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School of Chemistry and Biochemistry,
School of Chemistry & Biochemistry
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Efficient Synthesis of 4,5,9,10-Tetrahydropyrene: A Useful Synthetic Intermediate for the Synthesis of 2,7-Disubstituted Pyrenes.
The Journal of organic chemistry Sep, 1999 | Pubmed ID: 11674701
Carbon dioxide as a solubility "switch" for the reversible dissolution of highly fluorinated complexes and reagents in organic solvents: application to crystallization.
Inorganic chemistry Jul, 2002 | Pubmed ID: 12079465
Phase-transfer catalyst separation by CO2 enhanced aqueous extraction.
Chemical communications (Cambridge, England) May, 2002 | Pubmed ID: 12122712
Use and recovery of a homogeneous catalyst with carbon dioxide as a solubility switch.
Chemical communications (Cambridge, England) Dec, 2003 | Pubmed ID: 14703813
The reaction of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) with carbon dioxide.
The Journal of organic chemistry Jun, 2005 | Pubmed ID: 15960544
Green chemistry: reversible nonpolar-to-polar solvent.
Nature Aug, 2005 | Pubmed ID: 16121169
The path forward for biofuels and biomaterials.
Science (New York, N.Y.) Jan, 2006 | Pubmed ID: 16439654
Biocatalytic reaction and recycling by using CO2-induced organic-aqueous tunable solvents.
Angewandte Chemie (International ed. in English) Jul, 2006 | Pubmed ID: 16789050
Probing the cybotactic region in gas-expanded liquids (GXLs).
Accounts of chemical research Aug, 2006 | Pubmed ID: 16906749
Switchable surfactants.
Science (New York, N.Y.) Aug, 2006 | Pubmed ID: 16917059
Molecular dynamics simulation of the cybotactic region in gas-expanded methanol-carbon dioxide and acetone-carbon dioxide mixtures.
The journal of physical chemistry. B Nov, 2006 | Pubmed ID: 17125382
Reversible in situ catalyst formation.
Accounts of chemical research Mar, 2008 | Pubmed ID: 18251512
A spectroscopic and computational exploration of the cybotactic region of gas-expanded liquids: methanol and acetone.
The journal of physical chemistry. B Apr, 2008 | Pubmed ID: 18358022
Local polarity in CO2-expanded acetonitrile: a nucleophilic substitution reaction and solvatochromic probes.
The Journal of organic chemistry May, 2008 | Pubmed ID: 18363361
Effects of solute structure on local solvation and solvent interactions: results from UV/vis spectroscopy and molecular dynamics simulations.
The journal of physical chemistry. B Nov, 2008 | Pubmed ID: 18975884
One-component, switchable ionic liquids derived from siloxylated amines.
Chemical communications (Cambridge, England) Jan, 2009 | Pubmed ID: 19082017
Charge screening in the S(N)2 reaction of charged electrophiles and charged nucleophiles: an ionic liquid effect.
The Journal of organic chemistry Mar, 2009 | Pubmed ID: 19178145
Combining homogeneous catalysis with heterogeneous separation using tunable solvent systems.
The journal of physical chemistry. A Mar, 2010 | Pubmed ID: 20235608
Organic aqueous tunable solvents (OATS): a vehicle for coupling reactions and separations.
Accounts of chemical research Sep, 2010 | Pubmed ID: 20565064
Combining the benefits of homogeneous and heterogeneous catalysis with tunable solvents and nearcritical water.
Molecules (Basel, Switzerland) Nov, 2010 | Pubmed ID: 21081860
Novel solvents for sustainable production of specialty chemicals.
Annual review of chemical and biomolecular engineering , 2011 | Pubmed ID: 22432616
The synthesis and the chemical and physical properties of non-aqueous silylamine solvents for carbon dioxide capture.
ChemSusChem Nov, 2012 | Pubmed ID: 22927114
Production of tartrates by cyanide-mediated dimerization of glyoxylate: a potential abiotic pathway to the citric acid cycle.
Journal of the American Chemical Society Sep, 2013 | Pubmed ID: 23914725
Design, Synthesis, and Evaluation of Nonaqueous Silylamines for Efficient CO2 Capture.
ChemSusChem Nov, 2013 | Pubmed ID: 24203891
Georgia Institute of Technology
Pamela Pollet1,
Amy L. Ethier2,
James C. Senter2,
Charles A. Eckert2,
Charles L. Liotta1
1School of Chemistry and Biochemistry, Georgia Institute of Technology,
2School of Chemical and Biomolecular Engineering, Georgia Institute of Technology
Alex Aw1,
Marshall Fritz2,
Jonathan W. Napoline1,
1School of Chemistry & Biochemistry, Georgia Institute of Technology,
2School of Chemical & Biomolecular Engineering, Georgia Institute of Technology
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