K. Remmers et al., INTERNAL-ROTATION EFFECTS IN THE ROTATIONALLY RESOLVED S-1(L-1(B))[-S-0 ORIGIN BANDS OF 3-METHYLINDOLE AND 5-METHYLINDOLE, The Journal of chemical physics, 108(20), 1998, pp. 8436-8445
The rotationally resolved ultraviolet (UV) excitation spectra of the S
-1(L-1(b))<--S-0 origin bands of 3-methylindole and 5-methylindole hav
e been measured and analyzed. As a result of an internal rotation of t
he methyl group, each spectrum consists of rotational lines of overlap
ping 0a(1)<--0a(1) and 0e<--0e torsional transitions. Like indole, 3-m
ethylindole and 5-methylindole undergo axis reorientation upon electro
nic excitation. The Hamiltonian used to describe all observed spectral
features includes a pure rotational part, a pure torsional part, and
terms describing the interaction between the internal rotation and the
overall rotation. It also accounts for the axis reorientation effect.
Values for the barrier heights of the methyl torsion, the angle of th
e methyl top axis with the inertial axes, and the rotational constants
are obtained for both the S-0 and the S-1 state. From an analysis of
the intensities of the rotational transitions, the direction of the tr
ansition moment and the axis reorientation angle are obtained. Due to
quantum interference effects in the 5-methylindole spectrum the sign o
f these angles could be determined. (C) 1998 American Institute of Phy
sics. [S0021-9606(98)02120-5]