Nickel (II) complex [NiCl2(DMF)(2)L-2] bearing diaminobenzene and sulfonamide: Crystal structure and catalytic application in the reduction of nitrobenzenes


DAYAN S., Kayaci N., DAYAN S., ÖZDEMİR N., ÖZPOZAN N.

POLYHEDRON, vol.175, 2020 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 175
  • Publication Date: 2020
  • Doi Number: 10.1016/j.poly.2019.114181
  • Journal Name: POLYHEDRON
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Chimica
  • Çanakkale Onsekiz Mart University Affiliated: No

Abstract

A new Bis[N-(2-aminophenyl)benzenesulfonamidej-di-chloro-Bis[O'-N,N-dimethyl-formamide]-nickel (II) complex [NiCl2(DMF)(2)L2] was synthesized in DMF solution in reflux media with NiCl2.2H(2)O and the pre-prepared N-(2-aminophenyl)benzenesulfonamide and the [NiCl2(DMF)(2)L-2] complex was crystallized in DMF/diethyl ether solution, for its single crystal. The complex characterized by FT-IR, elemental analysis, TG-DTA and UV Vis spectrophotometry methods, and its single crystal study were also performed by X-ray spectroscopy. Additionally, the catalytic efficiency of the fabricated [NiCl2(DMF)(2)L-2] complex was determined by UV Vis spectrophotometry in the reduction reaction of 2-nitroaniline (2-NA), 4-nitroaniline (4-NA) and nitrobenzene (NB) in presence of NaBH4 in water. The best conversion obtained as a result of the reduction of nitroarenes in the short time of 10 min. was 62.5 %, which was obtained at the 2-NA reduction. The conversion obtained from of the reduction of nitroarenes, are sequenced as 2-NA (62.5 %) > NB (56.5 %) > 4-NA (25.5%) in 10 min. In addition, the reaction products, both aqueous and short-term, are harmless to the environment, which will provide a significant reaction variety in terms of green chemistry. (C) 2019 Elsevier Ltd. All rights reserved.