Synthesis of bis(thiosemicarbazone) derivatives: Definition, crystal structure, biological potential and computational analysis

[ X ]

Tarih

2018

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Taylor and Francis Ltd.

Erişim Hakkı

info:eu-repo/semantics/closedAccess

Özet

(2-(2-(2-methoxyphenyl)hydrazono)cyclohexane-1,3-diylidene) bis(hydrazine carbothioamide) (L1), 4-(2-(-2,-6-bis(2-carbamothioylhydrazono) cyclohexylidene) hydrazinyl)benzoic acid (L2), and (2-(2-(4-bromophenyl) hydrazono) cyclohexane-1,3-diylidene) bis(hydrazinecarbothioamide) (L3) bis(thiosemicarbazone) derivative compounds were synthesized by the condensation reaction of thiosemicarbazide and various ketone compounds. The structures of synthesized compounds were characterized by using FT-IR, 1H and 13C-NMR spectra, elemental analysis and mass spectra. Also, the structure of L1 has been determined by X-ray crystallographic analysis. Additionally, the antioxidant activities (free radical (DPPH) scavenging, iron chelating and reducing power) of compounds were evaluated. Especially, L3 displayed good DPPH activity (84.13%) at 100 mg/L. Moreover, pBR322 plasmid DNA cleavage activity was examined and all of the compounds were able to cleave the plasmid DNA. Finally, the ground state geometries of the thiosemicarbazone derivatives were optimized using Density Functional Theory applications at B3LYP/6-31G (d,p) level in order to obtain information about the 3D geometries and electronic structure, © 2018 Taylor & Francis Group, LLC.

Açıklama

Anahtar Kelimeler

Antioxidant, Computational Analysis, Crystal Structure, DNA Cleavage, Thiosemicarbazone

Kaynak

Phosphorus, Sulfur and Silicon and the Related Elements

WoS Q Değeri

N/A

Scopus Q Değeri

Q3

Cilt

193

Sayı

1

Künye

Ateş, D., Gülcan, M., Gümüş, S., Şekerci, M., Özdemir, S., Şahin, E., Çolak, N. (2018). Synthesis of bis (thiosemicarbazone) derivatives: Definition, crystal structure, biological potential and computational analysis. Phosphorus, Sulfur, and Silicon and the Related Elements, 193(1), 14-22.