Journal
CHEMICAL COMMUNICATIONS
Volume 50, Issue 73, Pages 10626-10629Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc03332a
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Funding
- NSF [CHE-0911081]
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An electron-transfer series of octahedral alpha-diimine complexes [(L-H(Cy))(3)Cr](n+)(BARF)(n) (n = 2, 1, 0) has been synthesized and crystallographically characterized. Cyclic voltammetry indicated additional formation of [(L-H(Cy))(3)Cr](3+). The molecular structures suggested that all redox processes were ligand-based. Magnetic moments were consistent with spin ground states of S = 0 for [(L3Cr)-L-H-Cr-Cy](0), S = 1/2 for [(L3Cr)-L-H-Cr-Cy](+1), and S = 1 for [(L3Cr)-L-H-Cr-Cy](+2). The experimental data is consistent with chromium maintaining the +III oxidation state throughout, while being coordinated by varying numbers of neutral diimines (L-H(Cy)) and diimine radical anions (L-H(Cy center dot-)).
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