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Achieving colour tuneable and white-light luminescence in a large family of dual-emission lanthanide coordination polymers.

Jun-Feng QianHuangjie LuZhaofa ZhengMiaomiao XuYuan QianZhi-Hui ZhangJian-Qiang WangMing-Yang HeJian Lin
Published in: Dalton transactions (Cambridge, England : 2003) (2021)
Expanding the family of lanthanide terpyridine coordination polymers has yielded eighteen new complexes with two different phases, Ln(TPC)2(HCOO)(H2O) (Ln-1) and Ln(TPC)(HCOO)2 (Ln-2) (Ln = Sm-Lu, except Tm). Both structures are composed of lanthanide cations interconnected by 2,2':6',2''-terpyridine-4'-carboxylate ligands to yield one-dimensional chain topologies. However, the incorporation of an additional crystallographically unique decorative TPC ligand into Ln-1 gives rises to a distinct phase. The encapsulation of both metal- and ligand-based phosphors within single coordination polymers leads to dual-emission of the afforded materials. Furthermore, judicious lanthanide doping in heterometallic Ln-1 and Ln-2 allows for fine-tuning the photoluminescent colours over a wide range of gamut. Such a combination showcases the capability to fine-tune the emission colours from deep green, to red, and to blue. In addition, direct white-light emission upon UV excitation can be achieved in the SmxGd1-x-1 system.
Keyphrases
  • energy transfer
  • single molecule
  • metal organic framework
  • air pollution
  • quantum dots
  • ionic liquid
  • mass spectrometry