Publication:
New N,N'-bis(thioamido)thiocarbohydrazones and carbohydrazones: synthesis, structure characterization, antioxidant activity, corrosion inhibitors and DFT studies

dc.contributor.authorÇavuş M.S., Yakan H., Özorak C., Muğlu H., Bakır T.K.
dc.contributor.authorCavus, MS, Yakan, H, Ozorak, C, Muglu, H, Bakir, TK
dc.date.accessioned2023-05-09T15:48:24Z
dc.date.available2023-05-09T15:48:24Z
dc.date.issued2022-04-01
dc.date.issued2022.01.01
dc.description.abstractNew symmetric N,N'-bis(thioamido)thio/carbohydrazones (1–4) were prepared from thio/carbohydrazide and various isothiocyanates with high yields and characterized the structures of the compounds. The compounds were evaluated as new corrosion inhibitors for corrosion of mild steel in 0.1 M HCl solutions using polarization and electrochemical impedance spectroscopy (EIS) techniques, and all compounds showed effective inhibitory properties. Antioxidant activity values determined using the DPPH method for all compounds showed higher antioxidant activity than the standard Trolox (5.89 µM). The IC50 values of the compounds were obtained between 3.45 and 4.25 µM, and also showed a ranking of 4 > 2 > 3 > 1 > Trolox , with antioxidant activities better than Trolox. Compound 4 (1,5-bis((3-fluorophenyl)carbamothioyl)carbonohydrazide) exhibited the highest activity in terms of both antioxidant and anti-corrosion properties. DFT calculations were also performed to determine the spectroscopic properties of the compounds and to analyze the structure–activity relationship for their antioxidant characteristics. It was investigated how DPPH reactions are affected by the dependence of delocalization indices and charge densities of N–H bonds on intramolecular interactions. As well as the calculations of intramolecular interactions and some QTAIM parameters, Laplacian bond order and bond polarity index (BPI) analysis were also performed to examine the electronic properties of reactive N–H bonds. Graphical abstract: New symmetric N,N'-bis(thioamido)thio/carbohydrazones were obtained. Structures of all compounds were elucidated using spectroscopic approaches. Antioxidant activities of the compounds were determined by DPPH method. QTAIM analyses were used to examine the relationship between the electronic properties and antioxidant activity. The compounds were evaluated as new corrosion inhibitors for corrosion of mild steel in 0.1 M HCl.[Figure not available: see fulltext.].
dc.identifier.doi10.1007/s11164-022-04659-z
dc.identifier.eissn1568-5675
dc.identifier.endpage1613
dc.identifier.issn0922-6168
dc.identifier.scopus2-s2.0-85123496570
dc.identifier.startpage1593
dc.identifier.urihttps://hdl.handle.net/20.500.12597/12622
dc.identifier.volume48
dc.identifier.wosWOS:000746289700001
dc.relation.ispartofResearch on Chemical Intermediates
dc.relation.ispartofRESEARCH ON CHEMICAL INTERMEDIATES
dc.rightsfalse
dc.subjectAntioxidant | Carbothioamides | Corrosion inhibitor | DFT analysis | Spectroscopic elucidation
dc.titleNew N,N'-bis(thioamido)thiocarbohydrazones and carbohydrazones: synthesis, structure characterization, antioxidant activity, corrosion inhibitors and DFT studies
dc.titleNew N,N '-bis(thioamido)thiocarbohydrazones and carbohydrazones: synthesis, structure characterization, antioxidant activity, corrosion inhibitors and DFT studies
dc.typeArticle
dspace.entity.typePublication
oaire.citation.issue4
oaire.citation.volume48
relation.isScopusOfPublication7d54fb74-4285-46a0-bc08-71105455d650
relation.isScopusOfPublication.latestForDiscovery7d54fb74-4285-46a0-bc08-71105455d650
relation.isWosOfPublication53dc61d6-7c9c-4dc1-9b12-07f5921a31b0
relation.isWosOfPublication.latestForDiscovery53dc61d6-7c9c-4dc1-9b12-07f5921a31b0

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