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A Quadruply Bridged Non-Offset Face-to-Face Porphyrin Dimer and Cross-Shaped Pentameric Porphyrin Tapes Based on 2,7,12,17-Tetrakis(pinacolatoboryl) Ni II Porphyrin.

Meng YeFangling DengLing XuYutao RaoBangshao YinMingbo ZhouRyo KurosakiNaoki ArataniAtsuhiro OsukaJianxin Song
Published in: Angewandte Chemie (International ed. in English) (2023)
2,7,12,17-Tetrakis(pinacolatoboryl) Ni II porphyrin 5 Ni was synthesized in 75 % yield by Ir-catalyzed borylation of porphine followed by Ni II metalation and has been demonstrated to be a useful synthon, giving 2,7,12,17-tetraaryated Ni II porphyrins 6 a-d, peripherally octaarylated Ni II porphyrins 8 a-d, quadruply bridged face-to-face non-offset Ni II -porphyrin dimer 12, and cross-shaped β-meso singly linked porphyrin pentamers and nonamers. Oxidation of cross-shaped β-meso singly linked porphyrin pentamers 14 Ni and 14 Zn gave fused pentameric tapes 15 Ni and 15 Zn. The structures of 12, 14 Zn, and 15 Ni have been revealed by X-ray diffraction analysis. Optical separation of 12 has been accomplished, showing a bisignate coupling pattern for exciton-coupled blue-shifted Soret band. Pentameric porphyrin tape 15 Zn exhibits a red-shifted absorption band at 1156 nm and seven reversible redox waves.
Keyphrases
  • metal organic framework
  • photodynamic therapy
  • electron transfer
  • energy transfer
  • transition metal
  • high resolution
  • heavy metals
  • magnetic resonance imaging
  • hydrogen peroxide
  • room temperature
  • light emitting