First name,Last name,Preferred title,Overview,Position,Department,Individual
John,Gladysz,Distinguished Professor,"My research has traditionally been centered around organometallic chemistry, and from this core area branches into catalysis, organic synthesis, enantioselective reactions, stereochemistry, mechanism, and materials chemistry. About half of my group is involved with catalysis projects. Areas receiving emphasis include (a) structurally novel new families of highly enantioselective catalysts, (b) metal-containing ""organocatalysts"" and (c) recoverable catalysts, particularly those with ""ponytails"" of the formula (CH2)m(CF2)nF; these can be recycled via ""fluorous"" liquid or solid phases, such as Teflon. The other half of my group synthesizes organometallic building blocks for molecular devices. These include (a) molecular wires composed of metal endgroups and linear (sp) carbon chains, including stable species with C28 bridges, (b) analogs in which the charge-transmitting bridges are insulated by a pair of polymethylene or (CH2)n chains that adopt a double-helical conformation, (c) polygons and multistranded molecular wires based upon such building blocks, and (d) molecular gyroscopes and compasses consisting of a rotating MLn fragment and an external cage (stator) that insulates the rotator from neighboring molecules, exactly as with the commercial gyroscopes used for aircraft and space-station navigation.",Faculty Affiliate||Distinguished Professor,Energy Institute||Chemistry,https://scholars.library.tamu.edu/vivo/display/n05e5403e
Donald,Darensbourg,Distinguished Professor,"The fundamentally interesting and challenging chemistry associated with carbon dioxide, coupled with its high potential as a source of chemical carbon, provides adequate justification for comprehensive investigations in this area. In our research program we have attempted to establish a clearer mechanistic view of carbon-hydrogen, carbon-carbon, and carbon-oxygen bond forming processes resulting from carbon dioxide insertion into M-H, M-C, and M-O bonds.
Relevant to the latter process our research has addressed the utilization of carbon dioxide in the development of improved synthetic routes for the production of polycarbonates. The hazardous and expensive production process currently in place industrially for these materials involves the interfacial polycondensation of phosgene and diols, accentuates the need for these studies. Although we and others have made significant advances in the synthesis of these useful thermoplastics from carbon dioxide and epoxides much of the fundamental knowledge concerning the reaction kinetics of these processes is lacking, due in part to the practical challenges associated with sampling and analyzing systems at elevated temperatures and pressures. This information is needed for making this process applicable to the synthesis of a variety of copolymers possessing a range of properties and uses. Our studies are examining in detail the mechanistic aspects of metal catalyzed carbon dioxide/epoxide coupling reactions employing in situ spectroscopy methods. For this purpose Fourier-transform infrared attenuated total refluctance (FTIR/ATR) spectroscopy is being utilized. Other related investigations involve the development of structural and reactivity models for the industrially prevalent double metal cyanide catalysts(DMC) used in polyethers and polycarbonate synthesis from epoxides or CO2/epoxides, respectively.",Distinguished Professor||Faculty Affiliate,Energy Institute||Chemistry,https://scholars.library.tamu.edu/vivo/display/n06bf3bf8
Robert,Lucchese,Professor,"We study various processes which involve electrons being scattered by or ejected from molecules. These processes include ectron-molecule collision, electron impact ionization, and photoionization. Recently we have worked closely with experimental groups around the world to study molecular frame photoelectron angular distributions. In these studies we can make detailed comparisons of experimental data and theoretical predictions of the probability of the emission of the photoelectron in specific directions relative to the orientation of the molecule. We have also considered electron scattering from cage molecules such as C60 and C20. In these systems we have found a new class of scattering resonances where the electron is trapped inside the cage. These processes are important in such physical systems as upper atmospheres, plasma processing of semiconductors, and surface analysis.
A second area of interest is the structure and dynamics of hydrogen bonded clusters. This work is done in collaboration with Professor J. W. Bevan's research group where the corresponding systems are studied experimentally. We develop potential energy surfaces using both experimental data and by performing quantum mechanical electronic structure calculations. These potentials are then used in quantum mechanical calculations of the vibrational motion of the complexes with particular attention being focused on the large amplitude motion found in hydrogen bonded systems. Currently we are studying the complexes CO--HI and (HBr)2. The results of this work will give a better understanding of important hydrogen bonded systems including liquid water and many systems of biological interest.",Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n0b4070b0
Francois,Gabbai,Professor,"Our research is concerned with the chemistry of both organic and organometallic polyfunctional Lewis acids. While an important component of our work deals with the synthesis of new examples of such polyfunctional Lewis acids, it is our ultimate intent to harness and utilize the cooperative effects occurring in such systems for the discovery of unusual structures, bonding modes, supramolecules and reactivities. Our research efforts present important ramifications in the domain of molecular recognition, supramolecular materials and catalysis.",Faculty Affiliate||Professor,Energy Institute||Chemistry,https://scholars.library.tamu.edu/vivo/display/n0d5d68bb
David,Russell,Professor,"My research focuses on proteomics, lipidomics, biophysical chemistry and application and development of mass spectrometry, such as ""label-free"" nano-particle based biosensors and novel peptide/protein isolation and purification strategies. We are also investigating the structure(s) of model peptides in an effort to better describe folding/unfolding and structure of membrane and intrinsically disordered (IDP) proteins. Peptides take on very different 2?, 3? and 4? structure, which determine or influence bio-activity. In the presence of lipid vesicles peptides can exist as solution-phase species, ""absorbed"" on lipid bilayers or ""inserted"" (as a monomer or multimer) in lipid bilayers. By what mechanism do peptides interact with lipid membranes to affect these structural changes, how do peptide-lipid interactions promote self-assembly to form intermediates that eventually yield aggregates, i.e., amyloid fibrils, or how does metal ion coordination affect the structure of metalloproteins? Mass spectrometry-based experiments, hydrogen/deuterium (H/D) exchange, chemical 'foot-printing' and gas-phase (ion-molecule and ion-ion reaction chemistry) and solution-phase chemical modifications, have expanded our abilities to address such questions, and new instrumental approaches, esp. ion mobility spectrometry (IMS) combined with enhanced molecular dynamics simulations (MDS), have become standard tools for structural-mass spectrometry studies. Over the past several years we have either acquired or developed novel, next-generation IM-MS instruments that are redefining cutting-edge structural-mass spectrometry research as well as cutting-edge computational tools essential to carry out these studies. Our new laboratories in the Interdisciplinary Life Sciences Building (ILSB) provides exciting opportunities for collaborative, interdisciplinary research with chemical-biologists, biochemists and other chemists.",Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n280e03e6
Lane,Baker,Professor,,Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n3b0176ae
James,Batteas,Professor,"The research in our group is organized around three main projects: nanoscale materials and devices, biological surfaces and interfaces and nanotribology,
with the overarching goal of developing custom engineered surfaces and interfaces. This requires obtaining a fundamental (molecular level) understanding of the underlying chemistry and physics of the systems in question to afford rational approaches to test and develop new technologies. In much of our research we employ a range of scanned probe microscopies such as scanning tunneling microscopy (STM) and atomic force microscopy (AFM) to probe structure and to manipulate materials at the nanoscale.",Faculty Affiliate||Professor||Faculty Fellow||D. Wayne Goodman Professor of Chemistry,Center for Health Systems and Design||Energy Institute||Chemistry||Chemistry,https://scholars.library.tamu.edu/vivo/display/n413d1dff
Tadhg,Begley,Distinguished Professor,"The Begley Group is interested in the mechanistic chemistry and enzymology of complex organic transformations, particularly those found on the vitamin biosynthetic pathways. We are currently working on the biosynthesis of thiamin, molybdopterin, pyridoxal phosphate and menaquinone. Our research involves a combination of molecular biology, protein biochemistry, organic synthesis and structural studies and provides a strong training for students interested in understanding the organic chemistry of living systems and in pursuing careers in biotechnology, drug design or academia.
