15min:

JUSTIN L. NEILL, MATT T. MUCKLE AND BROOKS H. PATE, Department of Chemistry, University of Virginia, Charlottesville, VA 22904; RYAN G. BIRD AND DAVID W. PRATT, Department of Chemistry, University of Pittsburgh, Pittsburgh, PA 15260.

The neurotransmitter p-methoxyphenylethylamine (pMPEA) has been well-studied by ultraviolet and microwave spectroscopy. Seven conformers of this molecule have been assigned in total, showing good agreement with ab intio rotational constants, relative dipole moments, ¹⁴N quadrupole coupling constants, and relative energies. In this talk, we present the assignment of two conformations of the water complex of pMPEA by chirped pulse Fourier transform microwave spectroscopy. These two structures are the two lowest energy conformations of the pMPEA monomer, with a water molecule donating a hydrogen bond to the nitrogen atom. Good agreement between ab initio and experimental parameters is observed. In addition, ultraviolet-microwave double resonance spectra have been collected on a Balle-Flygare type cavity to determine the electronic band origins of these complexes, confirming that these water clusters are the same as those previously observed by Unamuno et al .\footnoteI.Unamuno, J.A.Fernández, C.Landajo, A.Longarte, F.Castaño, Chem.~Phys. \textbf271 (2001) 55-69.