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Anion Recognition-Directed Supramolecular Catalysis with Functional Macrocycles and Molecular Cages. | LitMetric

Anion Recognition-Directed Supramolecular Catalysis with Functional Macrocycles and Molecular Cages.

Acc Chem Res

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

Published: November 2024

AI Article Synopsis

  • The text discusses the advancements in supramolecular chemistry, particularly focusing on how host molecules and noncovalent interactions can enhance catalytic processes through supramolecular catalysis.
  • It highlights the significance of macrocyclic and cage-like compounds which mimic enzymes and possess unique recognition features, emphasizing the underutilization of directional binding sites in traditional host molecules.
  • The study introduces a novel approach using tailor-made functionalized macrocycles and cages specifically designed for anion recognition, which enhances catalytic efficiency and stereocontrol in reactions by leveraging strong anion binding and cooperative interactions.

Article Abstract

ConspectusThe development of supramolecular chemistry has provided a variety of host molecules and noncovalent tools for boosting catalytic processes, stimulating the emergence and advance of supramolecular catalysis, among which macrocyclic and cage-like compounds have attracted great attention due to their possession of an enzyme-mimetic cavity and recognition ability. While the privileged scaffolds such as crown ethers, cyclodextrins, cucurbiturils, calixarenes, and metal-coordinated cages have been widely used, their skeletons usually do not contain a directional binding site; binding and activation mainly rely on cation-associated interactions or hydrophobic effects. In this context, the recent advance of anion supramolecular chemistry has drawn our attention to developing an anion recognition-directed approach by using tailor-made functionalized macrocycles and cages. Anions are important widely existing species in both biological and chemical systems and play an important role in regulating the structure and function of enzymes. We envisioned that by taking advantage of anions, including their rich variety, diverse geometry, and multiple interaction sites, the sophisticated cooperation of multiple noncovalent interactions can be manipulated in a confined cavity for directing efficient and selective catalysis.Following this concept, we initiated our study by introducing typical thiourea H-bonding groups to design and synthesize a series of bis-thiourea macrocycles, especially chiral macrocycles, by incorporating chiral linkers. Taking advantage of the obtained strong, cooperative anion binding, a macrocycle-enabled counteranion trapping strategy was developed, which afforded greatly enhanced catalytic efficiency and excellent stereocontrol in acid-catalyzing reactions. Furthermore, inspired by sulfate-induced macrocyclic dimerization assembly, we built a substrate-induced assembly system, enabling an induced-fit cooperative activation network for efficient and enantioselective catalysis. In addition, anion recognition-driven chirality gearing with a more sophisticated trithiourea cage was revealed, which could provide a basis for implementing anion-triggered allosteric catalysis within the induced helical space. Not limited to hydrogen bonding, the emerging anion-π interactions were largely exploited. A series of triazine-based prism cages containing three V-shaped electron-deficient π-cavities were constructed, and their anion-π binding properties were studied. Based on this system, cooperative anion-π activation was established for driving highly efficient and selective catalysis, which paved a way to push anion-π interactions toward more practical and useful catalyst design.These results demonstrated that the anion-recognition direction can serve as a powerful, versatile approach for boosting highly efficient and selective supramolecular catalysis. It is feasible not only for employing exogenous anions (e.g., counteranion) as a handle but also for recognition and regulation of anionic active intermediates/transition states, from use in conventional H-bonding to emerging anion-π recognition.

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Source
http://dx.doi.org/10.1021/acs.accounts.4c00583DOI Listing

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