Thiamin pyrophosphate plays a key role in the stabilization of the acyl carbanion synthon in carbohydrate and amino acid metabolism. The biosyntheses of the thiamin pyrimidine and thiazole are complex and are different from any of the characterized chemical or biochemical routes to these heterocycles. We are particularly interested in cellular physiology and the mechanistic enzymology of thiamin biosynthesis. As an example of one of the complex transformations on this pathway, the figure below shows the structure of the pyrimidine synthase catalyzing the complex rearrangement of aminoimidazole ribotide (left) to the thiamin pyrimidine (right).",Distinguished Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n498aa35b
Arthur,Laganowsky,Associate Professor,"A long-term research goal of our group is to determine the molecular basis behind protein-lipid interactions and how these interactions can modulate the structure and function of membrane proteins, including their interactions with signaling molecules. What determines the selectivity of membrane proteins towards lipids, and the coupling between lipid binding events and function remains a key knowledge gap in the field; one that if addressed will significantly advance our understanding of how lipids participate in both normal and pathophysiological processes of membrane proteins. Therefore, there is a critical need to expand our fundamental knowledge in this emerging field by applying and developing innovative approaches to elucidate how lipids modulate the structure function of membrane proteins. To this end, we are studying a number of ion channels, receptors and other types of membrane proteins.",Associate Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n542411e4
Wenshe,Liu,Bovay Chair and Professor in Chemistry,"Our research interest is to design methods for the genetic incorporation of noncanonical amino acids into proteins in living cells and apply these methods in three major directions: deciphering functions of protein posttranslational modifications, small molecule sensing, and expanding chemical diversities of phage display libraries. To study protein posttranslational modifications, we have constructed methods for the site-specific installation of lysine acetylation and methylation in proteins and will apply them to study functional roles of these two modifications on p53, a tumor suppressor protein. We have also developed a strategy to site-specifically install two noncanonical amino acids into one protein in E. coli and are applying this approach to construct biosensors for small organic molecules and metal ions. Phage display is an efficient method to identify peptides for therapeutic interventions. However, a phage display peptide library has limited structure motifs and functional groups because only 20 natural amino acids can be used to generate a library. We plan to expand the chemical diversity of a phage display library by incorporating multiple noncanonical amino acids and chemically modifying them to extend functional diversities. Screening this unnatural phage display library against therapeutic targets such as c-Abl tyrosine kinase is expected to identify highly potent inhibitors.",Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n5d9506ea
Abraham,Clearfield,Distinguished Professor,"Our research interests are focused in solid state and materials chemistry and encompass a wide variety of projects. An important goal is the ability to design and synthesize new materials whose structure and properties can be predicted and controlled. Layered compounds are amenable to manipulation to produce new structures because of the weak forces between layers. We have learned how to separate the layers of several classes of compounds and are reconstituting them into novel materials. For example, we have prepared staged materials in which alternating layers are hydrophobic and hydrophilic.
The surfaces of our layered materials react with a variety of molecules to bond them to the surface. We are developing such materials for drug delivery, heterogeneous catalysis, and polymer-nanoparticle composites.
