3 results match your criteria: "Department of Chemistry Towson University[Affiliation]"
Chem Commun (Camb)
July 2024
Department of Chemistry Towson University, 8000 York Road, Towson, MD 21252, USA.
A methodology is described herein for the synthesis of 2-aryl acetaldehydes from aryl aldehydes using TMSCHN under Au(I) catalysis. A diazoorgano Au(I) complex was shown to be an intermediate that reacts with ArCHO to give ArCHCHO products. This homologation protocol was used to synthesize a wide range of 2-aryl acetaldehydes with high functional group compatibility.
View Article and Find Full Text PDFDalton Trans
March 2024
Department of Chemistry Towson University, 8000 York Road, Towson, MD 21252, USA.
Rare examples of trinuclear [Ni-N-M-N-Ni] core (M = Ca, Mg) with linear bridged dinitrogen ligands are reported in this work. The reduction of [PrNN]Ni(μ-Br)Li(thf) (1) (PrNN = 2,4-bis-(2,6-diisopropylphenylimido)pentyl) with elemental Mg or Ca in THF under an atmosphere of dinitrogen yields the complex {PrNNNi(μ-N)}M (thf) (M = Mg, complex 2 and M = Ca, complex 3). The bridging end-on (μ-N)M(thf) moiety connects the two [PrNNNi] nickelate fragments.
View Article and Find Full Text PDFJ Phys Chem B
February 2016
Department of Chemistry Towson University, Towson, Maryland 21252 United States.
We present a study to probe the formation of localized aromatic sextets and their effects on the charge transport properties in polymers with acene cores. Bithiophene-acene copolymers containing benzene, naphthalene, or anthracene as acene cores were synthesized using Yamamoto polymerization. Drop-casted polymer films were chemically doped and analyzed using high frequency saturation transfer EPR (HF ST-EPR), a method which has proven useful in the study of conducting polymers.
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