Structural elucidation, DFT calculations and catalytic activity of dioxomolybdenum(VI) complexes with NN donor ligand: Role of halogen atom coordinated to the molybdenum centre

• Published in: Polyhedron 2021-05, Vol.200, Article 115144
• Main Authors: Roy, Malini, Biswal, Debanjana, Pramanik, Nikhil Ranjan, Drew, Michael G.B., Paul, Suvendu, Kachhap, Payal, Haldar, Chanchal, Chakrabarti, Syamal
• Format: Article
• Language: English
• Subjects: Catalytic activities; Crystal structure; Dioxomolybdenum(VI); Hirshfeld surface analysis; N[sbnd]N donor ligand
• ISSN: 0277-5387
• DOI: 10.1016/j.poly.2021.115144

Two dioxomolybdenum(VI) complexes containing a NN donor ligand (L) of the general formula MoO2X2L [X = Cl(1), Br(2)] have been characterized by electrochemistry and single crystal XRD. DFT calculations, Hirshfeld surface analysis and catalytic activities of the complexes have also been studied. [Display omitted] Two new isostructural mononuclear dioxomolybdenum(VI) complexes of the formula MoO2X2L [where, X  = Cl (1), Br (2)] have been synthesized with a NN donor 2-(3-methyl-5-phenyl pyrazol-1-yl) benzthiazole ligand (L). The reaction is carried out in open air and the MoVO3+ centre in the precursor molecule, MoOX3L undergoes spontaneous aerial oxidation, leading to the formation of molybdenum(VI) complexes 1 and 2. The complexes are characterized by a wide range of spectroscopic techniques (IR, UV–Vis and 1H NMR) and elemental analyses. Crystal structures of the ligand and complexes 1 and 2 have been determined by single crystal X-ray diffraction which reveal a distorted octahedral geometry around the molybdenum(VI) centre in both the complexes. The ligand and the complexes build up fascinating supramolecular assembly via several non-covalent interactions including hydrogen bonding, CH···π and π···π interactions. Further, a detailed study of Hirshfeld surface analysis and fingerprint plots of complexes 1 and 2 are presented for understanding the intermolecular interactions involved in building self-assembled frameworks. Supportive DFT and TD-DFT calculations have also been carried out. Electrochemical properties of the complexes have been examined by cyclic voltammetry. Catalytic performance of the synthesized complexes has been evaluated for the oxidation of different olefins in the presence of hydrogen peroxide.