An Acceptor-Substituted N-Heterocyclic ortho-Quinodimethane: Pushing the Boundaries of Polarization in Donor–Acceptor-Substituted Polyenes

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Abstract
We report the synthesis, isolation, and characterization of a stable donor-acceptor substituted ortho-quinodimethane (oQDM). This system with an imidazolidine scaffold as the donor can also be referred to as acceptor-substituted ortho-N-heterocyclic quinodimethane (oNHQ). We have examined the extent of polarization of the conjugated pi-system using single-crystal X-ray diffraction, NMR and UV/vis spectroscopy, cyclic voltammetry, and DFT computations. The bond lengths in the phenyl linker do not exhibit the alternation typical of oQDMs. In addition, the 13C and 15N NMR shifts suggest significant charge separation, an interpretation supported by the diatropic ring current determined by NICSZZ(r) computations, which is characteristic of aromatic compounds. DFT calculations show that polarization is an electronic effect that is amplified by steric influences. More strikingly, the oxidation and reduction potentials of the push-pull substituted oQDM are virtually identical to those of authenticated anionic and cationic derivatives. The results therefore indicate that an aromatic zwitterionic structure represents the electronic structure more accurately than a neutral quinoidal Lewis structure, which indicates that the acceptor-substituted oNHQ is a rare example of an organic zwitterion in which the centers of charge are in conjugation. The ambiphilic reactivity of the acceptor-substituted oNHQ, which is evidenced by the dehydrogenation of ammonia borane and the addition of phenylacetylene via heterolytic C-H bond cleavage, further supports its notation as an organic zwitterion and is reminiscent of frustrated Lewis pairs (FLPs). Thus, the acceptor-substituted oNHQ can be considered to be an intramolecular carbogenic FLP in terms of its reactivity.
Funding Information
  • Deutsche Forschungsgemeinschaft (GE 3117/1-1, GE 3117/1-2)
  • Verband der Chemischen Industrie
  • Aventis Foundation

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