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Organometallic Materials for Optical Computers
Photochromic materials are substances that change color when irradiated
at one frequency and return to the original color when irradiated at
another frequency. These materials can be used for data storage and if
they respond rapidly could be useful for random access memory components
of an optical computer. Results for our new materials suggest a
potential writing speed of 107 MHz!

The photochromic compound idealized in Scheme 1 is a long-term goal
of this project. In our model the M-L and M-L’ bonds must not be labile,
except upon photolysis. Ring closure with L’ must be exceedingly fast to
compete with L recombination. A desirable characteristic is that the
product does not absorb v1, or if it does, no net
chemistry occurs. The same analysis applies to the reactant and v2.
We now
have compounds with some of the essential features in Scheme 1. The
first phase of this work is to develop materials that have high quantum
yields for ligand dissociation and efficient ring closure. We are using
organometallics for this application and various target compounds are
being synthesized and characterized for their photochromic properties.
There are number of advantages to using organometallics:
1) absorption in the UV, visible and the infrared are often very strong
and achievable with low molecular weight compounds
2) metal-ligand bonds are rarely >70 kcal/mol thus high energy
irradiation is unnecessary
3) hundreds of ligands may be used allowing modification of optical,
thermal, physical, chemical and kinetic properties
4) ultrafast spectroscopic methods have become available to investigate
the early steps that determine paths of excited states
For this project various target compounds are being synthesized and
characterized for their photochromic properties.
Other Studies in the Burkey Laboratory
We are undertaking several studies that support the development of
photochromic organometallics.
1) In designing photochromic compounds we need to know which ligand is
going to dissociates upon photolysis; this is normally the ligand with
the weakest metal-ligand bond. Bond energies are determined in our
laboratory using Laser photoacoustic calorimetry (LPAC, see below).
2) Ring closure must be fast to compete with the recombination of the
dissociated ligand. We can determine the kinetics of ring closure and
reactions with ligands by LPAC. Some of these experiments are done in
collaboration with other laboratories.
3) Different metal complexes have environmental, economic, and other
practical advantages. We survey the photochemical properties of various
metal complexes.
Selected Publications:
- T. Jiao, Z. Pang, T. J. Burkey, R. F. Johnston, T. A.
Heimer, V. D. Kleinman, E. J. Heilweil, J "Ultrafast Ring
Closure Energetics and Dynamics of Cyclopentadienyl
Manganese Tricarbonyl Derivatives" J. Am. Chem. Soc.
1999, 121, 4618.
- T .J. Jiao, G.-L. Leu, G. J. Farrell and T. J. Burkey,
"Photoacoustic Calorimetry and Quantum Yields of Mo(CO)6
Ligand Exchange in Linear Alkanes: Determination of Volume
of Reaction, Energetics, and Kinetics of Nucleophile
Displacement of Alkane from Mo(CO)5(Alkane)"
J. Am. Chem. Soc. 2001, 123, 4960-4965.
- G. J. Farrell and Theodore J. Burkey, "High-Pressure
Photoacoustic Calorimetry of Chromium Hexacarbonyl: Volumes
of Heptane Displacement at Chromium Pentacarbonyl Heptane"
J. Photochem. Photobiol. A: Chemistry, 2000,
137, 135-139.
- S. Gittermann, T. Jiao
and T. J. and Burkey "Volume of Reaction, Energetics, and
Kinetics of Tetrahydrothiophene Displacement of Solvent from
Mo(CO)5(alkane)", S. Gittermann, Photochem.
Photobiol. Sci. 2003, 2, 817-820.
- J. S.
Yeston, T. T. To, T. J. Burkey, E. J. Heilweil,
"Ultrafast Chelation Dynamics of Cyclopentadienyl Manganese
Tricarbonyl Derivatives with Pendant Sulfides", J. Phys.
Chem B. 2004, 108, 4582-4585.
- T. T. To, C. E. Barnes, and T. J. Burkey
"Bistable Photochromic Organometallics Based on
Linkage Isomerization: Photochemistry of Dicarbonyl(η5-methylcyclopentadienyl)manganese(I)
derivatives with a Bifunctional, Non-Chelating Ligand",
Organometallics, 2004, 23, 2708-2714.
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