10min:

SEAN A. PEEBLES, REBECCA A. PEEBLES, AMANDA L. STEBER AND DANIEL A. OBENCHAIN, Department of Chemistry, Eastern Illinois University, 600 Lincoln Avenue, Charleston, IL 61920; GAMIL A. GUIRGIS, Department of Chemistry and Biochemistry, The College of Charleston, 66 George Street, Charleston, SC 29424; HOWARD D. STIDHAM, Department of Chemistry, University of \hboxMassachusetts, 710 North Pleasant Street, Amherst, MA 01003.

Rotational spectra for the five naturally occurring germanium isotopologues of the anti-anti conformer of n-butylgermane have been measured using a Fourier-transform microwave spectrometer operating in the 4-18 GHz range. This conformer, determined by ab initio calculations at the MP2/6-311++G(2d,2p) level to be the most stable of five possible conformers, has a heavy atom planar structure and dipole moment values (for the ⁷⁴Ge species) of µ_a = 0.7332(85) D and µ_b = 0.489(46) D, with µ _total = 0.881(26) D.

Nuclear quadrupole coupling constants have also been determined for the I = 9/2 ⁷³Ge nucleus and are in reasonable agreement with ab initio calculations. Small splittings, which were particularly apparent on the very weak b-type transitions for all isotopic species, are presumably due to rotation of one or both of the internal rotors (CH₃ and GeH₃) although these splittings have not yet been resolved sufficiently well to allow determination of any internal rotation parameters. The spectroscopic data will be discussed in relation to ab initio results and compared with results for similar species.