Issue 30, 2024

Tuning the dimensionality in chiral and racemic organic/tin hybrids with halides

Abstract

Chiral 1D tin iodides EBASnI3 were synthesized while incorporating enantiomerically pure and racemic ethylbenzylammonium (EBA) cations between the 1D shared inorganic corners. The dimensionality was reduced to 0D when replacing iodine with bromine. In all the cases, the presence of hydrogen bonds was observed between the organic part and the inorganic part, while transfer of chirality was evidenced for the EBASnI3 enantiomerically pure compounds.

Graphical abstract: Tuning the dimensionality in chiral and racemic organic/tin hybrids with halides

Supplementary files

Article information

Article type
Paper
Submitted
05 Jun 2024
Accepted
01 Jul 2024
First published
18 Jul 2024
This article is Open Access
Creative Commons BY-NC license

Dalton Trans., 2024,53, 12755-12763

Tuning the dimensionality in chiral and racemic organic/tin hybrids with halides

L. Caussin, A. Jouaiti, D. Chartrand, W. G. Skene and S. Ferlay, Dalton Trans., 2024, 53, 12755 DOI: 10.1039/D4DT01645A

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