Single crystal X-ray diffraction has been the key tool in elucidating the structure of solids. For many compounds, single crystals are unavailable so that indirect methods need to be used. We pioneered the solution of crystal structures from X-ray powder data and have had considerable success. The methods need to be improved and extended to more complex systems such as poorly crystallized materials. Combined use of X-ray, neutron and synchrotron methods are in progress and extension to EXAFS and amorphous scattering techniques is contemplated.",Distinguished Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n6dc4bd81
Marcetta,Darensbourg,Distinguished Professor,"Bio-inspired Catalysts for Hydrogen Production: The ultimate, home-run, goal of our work is to synthesize and develop a robust, highly active hydrogen-producing catalyst comprised of earth-abundant transition metals within a ligand environment that is inspired by the biological Figure 3hydrogenase (H2ase) enzyme active sites. Progress in precise structural modeling of the illusive ""rotated"" structure displayed in the as-isolated, mixed-valent FeIIFe state in the past decade has permitted in depth analysis of electronic structure by Mo ssbauer, EPR (ENDOR), and computational chemistry. New electrocatalysts for hydrogen production: The connection between the Fe(NO)2 unit and the Fe(CX)3 (X = O or N) unit found in hydrogenase enzyme active sites offers opportunity for design of new catalysts, one of which is shown. In this regard we explore the ability of N2S2 metal complexes to bind as metallodithiolate ligands to various metal acceptors. The properties of such complexes vary The connection of these to light harvesting molecules for dye sensitized, sacrificial electron donor, hydrogen production is also of interest. When Iron Meets Nitric Oxide: Good Chemistry, Intriguing Biology. The affinity of iron for diatomic molecules, O2, CO, N2, and NO, is central to the most important of life processes, including those of human physiology. Figure 6In this research area we target synthetic chemistry involving dinitrosyl iron complexes (DNICs) that serve as biomimetics of products of FeS cluster degradation by excesses of NO, or as derived from the chelatable iron pool (CIP) in cells. The electronic ambivalence of the DNIC unit is expressed in the ease with which it interconverts between oxidized and reduced forms, {Fe(NO)2}9 and {Fe(NO)2}10, respectively (Enemark/Feltham notation), and serves as impetus to explore analogous reactions known to involve the CuII/CuI redox couple. The accessory ligands which stabilize one redox level over the other, including N-heterocyclic carb",Distinguished Professor||Faculty Affiliate,Energy Institute||Chemistry,https://scholars.library.tamu.edu/vivo/display/n6f445741
Christine,Mullen,Senior Lecturer,,Senior Lecturer,Chemistry,https://scholars.library.tamu.edu/vivo/display/n79b0381c
Karen,Wooley,Distinguished Professor,"Our research activities combine organic syntheses, polymerization strategies and polymer modification reactions in creative ways to afford unique macromolecular structures, which have been designed as functional nanostructures, polymer systems having unique macromolecular architectures, and/or degradable polymers. The emphasis is upon the incorporation of functions and functionalities into selective regions of polymer frameworks. In some cases, the function is added at the small molecule, monomer, stage, prior to polymerization, whereas, in other cases, chemical modifications are performed upon polymers or at the nanostructure level; each requires a strategic balance of chemical reactivity and the ultimate composition and structure.",Distinguished Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n7d5d2fbd
David,Barondeau,Associate Professor,Our group conducts research on Fe-S cluster biogenesis.,Associate Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n83588e44
Quentin,Michaudel,Assistant Professor,,Assistant Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n83f25144
Christian,Hilty,Professor,"We are developing and applying Magnetic resonance techniques for the investigation of rapid processes and molecular dynamics. Hyperpolarization of nuclear spins yields unprecedented levels of signal, which enables us to acquire NMR spectra of reactions as they occur, in real time. Applications of these techniques include the fields of enzyme catalysis, reactions in organic chemistry, polymers, and more.
To enable the use of hyperpolarization in NMR, we develop new hardware and specially adapted NMR experiments, and investigate the dynamics of hyperpolarized spin systems.
