Peter Gantzel
University of California, San Diego
75 Papers
1.5K Citations
Peter Gantzel is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Carbene & Ligand. The author has an hindex of 33, co-authored 75 publications. Previous affiliations of Peter Gantzel include San Diego Supercomputer Center.
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Papers
Uranium Tris-aryloxide Derivatives Supported by Triazacyclononane: Engendering a Reactive Uranium(III) Center with a Single Pocket for Reactivity
TL;DR: It is shown that the deeply colored uranium(III) and uranium(V) species are stabilized via pi-bonding interaction, involving uranium f-orbitals and the axial acetonitrile and imido ligand, respectively.
197
Structures of the Copper(I) and Copper(II) Complexes of 2,9-Diphenyl-1,10-phenanthroline: Implications for Excited-State Structural Distortion.
TL;DR: Solution-state absorption and (1)H NMR spectra indicate that the [Cu(dpp)(2)](+) complex is fluxional in solution, rocking between two enantiomeric structures of C(2) molecular symmetry through an intermediate ofC(s)() symmetry.
184
Single-Molecule Magnets: Jahn−Teller Isomerism and the Origin of Two Magnetization Relaxation Processes in Mn12 Complexes
Sheila M. J. Aubin,Ziming Sun,Hilary J. Eppley,Evan Rumberger,Ilia A. Guzei,Kirsten Folting,Peter Gantzel,Arnold L. Rheingold,George Christou,David N. Hendrickson +9 more
TL;DR: In this article, the origin of the magnetization relaxation processes was systematically examined in single-molecule magnets with the composition [Mn12O12(O2CR)16(H2O)x] (x = 3 or 4).
156
Effects of Sterics and Electronic Delocalization on the Photophysical, Structural, and Electrochemical Properties of 2,9-Disubstituted 1,10-Phenanthroline Copper(I) Complexes.
TL;DR: The syntheses, crystal structures, electronic absorption spectra, electrochemical properties, and photophysical properties of a series of copper(I) bis(phenanthroline) complexes are reported and demonstrate that the copper coordination environment is more sterically encumbered and more rigid in these two complexes than the coordination environment in the comparison molecule.
156