Chemical Physics: Molecular beam microwave spectroscopy; structure and dynamics of weakly bound complexes, conformations of floppy molecules; high resolution spectroscopy of free radicals.
The major thrust of our work is the study of "exotic" molecules. These can include highly reactive free radicals; ions; high temperature species; short-lived "intermediates"; and very weakly bound complexes, van der Waals and hydrogen bonded molecules. The free radicals and carbenes we study are important in the chemistry of the interstellar medium.

We use high vacuum techniques to produce molecular beams which are probed by microwave spectroscopy. For example it is possible to reach the low temperature necessary for the production of van der Waals complexes by expansion of a gas through a supersonic nozzle into a vacuum chamber. By exciting molecules exiting the nozzle with a corona discharge, free radicals and other reactive intermediates are produced.

The microwave spectroscopic technique we employ in the laboratory is called pulsed-jet Fabry-Perot Fourier Transform microwave spectroscopy (FTMS). An intense pulsed jet of gas is produced at temperatures within 1 degree of zero Kelvin by standard pulsed supersonic techniques. This cold jet flows through a Fabry-Perot microwave cavity created by two large spherical aluminum mirrors whose separation ensures a high Q cavity tunable within the 6 to 26 GHz range. A pulse of microwave radiation timed to coincide with the arrival of the gas pulse, is introduced into the tuned cavity. If the molecules in the jet have a spectral transition within the 1 MHz spectral width of the cavity they can absorb the radiation and a macroscopic polarization of the molecules is induced. It is the free induction decay (FID) of this radiation that is detected. The results of many pulses and decays can be added together. The jet can be pulsed, say, ten times a second, so the result of two hundred pulses, polarization, FID's, can be collected within twenty seconds. These summed FID's are then Fourier transformed to produce a small piece of the molecular spectrum. The full microwave spectrum is gathered by retuning the cavity mechanically with a stepping motor to the next, say, 500 kHz window, stepping the master oscillator up by 500 kHz, and starting the pulsing sequence again. All this is accomplished automatically under computer control.

Weakly bound complexes are indeed rather complex molecules. Due to their extremely weak bonding, the molecules can and so undergo wild internal motions including extremely wide amplitude motions, and even inversions which make and break the weak bond. And yet, for these systems, the bonding geometry seems rather well predicted by chemical models similar to those which have proved so successful for the strongly bound covalent molecules.

A detailed understanding of the nature of these systems will have a fundamental impact on a host of chemical and physical problems including: transition state structures and dynamics, hydrogen bonding selectivity and directionality, crystal structures, reaction mechanisms, catalysis and surface interactions.

Group Members

Visitors to the Laboratory

Publications since 1990

Education

B.S. 1967 State University of New York, Stony Brook, Ted Goldfarb
M.A. 1968 Harvard University, Harvard Chemistry
Ph.D. 1973 Harvard University, William Klemperer   
Post Doctoral Research Associate, Joint Institute for Laboratory Astrophysics Carl Lineberger
BIBLIOGRAPHY OF ROTATIONAL SPECTRA OF WEAKLY BOUND COMPLEXES

Below are photographs from Professor William Klemperer's 65th birthday celebration in 1992, from his Retiral celebration in May 2002, and from his 80th birthday symposium on October 6, 2007.

The fourth photo is from the 70th birthday celebration and group reunion for W. Carl Lineberger, held in Boulder, Colorado on June 13, 2009. 40 years of ion chemistry.

  
 

[Chemistry] [Wesleyan]

Last updated: January 21, 2010 (sn)