Unravelling the Photochemical Transformations of Chromium(I) 1,3 Bis(diphenylphosphino), [Cr(CO)4(dppp)]+, by EPR Spectroscopy

UV-induced photochemical transformations of the paramagnetic [Cr­(CO)4(Ph2PCH2CH2CH2PPh2)]+ complex (abbreviated [Cr­(CO)4(dppp)]+) in dichloromethane was investigated by CW EPR spectroscopy. Room-temperature UV irradiation results in the rapid transformation of [Cr­(CO)4(dppp)]+ into trans-[Cr­(CO)...

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Veröffentlicht in:Organometallics 2019-06, Vol.38 (12), p.2523-2529
Hauptverfasser: Luckham, Stephen L. J, Folli, Andrea, Platts, James A, Richards, Emma, Murphy, Damien M
Format: Artikel
Sprache:eng
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Zusammenfassung:UV-induced photochemical transformations of the paramagnetic [Cr­(CO)4(Ph2PCH2CH2CH2PPh2)]+ complex (abbreviated [Cr­(CO)4(dppp)]+) in dichloromethane was investigated by CW EPR spectroscopy. Room-temperature UV irradiation results in the rapid transformation of [Cr­(CO)4(dppp)]+ into trans-[Cr­(CO)2(dppp)2]+. However, low-temperature (77–120 K) UV irradiation reveals the presence of an intermediate mer-[Cr­(CO)3(κ1-dppp)­(κ2-dppp)]+ complex which photochemically transforms into trans-[Cr­(CO)2(dppp)2]+. The derived spin Hamiltonian parameters for these complexes were confirmed by DFT calculations. The photoinduced reaction is shown to be concentration-dependent, leading to a distribution of the three complexes ([Cr­(CO)4(dppp)]+, mer-[Cr­(CO)3(κ1-dppp)­(κ 2-dppp)]+, and trans-[Cr­(CO)2(dppp)2]+). A bimolecular photoinduced mechanism is proposed to account for the formation of mer-[Cr­(CO)3(κ1-dppp)­(κ2-dppp)]+ and trans-[Cr­(CO)2(dppp)2]+.
ISSN:0276-7333
1520-6041
DOI:10.1021/acs.organomet.9b00226