A Density Functional Theory Investigation of d8 Transition Metal(II) (Ni, Pd, Pt) Chloride Complexes of Some Vic-dioximes Derivatives

Content Provider	Semantic Scholar
Author	Nogheu, Ludovid Ngouo Ghogomu, Julius Numbonui Nkungli, Nyiang Kennet Mama, Désiré Bikélé Younang, Elie
Copyright Year	2017
Abstract	Herein, a theoretical study on the stability of some vic-dioxime complexes of Ni(II), Pd(II) and Pt(II) in gas and aqueous phases is reported. The DFT/M06/SDD and DFT/M06/6-31G+(d,p) levels of theory were adopted for the metal ions and for every other element respectively. Structural analyses of investigated complexes have revealed square planar geometries stabilized by two O–H⋯Cl hydrogen bonds. Analysis of hydrogen bond energies calculated via quantum theory of atoms in molecules (QTAIM) and computed chemical hardness values has revealed that the stability of the complexes is determined by the hydrogen bond strength. Natural population analysis has revealed ligand-metal charge transfer in the complexes investigated. A good linear agreement with correlation coefficient 0.992 has been found between calculated and experimental IR vibrational frequencies, indicating the validity of the theoretical method employed herein. Negative binding energies obtained are indicative of the stability of the complexes, thus affirming the use of vic-dioximes ligands as potential d8 transition metal eliminating agents in solution.
Starting Page	737
Ending Page	754
Page Count	18
File Format	PDF HTM / HTML
DOI	10.22036/pcr.2017.87581.1381
Volume Number	5
Alternate Webpage(s)	http://www.physchemres.org/article_49275_d60ba220c05415888cffc6fe4a643746.pdf
Alternate Webpage(s)	https://doi.org/10.22036/pcr.2017.87581.1381
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article