Charles L. Liotta

ORCID: 0000-0002-7450-6640
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About
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Research Areas
  • Ionic liquids properties and applications
  • Phase Equilibria and Thermodynamics
  • Inorganic and Organometallic Chemistry
  • Catalysis and Oxidation Reactions
  • Subcritical and Supercritical Water Processes
  • Carbon dioxide utilization in catalysis
  • Chemical Synthesis and Reactions
  • Microwave-Assisted Synthesis and Applications
  • Analytical Chemistry and Chromatography
  • Molecular Sensors and Ion Detection
  • Chemical Reaction Mechanisms
  • Photochemistry and Electron Transfer Studies
  • Chemical Synthesis and Analysis
  • Carbon Dioxide Capture Technologies
  • Various Chemistry Research Topics
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • Asymmetric Hydrogenation and Catalysis
  • Chemistry and Chemical Engineering
  • Origins and Evolution of Life
  • Zeolite Catalysis and Synthesis
  • Spectroscopy and Quantum Chemical Studies
  • Fluorine in Organic Chemistry
  • Catalysis for Biomass Conversion
  • Microbial Metabolic Engineering and Bioproduction
  • Chemical Reactions and Isotopes

Georgia Institute of Technology
2014-2023

AID Atlanta
2014-2020

Foundation for Applied Molecular Evolution
2018

Auburn University
2010

Imperial College London
2006-2009

Queen's University
2005-2007

University of Kansas
2007

RWTH Aachen University
2007

University of Regensburg
2005

University of California, Davis
2001-2002

Fourier transform IR spectroscopy has been used to investigate the interaction of carbon dioxide with polymers. transmission and attenuated total reflectance spectra were obtained for CO2 impregnated into polymer films. It shown that polymers possessing electron-donating functional groups (e.g., carbonyl groups) exhibit specific interactions CO2, most probably Lewis acid−base nature. An unusual aspect is use bending mode (ν2) probe polymer−CO2 interactions. The evidence observation splitting...

10.1021/ja950416q article EN Journal of the American Chemical Society 1996-01-01

Many industrial applications that rely on emulsions would benefit from an efficient, rapid method of breaking these at a specific desired stage. We report long-chain alkyl amidine compounds can be reversibly transformed into charged surfactants by exposure to atmosphere carbon dioxide, thereby stabilizing water/alkane or, for the purpose microsuspension polymerization, styrene-in-water emulsions. Bubbling nitrogen, argon, or air through amidinium bicarbonate solutions 65 degrees C reverses...

10.1126/science.1128142 article EN Science 2006-08-17

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTAsymmetric Hydrogenation and Catalyst Recycling Using Ionic Liquid Supercritical Carbon DioxideRichard A. Brown, Pamela Pollet, Erin McKoon, Charles Eckert, L. Liotta, Philip G. JessopView Author Information Department of Chemistry, University California Davis, 95616-5295 Schools Chemistry Chemical Engineering Georgia Institute Technology, Atlanta, 30332-0100 Cite this: J. Am. Chem. Soc. 2001, 123, 6, 1254–1255Publication Date (Web):January...

10.1021/ja005718t article EN Journal of the American Chemical Society 2001-01-17

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTChemistry of naked anions. I. Reactions the 18-crown-6 complex potassium fluoride with organic substrates in aprotic solventsCharles L. Liotta and Henry P. HarrisCite this: J. Am. Chem. Soc. 1974, 96, 7, 2250–2252Publication Date (Print):April 1, 1974Publication History Published online1 May 2002Published inissue 1 April 1974https://pubs.acs.org/doi/10.1021/ja00814a044https://doi.org/10.1021/ja00814a044research-articleACS PublicationsRequest reuse...

10.1021/ja00814a044 article EN Journal of the American Chemical Society 1974-04-01

This review highlights solvent systems that were designed to simultaneously address reaction, separation and recycling challenges.

10.1039/c3gc42302f article EN Green Chemistry 2013-12-20

Amidines have been reported to react with CO(2) form a stable and isolable zwitterionic adduct but previous studies were performed in the presence of at least some water. However, spectroscopy reaction between DBU detects rapid formation bicarbonate salt when wet is exposed does not indicate that an forms either or absence

10.1021/jo0503759 article EN The Journal of Organic Chemistry 2005-05-26

Liquids that consist of a mixture an alcohol and either amidine or guanidine have been developed to switch from low-polarity form high-polarity ionic liquid upon treatment with CO2 at atmospheric pressure. Treatment N2 and/or mild heat (50−60 °C) reverses the process. These liquids can be used as switchable solvents dissolve then precipitate solute reagents for chemical synthesis product.

