Research interest(s)/area of expertise
Lanthanide chemistry, contrast agents for magnetic resonance imaging, catalysis, molecular imaging, coordination chemistry
Research in the Allen laboratory explores the chemistry of magnetic resonance imaging (MRI) and asymmetric catalysis. We are at the frontier of inorganic chemistry intersecting with organic synthesis, analytical chemistry, and biology. Because of the multidisciplinary approach to science in the laboratory, group members are exposed to a wide variety of synthetic and analytical techniques from chemical and biological disciplines. Specifically, projects in the group require the synthesis of inorganic and organic molecules; characterization of these compounds using a variety of techniques including multinuclear NMR spectroscopy, mass spectrometry, fluorescence spectroscopy, and cyclic voltammetry; and compound testing through catalytic transformations or in vitro and in vivo imaging experiments.
Two major aims in the group are (1) to overcome critical barriers to the advanced use of lanthanide-based contrast agents for MRI and (2) to elucidate mechanistic details of water-tolerant lanthanide-catalyzed organic reactions with the goal of generating improved catalysts.
(1) Magnetic Resonance Imaging: MRI can be used to noninvasively visualize the inside of living organisms. This property of MRI has greatly advanced the ability to diagnose disease and evaluate medical conditions. Lanthanide complexes can enhance inherent contrast in MR images through interactions with solvent molecules. Through the selective enhancement of contrast, MRI can be converted into an even more powerful tool for imaging biological events on the molecular level (molecular imaging); however, there are major limitations to the use of existing rare earth complexes in improving the diagnostic capabilities of MRI and in the study of complicated biological systems. To overcome these limitations, our laboratory uses novel coordination chemistry to manipulate the properties of lanthanide ions. Specifically, we are interested in controlling the magnetic and electronic interactions of lanthanide ions with their surrounding environment and in stabilizing unstable oxidation states. These projects will illuminate fundamental properties of lanthanides. Additionally, they are an inroad toward greatly enhancing the molecular imaging and diagnostic capabilities of MRI.
(2) Asymmetric Catalysis: The use of water-tolerant catalysts is of great consequence in synthesizing organic molecules in a more environmentally benign manner. The Allen laboratory is interested in the study of lanthanide-based, water-tolerant, asymmetric catalysts for organic transformations including aldol, Mannich, and Diels-Alder reactions. Over the last decade, the use of lanthanide triflates as water-tolerant catalysts for organic transformations has been developed; however, mechanistic details of these reactions are largely unknown. During the development of these catalysts, the field of MRI inspired the generation of advanced techniques for characterizing and manipulating the properties of lanthanide ions. Our group is working at the intersection of these two fields to design and study lanthanide triflate-based catalysts with high enantioselectivity and water-stability. By studying and improving lanthanide-based catalysts, we hope to increase the quality and number of more environmentally benign catalysts for the synthesis of organic molecules.
- B.S., Purdue University, 1998
- Ph.D., California Institute of Technology, 2004
- NIH Postdoctoral Fellow, University of Wisconsin-Madison, 2004-2007
Ekanger, L. A.; Basal, L. A.; Allen, M. J.* The Role of Coordination Environment and pH in Tuning the Oxidation Rate of Europium(II). Chem. Eur. J. 2017, 23, 1145–1150
Tu, Y.-J.; Allen, M. J.; Cisneros, G. A.* Simulations of Water Exchange Dynamics on Lanthanide Ions in 1-Ethyl-3-Methylimidazolim Ethyl Sulfate ([EMIm][EtSO4]) and Water. Phys. Chem. Chem. Phys. 2016, 18, 30323–30333.
White, S. A.; Piechocki, J. A., Jr.; Allen, M. J.* Building an Outstanding ACS Student Chapter. In Building and Maintaining Award-Winning ACS Student Member Chapters Volume 1: Holistic Viewpoints; Mio, M. J., Benvenuto, M. A., Eds.; ACS Symposium Series 1229; American Chemical Society: Washington, DC, 2016; Chapter 1, pp 1–14.
Jin, G.; Bailey, M. D.; Allen, M. J.* Unique Eu(II) Coordination Environments with a Janus Cryptand. Inorg. Chem. 2016, 55, 9085–9090.
Ekanger, L. A.; Mills, D. R.; Ali, M. M.; Polin, L. A.; Shen, Y.; Haacke, E. M.; Allen, M. J.* Spectroscopic Characterization of the +3 and +2 Oxidation States of Europium in a Macrocyclic Tetraglycinate Complex. Inorg. Chem. 2016, 55, 9981–9988.
CHM 2999 Honors Research, 2-4 credit hours, W2020
CHM 5998 Honours Thesis Research, 2-4 credit hours, W2020
CHM 5999 Research in Chemistry, 2-4 credit hours, W2020
CHM 6990 Directed Study, 1-4 credit hours, W2020
CHM 6991 Internship in Chemistry, 1 credit hour, W2020
CHM 7990 Directed Study, 1-4 credit hours, W2020
CHM 8700 Research: Chemistry, 1-4 credit hours, W2020
CHM 9990 Predoctorate Candidate Research, 1-8 credit hours, W2020
CHM 9991 Doctorate Candidate Status 1, 7.5 credit hours, W2020
CHM 9992 Doctorate Candidate Status 2, 7.5 credit hours, W2020
CHM 9993 Doct Cand Maint Stat 3, 7.5 credit hours, W2020
CHM 9994 Doctorate Candidate Status 2, 7.5 credit hours, W2020
CHM 9995 Doctorate Candidate Status 3, 7.5 credit hours, W2020
CHM 2999 Honors Research, 2-4 credit hours, W2019
CHM 5998 Honours Thesis Research, 2-4 credit hours, W2019
CHM 5999 Research in Chemistry, 2-4 credit hours, W2019
CHM 6990 Directed Study, 1-4 credit hours, W2019
CHM 6991 Internship in Chemistry, 1 credit hour, W2019
CHM 7990 Directed Study, 1-4 credit hours, W2019
CHM 8700 Research: Chemistry, 1-4 credit hours, W2019
CHM 8990 Masters Thesis Research & Directed Study, 1-8 credit hours, W2019
CHM 9990 Predoctorate Candidate Research, 1-8 credit hours, W2019
CHM 9991 Doctorate Candidate Status 1, 7.5 credit hours, W2019
CHM 9992 Doctorate Candidate Status 2, 7.5 credit hours, W2019
CHM 9993 Doctorate Candidate Status 3, 7.5 credit hours, W2019