Eric Anslyn | |
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Born | Eric Van Anslyn June 9, 1960 |
Alma mater | California Institute of Technology |
Awards | Centenary Prize, Arthur C. Cope Scholar Award |
Scientific career | |
Fields | Physical organic chemistry |
Institutions | The University of Texas at Austin |
Thesis | Mechanistic, Synthetic and Theoretical Studies of High Valent Metallacycles and metal Alkylidenes (1987) |
Doctoral advisor | Robert Grubbs |
Eric V. Anslyn (born June 9, 1960, Santa Monica, California) is an American chemist , University Distinguished Teaching Professor, and Welch Regents Chair in Chemistry at the University of Texas at Austin. [1] He previously held the Norman Hackerman Professorship[ citation needed ]. Anslyn is co-author of Modern Physical Organic Chemistry, an introductory graduate textbook. [2]
Anslyn is notable for his work in developing designed receptors and sensor arrays by incorporating principal component analysis and discriminant analysis to mimic human taste and smell. [3] [4] [5] Prof. Anslyn developed a colorimetric sensor to distinguish flavonoids (hydrolysis products of tannins) between varietals of red wines. An analogous colorimetric sensor was developed to mimic human taste by positioning polymer microbeads on a silicon chip.[ citation needed ] In related research, Prof. Anslyn designed a fluorometric chemical sensor consisting of a light-tight lego box and a smart phone to detect nerve agents such as VX and sarin. [6]
Anslyn received one of the American Chemical Society Arthur C. Cope Scholar Awards awarded in 2006 for his research in pattern recognition and supramolecular chemistry [7] and the Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry in 2013. [8]
This section of a biography of a living person needs additional citations for verification .(January 2020) |
Research: Mechanistic studies of ribonuclease A mimics. Detailed kinetics analyses of imidazole catalyzed 3'→5' UpU hydrolysis and isomerization. Synthesis and kinetics studies of bis-imidazole β-cyclodextrin catalyzed phosphodiester hydrolyses.
Research: Mechanistic and theoretical studies of olefin metathesis and ring-opening metathesis polymerizations catalyzed by group IV and VI metals.
Charles John Pedersen was an American organic chemist best known for discovering crown ethers and describing methods of synthesizing them during his entire 42-year career as a chemist for DuPont at DuPont Experimental Station in Wilmington, Delaware, and at DuPont's Jackson Laboratory in Deepwater, New Jersey. Often associated with Reed McNeil Izatt, Pedersen also shared the Nobel Prize in Chemistry in 1987 with Donald J. Cram and Jean-Marie Lehn. He is the only Nobel Prize laureate born in Korea other than Peace Prize laureate Kim Dae-jung.
In chemistry, homogeneous catalysis is catalysis where the catalyst is in same phase as reactants, principally by a soluble catalyst a in solution. In contrast, heterogeneous catalysis describes processes where the catalysts and substrate are in distinct phases, typically solid-gas, respectively. The term is used almost exclusively to describe solutions and implies catalysis by organometallic compounds. Homogeneous catalysis is an established technology that continues to evolve. An illustrative major application is the production of acetic acid. Enzymes are examples of homogeneous catalysts.
Grubbs catalysts are a series of transition metal carbene complexes used as catalysts for olefin metathesis. They are named after Robert H. Grubbs, the chemist who supervised their synthesis. Several generations of the catalyst have also been developed. Grubbs catalysts tolerate many functional groups in the alkene substrates, are air-tolerant, and are compatible with a wide range of solvents. For these reasons, Grubbs catalysts have become popular in synthetic organic chemistry. Grubbs, together with Richard R. Schrock and Yves Chauvin, won the Nobel Prize in Chemistry in recognition of their contributions to the development of olefin metathesis.
In organic chemistry, olefin metathesis is an organic reaction that entails the redistribution of fragments of alkenes (olefins) by the scission and regeneration of carbon-carbon double bonds. Because of the relative simplicity of olefin metathesis, it often creates fewer undesired by-products and hazardous wastes than alternative organic reactions. For their elucidation of the reaction mechanism and their discovery of a variety of highly active catalysts, Yves Chauvin, Robert H. Grubbs, and Richard R. Schrock were collectively awarded the 2005 Nobel Prize in Chemistry.
