Coronene (also known as superbenzene and cyclobenzene) is a polycyclic aromatic hydrocarbon (PAH) comprising seven peri-fused benzene rings. [10] Its chemical formula is C 24 H 12. It is a yellow material that dissolves in common solvents including benzene, toluene, and dichloromethane. Its solutions emit blue light fluorescence under UV light.

Jan 22, 2009 · Coronene is a ortho- and peri-fused polycyclic arene that consists of six peri-fused benzene rings. Coronene is one of over 100 different polycyclic aromatic hydrocarbons (PAHs). PAHs are chemicals that are formed during the incomplete burning organic substances, such as …

Coronene, C24H12, is a D6h symmetric polycyclic compound composed from one central and six adjacent C6-rings. From: Advances in Organometallic Chemistry, 2013

Mar 22, 2023 · Single aromatic ring benzene and coronene, in which benzene is fully enclosed by a layer of outer fused rings, are readily available, but the next molecule in the series — circumcoronene, fully...

ChemSpider record containing structure, synonyms, properties, vendors and database links for Coronene, 191-07-1, 658468, VPUGDVKSAQVFFS-UHFFFAOYSA-N

Apr 3, 2013 · Gas basicity (review) (kJ/mol) Reference Comment; 836.8: Aue, Guidoni, et al., 2000: Experimental literature data re-evaluated by the authors using ab initio protonation entropies; MM

Feb 1, 2021 · In the present review, we highlight the modern aspects of syntheses related to or different from the strategies used in the early era of coronene research. Systematic extension and expansion of coronene backbones to wide categories of angular PAHs are covered.

May 10, 2016 · Here we show that by crystallizing the polyaromatic hydrocarbon coronene in the presence of a magnetic field, a polymorph is formed in a β-herringbone structure instead of the ubiquitous...

Aldrich-C84801; Coronene 0.97; CAS Number: 191-07-1; Linear Formula: C24H12; find related products, papers, technical documents, MSDS & more at Sigma-Aldrich.

Mar 15, 2021 · In the present review, we highlight the modern aspects of syntheses related to or different from the strategies used in the early era of coronene research. Systematic extension and expansion of coronene backbones to wide categories of angular PAHs are covered.