Role of Supramolecular Strucutres in Mechanisms of Catalytic Oxidation and Action of Ni(Fe)ARD Dioxygenases on Model Systems

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dc.citation.epage311
dc.citation.issue3
dc.citation.spage304
dc.contributor.affiliationEmanuel Institute of Biochemical Physics, Russian Academy of Sciences
dc.contributor.authorMatienko, Ludmila
dc.contributor.authorBinykov, Vladimir
dc.contributor.authorMil, Elena
dc.contributor.authorZaikov, Gennady
dc.coverage.placenameЛьвів
dc.coverage.placenameLviv
dc.date.accessioned2024-01-09T08:54:40Z
dc.date.available2024-01-09T08:54:40Z
dc.date.created2020-03-16
dc.date.issued2020-03-16
dc.description.abstractЗа допомогою методу АСМ досліджено можливість утворення супрамолекярних структур внаслідок водневих зв‘язків на основі Ni(або Fe)(асас)n-систем, які є каталізаторами окиснення етилбензену, а також моделями Ni(Fe)ARD діоксигеназ: потрійні системи {М(асас)п + L2 + L3} (М = NiII, FeIII, L2 = NMP (NMP = N-метил-2-піролідон), L-гістидин, L3 = PhOH, L-тирозин), п = 2, 3). Визначено роль Н-зв‘язків і супрамолекулярних структур при окисненні алкіларенів (етилбензен), який каталізується Ni(або Fe)-комплексними каталізаторами, а також роль супрамолекулярних структур і Tyr-фрагменту в механізмах дії Ni(Fe)ARD діоксигеназ.
dc.description.abstractThe AFM technique was used to research the possibility of the supramolecular structures formation due to H-bonds based on Ni(Fe)(acac)n-systems, that are catalysts of alkylarens oxidations and also models Ni(Fe)ARD dioxygenases: {M(acac)n+L2+L3} triple systems (M=NiII, FeIII , L2 = NMP (NMP = N-methyl-2-pirrolidone), L-histidine, L3 = PhOH, L-tyrosine), n = 2, 3). Role of H-bonding and supramolecular structures in alkylarens oxidations, catalyzed with Ni(or Fe) complexes catalysts, and also role of supramolecular structures and Tyrfragment in mechanisms of Ni(Fe)ARD-actions is discussed.
dc.format.extent304-311
dc.format.pages8
dc.identifier.citationRole of Supramolecular Strucutres in Mechanisms of Catalytic Oxidation and Action of Ni(Fe)ARD Dioxygenases on Model Systems / Ludmila Matienko, Vladimir Binykov, Elena Mil, Gennady Zaikov // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2020. — Vol 14. — No 3. — P. 304–311.
dc.identifier.citationenRole of Supramolecular Strucutres in Mechanisms of Catalytic Oxidation and Action of Ni(Fe)ARD Dioxygenases on Model Systems / Ludmila Matienko, Vladimir Binykov, Elena Mil, Gennady Zaikov // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2020. — Vol 14. — No 3. — P. 304–311.
dc.identifier.doidoi.org/10.23939/chcht14.03.304
dc.identifier.urihttps://ena.lpnu.ua/handle/ntb/60681
dc.language.isoen
dc.publisherВидавництво Львівської політехніки
dc.publisherLviv Politechnic Publishing House
dc.relation.ispartofChemistry & Chemical Technology, 3 (14), 2020
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dc.relation.referencesen[1] Matienko L., Mosolova L., Zaikov G., Russ. Chem. Rev., 2009, 78, 211. https://doi.org/10.1070/RC2009v078n03ABEH003919
dc.relation.referencesen[2] Matienko L., Mosolova L., Zaikov G., Selective Catalytic Hydrocarbons Oxidation. New Perspectives. Nova Science Publ. Inc., New York 2010.
dc.relation.referencesen[3] Beletskaya I., Tyurin V., Tsivadze A. et al: Chem. Rev., 2009, 109, 1659. https://doi.org/10.1021/cr800247a
dc.relation.referencesen[4] Slater A., Perdigao L., Beton P., Champness N., Acc. Chem. Res., 2014, 47, 3417. https://doi.org/10.1021/ar5001378
dc.relation.referencesen[5] Matienko L., Mosolova L., Oxid. Commun., 2014, 37, 20.
dc.relation.referencesen[6] Matienko L., Mosolova L., Binyukov V. et al: Ch. 8 [in:] Pearce E., Howell B., Pethrick R., Zaikov G. (Eds.), Physical Chemistry Research for Engineering and Applied Sciences. V.3. High PerformanceMaterials andMethods. Apple Academic Press Inc., Toronto, New Jersey 2015, 63.
dc.relation.referencesen[7] Matienko L., Mosolova L., Binyukov V. et al: J. Biol. Res., 2012, 1, 37.
