Crystallographic and Vibrational Spectroscopic Studies of Octakis(DMSO)lanthanoid(III) Iodides

Abstract

The octakis(DMSO) (DMSO = dimethylsulfoxide) neodymium(III), samarium(III), gadolinium(III), dysprosium(III), erbium(III), and lutetium(III) iodides crystallize in the monoclinic space group P21/n (No. 14) with Z = 4, while the octakis(DMSO) iodides of the larger lanthanum(III), cerium(III), and praseodymium(III) ions crystallize in the orthorhombic space group Pbca (No. 61), Z = 8. In all [Ln(OS(Me2)8]I3 compounds the lanthanoid(III) ions coordinate eight DMSO oxygen atoms in a distorted square antiprism. Up to three of the DMSO ligands were found to be disordered and were described by two alternative configurations related by a twist around the metal-oxygen (Ln-O) bond. To resolve the atomic positions and achieve reliable Ln-O bond distances, complete semirigid DMSO molecules with restrained geometry and partial occupancy were refined for the alternative sites. This disorder model was also applied on previously collected data for the monoclinic octakis(DMSO)yttrium(III) iodide. At ambient temperature, the eight Ln-O bond distances are distributed over a range of about 0.1 A. The average value increases from Ln-O 2.30, 2.34, 2.34, 2.36, 2.38, 2.40 to 2.43 A (Ln = Lu, Er, Y, Dy, Gd, Sm, and Nd) for the monoclinic [Ln(OSMe2)8]I3 structures, and from 2.44, 2.47 to 2.49 A (Ln = Pr, Ce, and La) for the orthorhombic structures, respectively. The average of the La-O and Nd-O bond distances remained unchanged at 100 K, 2.49 and 2.43 A, respectively. Despite longer bond distances and larger Ln-O-S angles, the cell volumes are smaller for the orthorhombic structures (Ln = Pr, Ce, and La) than for the monoclinic structure with Ln = Nd, showing a more efficient packing arrangement. Raman and IR absorption spectra for the [Ln(OS(CH3)2)8]I3 (Ln = La, Ce, Pr, Nd, Gd, Tb, Dy, Er, Lu, and Y) compounds, also deuterated for La and Y, have been recorded and analyzed by means of normal coordinate methods. The force constants for the Ln-O and S-O stretching modes in the complexes increase with decreasing Ln-O bond distance and show increasing polarization of the bonds for the smaller and heavier lanthanoid(III) ions.

Lanthanide–Bismuth Heterometallics Combined Lanthanide Metal Complexes with Bismuth Iodides: Structures and Properties

“…2). Similar stereochemistries have been found in other 8-coordinate lanthanide compounds [23][24][25]. As observed previously for other 8- (Table 4 and (10) Bi(1)-I(4) 3.2609 (11) Bi(1)-I(6) 3.2451 (12) Bi (2) 1-x,0.5 ?…”

Ambidentate coordination in hydrogen bonded dimethyl sulfoxide, (CH3)2SO⋯H3O+, and in dichlorobis(dimethyl sulfoxide) palladium(ii) and platinum(ii) solid solvates, by vibrational and sulfur K-edge X-ray absorption spectroscopy

“…Normal coordinate force field calculations were performed to compare the force constants of square planar MCl 4 2-complexes with those of the M(Me 2 SO) 2 Cl 2 , M = Pd and Pt, solvates.…”

A Coordination Chemistry Study of Solvated Thorium(IV) Ions in Two Oxygen‐Donor Solvents

“…[18] As a space-demanding ligand upon coordination, dmpu often causes metal ions to attain a lower coordination number (CN) in comparison to the corresponding hydrates and dmso solvates. [19][20][21][22][23][24][25][26] [3] ).…”