Title: Hines Lab

URL: http://hines.chem.cornell.edu/

Collection: Cornell University Archives Web Archive

Description: "The goal of our research is to use atomic-scale images of surfaces to quantitatively understand and control their reactivity. We use scanning tunneling microscopy (STM), surface spectroscopies, as well as density functional theory (DFT) and Monte Carlo simulations to understand and control chemical reactivity at the nanoscale. Much of our current research is aimed at developing a new surface-science approach to understanding sustainable nanocatalysis and photocatalysis on earth-abundant metal oxides under technologically relevant conditions. This research probes catalytically active sites with atomic-scale spatial resolution and submonolayer spectroscopic sensitivity — studies that have been previously infeasible due to technical limitations. Although TiO2 is our current focus, our goal is to use these techniques on a much wider variety of sustainable metal oxide nanocatalysts, such as oxygen evolution catalysts, envioronmental remediation photocatalyst, and electroactive materials for battery applications."--taken from website 2023.09.25

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Subject:   Chemistry,  Cornell University -- Research groups,  Research groups,  Cornell University. Department of Chemistry and Chemical Biology ,  Nanoscience -- Research

Title: Marohn Group

URL: http://marohn.chem.cornell.edu/

Collection: Cornell University Archives Web Archive

Description: "There are two major thrusts to the Marohn group's research. The first is understanding circuits and solar cells that are made from plastics. Here we use custom-built scanned probe microscopes to record 100 nm resolution maps of electrostatic potential, capacitance, photo-generation of charge, and electric field fluctuations in working organic devices. The second thrust of the group's research is developing approaches for imaging single molecules such as, for example, an individual membrane protein. Here the approach is to push magnetic resonance imaging to nanometer resolution by detecting magnetic resonance mechanically, using tiny silicon cantilevers. Please explore our Research section for details on each project."--taken from website 2023.09.25

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Subject:   Research groups,  Cornell University. Department of Chemistry and Chemical Biology ,  Cornell University -- Research groups,  Chemistry,  Physics,  Biology,  Materials science -- Research

Title: National Biomedical Center for Advanced ESR Technology

URL: http://www.acert.cornell.edu/

Collection: Cornell University Archives Web Archive

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Subject:   Cornell University. Department of Chemistry and Chemical Biology ,  Chemical technology,  Biology,  Biomedical engineering -- Research,  Public health,  Technology

Title: Cerione Lab

URL: http://www.cerionelab.com/

Collection: Cornell University Archives Web Archive

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Subject:   Cornell University. Department of Chemistry and Chemical Biology

Title: Abruña Group

URL: https://abruna.chem.cornell.edu/

Collection: Cornell University Archives Web Archive

Description: "The Abruña group performs cutting-edge, interdisciplinary research to address problems of electrochemical interest, from fundamental studies of battery and fuel cell systems to molecular electronics. We employ standard electrochemical techniques in addition to X-ray methods, scanned probe microscopies (STM, SECM), NMR, nanoscale fabrication, electron microscopy (SEM, TEM), DEMS, and a variety of spectroscopic techniques (UV-vis, IR, Raman). Our group also synthesizes novel, tailored inorganic complexes and organic battery materials to drive discovery of new chemical and electrochemical properties."--taken from website 2023.09.25

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Subject:   Research groups,  Cornell University -- Research groups,  Chemistry,  Biology,  Cornell University. Department of Chemistry and Chemical Biology ,  Electrochemistry--Research

Title: Steve Ealick's Research Group

URL: https://arginine.chem.cornell.edu/

Collection: Cornell University Archives Web Archive

Description: "We use X-ray crystallography to study the three-dimensional structures of proteins. The structural information is used for drug design, protein engineering, to understand catalytic mechanisms, and to explore protein evolution. Our group is also involved in the development of tools and techniques associated with synchrotron radiation, especially multiple wavelength anomalous diffraction (MAD), single wavelength anomalous diffraction (SAD) and microdiffraction. Our main projects include studies of enzymes involved in purine nucleotide metabolism and pyrimidine nucleotide metabolism, studies of enzymes involved in cofactor biosynthesis, especially thiamin biosynthesis and pyridoxal 5'-phosphate PLP biosynthesis and enzymes involved in polyamine biosynthesis, purine biosynthesis, pyrimidine biosynthesis, and diphthamide biosynthesis."--taken from website 2023.09.25

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Subject:   Biophysics,  Research groups,  Cornell University -- Research groups,  Cornell University. Department of Chemistry and Chemical Biology

