Highly distorted octahedral molybdenum(II) complexes: Synthesis, crystal structure, and properties of [Mo(S2C6H4)(CO)2(PMenPh3−n)2] (n = 0–3). (15th October 2016)

• Record Type: Journal Article
• Authors: Tsukada, Satoru; Abe, Naoya; Gunji, Takahiro
• Is Part Of: Polyhedron. Volume 117(2016)
• Page Start: 73
• Page End: 79
• Publication Date: 2016-10-15
• Subjects: Metalladithiolene complex -- Highly distorted octahedral -- Crystal structure -- Molybdenum -- Phosphine ligand; Chemistry, Inorganic -- Periodicals; Chimie inorganique -- Périodiques; Organometaalverbindingen; Anorganische chemie; 546.05
• DOI: 10.1016/j.poly.2016.05.035
• Languages: English
• ISSNs: 0277-5387

Abstract

Graphical abstract: A series of highly distorted octahedral 6-coordinate molybdenum complexes were synthesized and their structures successfully characterized by single crystal X-ray diffraction. Abstract: Four hexacoordinated molybdenum complexes, [Mo(S2 C6 H4 )(CO)2 (PMe n Ph3− n )2 ] ( n = 0 (1 ), 1 (2 ), 2 (3 ), 3 (4 )), were synthesized via the one-pot reaction of [Mo( η 3 -C3 H5 )(Br)(CH3 CN)2 (CO)2 ], 1, 2-H2 bdt (bdt = benzenedithiolate), and phosphines. The structure of all complexes was successfully characterized by single crystal X-ray diffraction. For the stabilization these complexes, the bdt ligand and the axial phosphine ligands are not located on the ideal vertexes of octahedron in order to reduce the destabilizing overlapping of molecular orbitals. Therefore, six-coordinated complexes generally adopt an octahedral geometry, the complexes1–4 showed structures intermediate between a distorted octahedron and a regular trigonal prism, i.e. configurations far from the ideal octahedral geometry. All complexes underwent a two-step 2e − reduction reaction, with the reduction potential of the Mo center shifting towards negative values moving from compound1 to compound4 .