

Publisher: John Wiley & Sons Inc
E-ISSN: 1521-3765|21|29|10566-10575
ISSN: 0947-6539
Source: CHEMISTRY - A EUROPEAN JOURNAL, Vol.21, Iss.29, 2015-07, pp. : 10566-10575
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
AbstractA rational synthetic procedure for the preparation of a series of pyrene‐based neutral and dicationic bis‐azole compounds is reported. The method allows the tailored design of pyrene‐based azoles with different substituents at the nitrogen atoms of the heterocycles, for which the relative conformation of the resulting bis‐azoles can be easily controlled. The bis‐azoliums were used for the preparation of the related diplatinum complexes by reaction with [{Pt(ppy)(μ‐Cl)2}2] (ppy=2‐phenylpyridinate). The X‐ray molecular structure of one of the resulting compounds, a diplatinum(II) bis(N‐heterocyclic carbene) complex, is described. Studies on the photophysical properties of all new species are described. The emission of the bis‐azole‐based compounds seems to be independent of their substitution patterns, which basically indicates that physical properties such as solubility, melting point, and viscosity can be fine‐tuned while maintaining the luminescence properties. Finally, the energies associated with the HOMO and LUMO levels suggest that this family provides versatility to match the energy levels of a wide range of host materials, which is important for the preparation of organic light‐emitting devices.
Related content








By Hirose Takuji Shibano Yuki Miyazaki Yutaro Sogoshi Norihito Nakabayashi Seiichiro Yasutake Mikio
Molecular Crystals and Liquid Crystals, Vol. 534, Iss. 1, 2011-01 ,pp. :