A profusion of phospholes: Diacenaphtho[1,2-b:1',2'-d]phospholes, a new class of arene-fused phosphole π-systems, were synthesized and their structural and electrochemical properties studied. The P-sulfide derivative has a high electron-transporting ability (μ(E) =2.4×10(-3) cm(2) V(-1) s(-1)) in a vacuum-deposited film.
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http://dx.doi.org/10.1002/anie.201102782 | DOI Listing |
Chempluschem
January 2021
Department of Molecular Engineering, Graduate School of Engineering, Kyoto University Nishikyo-ku, Kyoto, 615-8510, Japan.
For polycyclic aromatics with heterole-fused structures, the orientation of fused heterole rings as well as the geometry of their fused structures has a large impact on the physicochemical properties. In this study, a series of isomers of thiophene-fused naphthodiphospholes was designed and synthesized. Systematic investigation unveiled the explicit impact of heterole-fused structures on their structural and electronic properties.
View Article and Find Full Text PDFOrg Lett
May 2019
Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences , Nanyang Technological University, Singapore 637371 , Singapore.
Angew Chem Int Ed Engl
August 2011
Department of Molecular Engineering, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Japan.
A profusion of phospholes: Diacenaphtho[1,2-b:1',2'-d]phospholes, a new class of arene-fused phosphole π-systems, were synthesized and their structural and electrochemical properties studied. The P-sulfide derivative has a high electron-transporting ability (μ(E) =2.4×10(-3) cm(2) V(-1) s(-1)) in a vacuum-deposited film.
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