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Christos P. Constantinides

Researcher at University of Michigan

Publications -  41
Citations -  1070

Christos P. Constantinides is an academic researcher from University of Michigan. The author has contributed to research in topics: Radical & Magnetic susceptibility. The author has an hindex of 18, co-authored 35 publications receiving 877 citations. Previous affiliations of Christos P. Constantinides include University of Cambridge & University of Cyprus.

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Characterization and magnetic properties of a "super stable" radical 1,3-diphenyl-7-trifluoromethyl-1,4-dihydro-1,2,4-benzotriazin-4-yl.

TL;DR: In this paper, it was shown that 1,3-Diphenyl-7-trifluoromethyl-1,4-dihydro, 1,2, 4-benzotriazin-4-yl (4), prepared in high yield via the catalytic oxidation of the corresponding amidrazone 5 by using Pd/C (1.6 mol %) and 1,8-diazabicyclo[5.0]undec 7-ene (0.1 equiv) in air,
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A DFT study of the ground state multiplicities of linear vs angular polyheteroacenes.

TL;DR: An analysis based on the SOMO-SOMO energy splittings, their spatial distributions, and the spin density populations for the triplet states is presented to clarify the factors that determine their ground state multiplicities.
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Route to benzo- and pyrido-fused 1,2,4-triazinyl radicals via N'-(het)aryl-N'-[2-nitro(het)aryl]hydrazides.

TL;DR: A two-step route to 1,3-disubstituted benzo- and pyrido-fused 1,2,4-triazinyl radicals is presented and requires a modification for aceto- and trifluoroacetohydrazides that involved a multistep synthesis of asymmetrically 1,1-diaryl-substituting hydrazines.
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Multifunctional Dithiadiazolyl Radicals: Fluorescence, Electroluminescence, and Photoconducting Behavior in Pyren-1'-yl-dithiadiazolyl.

TL;DR: Comparative studies between the energies of the frontier orbitals of pyren-1'-yl nitronyl nitroxide and 1 reveal that the energy mismatch and poor spatial overlap between the DTDA radical SOMO and the pyrene π manifold in 1 efficiently inhibit the non-radiative electron-electron exchange relaxation pathway previously described for 2.
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Preparation of Blatter Radicals via Aza-Wittig Chemistry: The Reaction of N-Aryliminophosphoranes with 1-(Het)aroyl-2-aryldiazenes.

TL;DR: Reacting N-aryliminophosphoranes with 1-(het)aroyl-2-aryldiazenes in preheated diphenyl ether at 150-250 °C for 5-25 min affords in most cases the 1,3-diaryl-1,4-dihydrobenzo[e][1,2,4]triazin-4-yls (aka Blatter radicals) in moderate to good yields.