Spin-Delocalization in a Helical Open-Shell Hydrocarbon
datasetposted on 03.11.2016, 00:00 by Prince Ravat, Peter Ribar, Michel Rickhaus, Daniel Häussinger, Markus Neuburger, Michal Juríček
Neutral open-shell molecules, in which spin density is delocalized through a helical conjugated backbone, hold promise as models for investigating phenomena arising from the interplay of magnetism and chirality. Apart from a handful of examples, however, the chemistry of these compounds remains largely unexplored. Here, we examine the prospect of extending spin-delocalization over a helical backbone in a model compound naphtho[3,2,1-no]tetraphene, the first helically chiral open-shell hydrocarbon, in which one benzene ring is fused to helicene, forming a phenalenyl subunit. The unpaired electron in this molecule is delocalized over the entire helical core composed of six rings, albeit in a nonuniform fashion, unlike in phenalenyl. In the case of a monosubstituted derivative, the uneven spin-distribution results in a selective σ-dimer formation in solution, as confirmed by 2D NMR spectroscopy. In contrast, the dimerization process is suppressed entirely when four substituents are installed to sterically hinder all reactive positions. The persistent nature of the tetrasubstituted derivative allowed its characterization by EPR, UV–vis, and CD spectroscopies, validating spin-delocalization through a chiral backbone, in accord with DFT calculations. The nonuniform spin-distribution, which dictates the selectivity of the σ-dimer formation, is rationalized by evaluating the aromaticity of the resonance structures that contribute to spin-delocalization.
Read the peer-reviewed publication
EPRhelical coredimerization process2 D NMR spectroscopyphenalenyl subunitcompoundchiral backbonenonuniform spin-distributionreactive positionsσ- dimer formationhelical backbonespin-distribution resultsHelical Open-Shell Hydrocarbon Neutral open-shell moleculesdelocalizedhelically chiral open-shell hydrocarbonbenzene ringUVCD spectroscopiesnonuniform fashionDFT calculationsspin-delocalizationresonance structuresmodel