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faculty
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Roseanne
J. Sension
Professor of Chemistry
Ph.D., University of California-Berkeley
Physical
Chemistry, Ultrafast Laser Spectroscopy and
Chemical Reaction Dynamics
Phone: (734) 763-6074
E-mail: rsension@umich.edu
Research
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The
majority of interesting reactions from a biological,
environmental, or engineering perspective occur
in fluid condensed phase environments. In such
an environment a chemical reaction is controlled
by intermolecular interactions with the surrounding
solvent bath as well as by the intramolecular Hamiltonian.
Interaction with the solvent often results in a
situation where reactions are controlled by the
competition between intramolecular and intermolecular
energy relaxation on time scales ranging from femtoseconds
to picoseconds.
In
the laboratory, state-of-the-art ultrafast lasers
and spectroscopic techniques are employed in the
observation and control of photoinitiated reactions.
These investigations are made possible by the continuing
development of tunable femtosecond light sources
from the far UV to the near IR, and the development
of techniques to precisely control the phase and
amplitude of coherent light pulses The
principle objectives of the research program in
our group are: (1)
To develop a detailed understanding of the fundamental
processes which govern chemical reaction dynamics
in fluid environments. Studies of small molecules
permit connections between theoretical calculations
and experimental measurements. We are using ultrafast
spectroscopy and theoretical modeling to investigate
isomerization dynamics in small polyene molecules.
(2)
To use "designer" light pulses to control chemical
reactions in condensed phases. Bond-selective
control of chemical reactions has been a long
standing goal of modern chemical physics. Early
attempts using selective laser excitation were
thwarted by fast intramolecular energy redistribution.
Now ultrafast laser pulses, optical pulse shaping,
and feedback algorithms have been successfully
combined to control bond dissociation reactions
in simple isolated molecules. We are using
coherent sculpted light pulses to control unimolecular
bond dissociation, and isomerization reactions
in solution.
(3)
To use short pulses to establish synchronization
and study enzyme mechanism in complicated biological
systems. Our current investigations are concentrating
on the bond-cleavage mechanism in B12 dependent
enzymes. this critical system.
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AWARDS
- LS&A
Excellence in Education Award-2005
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REPRESENTATIVE PUBLICATIONS
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Harris, D. A., Orozco, M. B., and Sension, R. J., 2006, "Solvent dependent conformational relaxation of cis-1,3,5 hexatriene" Journal of Physical Chemistry A, v110 (30) 9325-9333.
- Florean, A. C., Carroll, E.C. Spears, K.G., Sension, R.J. and Bucksbaum P.H., 2006, "Optical control of excited state vibrational coherences of a molecule in solution: The influence of the excitation pulse spectrum and phase in LD690." Journal of Physical Chemistry B, available in ASAP.
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Carroll, E. C., Pearson,
B. J., Florean, A. C., Bucksbaum, P. H., and
Sension, R. J., 2006, "Spectral phase effects
on nonlinear resonant photochemistry of 1,3-cyclohexadiene
in solution" The Journal of Chemical Physics,
v124 (11) 114506 (10 pages).
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Shiang, J. J., Cole,
A. G., Sension, R. J., Hang, K., Weng, Y.,
Trommel, J. S., Marzilli, L. G. and Lian,
T., 2006, "Ultrafast Excited State Dynamics in Vitamin B12
and Related Cob(III)alamins" Journal of the
American Chemical Society, v128 (3) 801-808.
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Sension,
R. J., Harris, D. A., and Cole, A. G., 2005 "Time-Resolved
Spectroscopic Studies of B12 Coenzymes: A Comparison
of the Influence of Solvent on the Primary Photolysis
Mechanism and Geminate Recombination of Methyl-, Ethyl-,
n-Propyl-, and 5'-Deoxyadenosylcobalamin" Journal of Physical
Chemistry B, v109 (46) 21954-21962.
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Sension,
R. J., Harris, D. A., Stickrath, A. B., Cole,
A. G., Fox, C. C., Marsh, E. N. G., 2005 "Time Resolved
Measurements of the Photolysis and Recombination of Adenosyl-cobalamin
Bound to Glutamate Mutase" Journal of Physical
Chemistry B, v109 (38) 18146-18152.
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