Abstract

In the title complex, [NiCl2(C12H9N3)2]·H2O, a divalent nickel atom is coordinated by two 2-(pyridin-2-yl)-1H-benzimidazole ligands in a slightly distorted octa-hedral environment defined by four N donors of two N,N'-chelating ligands, along with two cis-oriented anionic chloride donors. The title complex crystallized with a water mol-ecule disordered over two positions. In the crystal, a combination of O-H⋯Cl, O-H.·O and N-H⋯Cl hydrogen bonds, together with C-H⋯O, C-H⋯Cl and C-H⋯π inter-actions, links the complex mol-ecules and the water mol-ecules to form a supra-molecular three-dimensional framework. The title complex is isostructural with the cobalt(II) dichloride complex reported previously [Das et al. (2011 ▸). Org. Biomol. Chem. 9, 7097-7107].

Highlights

  • In the paper by MacNeil et al (2020), the address of the second author, Aloice O

  • Complexes of precious metals (Rh, Ir, and Ru) have been the preferred catalysts for TH owing to their high activity and commercial availability (Raja et al, 2012; Wang et al, 2015; Li et al, 2015)

  • Cg1, Cg2, Cg3, Cg4 and Cg5 are the centroids of the C7–C12, N5/N6/C18/C19/ C24, N1/C1–C5, N4/C13–C17 and C19–C24 rings, respectively

Read more

Summary

Structure description

Transition-metal-catalyzed transfer hydrogenation (TH) is an effective method of reducing ketones to the corresponding secondary alcohols (Zhu et al, 2014). The method is operationally simple, selective, and sources hydrogen from alcohols, avoiding high pressures of H2 gas (Zhu et al, 2014). Complexes of precious metals (Rh, Ir, and Ru) have been the preferred catalysts for TH owing to their high activity and commercial availability (Raja et al, 2012; Wang et al, 2015; Li et al, 2015). With growing concern surrounding the economic and environmental impact of using precious metals in chemistry, a renewed interest in Earth-abundant metal catalysis has prompted our research into TH catalysts featuring first-row transition metals, such as iron, cobalt, or nickel Cg1, Cg2, Cg3, Cg4 and Cg5 are the centroids of the C7–C12, N5/N6/C18/C19/ C24, N1/C1–C5, N4/C13–C17 and C19–C24 rings, respectively

DÁ Á ÁA
Absorption correction
Funding information
Data collection
Special details

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.