Reports: UR653451-UR6: The Characterization and Conformational Preferences of Long Alkyl Chains Using Advanced Broadband Microwave Spectroscopy
Stephen A. Cooke, PhD, State University of New York, College at Purchase
Briefly, ethyl methyl ether exists in a trans conformer in its lowest energy configuration. The next member of the series, propyl methyl ether, has, curiously, only been studied as the trans-trans conformer, with the aim of that study being to compare geometric parameters to ethyl methyl ether. This is curious because the lowest energy conformer of propyl methyl ether is the trans-gauche configuration, i.e. the O-C-C-C dihedral is approximately 60o. Butyl methyl ether, and the higher members have not been the subject of any prior microwave spectroscopic studies. We proposed to study these molecules using microwave spectroscopy with the goal of establishing the conformations of the alkyl chain.
We have successfully recorded the pure rotational spectrum of butyl methyl ether. Furthermore, we have synthesized the pentyl methyl ether and recorded its rotational spectrum. The synthesis of hexyl methyl ether is complete, and its microwave spectrum is next to be recorded. Through the analysis of the rotational spectrum for butyl methyl ether, performed by our students, we have located the lowest energy conformer also contains the O-C-C-C dihedral angle of approximately 60 degrees. The analysis of the pentyl methyl ether is ongoing, as is the analysis of the observable effects of the methoxy internal rotation in these molecules.
In regards to impact upon the personnel’s careers both undergraduates who have been supported by this award are making applications to graduate school to pursue advanced degrees in the field of chemistry. The third involved undergraduate is in the process of applying to medical school. The data obtained will be publishable in a peer reviewed journal such as the Journal of Molecular Spectroscopy or Journal of Molecular Structure.