4.8 Article

Heteroleptic [Bis(oxazoline)](dipyrrinato)zinc(II) Complexes: Bright and Circularly Polarized Luminescence from an Originally Achiral Dipyrrinato Ligand

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 55, Issue 4, Pages 1377-1381

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201509411

Keywords

absorption; chirality; fluorescence; N ligands; zinc

Funding

  1. MEXT of Japan [25107510, 26708005, 26107510, 26620039, 15H00862, 2406, 2506]
  2. Murata Science Foundation
  3. Japan Prize Foundation
  4. Tokuyama Science Foundation
  5. Iketani Science and Technology Foundation
  6. Ogasawara Foundation for the Promotion of Science Engineering
  7. Kao Foundation for Arts and Sciences
  8. Asahi Glass Foundation
  9. Noguchi Institute
  10. Japan Association for Chemical Innovation
  11. MIKIYA Science and Technology Foundation
  12. Yazaki Memorial Foundation for Science and Technology
  13. Shorai Foundation for Science and Technology
  14. LIXIL JS Foundation
  15. Iwatani Naoji Foundation
  16. JSPS
  17. Grants-in-Aid for Scientific Research [26107510, 26620039, 2506, 25248019, 15H00862, 25107510, 26220801, 26410093, 26708005] Funding Source: KAKEN

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Heteroleptic zinc(II) complexes synthesized using achiral dipyrrinato and chiral bis(oxazoline) ligands show bright fluorescence with quantum efficiencies of up to 0.70. The fluorescence originates from the (1)pi-pi* photoexcited state localized exclusively on the dipyrrinato ligand. Furthermore, the luminescence is circularly polarized despite the achirality of the dipyrrinato ligand. Single-crystal X-ray structure analysis discloses that the chiral bis(oxazoline) ligand undergoes intramolecular pi-pi stacking with the dipyrrinato ligand, inducing axial chirality in the dipyrrinato moiety.

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