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A novel 22π-aromatic sapphyrin isomer endowed with an acene moiety was designed and realised for the first time as a core-modified monothia analogue. This macrocycle exhibited absorption and emission in… Click to show full abstract
A novel 22π-aromatic sapphyrin isomer endowed with an acene moiety was designed and realised for the first time as a core-modified monothia analogue. This macrocycle exhibited absorption and emission in the near-infrared region. It was diprotonated under strongly acidic conditions and bound to anions like sapphyrin. It showed unusual coordination chemistry, acting as a neutral ligand and undergoing large out-of-plane deformation to bind Pd(II) ions.
Keywords:
core modified;
pentaphyrin core;
sapphyrin;
modified isomer;
monothia pentaphyrin
Journal Title: Dalton transactions
Year Published: 2022
Link to full text (if available)
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Journal Title: Dalton transactions
Year Published: 2022
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!