4.7 Article

Highly cooperative double metalation of a bis(N2O2) ligand based on bipyridine-phenol framework driven by intramolecular pi-stacking of square planar nickel(II) complex moieties

Journal

DALTON TRANSACTIONS
Volume 40, Issue 34, Pages 8507-8509

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1dt10124b

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan
  2. Grants-in-Aid for Scientific Research [23750055] Funding Source: KAKEN

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Highly cooperative double metalation took place when a novel ligand based on a bipyridine-phenol framework was allowed to react with nickel(II) acetate. The pi-stacking of the square planar metal complex moieties is responsible for the highly cooperative double metalation judging from the X-ray crystal structure in which two complex moieties stack on top of each other in a parallel fashion.

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