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Structural, magnetic, and computational correlations of some imidazolo-fused 1,2,4-benzotriazinyl radicals

By Christos P. Constantinides, Andrey A. Berezin, Maria Manoli, Gregory M. Leitus, Georgia A. Zissimou, Michael Bendikov, Jeremy M. Rawson and Panayiotis A. Koutentis


1,3,7,8‐Tetraphenyl‐4,8‐dihydro‐1H‐imidazolo[4,5g][1,2,4]benzotriazin‐4‐yl (5), 8‐(4‐bromophenyl)‐1,3,7‐triphenyl‐4,8‐dihydro‐1H‐imidazolo[4,5g][1,2,4]benzotriazin‐4‐yl (6), and 8‐(4‐methoxyphenyl)‐1,3,7‐triphenyl‐4,8‐dihydro‐1H‐imidazolo[4,5g][1,2,4]benzotriazin‐4‐yl (7) were characterized by using X‐ray diffraction crystallography, variable‐temperature magnetic susceptibility studies, and DFT calculations. Radicals 5–7 pack in 1 D π stacks made of radical pairs with alternate short and long interplanar distances. The magnetic susceptibility (χ vs. T) of radicals 5 and 6 exhibit broad maxima at (50±2) and (50±4) K, respectively, and are interpreted in terms of an alternating antiferromagnetic Heisenberg linear chain model with average exchange‐interaction values of J=−31.3 and −35.4 cm−1 (gsolid=2.0030 and 2.0028) and an alternation parameter a=0.15 and 0.38 for 5 and 6, respectively. However, radical 7 forms 1 D columns of radical pairs with alternating distances; one of the interplanar distances is significantly longer than the other, which decreases the magnetic dimensionality and leads to discrete dimers with a ferromagnetic exchange interaction between the radicals (2J=23.6 cm−1, 2zJ′=−2.8 cm−1, gsolid=2.0028). Magnetic exchange‐coupling interactions in 1,2,4‐benzotriazinyl radicals are sensitive to the degree of slippage and inter‐radical separation, and such subtle changes in structure alter the fine balance between ferro‐ and antiferromagnetic interactions

Publisher: Wiley
Year: 2014
DOI identifier: 10.1002/chem.201304538
OAI identifier: oai:
Provided by: ORCA
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