Research as a Driver of Educational Innovation: Some Reflections on the Outreach Program of an NSF Collaborative Research in Chemistry Project Dennis H. Evans Department of Chemistry, University of Arizona, Tucson, AZ 85721 (USA) Supported by NSF, CHE-0527003
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Research as a Driver of Educational Innovation: Some Reflections on the Outreach Program of an NSF Collaborative Research in Chemistry Project Dennis H.
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Research as a Driver of Educational Innovation: Some Reflections on the
Outreach Program of an NSF Collaborative Research in Chemistry
Project
Dennis H. Evans Department of Chemistry, University of Arizona,
Tucson, AZ 85721 (USA)
Supported by NSF, CHE-0527003
…or, how I spent my summer vacation (seriously)
J. Am. Chem. Soc. 1984, 106, 3039-3041.
National Science Foundation
Collaborative Research in Chemistry
“Coupling Redox Processes to Drive Chemical Reactivity: New Catalysts for Hydrogen Production”
Principal Investigators: Dennis H. Evans, Richard S. Glass and Dennis L. Lichtenberger, Department of Chemistry, University of Arizona
The science:
…To overcome these obstacles, this proposal derives inspiration from Nature. Hydrogenases are naturally occurring enzymes that couple low potential redox reactions to generate hydrogen. Iron-only hydrogenases utilize a cheap and abundant metal and operate in ambient conditions. The active site in the enzyme is a diiron center. The scientific challenge is to couple low potential redox reactions with reduction of a diiron center, an energetically unfavorable process. The proposed solution is to electronically couple a functional diiron system to a low potential redox ligand, and then drive the energetically unfavorable electron-transfer from the redox ligand to the diiron system by coupling it to an irreversible chemical reaction, that is, protonation and generation of H2…
The outreach:
…be mentored in the skills essential for multidisciplinary team approaches to problem-solving. A program to inspire underrepresented high school students to pursue careers in science, which takes advantage of Tucson’s large Hispanic and long-standing Native American populations (two minorities woefully underrepresented in science), is an integral part of this endeavor.
SUMMER PROGRAM IN HYDROGEN RESEARCH
FOR HIGH SCHOOL STUDENTSJune 5-July 14, 2006
The CRC Hydrogenase TeamSynthesis:
Professor Richard Glass (Co-PI)Dr. Jinzhu Chen (Postdoc)Dr. Rudresha Kottani (Postdoc)
Ms. Uzma Zakai (Graduate Student)Mr. Matt Swenson (Graduate Student)
Electrochemistry:
Professor Dennis Evans (Co-PI)
Dr. Greg Felton (Postdoc)
PES/Computations:
Professor Dennis Lichtenberger (Co-PI)Ms. Tori Moser (Graduate Student)Mr. Taka Sakamoto (Graduate Student)Mr. Aaron Vannucci (Graduate Student)Mr. Ben Petro (Graduate Student)
The PromiseHydrogen as our energy source benefits us because it is renewable,environmentally friendly and removes our dependence on foreign oil.
The ChallengeTo make a hydrogen energy economy a reality major obstacles must be overcome that require new scientific knowledge. One such obstacle is the need for cheap, efficient, readily available catalysts for chemically combining two electrons (2e-) and two protons (2H+) from water to produce molecular hydrogen (H2) as well as catalysts for the burning of H2 in fuel cells to yield energy and water.
The IdeaTo invent a catalyst we have been inspired by nature's catalyst,hydrogenase. As illustrated, Fe-hydrogenase is a complex protein which bears a catalytic core, the diiron active site, and electron transfer centers connecting the buried core to the electron donors at the protein surface. By directly attaching a versatile and easily made electron donor directly to a simple chemical analogue of the diiron active sitethe need for protein and electron transfer centers vanishes. As shown, two electrons (2e-) enter the donor site, which then delivers them to the catalytic diiron site to combine with 2H+ to produce H2. This design requires new basic scientific knowledge because the internal 2e- transfer requires a conduit, a driving force to propel them energetically uphill, and the 2H+ must be delivered selectively at the diiron site to rapidly form H2. Spectroscopic and electrochemical data on the chemically synthesized catalyst candidates will afford the real-world measurements and the essential scientific understanding required for inventing a successful catalyst.
2H2 + O2 2H2O + Energy
CysS
FeFeCO
CN
SS
CO
CO
CN
2e-
2H+
Fe-Hydrogenase
H2
computations
synthesiselectrochemistry
Richard S. Glass, Dennis H. Evans, and Dennis L. LichtenbergerThe University of Arizona
Diiron active site
The NSF “Nugget”:
Hydrogenase Active Site
http://metallo.scripps.edu/PROMISE/FEHASE.html
X = OH¯ or H2O; Y = O or N
Quinone Derivatives
• Quinone/Hydroquinone derivatives of the disulfidocompound are of special interest because of their potential redox properties.