15min:

DAMIAN M. GOODRIDGE, Department of Chemistry and Biochemistry, The Arizona State University, Tempe, AZ 85287; DANIEL F. HULLAH, RICHARD F. BARROW AND JOHN M. BROWN, The Physical and Theoretical Chemistry Laboratory, South Parks Road, Oxford, OX1 3QZ, UK.

The visible spectrum of FeH is dominated by two strong band systems, one in the blue at around 493 nm and one in the green at around 532 nm ^,. High resolution studies, carried out on room temperature samples, have established that these bands arise primarily from the g⁶-a⁶ and e⁶-a⁶ transitions respectively.

Extensive dispersed fluorescence studies have been carried out on rovibrational lines in the three lowest energy spin components of the (0,0) vibrational band of the e⁶-a⁶ system of FeH. These have revealed the positions of the (0,1) band and two further, very weak systems at around 600 nm and 630 nm. The 600 nm system has been assigned as the e⁶-c⁶⁺ transition, whilst the lines around 630 nm have been tentatively identified with the e⁶-b⁶ transition. Characterisation of the c⁶⁺ state has enabled the first parity assignments in FeH and represents the first identification of all six of the spin components in a sextet state of this radical. Following on from this, attempts are currently being made to observe e⁶-c⁶⁺ transitions involving the three highest energy spin components of the e⁶ state. A review of data collected in the early, high temperature study^a,b is also being carried out in the light of the assignments made during this work.