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001-es BibID:BIBFORM078704
Első szerző:Buglyó Péter (vegyész)
Cím:Tuning the redox potentials of ternary cobalt(III) complexes containing various hydroxamates / Buglyó Péter, Kacsir István, Kozsup Máté, Nagy Imre, Nagy Sándor, Bényei Attila Csaba, Kováts Éva, Farkas Etelka
Dátum:2018
ISSN:0020-1693
Megjegyzések:Sixteen cobalt(III) complexes incorporating one of the investigated 4N donor tripodal amines in the presence or absence of differently substituted hydroxamates have been synthesized and the effect of the nature of the N-donor, size of the chelates formed and the effect of the type of the substituent(s) at the hydroxamate moiety on the redox properties of the complexes have been studied. The crystal and molecular structures of the new complexes, [Co(unspenp)(H2O)Cl]Cl2.H2O (4), [Co(tren)(phebha)](ClO4)2 (11), [Co(tpa)(bha)](ClO4)2?C2H5OH?H2O (15) and [Co(tpa)(phebha)](ClO4)2 (16) have also been determined by single crystal X-ray diffraction method. Cyclic voltammetric (CV) results indicated the irreversible reduction of Co(III) in all the investigated complexes. Out of the four studied tripodal amines, abap was found to decrease the Co(III/II) reduction potential far below the region of bioreductants. Decreasing of two of the chains by one CH2 in tren compared to abap resulted in less negative reduction potential of the corresponding complex. Further positive shift was observed by introducing two (uns-penp), and especially three (tpa) ?-back-bonding pyridyl rings into the chains of tetramines. In agreement with literature results, the 3+ oxidation state of the central cobalt ion was found to be extremely stabilized in the ternary complexes containing the doubly deprotonated benzohydroximate, but the metal ion is significantly more reducible in the ternary complexes with mono-deprotonated benzohydroxamate/derivative ligands. Measurable effect was not found on the redox potential via introduction of chloro or nitro substituents in para position into the phenyl moiety of bha? (Cl-bha? and NO2-bha? ). Significant positive shift (ca. 200 mV) was obtained, however, when RN = H was replaced by a phenyl ring in phebha? therefore complexes with this latter ligand can be likely candidates for the in vitro releasing of hydroxamates with proven biological activity.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Inorganica Chimica Acta. - 472 (2018), p. 234-242. -
További szerzők:Kacsir István (1994-) (vegyész) Kozsup Máté (1992-) (Okleveles vegyész) Nagy Imre (1992-) (vegyész analitikus) Nagy Sándor (1993-) (vegyész) Bényei Attila (1962-) (vegyész) Kováts Éva (1977-) (vegyész) Farkas Etelka (1948-) (vegyész)
Pályázati támogatás:GINOP-2.3.2-15-2016-00008
GINOP
OTKA-112317
OTKA
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2.

001-es BibID:BIBFORM099415
035-os BibID:(cikkazonosító)3586 (WoS)000666566100001 (Scopus)85108329799
Első szerző:Nagy Sándor (vegyész)
Cím:Donor Atom Preference of Organoruthenium and Organorhodium Cations on the Interaction with Novel Ambidentate (N,N) and (O,O) Chelating Ligands in Aqueous Solution / Nagy Sándor, Ozsváth András, Bényei Attila Cs., Farkas Etelka, Buglyó Péter
Dátum:2021
ISSN:1420-3049
Megjegyzések:Two novel, pyridinone-based chelating ligands containing separated (O,O) and (Namino,Nhet) chelating sets (Namino = secondary amine; Nhet = pyrrole N for H(L3) (1-(3-(((1H-pyrrole-2-yl)methyl)-amino)propyl)-3-hydroxy-2-methylpyridin-4(1H)-one) or pyridine N for H(L5) (3-hydroxy-2-methyl-1-(3-((pyridin-2-ylmethyl)amino)propyl)pyridin-4(1H)-one)) were synthesized via reduction of the appropriate imines. Their proton dissociation processes were explored, and the molecular structures of two synthons were assessed by X-ray crystallography. These ambidentate chelating ligands are intended to develop Co(III)/PGM (PGM = platinum group metal) heterobimetallic multitargeted complexes with anticancer potential. To explore their metal ion binding ability, the interaction with Pd(II), [(?6-p-cym)Ru]2+ and [(?5-Cp*)Rh]2+ (p-cym = 1-methyl-4-isopropylbenzene, Cp* = pentamethyl-cyclopentadienyl anion) cations was studied in aqueous solution with the combined use of pH-potentiometry, NMR and HR ESI-MS. In general, organorhodium was found to form more labile complexes over ruthenium, while complexation of the (N,N) chelating set was slower than the processes of the pyridinone unit with (O,O) coordination. Formation of the organoruthenium complexes starts at lower pH (higher thermodynamic stabilities of the corresponding complexes) than for [(?5-Cp*)Rh]2+ but, due to the higher affinity of [?6-p-cym)Ru]2+ towards hydrolysis, the complexed ligands are capable of competing with hydroxide ion in a lesser extent than for the rhodium systems. As a result, under biologically relevant conditions, the rhodium binding effectivity of the ligands becomes comparable or even slightly higher than their effectivity towards ruthenium. Our results indicate that H(L3) is a less efficient (N,N) chelator for these metal ions than H(L5). Similarly, due to the relative effectivity of the (O,O) and (N,N) chelates at a 1:1 metal-ion-to-ligand ratio, H(L5) coordinates in a (N,N) manner to both cations in the whole pH range studied while, for H(L3), the complexation starts with (O,O) coordination. At a 2:1 metal-ion-to-ligand ratio, H(L3) cannot hinder the intensive hydrolysis of the second metal ion, although a small amount of 2:1 complex with [(?5-Cp*)Rh]2+ can also be detected.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
ruténium
ródium
komplex
piridinon
maltol
Megjelenés:Molecules. - 26 : 12 (2021), p. 1-23. -
További szerzők:Ozsváth András (1992-) (vegyész) Bényei Attila (1962-) (vegyész) Farkas Etelka (1948-) (vegyész) Buglyó Péter (1965-) (vegyész)
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3.

001-es BibID:BIBFORM096865
035-os BibID:(cikkazonosító)111372 (WoS)000651369100004 (Scopus)85105285700
Első szerző:Nagy Sándor (vegyész)
Cím:Effect of the replacement of tripodal 4N donors by two 2N chelators on the redox and cytotoxic activity of maltolato and deferipronato containing Co(III) complexes / Nagy Sándor, Tóth Emese, Kacsir István, Makai Attila, Bényei Attila Csaba, Buglyó Péter
Dátum:2021
ISSN:0162-0134 1873-3344
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Journal of Inorganic Biochemistry. - 220 (2021), p. 1-10. -
További szerzők:Tóth Emese (1988-) (biotechnológus) Kacsir István (1994-) (vegyész) Makai Attila Bényei Attila (1962-) (vegyész) Buglyó Péter (1965-) (vegyész)
Pályázati támogatás:GINOP-2.3.2-15-2016-00008
GINOP
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