Molecular Dynamics In Real Time | March 8, 2010 Issue - Vol. 88 Issue 10 | Chemical & Engineering News
Volume 88 Issue 10 | pp. 14-15
Issue Date: March 8, 2010

Cover Stories: Nifty At Fifty

Molecular Dynamics In Real Time

Department: Science & Technology
News Channels: Analytical SCENE
Keywords: femtosecond, pump-probe, reaction dynamics
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CONFORMATION
In ethyl acetate, cyclopentadienylmolybdenum(II) tricarbonyl dimers adopt trans and gauche conformations. By breaking the Mo-Mo bond and probing the products with laser-driven two-dimensional infrared spectroscopy, a team led by Kevin J. Kubarych of the University of Michigan found that the monomers (C is blue; H is white; O is red; Mo is green) rebind on the picosecond timescale in the trans configuration only.
Credit: Kevin Kubarych
8810cov_figure
 
CONFORMATION
In ethyl acetate, cyclopentadienylmolybdenum(II) tricarbonyl dimers adopt trans and gauche conformations. By breaking the Mo-Mo bond and probing the products with laser-driven two-dimensional infrared spectroscopy, a team led by Kevin J. Kubarych of the University of Michigan found that the monomers (C is blue; H is white; O is red; Mo is green) rebind on the picosecond timescale in the trans configuration only.
Credit: Kevin Kubarych
Kevin Kubarych
Click below to hear thoughts from laser spectroscopists on the advances in chemistry knowledge that have come -and may come in the future- from laser-based research.
Credit: University of Michigan
8810audkubarych
 
Kevin Kubarych
Click below to hear thoughts from laser spectroscopists on the advances in chemistry knowledge that have come -and may come in the future- from laser-based research.
Credit: University of Michigan
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Advanced laser methods for chemical spectroscopy.

 


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Early in their education, chemistry students learn about reaction intermediates that exist for fleeting moments as molecules undergo transformations en route to forming reaction products. For molecules in motion, "fleeting" is on the femtosecond (10–15 second) timescale. Time resolution on that scale was achieved over the course of decades as the millisecond flash photolysis method of the 1950s gave way slowly to picosecond (10–12 second) lasers in the 1970s and lasers with femtosecond pulses in the 1980s.

To apply femtosecond technology to chemical systems, Ahmed H. Zewail's group at California Institute of Technology developed methods for exciting sample molecules with a "pump" laser beam and then quickly probing them with a second laser pulse. By tuning the interval between the pump and probe pulses, the group was able to record series of snapshots that captured reactants evolving into products. In a key demonstration of that technique, Zewail's group monitored the dissociation of iodine cyanide into an iodine atom and a cyano radical and caught the 50-femtosecond-long transition state in which the C–I bond is nearly broken (J. Chem. Phys. 1987, 87, 2395).

The Caltech team used similar methods to record the "birth" of •OH from the reaction of a hydrogen atom with CO2 and to show that tetrafluorodiiodoethane (CF2ICF2I) transforms into tetrafluoroethylene by way of consecutive C–I bond-breaking steps. In recognition of the importance of femtochemistry innovations to molecular reaction dynamics, Zewail was honored with the 1999 Nobel Prize in Chemistry.

As often happens in scientific discovery, the early femtosecond experiments on relatively simple systems—small gas-phase molecules—inspired researchers to apply ultrafast laser methods to study dynamics in a range of increasingly complex systems. Examples include liquid-phase molecules, metal-centered complexes, clusters, and a variety of biomolecules, including proteins and DNA.

Reflecting today on the advances in laser technology that helped bring about this burgeoning research field, Zewail says, "We could not have dreamed 50 years ago that one day we would be able to reach the ultrashort time domain required to study the motions of atoms and molecules in real time."

 
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