Solvent Induced Helix Folding of Defined Indolenine Squaraine Oligomers

Turkin A, Holzapfel M, Agarwal M, Fischermeier D, Mitric R, Schweins R, Gröhn F, Lambert C (2021)


Publication Type: Journal article

Publication year: 2021

Journal

DOI: 10.1002/chem.202101063

Abstract

A protecting group strategy was employed to synthesise a series of indolenine squaraine dye oligomers up to the nonamer. The longer oligomers show a distinct solvent dependence of the absorption spectra, that is, either a strong blue shift or a strong red shift of the lowest energy bands in the near infrared spectral region. This behaviour is explained by exciton coupling theory as being due to H- or J-type coupling of transition moments. The H-type coupling is a consequence of a helix folding in solvents with a small Hansen dispersity index. DOSY NMR, small angle neutron scattering (SANS), quantum chemical and force field calculations agree upon a helix structure with an unusually large pitch and open voids that are filled with solvent molecules, thereby forming a kind of clathrate. The thermodynamic parameters of the folding process were determined by temperature dependent optical absorption spectra.

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APA:

Turkin, A., Holzapfel, M., Agarwal, M., Fischermeier, D., Mitric, R., Schweins, R.,... Lambert, C. (2021). Solvent Induced Helix Folding of Defined Indolenine Squaraine Oligomers. Chemistry - A European Journal. https://doi.org/10.1002/chem.202101063

MLA:

Turkin, Arthur, et al. "Solvent Induced Helix Folding of Defined Indolenine Squaraine Oligomers." Chemistry - A European Journal (2021).

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