Hand-in-hand with hyperpolarization, we use modern multi-dimensional NMR for the investigation of basic determinants of protein structure and function, including of membrane proteins.",Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n83f91df7
Simon,North,Professor and Head,"Our research involves trying to understand chemical reactivity on a microscopic quantum-state resolved level. We focus on isolated molecules in the gas-phase to develop a detailed description of the factors which influence the rates, energy disposal, and final products in a reaction. In order to address these issues we use lasers to carefully control the preparation of excited molecules and to probe all the properties of the reaction products. chemical reactivity on a microscopic quantum-state resolved level. Our specific interests include understanding atmospheric photochemistry, the tropospheric oxidation of biogenic hydrocarbons, and laser diagnostic development for flow field characterization. The laboratory contains equipment to perform state-of-the-art experiments in chemical dynamics and kinetics and is associated with several interdisciplinary University Research Centers. Our photochemistry experiments combine molecular beam and state-resolved ionization techniques with position-sensitive ion imaging to determine the identity and energy content of photochemical products in the absence of secondary collisions. Studies focus on the photodissociation of jet-cooled radicals of atmospheric relevance and preliminary results have already stimulated collaboration with several theoretical groups. The experiments provide a stringent test for modern theory and allow assessment of the impact that the photochemistry has on atmospheric modeling.",Professor and Head,Chemistry,https://scholars.library.tamu.edu/vivo/display/n8c54a7a4
Oleg,Ozerov,Professor,"The projects in our group typically involve transition metal or main group organometallic chemistry but are diverse and cover a wide variety of synthetic and mechanistic work. The ideal-case research scheme consists of: 1) discovery of a new reaction or a structural environment; 2) demonstration of unusual reactivity, structural, or electronic novelty; 3) application of these findings to develop a new catalytic process. The training of students in our group is not built around a narrow research theme but instead aims to help students mature into problem-solving practicing synthetic chemists through exposure to diverse research experiences.",Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n8f8f768d
Jack,Waas,Lecturer,,Lecturer,Chemistry,https://scholars.library.tamu.edu/vivo/display/n956db11d
Coran,Watanabe,Associate Professor,"Our research group is actively characterizing the biosynthetic genes of this pathway, which involves a variety of techniques and strategies including: cloning and overexpression of genes, disruption/knockout of genes, enzymology, as well as chemical synthesis/isotopic labeling studies. Functional characterization of the genes of the pathway will not only shed light on the mechanism of azabicycle formation but will also pave the way for genetic engineering of the pathway and the development of new therapeutic methodologies.
We have also been investigating the biosynthesis and cellular effects of cycloterpenals and their derivatives. Cycloretinal (all-trans retinal dimer), a representative member of this family of natural products is attributed to causing age-related macular degeneration (AMD). AMD is the leading cause of blindness in adults over the age of 50 that can lead to the loss of central vision. One of the most common early characteristic features of AMD (the dry form) is the accumulation of yellow deposits in the eye called drusen. A more severe form of the disease, the wet form, is characterized by neovascularization (abnormal blood vessel formation). Our research group aims to study the role of beta-lactoglobulin in cycloretinal synthesis in the eye as an environmental (dietary), non-genetic contributor of AMD. This involves tracking BLG in the eye, monitoring the formation of cycloretinal, and elucidating the mechanism of cycloretinal formation. Research strategies include: chemical synthesis, enzymology, fluorescence/confocal microscopy, PET imaging, dual modality OCT/fluorescence lifetime imaging.",Associate Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n9a83891f
Daniel,Singleton,Professor,"The central focus of the Singleton research group is the study of organic, organometallic, and bioorganic reaction mechanisms, and the key tool that we use in these studies is the determination o kinetic isotope effects (KIEs). In the mid-1990's, we developed a method for the high precision combinatorial determination of small KIEs at natural abundance by NMR. Its direct applicability to complex unlabeled reactants makes this methodology 1-2 orders of magnitude faster than studies requiring labeling. At the same time, it is much more versatile - our technique can look at a great number of reactions that would have been impractical or impossible to study by labeling or mass spectral methods, and the choice of reactants can be readily changed in response to each new experimental result. The simultaneous determination of a complete set of 13C, 2H, and 17O isotope effects possible with our methodology provides a much greater level of information than available from conventional methods. In addition, substantial evidence has accumulated supporting the reliable accuracy of our results.",Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/na0239851
Frank,Raushel,Distinguished Professor,"Enzymes catalyze a remarkable variety of chemical reactions with extremely high rate enhancements and very selective substrate specificity. The research efforts in our laboratory are directed towards a more complete understanding of the fundamental principles involved in enzyme-catalyzed chemistry and the dependence on protein structure. The pursuit of this information will provide the framework for the rational and combinatorial redesign of these complex molecules in an effort to exploit and develop the properties of enzyme active sites for a variety of chemical, biological, and medicinal uses. The techniques that we are using to solve these problems include steady-state and stopped-flow kinetics, NMR and EPR spectroscopy, X-ray crystallography, and the synthesis of inhibitors and suicide substrates. We are also using recombinant DNA methods to construct new proteins with novel catalytic properties. These efforts are currently being directed to the reactions catalyzed by phosphotriesterase and enzymes involves in the degradation of lignin and the metabolism of novel carbohydrates from the human gut microbiome.
