π-Extended Diaza[7]helicenes by Hybridization of Naphthalene Diimides and Hexa-peri-hexabenzocoronenes.
Carolin DusoldDmitry I SharapaFrank HampelAndreas HirschPublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2020)
The synthesis of an unprecedented, π-extended hexabenzocorene (HBC)-based diaza[7]helicene is presented. The target compound was synthesized by an ortho-fusion of two naphthalene diimide (NDI) units to a HBC-skeleton. A combination of Diels-Alder and Scholl-type oxidation reactions involving a symmetric di-NDI-tolane precursor were crucial for the very selective formation of the helical superstructure via a hexaphenyl-benzene (HPB) derivative. The formation of the diaza[7]helicene moiety in the final Scholl oxidation is favoured, affording the symmetric π-extended helicene as the major product as a pair of enantiomers. The separation of the enantiomers was successfully accomplished by HPLC involving a chiral stationary phase. The absolute configuration of the enantiomers was assigned by comparison of circular dichroism spectra with quantum mechanical calculations.
Keyphrases
- capillary electrophoresis
- mass spectrometry
- molecular dynamics
- density functional theory
- liquid chromatography
- ms ms
- hydrogen peroxide
- simultaneous determination
- molecular dynamics simulations
- tandem mass spectrometry
- high performance liquid chromatography
- nitric oxide
- single molecule
- solid phase extraction
- escherichia coli
- quantum dots
- candida albicans