Synthesis and structure of cis-dichlorobis(2-phenylazopyridine)chromium(II), an inert chromium(II) compound

Autor: Sine Larsen, Ronald A. Krause, V. Ferreira
Rok vydání: 1988
Předmět:
Zdroj: Inorganica Chimica Acta. 145:29-38
ISSN: 0020-1693
DOI: 10.1016/s0020-1693(00)82002-2
Popis: Recent studies have shown 2-phenylazopyridine (Azpy) to be a useful departure from polypyridyl type ligands in coordination chemistry; frequently lower oxidation states are stabilized by this ligand. We have prepared and studied [Cr(Azpy)2Cl2] which is surprisingly inert for a chromium(II) complex. The compound crystallizes in the space group P21/c with a = 7.953(3), b = 21.189(11), c = 12.922(12) A, β = 114.80(5)° and Z = 4. Based on 6777 reflections the structure has been refined to R = 0.030 and Rw = 0.038. The complex is six-coordinated with cis-chlorides, cis-azo and trans-pyridyl groups. The overall symmetry is close to C2. The azo NN distances are elongated to 1.282 and 1.314 A, significantly longer than observed in free azo groups. The magnetic moment of 2.8 BM is independent of temperature indicating an orbitally non-degenerate low-spin ground state. In acetonitrile the spectrum shows a band in the red at 1470 nm which is assigned as ligand-metal charge transfer, consistent with earlier interpretations on similar compounds. The compound is stable to air oxidation in acetonitrile or methylene chloride; cyclic voltammetry in these solvents yields potentials of 0.508 and −0.185 V, both appearing to be one electron transfers. The complex is a non-electrolyte in acetonitrile, nearly unchanged over 24 h. However, chloride ions are slowly replaced at 50 °C in this solvent by 2,2′-bipyridyl; this reaction is pseudo-first order in complex with a rate constant of 4.0 ± 0.3 × 10−7 s−1. All data indicate the presence of a strong chromium-Azpy pi-interaction.
Databáze: OpenAIRE