Synthesis and Properties of Conjugated Nanohoops Incorporating Dibenzo[a,e]pentalenes: [2]DBP[12]CPPs
Daniel Wassy, Manuel Pfeifer, Birgit Esser
Abstract
Daniel Wassy, Manuel Pfeifer, Birgit Esser
Abstract
Conjugated nanohoops allow studying the effect of cyclic conjugation and bending on the incorporated π-systems. To date, no such system containing antiaromatic units has been reported. We herein present [12]cycloparaphenylenes incorporating two dibenzo[ a, e ]pentalene units: [2]DBP[12]CPP nanohoops. Dibenzo[ a, e ]pentalene is a nonalternant hydrocarbon with antiaromatic character. The syntheses and optoelectronic properties of two different [2]DBP[12]CPP nanohoops with electronically modifying substituents are reported, accompanied by TDDFT calculations.
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Conjugated nanohoops allow studying the effect of cyclic conjugation and bending on the incorporated π-systems. To date, no such system containing antiaromatic units has been reported. We herein present [12]cycloparaphenylenes incorporating two dibenzo[ a, e ]pentalene units: [2]DBP[12]CPP nanohoops. Dibenzo[ a, e ]pentalene is a nonalternant hydrocarbon with antiaromatic character. The syntheses and optoelectronic properties of two different [2]DBP[12]CPP nanohoops with electronically modifying substituents are reported, accompanied by TDDFT calculations.
Key concepts: Pentalene, Antiaromaticity, Conjugated system, Chemistry, Computational chemistry, Stereochemistry, Aromaticity, Organic chemistry