Bio‐Templated Chiral Zeolitic Imidazolate Framework for Enantioselective Chemoresistive Sensing

Author:

Kim Minkyu1ORCID,Han Moon Jong1,Lee Hansol1,Flouda Paraskevi1ORCID,Bukharina Daria1ORCID,Pierce Kellina J.1,Adstedt Katarina M.1,Buxton Madeline L.1ORCID,Yoon Young Hee2,Heller William T.3ORCID,Singamaneni Srikanth4ORCID,Tsukruk Vladimir V.1ORCID

Affiliation:

1. School of Materials Science & Engineering Georgia Institute of Technology Atlanta GA 30332 USA

2. School of Chemical & Biomolecular Engineering Georgia Institute of Technology Atlanta GA 30332 USA

3. Neutron Scattering Division Oak Ridge National Laboratory Oak Ridge TN 37831 USA

4. Department of Mechanical Engineering and Materials Science Institute of Materials Science and Engineering Washington University in St. Louis St Louis MO 63130 USA

Abstract

AbstractChiral metal–organic frameworks (MOFs) have gained rising attention as ordered nanoporous materials for enantiomer separations, chiral catalysis, and sensing. Among those, chiral MOFs are generally obtained through complex synthetic routes by using a limited choice of reactive chiral organic precursors as the primary linkers or auxiliary ligands. Here, we report a template‐controlled synthesis of chiral MOFs from achiral precursors grown on chiral nematic cellulose‐derived nanostructured bio‐templates. We demonstrate that chiral MOFs, specifically, zeolitic imidazolate framework (ZIF), unc‐[Zn(2‐MeIm)2, 2‐MeIm=2‐methylimidazole], can be grown from regular precursors within nanoporous organized chiral nematic nanocelluloses via directed assembly on twisted bundles of cellulose nanocrystals. The template‐grown chiral ZIF possesses tetragonal crystal structure with chiral space group of P41, which is different from traditional cubic crystal structure of I‐43 m for freely grown conventional ZIF‐8. The uniaxially compressed dimensions of the unit cell of templated ZIF and crystalline dimensions are signatures of this structure. We observe that the templated chiral ZIF can facilitate the enantiotropic sensing. It shows enantioselective recognition and chiral sensing abilities with a low limit of detection of 39 μM and the corresponding limit of chiral detection of 300 μM for representative chiral amino acid, D‐ and L‐ alanine.

Funder

National Science Foundation

Air Force Office of Scientific Research

National Research Foundation of Korea

Publisher

Wiley

Subject

General Medicine

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