The phosphotriesterase enzyme catalyzes the hydrolysis of organophosphate insecticides and other toxic organophosphate nerve agents. We have discovered that the active site of this protein consists of a unique binuclear metal center for the activation of water. We are now investigating the structure and properties of this metal center as a model system for the evolution of enzyme structure and function. Toward this end we have mutated the active site of this enzyme in a research project to create novel enzymes with the ability to detect, destroy, and detoxify various chemical warfare agents such as sarin, soman, and VX. The Raushel laboratory is also engaged in a large scale research project that is focused on the development of novel strategies for the discovery of new enzymes.",Distinguished Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/na84f2fec
Kevin,Burgess,Professor,"We use novel strategies Exploring Key Orientations (EKO) that feature datamining to compare simulated preferred conformers of chemotypes we design with key features at protein-protein interfaces. Many chemotype candidates can be screened against one PPI, or one chemotype can be screened against all the PPI interfaces in the PDB. Virtual hit chemotypes are prepared in my lab, then tested against protein-protein interactions of biomedicinal interest using an array of biophysical and cellular assays.
We also design small molecules to target cell surface receptors that are selectively overexpressed in cancer cells. Much or our work has been focused on the TrkC receptor that is particularly important to metastatic breast cancer and melanoma. Going forwards we are interested in expanding the targets to include cell surface receptors that are overexpressed when cancer cells undergo aberrant epithelial to mesenchymal transitions (EMT) to produce circulating tumor cells and cancer stem cells. Much of this work involves design and synthesis of the small molecules for this targeting.",Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/nc4a5cad4
Paul,Lindahl,Professor,"One of our two current research areas involves iron metabolism in mitochondria. The iron imported into these organelles is assembled into iron-sulfur clusters and heme prosthetic groups. Some of these centers are exported into the cytosol, while others are installed into mitochondrial apo-proteins. All of these processes are regulated in healthy cells, but various genetic mutations giving rise to diseases can cause iron to accumulate (e.g. Friedreich's ataxia) or become depleted (e.g. Sideroblastic anemia). We have developed a biophysical approach involving Mossbauer, electron paramagnetic resonance, and electronic absorption spectroscopy, to study the entire iron content of intact mitochondria in healthy and genetically altered cells. This Systems Biology approach allows us to characterize the ""iron-ome"" of mitochondria at an unprecedented level of detail. We are also using analytical tools (e.g. liquid chromatography) to identify complexes that are involved in ""trafficking"" iron into and out of the organelle.
