Homohelical Self-Assembly of Trimer of α-Cyclodextrin and Octamolybdate.

Inorg Chem

Key Laboratory of the Ministry of Education for Advanced Catalysis Material, Institute of Physical Chemistry, College of Chemistry and Materials Science, Zhejiang Normal University, Jinhua 321004, China.

Published: November 2023

AI Article Synopsis

  • The study addresses the challenge of mimicking biomolecules to create homospiral structures using a blend of inorganic polyoxometalates (POMs) and organic cyclodextrin.
  • Chiral double-helical chains were successfully formed through a specific arrangement of complexes, allowing for chiral transfer from molecules to the larger superstructure.
  • This research enhances the understanding of POM-based materials and demonstrates their potential for selective interactions in chemical applications.

Article Abstract

The ability to conceptually mimic biomolecules to construct emergency-functional homospiral aggregates remains a long-standing challenge. Herein, we report artificial homohelical assembly by blending inorganic polyoxometalates (POMs) and organic cyclodextrin molecules. The chiral double-helical chains have been achieved by a left-hand arrangement of trimer-trimer. The trimer is formed by three {Mo}@α-CD inclusive complexes as a Whittaker-style paddle wheel. During the process of assembly, chiral transfer and amplification from molecule to superstructure were observed. The enantioselective adsorption of the homohelical aggregate toward (R/S)-1,1'-binaphthyl-2,2'-diamine was further demonstrated. The interaction of {Mo} and α-CD in solution was investigated. This work opens a wide scope for the design of a homohelix, enriching POM-based inorganic-organic materials.

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Source
http://dx.doi.org/10.1021/acs.inorgchem.3c03687DOI Listing

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