dc.relation.referencesen[8] Matienko L., Binyukov V., Mosolova L. et al: Chem. Chem. Technol., 2014, 8, 339. https://doi.org/10.23939/chcht08.03.339
dc.relation.referencesen[9] Deshpande A., Wagenpfail K., Pochapsky Th. et al: Biochemistry, 2016, 55, 1398. https://doi.org/10.1021/acs.biochem.5b01319
dc.relation.referencesen[10] Straganz G., Nidetzky B., J. Am. Chem. Soc., 2005, 127, 12306. https://doi.org/10.1021/ja042313q
dc.relation.referencesen[11] Deshpande A., Pochapsky Th., Ringe D., Chem. Rev., 2017, 117, 10474. https://doi.org/10.1021/acs.chemrev.7b00117
dc.relation.referencesen[12] Mbughuni M., Meier K., Münck E., Biochemistry, 2012, 51, 8743. https://doi.org/10.1021/bi301114x
dc.relation.referencesen[13] Zhang J., Klinman J., J. Am. Chem. Soc., 2011, 133, 17134. https://doi.org/10.1021/ja207467d
dc.relation.referencesen[14] Matienko L., Mosolova L., Binyukov V. et al., Oxid. Commun. 40, 569 (2017).
dc.relation.referencesen[15] Matienko L., Mosolova L., Binyukov V. et al: J. Pharm. Pharmacol., 2017, 5, 379. https://doi.org/10.17265/2328-2150/2017.06.010
dc.relation.referencesen[16] Zhang Y., HeinsenM., KosticM. et al., Bioorg. Med. Chem., 2004, 12, 3847. https://doi.org/10.1016/j.bmc.2004.05.002
dc.relation.referencesen[17] Allpress C., Grubel K., Szajna-Fuller E. et al., J. Am. Chem. Soc., 2013, 135, 659. https://doi.org/10.1021/ja3038189
dc.relation.referencesen[18] Nekipelov V., Zamaraev K., Coord. Chem. Rev., 1985, 61, 185. https://doi.org/10.1016/0010-8545(85)80005-9
dc.relation.referencesen[19] Belsky V., Bulychev V., Russ. Chem. Rev., 1999, 68, 119. https://doi.org/10.1070/RC1999v068n02ABEH000459
dc.relation.referencesen[20] Patel N., Ramachandran S., Azimov R. et al., Biochemistry, 2015, 54, 7320. https://doi.org/10.1021/acs.biochem.5b00988
dc.relation.urihttps://doi.org/10.1070/RC2009v078n03ABEH003919
dc.relation.urihttps://doi.org/10.1021/cr800247a
dc.relation.urihttps://doi.org/10.1021/ar5001378
dc.relation.urihttps://doi.org/10.23939/chcht08.03.339
dc.relation.urihttps://doi.org/10.1021/acs.biochem.5b01319
dc.relation.urihttps://doi.org/10.1021/ja042313q
dc.relation.urihttps://doi.org/10.1021/acs.chemrev.7b00117
dc.relation.urihttps://doi.org/10.1021/bi301114x
dc.relation.urihttps://doi.org/10.1021/ja207467d
dc.relation.urihttps://doi.org/10.17265/2328-2150/2017.06.010
dc.relation.urihttps://doi.org/10.1016/j.bmc.2004.05.002
dc.relation.urihttps://doi.org/10.1021/ja3038189
dc.relation.urihttps://doi.org/10.1016/0010-8545(85)80005-9
dc.relation.urihttps://doi.org/10.1070/RC1999v068n02ABEH000459
dc.relation.urihttps://doi.org/10.1021/acs.biochem.5b00988
dc.rights.holder© Національний університет “Львівська політехніка”, 2020
dc.rights.holder© Matienko L., Binykov V., Mil E., Zaikov G., 2020
dc.subjectАСМ
dc.subjectсупрамолекулярні структури
dc.subjectкаталітичне окиснення
dc.subjectO2
dc.subjectNi(або Fe)(acac)n
dc.subjectNi(Fe)ARD діоксигенази
dc.subjectAFM
dc.subjectsupramolecular structures
dc.subjectcatalytic oxidation
dc.subjectO2
dc.subjectNi(or Fe)(acac)n
dc.subjectNi(Fe)ARD dioxygenases
dc.titleRole of Supramolecular Strucutres in Mechanisms of Catalytic Oxidation and Action of Ni(Fe)ARD Dioxygenases on Model Systems
dc.title.alternativeРоль супрамолекулярних структур в механізмах каталітичного окиснення та дія діоксигеназ NI(FE)ARD на модельних системах
dc.typeArticle

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Chemistry & Chemical Technology. – 2020. – Vol. 14, No. 3