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Updated: Jan 29, 2026

Variations on Negative Stain Electron Microscopy Methods: Tools for Tackling Challenging Systems
Published on: February 6, 2018
A BN anthracene mimics the electronic structure of more highly conjugated systems
Jacob S A Ishibashi1, Clovis Darrigan, Anna Chrostowska
1Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, USA. shihyuan.liu@bc.edu.
Abstract:
9a,9-BN anthracene was synthesized using a simple three-step sequence involving intramolecular electrophilic borylation of 2-benzylpyridines. The same procedure can be applied to yield a number of substituted 9a,9-BN anthracenes. Spectroscopic characterization of the parental compound (UV-photoelectron spectroscopy, UV-vis absorption/emission) shows an electronic structure more similar to that of a larger conjugated system rather than anthracene, the direct all-carbon analogue.
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