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Correlation between Optical Activity and the Helical Molecular Orbitals of Allene and Cumulenes

Marc H. Garner, Clémence Corminbœuf

2020Organic Letters20 citationsDOIOpen Access PDF

Abstract

cumulenes. Chiral molecules are optically active, but while these molecules are single-handed chiral, π-orbitals of both helicities are present. Here we computationally examine whether the optical activity of chiral cumulenes is controlled by the axial chirality or the helicity of the electronic structure. We exploit hyperconjugation with alkyl, silaalkyl, and germaalkyl substituents to adjust the MO helicity without altering the axial chirality. For the same axial chirality, we observe an inversion of the helical MOs contribution to the electronic transitions and a change of sign in the electronic circular dichroism and optical rotation dispersion spectra. While the magnitude of the chiroptical response also increases, it is similar to that of chiral cumulenes without helical π-orbitals. Overall, helical π-orbitals correlate with the big chiroptical response in cumulenes, but are not a prerequisite for it.

Topics & Concepts

ChemistryChirality (physics)Molecular orbitalAxial chiralityOptical rotationCircular dichroismAtomic orbitalAlleneHelicityCumuleneComputational chemistryMolecular physicsMoleculeStereochemistryPhysicsEnantioselective synthesisOrganic chemistrySymmetry breakingElectronChiral symmetry breakingNambu–Jona-Lasinio modelParticle physicsCatalysisQuantum mechanicsMolecular spectroscopy and chiralitySynthesis and Properties of Aromatic CompoundsAxial and Atropisomeric Chirality Synthesis
Correlation between Optical Activity and the Helical Molecular Orbitals of Allene and Cumulenes | Litcius