EPR Spectra of [Cr(CO)2L(η-C6Me6)]+ (L = PEt3, PPh3, P(OEt)3, P(OPh)3):  Analysis of Line Widths and Determination of Ground State Configuration from Interpretation of 31P Couplings

• Published in: Organometallics Vol. 16; no. 20; pp. 4369 - 4376
• Main Authors: Castellani, Michael P, Connelly, Neil G, Pike, Robert D, Rieger, Anne L, Rieger, Philip H
• Format: Journal Article
• Language: English
• Published: American Chemical Society 30.09.1997
• ISSN: 0276-7333; 1520-6041
• DOI: 10.1021/om970251p

The preparation and characterization of [Cr(CO)2L(η-C6Me6)] (L = PEt3, PPh3, P(OEt)3 and P(OPh)3, are reported. One-electron oxidation affords unstable Cr(I) cations, [Cr(CO)2L(η-C6Me6)]+, EPR spectra of which are reported. Detailed analysis of the anisotropic 31P hyperfine interaction indicates that, in frozen CH2Cl2/THF, the phosphine and phosphite complexes have 2A‘ and 2A‘‘ ground states, respectively. The hyperfine anisotropy can be accounted for by dipolar interaction of the 31P nucleus with spin density on Cr and, in the case of the phosphite complexes, with ∼0.01 P 3p y spin density resulting from π-backbonding. Line width anomalies observed in EPR spectra of these and other Cr(I) and Mn(II) “piano stool” complexes can be understood in terms of molecular distortions resulting from solvation in frozen solutions.