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Contact Information

Office: NHB: 5.114A
Phone: 512-471-0068

Lab

Office: NHB: 5.120/5.110
Phone: 512-471-4781

Eric V. Anslyn

anslyn@austin.utexas.edu

University Distinguished Teaching Professor, Faculty
Norman Hackerman Professorship in Chemistry



Research Group

The Anslyn Group



Education

BS, California State University - Northridge, 1982
PhD, California Institute of Technology, 1987

Alfred P. Sloan Research Fellow (1994-6)



Awards

Saul Winstein Lecturer, UCLA, May 2014

Edward Leete Award, for Outstanding Contributions to Teaching and Research in Organic Chemistry, from The Organic Division of the ACS, Awarded on September 10th, 2013.

Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry, awarded at the 8th ISMSC in Washington DC, July 7th to 11th 2013.

Senior Visiting Fellow of the Institute for Advanced Study, Hong Kong University of Science and Technology, 2013-2014

Ta-shue Chou Award, For Outstanding Achievements in Physical Organic Chemistry, Feb. 21st 2012, Academia Sinica, Taiwan.

Gassman Lecturer, University Minnesota, Oct. 2011



Affiliations

Texas Institute for Drug and Diagnostics Development; Institute for Cellular and Molecular Biology; IGERT: Optical Biomedical Engineering; Environmental Science Institute; Texas Materials Institute



Understanding Molecular Interactions Using Bioorganic and Supramolecular Chemistry

My research group is interested in the physical and bioorganic chemistry of synthetic and natural receptors and molecular recognition. Using a combination of synthesis, combinatorial techniques, NMR, kinetics, computer modeling, and optical signaling, we design and implement studies oriented at the development of receptors for numerous real world applications. In specific, we focus upon receptors for diols, catechols, carbohydrates, enolates, and enantiomeric excess using single and multi-analyte sensing ensembles.

   
To this end, our group works on synthetic and designed receptors for the analysis of complex analytes in real-life settings by mimicking the mammalian senses of taste and smell.  As a means of developing sensors, we are pursuing the formation of combinatorial libraries of peptidic and non-peptidic structures augmented with elements of rational chemical design.  We have used receptors designed this way to generate fingerprints that differentiate between the individual members of a targeted class of molecules.  These types of receptors can be used to determine the identify of mixtures, enantiomeric excess of a reaction, or identify analytes in a mixture.
     
Finally, we are also pursuing the use of polymers and other large molecules for the creation of multicomponent assemblies that can be used in multianalyte sensing applications.  Different portions of the assembly impart the differential behavior and cross-reactivity, as well as bias toward the central recognition element for the target class of molecules.  While our group works in many different areas, each of our projects relies upon the principles of supramolecular, organic, and biological chemistry, to unite them together.

 



Representative Publications

 “The Use of Principle Component Analysis and Discriminant Analysis in Differential Sensing Routines” Stewart, S.; Adams, M.; Anslyn, E.V. Chem. Soc. Rev. 2014, 43, 70-84.

 

 “In-Situ Generation of Differential Sensors that Fingerprint Kinases and the Cellular Response to Their Expression” Zamora-Olivares, D.; Kaoud, T.; Dalby, K.; Anslyn, E.V. J. Am. Chem. Soc. 2013, 135, 14814-14820.

 

 “A Selective Turn-On Fluorescent Sensor for Sulfur Mustard Simulants” Kumar, V.; Anslyn, E.V. J. Am. Chem. Soc. 2013, 135, 6338-6344.

 

 “Dynamic Thiol Exchange with ß-Sulfido-α, ß-Unsaturated Carbonyl Compounds and Dithianes” Joshi, G.; Anslyn, E.V. Organic Letters 2012, 14,18, 4714-4717.

 

 “Exploration of plasticizer and plastic explosive detection and differentiation with serum albumin cross-reactive arrays” Adams-Ivy, M.; Gallagher, L.T.; Ellington, A.D.; Anslyn, E.V. Chemical Science 2012, 3, 1773-1779.

 

 “An Exciton-Coupled Circular Dichroism Protocol for the Determination of Identity, Chirality, And Enantiomeric Excess of Chiral Secondary Alcohols” You, L.; Pescitelli, F.; Anslyn, E.V.; Di Bari, L. J. Am. Chem. Soc. 2012, 134, 7117-7125

 

 “Correlating Sterics Parameters and Diastereomeric Ratio Values for a Multicomponent Assembly To Predict Exciton-Coupled Circular Dichroism Intensity and Thereby Enantiomeric Excess of Chiral Secondary Alcohols” You, L; Berman, J.S.; Lucksanawichien, A.; Anslyn, E.V. J. Am. Chem. 2012, 134, 7126-7134.