Dynamic covalent chemistry (DCvC) is a synthetic strategy employed by chemists to make complex molecular and supramolecular assemblies from discrete molecular building blocks. DCvC has allowed access to complex assemblies such as covalent organic frameworks, molecular knots, polymers, and novel macrocycles. Not to be confused with dynamic combinatorial chemistry, DCvC concerns only covalent bonding interactions. As such, it only encompasses a subset of supramolecular chemistries.
A molecular sensor or chemosensor is a molecular structure that is used for sensing of an analyte to produce a detectable change or a signal. The action of a chemosensor, relies on an interaction occurring at the molecular level, usually involves the continuous monitoring of the activity of a chemical species in a given matrix such as solution, air, blood, tissue, waste effluents, drinking water, etc. The application of chemosensors is referred to as chemosensing, which is a form of molecular recognition. All chemosensors are designed to contain a signalling moiety and a recognition moiety, that is connected either directly to each other or through a some kind of connector or a spacer. The signalling is often optically based electromagnetic radiation, giving rise to changes in either the ultraviolet and visible absorption or the emission properties of the sensors. Chemosensors may also be electrochemically based. Small molecule sensors are related to chemosensors. These are traditionally, however, considered as being structurally simple molecules and reflect the need to form chelating molecules for complexing ions in analytical chemistry. Chemosensors are synthetic analogues of biosensors, the difference being that biosensors incorporate biological receptors such as antibodies, aptamers or large biopolymers.
Maurice S. Brookhart is an American chemist, and professor of chemistry at the University of Houston since 2015.
Myron Lee Bender (1924–1988) was born in St. Louis, Missouri. He obtained his B.S. (1944) and his Ph.D. (1948) from Purdue University. The latter was under the direction of Henry B. Hass. After postdoctoral research under Paul D. Barlett, and Frank H. Westheimer, he spent one year as a faculty member at the University of Connecticut. Thereafter, he was a professor of Chemistry at Illinois Institute of Technology in 1951, and then at Northwestern University in 1960. He worked primarily in the study of reaction mechanisms and the biochemistry of enzyme action. Myron L. Bender demonstrated the two-step mechanism of catalysis for serine proteases, nucleophilic catalysis in ester hydrolysis and intramolecular catalysis in water. He also showed that cyclodextrin can be used to investigate catalysis of organic reactions within the scope of host–guest chemistry. Finally, he and others reported on the synthesis of an organic compound as a model of an acylchymotrypsin intermediate.
The Taft equation is a linear free energy relationship (LFER) used in physical organic chemistry in the study of reaction mechanisms and in the development of quantitative structure–activity relationships for organic compounds. It was developed by Robert W. Taft in 1952 as a modification to the Hammett equation. While the Hammett equation accounts for how field, inductive, and resonance effects influence reaction rates, the Taft equation also describes the steric effects of a substituent. The Taft equation is written as:
Jeremy Keith Morris Sanders is a British chemist and Emeritus Professor in the Department of Chemistry at the University of Cambridge. He is also Editor-in-Chief of Royal Society Open Science. He is known for his contributions to many fields including NMR spectroscopy and supramolecular chemistry. He served as the Pro-Vice-Chancellor for Institutional Affairs at the University of Cambridge, 2011–2015.
Reed McNeil Izatt was an American chemist who was emeritus Charles E. Maw Professor of Chemistry at Brigham Young University in Provo, Utah. His field of research was macrocyclic chemistry and metal separation technologies.
Kim Kimoon is a South Korean chemist and professor in the Department of Chemistry at Pohang University of Science and Technology (POSTECH). He is the first and current director of the Center for Self-assembly and Complexity at the Institute for Basic Science. Kim has authored or coauthored 300 papers which have been cited more than 30,000 times and he holds a number of patents. His work has been published in Nature, Nature Chemistry, Angewandte Chemie, and JACS, among others. He has been a Clarivate Analytics Highly Cited Researcher in the field of chemistry in 2014, 2015, 2016.
