1
40. Method for the separation of mixtures following CO2 absorption, M. Ściążko, A. Sobolewski, L. Więcław-Solny, A. Tatarczuk, S. Baj, A. Chrobok, A. Siewniak, T. Krawczyk
PL 234603B1 (PL 394872A1)
41. Process for the preparation of ε-caprolactam, S. Baj, A. Chrobok
PL 217547B1 (PL 391682A1)
42. Process for the preparation of esters and lactones, S. Baj, A. Chrobok, A. Siewniak
PL 215318B1 (PL 391825A1)
43. Process for the preparation of aldehydes from primary alcohols, S. Baj, A. Chrobok, A. Jarzębski, W. Pudło
PL 210887B1 (PL 389527A1)
44. Method of obtaining esters and lactones in the environment of ionic liquids, S. Baj, A. Chrobok, R. Słupska
PL 217468B1 (PL 385859A1)
45. The manner of obtaining of esters and lactones in the environment of ionic liquids, S. Baj, A. Chrobok
PL 206383B1 (PL 383036A1)
46. Method for obtaining dialkyl peroxides and peroxy esters, S. Baj, A. Chrobok
PL 198573B1 (PL 368148A1)