Kurtis Carsch

Kurtis began his interest in chemistry by researching selective methane functionalization with Tom Cundari at the University of North Texas as a part of the Texas Academy of Mathematics and Science (TAMS) program. Kurtis then attended Caltech and received a joint B.S./M.S. in chemistry, where he conducted computational and experimental research on bio-inspired clusters of the oxygen-evolving complex in Photosystem II with Bill Goddard and Theo Agapie. During his undergraduate studies, Kurtis additionally worked at SAFCell Inc., UOP Honeywell, and examined the coordination chemistry of first-row transition metal ions in trigonal ligand fields with Susanne Mossin at the Technical University of Denmark.

As a Hertz Fellow and a NSF Graduate Research Fellow, Kurtis conducted his Ph.D. research with Ted Betley at Harvard, where he focused on understanding amination catalysis by copper nitrene intermediates through the lens of inverted ligand fields, receiving the Hertz Thesis Prize for his research. Kurtis was then an Arnold O. Beckman Postdoctoral Fellow at the Institute for Decarbonization Materials at the University of California, Berkeley, with Jeff Long, where he established elementary organometallic transformations in the context of chemical separations and discovered the field of high-temperature adsorption. ​

In January 2025, Kurtis returned back to Texas to start his independent research program at The University of Texas at Austin.

The Carsch Group at The University of Texas at Austin merges design principles from synthetic inorganic and organic chemistry, organometallic catalysis, chemical engineering and materials science to manipulate the electronic structures of coordinatively unsaturated metal ions in both molecular complexes and extended porous materials. The group's research advances catalysis, separations and materials processability, with a particular emphasis on designing transition metals with unusual electron counts and coordination environments to explore new bond activations and transformations.

The group's research program addresses topics including alkane homologation, C-H functionalization, ambient air separations, liquid chemisorption, microporous metallopolymers, ultramicroporous polycrystalline membranes, ligand field inversion, hyper-low-coordinate metal ions, frustrated metalloradical pair catalysis, multi-gas single-site binding, MOF gels and liquid porous materials.

Members of the group develop critical reasoning skills, gain interdisciplinary expertise and master synthesis and characterization techniques as they train to become independent scientists. The group employs a broad suite of spectroscopic and diffraction techniques, electrochemical methods, imaging probes and film-deposition approaches.