Title: Baird-Holowka Group Webpage

URL: https://baird.chem.cornell.edu/

Collection: Cornell University Archives Web Archive

Description: "The Baird-Holowka research laboratory integrates a broad range of experimental approaches to investigate molecular mechanisms of receptor-mediated cell signaling that enables cells to sense and respond to environmental cues. Much of our work has focused on the high affinity receptor (FcεRI) for immunoglobulin E (IgE), which sensitizes mast cells to antigen and thereby plays a pivotal role in initiating inflammatory and allergic immune responses. We employ quantitative microscopy and other biophysical methods to monitor changes in the distributions and dynamics of receptors and signaling components that accompany cellular response activities, which we measure in parallel. A particular area of interest is the role of cellular membranes in regulating and targeting signaling pathways. We have long worked to characterize IgE-FcεRI- mediated signaling in RBL mast cells as a model system for addressing fundamental questions of cellular response mechanisms initiated by other receptors and environmental factors. Similarly, we are translating the experimental techniques and cell response concepts developed in our work to elucidate mechanisms in other cell types, including those involved in cancer and neurodegenerative diseases. For example, our current work investigates pathological interactions of alpha synuclein associated with Parkinson’s Disease."--taken from webstie 2023.09.25

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Subject:   Research groups,  Cornell University -- Research groups,  Biophysics,  Biology,  Chemistry,  Cornell University. Department of Chemistry and Chemical Biology

Title: Coates Group

URL: https://coates.chem.cornell.edu/

Collection: Cornell University Archives Web Archive

Description: "The research focus of the Coates Group is the development of new synthetic strategies for producing polymers of defined structure. The control of polymer composition, architecture, stereochemistry, and molecular weight allows the indirect control of polymer properties via polymer morphology. Our research projects are interdisciplinary, addressing problems at the interface of organic, inorganic, organometallic, and polymer chemistry. Described in the links in the drop-down menu of the Research tab are a selected compilation of research topics that are being investigated in the group."--taken from website 2023.09.25

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Subject:   Research groups,  Cornell University -- Research groups,  Cornell University. Department of Chemistry and Chemical Biology ,  Polymer chemistry,  Chemistry

Title: Lin Group

URL: https://lin.chem.cornell.edu/

Collection: Cornell University Archives Web Archive

Description: "Our lab is interested in the function, regulation, and targeting of enzymes that control protein post-translational modifications (PTM). After the human genome is sequenced, a major challenge to understand biology and human diseases is to understand the function of all proteins. Proteins are not always expressed, and even if expressed, their activities are not always on. Their activities are often regulated by certain stresses and signals, which is crucial for all cell signaling events. Thus, to fully understand the function of a protein, it is also crucial to understand how it is regulated. We, therefore, focus on understanding the function and regulation of PTM enzymes and use the understanding to develop small molecule inhibitors for these enzymes as potential therapeutics for treating human diseases, including cancer, autoimmune diseases, and neurodegenerative diseases."--taken from website 2023.09.25

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Subject:   Research groups,  Cornell University. Department of Chemistry and Chemical Biology ,  Chemistry,  Cornell University -- Research groups,  Biology

Title: Lin Research Group

URL: https://songlin.chem.cornell.edu/

Collection: Cornell University Archives Web Archive

Description: "The Lin Lab is located in the Department of Chemistry and Chemical Biology at Cornell University. We are an organic chemistry lab with specific research interests in synthetic electrochemistry, asymmetric catalysis, and organic materials. We work to develop methodologies that expand both the scope and sustainability of synthetic chemistry using the unique capabilities offered by electrochemical systems. Particular emphases of our program include the rational design of catalysts and the creative use of electrochemistry to enable the conversion of readily available starting materials into value-added products, such as pharmaceuticals and polymers."--taken from website 2023.09.25

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Subject:   Research groups,  Cornell University -- Research groups,  Chemistry,  Biology,  Cornell University. Department of Chemistry and Chemical Biology ,  Electrochemistry--Research

Title: Lambert Group

URL: https://www.cyclopropenium.com/

Collection: Cornell University Archives Web Archive

Description: "Tristan was born in Madison, WI, in 1976 and grew up in the small town of Black Earth. He graduated from the University of Wisconsin at Platteville in 1998 with a B.S. in chemistry. The same year he began graduate studies at UC-Berkeley as one of Dave MacMillan’s first students. In 2000, Tristan moved with the MacMillan group to Caltech where he earned his Ph.D. for the development and application of novel Claisen rearrangements. In 2004, he began postdoctoral studies with Sam Danishefsky at the Memorial Sloan-Kettering Cancer Center in New York. At Sloan-Kettering he completed a total synthesis of UCS1025A, a putative telomerase inhibitor. In 2006, Tristan accepted a faculty position in the Department of Chemistry at Columbia University. In 2011 he was promoted to Associate Professor and in 2016 to Full Professor. In January 2018, he moved to the Department of Chemistry and Chemical Biology at Cornell University. His research group focuses on the study of intriguing chemical building blocks such as aromatic ions and their application to problems in the areas of catalysis, reaction design, and polymers."--taken from website 2024.02.05

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Subject:   Cornell University -- Faculty,  Cornell University -- Research groups,  Cornell University. Department of Chemistry and Chemical Biology ,  Chemistry

Title: X-Ray Diffraction Facility

URL: https://xray.chem.cornell.edu/

Collection: Cornell University Archives Web Archive

Description: News and accomplishments of students and research group participants.

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Subject:   Cornell University. Department of Chemistry and Chemical Biology ,  Chemistry,  X-rays -- Diffraction -- Research,  Biology,  Students