Abstract
In a series of thiaaceneporphyrinoids, their conformers exhibit macrocyclic π-conjugation pathways controlled by a dihedral angle between the porphyrin framework and acene planes. Conformational equilibria significantly affect the photophysical properties of these macrocycles.
Original language | English |
---|---|
Pages (from-to) | 8367-8369 |
Number of pages | 3 |
Journal | Chemical Communications |
Volume | 50 |
Issue number | 61 |
DOIs | |
Publication status | Published - 2014 Jul 3 |
All Science Journal Classification (ASJC) codes
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Chemistry(all)
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry