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Chirality Sensing of Amino Acid Esters by S-2-Methylbutanamido-Substituted m -Phthalic Diamide-Linked Zinc Bisporphyrinate.

Zhipeng LiYue ZhaoYong WangWen-Hua ZhangChuanjiang Hu
Published in: Molecules (Basel, Switzerland) (2024)
To understand the role of an additional coordination site in the linker in chirality sensing, we designed and synthesized an S-2-methylbutanamido-substituted m -phthalic diamide-linked zinc bisporphyrinate, [Zn 2 (S-MAABis)] and investigated its ability to sense the chirality of amino acid esters. The 1 H NMR spectra and the crystal structure showed that the amido oxygen adjacent to the chiral carbon was coordinated with zinc. NMR and UV-vis titration showed that the binding of [Zn 2 (S-MAABis)] to amino acid esters occurred via two equilibria, forming 1:1 and 1:2 host-guest complexes. The CD spectra suggested that [Zn 2 (S-MAABis)] can effectively recognize the absolute configuration of amino acid esters. The sign of the CD spectra remained unchanged during the titration, indicating that the corresponding 1:1 and 1:2 host-guest complexes had the same chirality. This is different from previously studied amino-substituted m -phthalic diamide-linked zinc bisporphyrinate [Zn 2 (AmBis)], which showed chirality inversion during titration. Theoretical calculations indicated that the additional coordination sites (amido or amino) in the 1:1 host-guest complexes played different roles, leading to differences in chirality. Our studies suggest that the introduction of a coordination site can influence the chirality transfer process, but the results of chirality transfers are dependent on the specific binding modes.
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