ArticleChemistry (Weinheim an der Bergstrasse, Germany)2022
Enhanced Optical Properties of Azaborole Helicenes by Lateral and Helical Extension.
Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Transformation of the Phosphorus Atom in Hexacyclic Polyaromates and Its Impact on Physicochemical Properties.The Journal of organic chemistry · 2026Article
- Taming boroloborinines: toward photostable polycyclic antiaromatic hydrocarbons.Chemical science · 2026Article
- Electrosynthetic access to unsymmetrical oxaza[8]helicenes with high chiral stability and strong circularly polarized luminescence (CPL).Beilstein journal of organic chemistry · 2026Article
- Quantum Chemistry Calculations of Circularly Polarized Luminescence (CPL): From Spectral Modeling to Molecular Design.Chemical reviews · 2025Review
- Boron-containing helicenes as new generation of chiral materials: opportunities and challenges of leaving the flatland.Chemical science · 2024Review
- Azaborahelicene fluorophores derived from four-coordinateOrganic chemistry frontiers : an international journal of organic chemistry · 2024Article
- Synthesis, Structures, and Chiroptical Properties of NBN-Doped Helicenes with Boron Atoms in the Inner Rims.Precision chemistry · 2024Article
- Boosting quantum yields and circularly polarized luminescence of penta- and hexahelicenes by doping with two BN-groups.Chemical science · 2024Article
- (BO)Angewandte Chemie (International ed. in English) · 2023Article
- Enhanced Optical Properties of Azaborole Helicenes by Lateral and Helical Extension.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022Article
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5 authors.
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Abstract
The synthesis and characterization of laterally extended azabora[5]-, -[6]- and -[7]helicenes, assembled from N-heteroaromatic and dibenzo[g,p]chrysene building blocks is described. Formally, the π-conjugated systems of the pristine azaborole helicenes were enlarged with a phenanthrene unit leading to compounds with large Stokes shifts, significantly enhanced luminescence quantum yields (Φ) and dissymmetry factors (g
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