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Synthesis of a Cyclophane Bearing Two Benz[a]anthracene Units Connected at the 5 and 7 Positions with Two Naphth-1,4-diyl Groups.

Haresh ThakellapalliBehzad FarajidizajiShuangjiang LiJosef C HellerYu ZhangNovruz G AkhmedovCarsten MilsmannJeffrey L PetersenKung K Wang
Published in: The Journal of organic chemistry (2018)
A synthetic pathway to a cyclophane bearing two benz[a]anthracene units connected at the 5 and 7 positions through two naphth-1,4-diyl groups was developed, and its structure was confirmed by X-ray structure analysis. Because of structural constraints, the two naphthyl groups are distorted from planarity and the bonds connecting them to the benz[a]anthracene units are bent significantly. The UV-vis and fluorescence spectra of the cyclophane are red-shifted from those of 7-(1-naphthalenyl)benz[a]anthracene, which is the corresponding monomeric polycyclic aromatic hydrocarbon.
Keyphrases
  • high resolution
  • single molecule
  • magnetic resonance imaging
  • density functional theory
  • magnetic resonance
  • dual energy
  • molecular dynamics
  • quantum dots
  • electron microscopy