LOWEST EXCITED STATES REORDERING IN (ARENE)M(CO)3, WHERE M = Cr or W, COMPLEXES

https://doi.org/10.22146/ijc.21572

Agus Abhi Purwoko(1*), Alistair J. Lees(2)

(1) Chemistry Education Study Program, Faculty of Teacher Training and Education, University of Mataram, Jl. Majapahit 62 Mataram Indonesia 83125
(2) Department of Chemistry, Binghamton University, New York, PO Box 6000, Binghamton, N.Y. USA 13902
(*) Corresponding Author

Abstract


A series of electronic spectral changes was observed when (arene)M(CO)3 complexes (where arene = benzene, chlorobenzene, phenyltrimethylsilane, acenaphthene, mesitylene, and M = Cr or W) were irradiated with 313 nm light in benzene solution at 298 K in the presence of excess pyridine. These photolysis were neatly leading to the formation of (arene)M(CO)2(py) without any interference from further net photoreaction or thermal reaction on the same time scale. The lower photoreactivity was exhibited by acenaphthene complex. The influences of ring substituents in these complexes and of entering ligands on their photoreactions are discussed in detail with respect to reordering of their electronic states.


Keywords


photolysis; arene metal tricarbonyl; excited states reordering

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DOI: https://doi.org/10.22146/ijc.21572

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Indonesian Journal of Chemisty (ISSN 1411-9420 / 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

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