10.1021/ie070552r article EN Industrial & Engineering Chemistry Research 2007-09-05

Bioethanol currently contributes ∼2% to the total US transportation fuels mix, and another ∼0.01% is based on biodiesel. To make a substantial contribution United States' energy portfolio, biofuels production needs grow substantially over next decade by factor of 10 or more. Although agro-energy crops agriculture waste for being intensively developed, potential forest products industry contribute this effort has been generally underestimated. The one few nationally industries that have...

10.1089/ind.2006.2.55 article EN Industrial Biotechnology 2006-03-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTPreparation and purification of 18-crown-6[1,4,7,10,13,16-hexaoxacyclooctadecane]George W. Gokel, Donald J. Cram, Charles L. Liotta, Henry P. Harris, Fred CookCite this: Org. Chem. 1974, 39, 16, 2445–2446Publication Date (Print):August 1, 1974Publication History Published online1 May 2002Published inissue 1 August 1974https://pubs.acs.org/doi/10.1021/jo00930a037https://doi.org/10.1021/jo00930a037research-articleACS PublicationsRequest reuse...

10.1021/jo00930a037 article EN The Journal of Organic Chemistry 1974-08-01

Phosphorylation of the nucleosides adenosine and uridine by simple mixing mild heating aqueous solutions organic compounds with synthetic analogs meteoritic mineral schreibersite, (Fe,Ni)3P under slightly basic conditions (pH ~9) is reported. These results suggest a potential role for phosphorus in origin development early life.

10.1038/srep17198 article EN cc-by Scientific Reports 2015-11-26

There are now available a variety of tunable solvents; these have been used extensively for extractions and in materials applications. Our focus has to apply techniques chemical reactions take advantage the special properties available, primarily sustainable technology, create processes that potentially more benign advantageous. We report here our work using supercritical fluids, near-critical gas-expanded liquids couple organic with separations. In this paper, we review applications...

10.1021/jp0487612 article EN The Journal of Physical Chemistry B 2004-09-14

Abstract The addition of cosolvents to supercritical fluid (SCF) solvents can have large effects on solubilities, giving engineers the ability tailor loadings and selectivities solutes for difficult separations. It is necessary a better understanding special intermolecular interactions that occur in SCF solutions predict cosolvents. We use chromatographic technique acquire database cosolvent variety solutes; examination shows evidence hydrogen bonding, charge transfer complex formation,...

10.1002/aic.690390206 article EN AIChE Journal 1993-02-01

Neoteric (new) solvents such as supercritical CO2 (scCO2), ionic liquids (ILs), ILs with cosolvents, and CO2-expanded (EILs) offer flexible physical properties, which allow chemists engineers to select the optimal solvent system for a specific reaction process. Homogeneously-catalyzed asymmetric hydrogenation of α,β-unsaturated carboxylic acids was chosen its economic interest multiple H2-concentration dependent behaviours. For example, ruthenium BINAP-type catalysts, type I substrates...

10.1039/b211894g article EN Green Chemistry 2003-03-25

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTChemistry of naked anions. III. Reactions the 18-crown-6 complex potassium cyanide with organic substrates in aprotic solventsFred L. Cook, Chauncey W. Bowers, and C. LiottaCite this: J. Org. Chem. 1974, 39, 23, 3416–3418Publication Date (Print):November 1, 1974Publication History Published online1 May 2002Published inissue 1 November 1974https://pubs.acs.org/doi/10.1021/jo00937a026https://doi.org/10.1021/jo00937a026research-articleACS...

10.1021/jo00937a026 article EN The Journal of Organic Chemistry 1974-11-01

Switchable solvents are a unique class of that were developed to facilitate both reaction and subsequent product separation. Their "built-in" separation ability for facile recovery is paramount achieving chemical processes economically competitive environmentally conscious. Two classes switchable discussed: 1) piperylene sulfone—a volatile recycle DMSO substitute 2) one two-component reversible ionic liquids—solvent systems can be switched back forth between molecular liquids liquids.

10.1039/c0sc00568a article EN Chemical Science 2011-01-01

A new class of one-component, thermally reversible, neutral to ionic liquid solvents derived from siloxylated amines is presented and characterized.

10.1039/b816267k article EN Chemical Communications 2008-11-19
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