Related Experiment Video
Updated: Jun 16, 2025

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Boron-doped double [6]carbohelicenes: a combination of helicene and boron-doped π-systems
Yujia Liu1, Liuzhong Yuan1, Zengming Fan1
1State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University Changchun 130012 P. R. China chuandong@jlu.edu.cn.
Abstract:
Helicenes, featuring unique helical structures, have a long history as three-dimensional polycyclic aromatic hydrocarbons (PAHs). Incorporation of heteroatoms into helicenes may alter their electronic structures and achieve unexpected physical properties. Here, we disclose fusion of boron-doped π-systems onto helicenes as an efficient strategy to design boron-doped carbohelicenes. Two boron-doped double [6]carbohelicenes were synthesized, which possess the C58B2 and C86B2 polycyclic π-skeletons containing two [6]helicene subunits, respectively. The C86B2 molecule thus represents the largest-size helicene-based boron-doped PAH. A thorough investigation reveals that the helicene moieties and boron atoms endow the polycyclic π-systems with delocalized electronic structures, and well-tunable ground-state and excited-state photophysical properties. It is notable that the C58B2 molecule displays excited-state stimulated emission behavior and amplified spontaneous emission (ASE) properties in not only the blend films with various doped concentrations but also the pure film. To our knowledge, it is the first example of ASE-active [n]helicene (n ≥ 6), and moreover, such robust ASE performance has rarely been observed in PAHs, demonstrating the promising utility of boron-doped carbohelicenes for laser materials.
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Hybridization of Atomic Orbitals I
π Molecular Orbitals of 1,3-Butadiene
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