Our other research area involves mathematical modeling of cellular self-replication on the mechanistic biochemical level. We collaborate on this multidisciplinary NSF-sponsored project with a mathematician at the University of Houston (Professor Jeffrey Morgan). We have developed a modeling framework that facilitates such modeling efforts, and have designed a number of very simple and symbolic in silico cells that exhibit self-replicative behavior. Our minimal in silico cell model includes just 5 components and 5 reactions. A second generation model includes a more realistic mechanism of mitotic regulation. One novel aspect of our approach is that cellular concentration dynamics impact (and are impacted by) cellular geometry. By minimizing membrane bending energies, we are now calculating cell geometry during growth and division. Our results suggest that the ""pinching"" observed in real cells is enforced by cytoskeletal structures.",Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/nc9ce621b
Jonathan,Sczepanski,Assistant Professor,"Our primary research goals are to develop and apply novel tools for studying DNA damage in the context of chromatin and to explore new avenues for RNA-based therapeutics and diagnostics. By combining expertise in chemical biology, molecular biology, and molecular evolution, our lab addresses challenges associated with studying and targeting noncoding RNAs from a unique perspective. In addition, we utilize modern chemical biology techniques to develop designer chromatin systems for studying DNA damage. We are seeking motivated individuals who wish to gain experience in chemical biology, molecular biology, and in vitro evolution techniques.",Assistant Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/ncc157d6e
Vytas,Bankaitis,Professor,"My laboratory is interested in the regulatory interfaces between novel lipid-mediated signal transduction pathways and important cellular functions. The focus of our work is the phosphatidylinositol/ phosphatidylcholine transfer proteins (PITPs), a ubiquitous but enigmatic class of proteins. Ongoing projects in the laboratory derive from a multidisciplinary approach that encompasses biochemical characterization of novel members of the metazoan PITP family, and the application of genetic, molecular and biophysical approaches to detailed structural and functional analyses of PITPs.",E.L. Wehner-Welch Foundation Chair||Professor||Professor,Cell Biology and Genetics||Biochemistry and Biophysics||Chemistry,https://scholars.library.tamu.edu/vivo/display/ncff8dc21
Jaan,Laane,Professor,Research efforts on a variety of projects concentrate on the use of fluorescence spectroscopy of jet-cooled molecules and Fourier transform infrared (FT-IR) and laser Raman spectroscopies. Computer methods for quantum mechanical calculations and on-line instrument control are also utilized and developed.,Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/nd19e1c2f
Kim,Dunbar,Distinguished Professor,"Research in the Dunbar group spans topics in synthetic, structural and physical inorganic and bioinorganic chemistry. The use of a range of tools including spectroscopy, X-ray crystallography, magnetometry, electron microscopy, mass spectrometry and electrochemistry reflect the breadth of problems under investigation.",Distinguished Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/ndd473437
Lei,Fang,Associate Professor,"The multi-disciplinary research programs in the Fang Group will focus on the bottom-up synthesis and processing of novel organic polymer materials -- namely, ladder and coplanar polymers, as well as microporous polymer networks -- for the applications on electronics and energy conversion/storage. Our thrust will be to gain profound understanding on the structure-property relationship of these materials at both the molecular and the macroscopic levels by employing the toolboxes of synthetic chemistry and device engineering. With this knowledge, we aim to establish a series of synthetically feasible, high performing, processable organic carbon-based material systems for field effect transistors, light emitting diodes, solar cells, supercapacitors, and batteries, and to be at the forefront in the enhancement of their efficiencies.",Faculty Affiliate||Associate Professor||Associate Professor,Energy Institute||Materials Science and Engineering||Chemistry,https://scholars.library.tamu.edu/vivo/display/ne3bd8752
Michael,Hall,Professor,"Our group applies ""state-of-the-art"" theoretical techniques to chemical problems of current interest to practicing inorganic, organometallic, and biological chemists. We also develop new algorithms that are especially suited to electronic structure problems in large transition metal molecules.",Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/ne91c0625
David,Powers,Professor,"Catalysis lies at the heart of many unmet chemical challenges. Research efforts in our group focus on development of new catalytic chemistry to impact both chemical synthesis as well as chemical storage of solar energy. Projects span organic, organometallic, and inorganic chemistries and rely on the tools of modern synthetic chemistry and spectroscopy, as well as advanced characterization techniques supported at synchrotron X-ray sources. Representative research interests include: shape-selective catalysis, solar energy storage in organic solar-thermal flow batteries, and aerobic oxidation chemistry for C-H functionalization reactions. We are seeking students who wish to gain expertise in synthetic chemistry and reaction mechanism elucidation.",Professor||Faculty Affiliate,Energy Institute||Chemistry,https://scholars.library.tamu.edu/vivo/display/nfa6c8878