Supramolecular catalysis is not a well-defined field but it generally refers to an application of supramolecular chemistry, especially molecular recognition and guest binding, toward catalysis. This field was originally inspired by enzymatic system which, unlike classical organic chemistry reactions, utilizes non-covalent interactions such as hydrogen bonding, cation-pi interaction, and hydrophobic forces to dramatically accelerate rate of reaction and/or allow highly selective reactions to occur. Because enzymes are structurally complex and difficult to modify, supramolecular catalysts offer a simpler model for studying factors involved in catalytic efficiency of the enzyme. Another goal that motivates this field is the development of efficient and practical catalysts that may or may not have an enzyme equivalent in nature.
The Agentase Chemical Agent Detection (CAD) Kit, formerly known as the Fido C1 CAD Kit, is an enzyme-based chemical detection kit that contains six different sensors that are designed to detect specific chemical warfare agents (CWAs) and other toxic chemical contaminants at trace levels. The kit is provided in a small pouch and can detect the presence of the chemical agents within five minutes.
Bruce C. Gibb is a professor of chemistry at Tulane University. He is notable for his work in aqueous supramolecular chemistry, with particular emphasis on self-assembly leading to compartmentalization, and contributing to fundamental understandings of the hydrophobic effect and Hofmeister effect Bruce C. Gibb received both his B.Sc. (1987) and Ph.D. degrees (1992) from Robert Gordon University. His Ph.D. Synthesis and Structural Examination of 3a,5-cyclo-5a-Androstane Steroids was carried out under the direction of Philip J. Cox and Steve M. MacManus. He accepted a gratis appointment as a post-doctoral researcher with John Sherman at the University of British Columbia (UBC) in 1993 where he "discovered" his interest in supramolecular chemistry. He worked at UBC through 1994, and subsequently as a post-doctoral researcher with James Canary at New York University from 1994-1996.
An artificial metalloenzyme (ArM) is a metalloprotein made in the laboratory which cannot be found in the nature and can catalyze certain desired chemical reactions. Despite fitting into classical enzyme categories, ArMs also have potential in chemical reactivity like catalyzing Suzuki coupling, metathesis and so on, which are never reported in natural enzymatic reaction. With the progress in organometallic synthesis and protein engineering, more and more new kind of design of ArMs came out, showing promising future in both academia and industrial aspects.
Geoffrey "Geoff" William Coates is an American chemist and the Tisch University Professor in the department of chemistry and chemical biology at Cornell University.
Roeland J. M. Nolte is a Dutch chemist, known for his work in the fields of organic chemistry, biochemistry, polymer chemistry, and supramolecular chemistry. He is an emeritus Royal Netherlands of Arts and Sciences professor and an emeritus professor of Organic Chemistry at Radboud University in Nijmegen, The Netherlands. Currently, he holds a special chair, i.e. professor of Molecular Nanotechnology, at this university. Nolte is considered to be one of the pioneers of the field of supramolecular chemistry, which encompasses the design and synthesis of new chemical structures from low molecular weight compounds and biopolymers using so-called non-covalent interactions. He published many studies on supramolecular assembly and biomimetic catalysts, which find applications in the field of nanomaterials and medicine.
A chemical sensor array is a sensor architecture with multiple sensor components that create a pattern for analyte detection from the additive responses of individual sensor components. There exist several types of chemical sensor arrays including electronic, optical, acoustic wave, and potentiometric devices. These chemical sensor arrays can employ multiple sensor types that are cross-reactive or tuned to sense specific analytes.
Virgil Percec is a Romanian-American chemist and P. Roy Vagelos Chair and Professor of Chemistry at the University of Pennsylvania. Expert in organic, macromolecular and supramolecular chemistry including self-assembly, biological membrane mimics, complex chiral systems, and catalysis. Pioneered the fields of liquid crystals with complex architecture, supramolecular dendrimers, Janus dendrimers and glycodendrimers, organic Frank-Kasper phases and quasicrystals, supramolecular polymers, helical chirality, Ni-catalyzed cross-coupling and multiple living and self-interrupted polymerizations. Most of these concepts were inspired by Nature and biological principles.