Photochemistry of (η5)-C5H5)Mn(CO)2[C(C6H5)2]. Generation of the diphenylcarbene radical anion |
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Authors: | R.E. Wright A. Vogler |
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Affiliation: | Universität Regensburg, Institut für Chemie, D-8400 Regensburg B.R.D. |
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Abstract: | The electronic absorption spectrum of (η5-C5H5)Mn(CO)2[C(C6H5)2]shows an intense maximum which is assigned to a MLCT transition in which the empty pπ orbital on the carbene carbon is populated. Upon irradiation of this band, the complex undergoes a decomposition with a disappearance quantum yield Φ = 0.10 ± 0.01 independent of solvent. In the CT excited state, the complex can be roughly described as containing d5 MnII and a diphenylcarbene radical anion ligand C(C6H5)2?. Due to the kinetic lability, the complex decomposes producing a MnII species and the free carbene radical anion, which then undergoes secondary reactions. In addition, small amounts of substitution product are observed. It is proposed that prior to total decomposition of the excited state, a radical pair (η5-C5H5)Mn(CO)2S+/C(C6H5)2?forms (S = solvent). A back electron transfer from C(C6H5)2?to the labile cation competes with decomposition to produce the substituted complex and free carbene. |
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