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

Org Biomol Chem

College of Pharmaceutical Sciences, Institute of Science and Engineering, Ritsumeikan University, Kusatsu, 525-8577, Japan.

Published: October 2010

Substituents at the boron unit of dipyrrolyldiketone boron complexes as pi-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 alpha-aryl moieties.

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http://dx.doi.org/10.1039/c0ob00044bDOI Listing

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