| Literature DB >> 27471860 |
Kenta Nishino1, Hideki Yamamoto1, Kazuo Tanaka1, Yoshiki Chujo1.
Abstract
The molecular design based on o-carborane dyads is described for preparing multifunctional luminescent molecules such as dual emissions, aggregation and crystallization-induced emission enhancements, and luminescent color changes. The pyrene-substituted o-carborane dyads were synthesized via the insertion reaction between decaborane and 1-ethynylpyrene in the presence of Lewis base in a good yield. Finally, extremely bright luminescent compounds with solid-state emission properties (ΦPL > 0.99) were obtained.Entities:
Year: 2016 PMID: 27471860 DOI: 10.1021/acs.orglett.6b01920
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005