Issue 19, 2010

Modification at a boron unit: tuning electronic and optical properties of π-conjugated acyclic anion receptors

Abstract

Substituents at the boron unit of dipyrrolyldiketone boron complexes as π-conjugated acyclic anion receptors play crucial roles for the tuning of solid-state molecular assemblies, anion-binding behaviour and electronic and optical properties. In particular, emission quantum yields can be significantly tunable by boron substituents and pyrrole α-aryl moieties.

Graphical abstract: Modification at a boron unit: tuning electronic and optical properties of π-conjugated acyclic anion receptors

Supplementary files

Article information

Article type
Paper
Submitted
26 Apr 2010
Accepted
17 Jun 2010
First published
30 Jul 2010

Org. Biomol. Chem., 2010,8, 4308-4315

Modification at a boron unit: tuning electronic and optical properties of π-conjugated acyclic anion receptors

H. Maeda, M. Takayama, K. Kobayashi and H. Shinmori, Org. Biomol. Chem., 2010, 8, 4308 DOI: 10.1039/C0OB00044B

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