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Full-Text Articles in Physical Sciences and Mathematics
Effect Of Ligands And Their Removal On The Au Nanoparticle-Catalyzed Reduction Of 4-Nitrophenol, Nicholas Langer, Ofer Kedem
Effect Of Ligands And Their Removal On The Au Nanoparticle-Catalyzed Reduction Of 4-Nitrophenol, Nicholas Langer, Ofer Kedem
Chemistry Faculty Research and Publications
The catalytic activity of gold nanoparticles (Au NPs) is strongly affected by the organic ligands coating them, which afford colloidal stability and are most commonly attached during the synthesis of the Au NPs. However, different ligands also produce Au NPs of different sizes and morphologies, complicating the study of the impact of the ligands themselves. Alternatively, postsynthetic ligand exchange risks incomplete exchanges and a mixed ligand shell, as well as colloidal instability. Here, Au NPs are immobilized on glass supports to afford truly ligand-free, solvent-stable Au nanoislands (NIs). The catalytic activity of Au NIs, uncoated and coated with a variety …
Investigation On The Synthesis, Application And Structural Features Of Heteroaryl 1,2-Diketones, Robert J. Wehrle, Alexander Rosen, Thu Vu Nguyen, Kalyn Koons, Eric Jump, Mason Bullard, Natalie Wehrle, Adam Stockfish, Patrick M. Hare, Abdurrahman Atesin, Tülay A. Ateşin, Lili Ma
Investigation On The Synthesis, Application And Structural Features Of Heteroaryl 1,2-Diketones, Robert J. Wehrle, Alexander Rosen, Thu Vu Nguyen, Kalyn Koons, Eric Jump, Mason Bullard, Natalie Wehrle, Adam Stockfish, Patrick M. Hare, Abdurrahman Atesin, Tülay A. Ateşin, Lili Ma
Chemistry Faculty Publications and Presentations
A set of unsymmetrical heteroaryl 1,2-diketones were synthesized by a heteroarylation/oxidation sequence with up to 65% isolated yields. Palladium catalyst XPhos Pd G4 and SeO2 were the key reagents used in this methodology, and microwave irradiation was utilized to facilitate an efficient and ecofriendly process. The application of heteroaryl 1,2-diketones is demonstrated through the synthesis of an unsymmetrical 2-phenyl-3-(pyridin-3-yl)quinoxaline (5a) from 1-phenyl-2-(pyridin-3-yl)ethane-1,2-dione (4a). The lowest energy conformations of 4a and 5a were located using Density Functional Theory (DFT) at the M06-2X/def2-TZVP level of theory. Two lowest energy conformations of 4a differ with respect to the position of the N atom …
Calcium Bistriflimide-Mediated Sulfur (Vi)–Fluoride Exchange (Sufex): Mechanistic Insights Toward Instigating Catalysis, Nicholas Ball, Brian Han, Samuel R. Khasnavis, Matthew Nwerem, Michael Bertagna, O Maduka Ogba
Calcium Bistriflimide-Mediated Sulfur (Vi)–Fluoride Exchange (Sufex): Mechanistic Insights Toward Instigating Catalysis, Nicholas Ball, Brian Han, Samuel R. Khasnavis, Matthew Nwerem, Michael Bertagna, O Maduka Ogba
Pomona Faculty Publications and Research
We report a mechanistic investigation of calcium bistriflimide-mediated sulfur(VI)–fluoride exchange (SuFEx) between sulfonyl fluorides and amines. We determine the likely pre-activation resting state─a calcium bistriflimide complex with ligated amines─thus allowing for corroborated calculation of the SuFEx activation barrier at ∼21 kcal/mol, compared to 21.5 ± 0.14 kcal/mol derived via kinetics experiments. Transition state analysis revealed: (1) a two-point calcium-substrate contact that activates the sulfur(VI) center and stabilizes the leaving fluoride and (2) a 1,4-diazabicyclo[2.2.2]octane additive that provides Brønsted-base activation of the nucleophilic amine. Stable Ca–F complexes upon sulfonamide formation are likely contributors to inhibited catalytic turnover, and a proof-of-principle redesign …
Valence-, Dipole-And Quadropole-Bound Electronically Excited States Of Closed-Shell Anions Formed By Deprotonation Of Cyano-And Ethynyl-Disubstituted Polycyclic Aromatic Hydrocarbons, Marie E. Strauss, Taylor J. Santaloci, Ryan C. Fortenberry
Valence-, Dipole-And Quadropole-Bound Electronically Excited States Of Closed-Shell Anions Formed By Deprotonation Of Cyano-And Ethynyl-Disubstituted Polycyclic Aromatic Hydrocarbons, Marie E. Strauss, Taylor J. Santaloci, Ryan C. Fortenberry
Faculty and Student Publications
Dicyano-functionalized benzene and naphthalene anion derivatives exhibit a relatively rich population of electronically excited states in stark contrast to many assumptions regarding the photophysics of anions in general. The present work has quantum chemically analyzed the potential electronically excited states of closed-shell anions created by replacing hydrogen atoms with valence-bound lone pairs in benzene and naphthalene difunctionalized with combinations of-CN and-C2H. Dicyanobenzene anion derivatives can exhibit dipole-bound excited states as long as the cyano groups are not in para position to one another. This also extends to cyanoethynylbenzene anions as well as deprotonated dicyano-and cyanoethynylnaphthalene anion derivatives. Diethynyl functionalization is …
Synthesis Of Highly Reactive Sulfone Iminium Fluorides And Their Use In Deoxyfluorination And Sulfur Fluoride Exchange Chemistry, James A. Vogel, Rania Hammami, Ara Ko, Hiya Datta, Yael N. Eiben, Karley J. Labenne, Ellis C. Mccarver, Ebrar Z. Yilmaz, Patrick R. Melvin
Synthesis Of Highly Reactive Sulfone Iminium Fluorides And Their Use In Deoxyfluorination And Sulfur Fluoride Exchange Chemistry, James A. Vogel, Rania Hammami, Ara Ko, Hiya Datta, Yael N. Eiben, Karley J. Labenne, Ellis C. Mccarver, Ebrar Z. Yilmaz, Patrick R. Melvin
Chemistry Faculty Research and Scholarship
We report the synthesis of sulfone iminium fluorides (SIFs), a reactive class of sulfur(VI) molecules. The synthesis is tolerant of a variety of substituents on the sulfur and nitrogen components. The SIF reagents were applied to the deoxyfluorination of alcohols and carboxylic acids, providing high yields of fluorinated products in 60 s at room temperature. The SIF reagents were then utilized in sulfur fluoride exchange (SuFEx), creating the first ionic SuFEx products to date.