A versatile electronic hole in one-electron oxidized NiIIbis-salicylidene phenylenediamine complexes
Chemical Communications2007Iss. 43, pp. 4462–4462
Citations Over TimeTop 11% of 2007 papers
Abstract
The nickel complexes 1(+)-3(+) exhibit a delocalized radical character, the extent of which depends on the electronic properties of the phenolate para-substituent.
Related Papers
- → Crystal Clear Structural Evidence for Electron Delocalization in 1,2-Dihydro-1,2-azaborines(2008)222 cited
- → Analysis of Electron Delocalization in Aromatic Systems: Individual Molecular Orbital Contributions to Para-Delocalization Indexes (PDI)(2006)35 cited
- → How does electron delocalization affect the electronic energy? A survey of neutral poly-nitrogen clusters(2011)23 cited
- → Lack of delocalization in compounds with the grouping CNNC(2000)19 cited
- → Proximate, “Parallel‐In‐Plane” Preoriented Bis(diazenes) − In‐Plane Delocalized Bis(homoconjugated) 4N/5(6)e Anions(2003)11 cited