4.7 Article

π-Type halogen bonding enhanced the long-lasting room temperature phosphorescence of Zn(ii) coordination polymers for photoelectron response applications

Journal

INORGANIC CHEMISTRY FRONTIERS
Volume 7, Issue 11, Pages 2224-2230

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0qi00191k

Keywords

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Funding

  1. National Natural Science Foundation of China [21971100, 21771097]
  2. Project of Central Plains Science and Technology Innovation Leading Talents of Henan Province [204200510001]
  3. Key Scientific Research Projects of Higher Education of Henan Province [20A150005]

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The development of non-noble metal ions with potential organic phosphor ligands through strong coordination bonds can afford an effective platform for achieving persistent and tunable phosphorescence at room temperature. However, successful examples of coordination polymers (CPs) or metal-organic frameworks (MOFs) exhibiting long-lasting phosphorescence emission are still rarely explored. In this work, a new strategy has been used for the first time to achieve long-lasting phosphorescence via pi-type halogen bonding in coordination polymers. By the selection of two isomers 5-BIPA and 4-BIPA with different Br atom substitution positions in isophthalic acid (IPA), two new Zn(ii)-based coordination polymers exhibiting long-lasting phosphorescence emission up to the order of magnitude of millisecond (ms) were presented, which were further revealed by theoretical calculations. Optoelectronic measurements indicated that 1 showed a high photoelectron response because the delocalized pi-type halogen bonding and long range order of pi-conjugated chains afforded large electron channels for efficient charge transport.

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