949173-40-4

Upstream product

• 949173-31-3 2,6-diisopropyl-phenyl-[1-(1H-pyrrol-2-yl)-ethylidene]-amine 
• 7646-79-9 cobalt(II) chloride 
• 53432-22-7 CoCl₂(trimethylphosphine) 
• 594-09-2 trimethylphosphane 

Relevant academic research and scientific papers

Synthesis, structure and magnetic behavior of five-coordinate bis(iminopyrrolyl) complexes of cobalt(II) containing PMe3 and THF ligands

The new bis-iminopyrrolyl five-coordinate Co(II) complexes [Co(κ2N,N′-NC4H3C(R)=N-2,6- iPr2C6H3)2(PMe 3)] (R = H 3a; Me 3b) were synthesized in high yields (ca. 80-90%), using THF and diethyl ether as solvents, respectively, by (a) treatment of CoCl2(PMe3)2 with the corresponding iminopyrrolyl Na salts (Ie or If) or (b) reaction of anhydrous CoCl2 and PMe3 with Ie or If. A third route was tested, involving the addition of excesses of PMe3 to the complexes [Co(κ 2N,N′-NC4H3C(R)=N-2,6-iPr 2C6H3)2] (R = H 1e; Me 1f), which was only successful for the synthesis of 3a, in lower yields (ca. 30%). The synthesis of 3b in THF was unfruitful because of the kinetic competition of the solvent, giving rise to mixtures of 1f and its coordinated THF adduct 4b. The synthesis of the new bis-iminopyrrolyl five-coordinate Co(II) complexes [Co(κ2N,N′-NC4H3C(R)=N-2,6- iPr2C6H3)2(THF)] (R = H 4a; Me 4b) were carried out in high yields (ca. 80-90%) by the reaction of CoCl2(THF)1.5 with the corresponding iminopyrrolyl Na salt. All the compounds have been characterized by X-ray diffraction, with 3a and 3b showing axially compressed trigonal bipyramidal geometry (with the PMe3 ligand lying on the equatorial plane), whereas complexes 4a and 4b exhibit distorted square pyramidal geometries with the THF molecule occupying the axial position. Complex 4a shows clearly a compressed geometry, but for complex 4b, two polymorphs were characterized, exhibiting molecules with different Co-O (THF) bond lengths, one of them being compatible with an elongated form. Magnetic measurements either in the solid or in the liquid phases indicate that complexes 3a and 3b have low-spin ground states (S = 1/2). In toluene solution, the geometry is fully confirmed by EPR data, which further indicates a dx2-y2/dxy, ground state. However, compounds 4a and 4b behave unusually because they show magnetic moments that are compatible with high-spin ground states (S = 3/2) in the solid state, but conform to low-spin ground states (S = 1/2) when both complexes are dissolved in toluene solutions. The low-spin ground states in toluene solution are confirmed by EPR spectroscopy, which further supports, for complexes 4a and 4b, an axially elongated square pyramidal geometry and a dz2 ground state. Thus the change in the ground-state and, consequently, in the geometry of complexes 4a and 4b from solid state to toluene solution might be a consequence of the elongation of the Co-O(THF) bond length. DFT studies performed on complexes 3 and 4 corroborate their different structure and magnetic behaviors and verify, for the latter complexes, the structural differences observed in the solid state and in toluene solution.

Synthesis and characterization of tetrahedral and square planar bis(iminopyrrolyl) complexes of cobalt(II)

A series of 2-iminopyrrole ligand precursors with increasing bulkiness [HNC4H3C(R)=N-2,6-R′2C6H 3] (R = R′ = H, 1a; R = Me, R′= H, 1b; R = H, R′ = Me, 1c; R = R′ = Me, 1d; R = H, R′ = iPr, 1e; R = Me, R′ = iPr, 1f) were synthesized and deprotonated with NaH to give the corresponding iminopyrrolyl sodium salts 2a-f. A set of homoleptic bis-ligand Co(II) complexes of the type [Co(κ2N,N′- NC4H3C(R)=N-2,6-R′2C6H 3)2] (R = R′= H, 3a; R = Me, R′= H, 3b; R = H, R′ = Me, 3c; R = R′ = Me, 3d; R = H, R′ = iPr, 3e; R = Me, R′ = Pr, 3f) was prepared by reaction of CoCl2 with the corresponding iminopyrrolyl sodium salts 2a-f. The new complexes were characterized by elemental analysis, magnetic susceptibility measurements, in powder and in solution, UV/vis/NIR, and, in some cases, X-ray crystallography. According to X-ray diffraction and magnetic measurements, the Co complexes 3a-e proved to be tetrahedral, which is the preferred geometry for Co(II) compounds. However, a square planar geometry is observed in the case of 3f, as determined by several characterization techniques. In this case, DFT calculations suggest the square planar geometry is slightly more stable than the tetrahedral one probably due to a combination of steric and electronic reasons.