Research Interests

Research Overview

              Our research goal is to develop broad-ranging, state-of-the-art programs based on organic synthetic chemistry and inorganic coordination chemistry and apply this to problems of both fundamental interest and practical importance. We have two main areas of focus: the development of new selective actinide coordination ligands for use in sensors and waste remediation, and the development of heterocyclic supported metal catalysts for improved reaction mechanisms, reduced wastes and "green" or sustainable chemistry.

Sensors and Extractants for Actinides

                One proposal to limit greenhouse gas emmisions is to increase the use of nuclear power; however, the potential for contamination of the environment with radioactive materials remains a concern. A resurgence of interest in actinide coordination chemistry (for example -  Thorium, Uranium, Neptunium, and Plutonium) has been inspired by the need to develop new sequestration technologies and to further our understanding of the chemistry of these radioactive, toxic heavy metals. New ligands and materials will be required that can coordinate, sense, manipulate, and purify actinides for waste remediation and for use in decontamination and detection applications. This could include sensors or "sensing" polymers for rapid detection and isolation these metals in the field without requiring complicated laboratory equipment. Given that the remediation of nuclear fuel wastes is made more difficult based on gaps that remain in our understanding of actinide chemistry, we investigate lanthanide and actinide complexes featuring soft-donor atoms (i.e., nitrogen, sulfur, and phosphorous) to probe the differences in the chemistry of the f-elements.

A video abstract of the sensors project - from the This is Auburn - This is Research feature - Jan 2016

  1. Niklas, J.E.Hunter, K. M.; Gorden, Anne E.V. "Bonding Interactions in Uranyl α-Diimine Complexes: A Spectroscopic and Electrochemical Study of the Impacts of Ligand Electronics and Extended Conjugation" Inorganic Chemistry 201958, 22, 15088-15100. 
  2. Grundhoefer, J.P; Hardy, E. E.; West, M.; Curtiss, A.B.; Gorden, A. E. V.; “Mononuclear Cu(II) and Ni(II) Complexes of Bis(napthalen-2-ol) Schiff Base Ligands,” Inorganica Chemica Acta 2019, 125-132.
  3. Hardy, E. E.; Wyss, K.M.; Gorden, John D.; Ariyarathna, Isuru R.; Miliordos,  Evangelos;  Gorden, Anne E.V. "Th(IV) and Ce(IV) Napthylsalophen Sandwich Complexes: Characterization of Unusual Thorium Fluorescence in Solution and Solid-state" Chemical Communications 2017 53, 11984-11987. 
  4. Niklas, J. E.; Farnum, B.D.; Gorden, John D.; Gorden, Anne E.V. “Structural Characterization and Redox Activity of a Uranyl Dimer and Transition Metal Complexes of a Tetradentate BIAN Ligand,” Organometallics 2017, 4626–4634. (DOI: 10.1021/acs.organomet.7b00454)
  5. Hardy, E. E.; Eddy, M.A.; Wyss, K.M.; Gorden, Anne E.V. “An example of unusual pyridine donor Schiff base uranyl (UO22+) complexes,” Chemical Communications, 2017, 53, 5718-5720
  6. Gorden, A.E. V.; DeVore, M. A., II; Maynard, B.A.; " Coordination Chemistry with f-Element Complexes for An Improved Understanding of Factors that Contribute to Extraction Selectivity," Inorg. Chem.201352 (7),  3445–3458.

Quinoxolinol supported catalysts

              As we become more aware of the impacts our activities have upon the environment, the simplification of syntheses and increased efficiency of chemical production will reduce waste streams. Thus, developing less-expensive, easier to use or more environmentally friendly catalysts is a promising trend for new synthetic methods. One way to approach this would be improving the stereoselectivity or regioselectivity of reactions, eliminating unwanted side products and reducing the amounts of solvents needed for purifications. Toward this end, we have developed a series of new ligands for metal catalyst supports based on heterocycles in the hopes that improved solubility and functionalization will provide options for specially tailored more efficient reactions taking advantage of bioessential or earth abundant metals like copper, as opposed to more expensive or toxic metals like chromium or rhodium. 

  1. Black, C.C.Gorden, Anne E.V. "Oxidative Mannich Reactions of Tertiary Amines Using a Cu(II) 2-Quinoxalinol Salen Catalyst," Journal of Organic Chemistry 2019,  84, (15), 9806-9810 
  2. Black, C. C.; Gorden, Anne E.V. “Propargylic C-H activation using a Cu(II) 2-quinoxalinol salen catalyst and tert-butyl hydroperoxide,”  Tetrahedron Letters 2018, 803-806.  
  3. Weerasiri, K.; Gorden, A. E. V.  “Cu(II) 2-Quinoxalinol Salen Catalyzed Oxidation of Propargylic, Benzylic , and Allylic alcohols using tert-Butyl Hydroperoxide in Aqueous Solutions” Tetrahedron 2014, 70 (43), 7962–7968
  4. Li, Y.; Lee, T. B.; Weerasiri, K.C.; Wang, T.Buss, E.E.; McKee, M.L.; Gorden, A. E. V. “2-Quinoxalinol Diamine Cu(II) Complex: Facilitating Catalytic Oxidation Through Dual Mechanisms”  Dalton Trans. 2014 (43) 13578 – 13583. 
  5. Weerasiri, K.C.; Gorden, A. E. V. "Oxidation of Propargylic Alcohols using a 2-Quinoxalinol Salen Copper (II) Complex and tert-Butyl Hydroperoxide " Eur. J. Org. Chem. 2013 (8) 1546–1550,