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Triple Helical Ir(ppy) Phenylene Cage Prepared by Diol-Mediated Benzannulation: Synthesis, Resolution, Absolute Stereochemistry and Photophysical Properties.

作者信息

Sato Hiroki, Blemker Michelle A, Hellinghausen Garrett, Armstrong Daniel W, Nafie Jordan W, Roberts Sean T, Krische Michael J

机构信息

Department of Chemistry, University of Texas at Austin, 105 E 24th St. (A5300, Austin, TX, 78712-1167, USA.

Department of Chemistry and Biochemistry, University of Texas at Arlington, 700 Planetarium Place, Arlington, Texas, 76019, USA.

出版信息

Chemistry. 2019 Jul 2;25(37):8719-8724. doi: 10.1002/chem.201902122. Epub 2019 May 27.

DOI:10.1002/chem.201902122
PMID:31070822
Abstract

Cyclometalation of a triple helical N-doped phenylene cage prepared by ruthenium(0)-catalyzed diol-diene benzannulation delivers a chiral, conformationally constrained Ir(ppy) analogue. Like the parent complex, fac-Ir(ppy) , the iridium-containing PAH-cage is phosphorescent, but displays enhanced resistance to oxygen quenching.

摘要

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