Induction of helical chirality in tetrahedral transition metal complexes with non-bridging monodentate oxazolines

Chirality on C4-atoms of non-bridging monodentate oxazolines direct stereoselective formation of helical chirality in [M(1)<sub>2</sub>X<sub>2</sub>] tetrahedral metal complexes of zinc(II), cadmium(II) and cobalt(II) halides, as revealed by their crystal structures. This feature was used to prepare a set of helically chiral derivatives with various structural motifs. In particular, bulkiness, non-covalent interactions and choice of point chirality combinations were found to strongly affect induction of chirality on the metal atom. The substituent influence on complexation and chiral induction was analyzed using XRD-diffraction studies, NMR, UV-Vis and CD spectroscopies, as well as DFT calculations.

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Publication Details

Journal
Dalton Transactions
Published
2025-01-01
DOI
https://doi.org/10.1039/d5dt02399h
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Induction of helical chirality in tetrahedral transition metal complexes with non-bridging monodentate oxazolines

Zoran Kokan, Srećko I. Kirin, Robert Vianello, Berislav Perić et al.
Dalton Transactions
Axial and Atropisomeric Chirality Synthesis
article

Induction of helical chirality in tetrahedral transition metal complexes with non-bridging monodentate oxazolines

Zoran Kokan, Srećko I. Kirin, Robert Vianello, Berislav Perić, Ernest Sanders, Tamara Rinkovec, Zoran Štefanić, Marija Bakija
article en

Abstract

Chirality on C4-atoms of non-bridging monodentate oxazolines direct stereoselective formation of helical chirality in [M(1)<sub>2</sub>X<sub>2</sub>] tetrahedral metal complexes of zinc(II), cadmium(II) and cobalt(II) halides, as revealed by their crystal structures. This feature was used to prepare a set of helically chiral derivatives with various structural motifs. In particular, bulkiness, non-covalent interactions and choice of point chirality combinations were found to strongly affect induction of chirality on the metal atom. The substituent influence on complexation and chiral induction was analyzed using XRD-diffraction studies, NMR, UV-Vis and CD spectroscopies, as well as DFT calculations.

Dalton TransactionsVol. 54(46)
Ruđer Bošković Institute (HR)
European Commission, Hrvatska Zaklada za Znanost, European Regional Development Fund
Openalex Percentile: Top 75%
Axial and Atropisomeric Chirality Synthesis
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Induction of helical chirality in tetrahedral transition metal complexes with non-bridging monodentate oxazolines — Zoran Kokan, Srećko I. Kirin, et al. · Dalton Transactions (2025) | TGRS Research Map | TGRS