# Click-Enabled Grafting for Adaptive Chiral Recognition in Porous Crystals

**Authors:** Guillermo Gómez-Tenés, Alechania Misturini, Neyvis Almora-Barrios, Sergio Tatay, Natalia M. Padial, Carlos Martí-Gastaldo

PMC · DOI: 10.1021/jacs.5c17377 · Journal of the American Chemical Society · 2026-01-07

## TL;DR

A new method allows for adaptive chiral recognition in porous crystals by grafting amino acid-derived moieties, improving enantioselectivity.

## Contribution

A modular click chemistry strategy enables adaptive chiral recognition in porous crystals through post-synthetic grafting.

## Key findings

- Histidine-functionalized UiO-68 frameworks show high enantioselectivity for cetirizine.
- Simulations show adaptive interaction pockets formed by local pore reorganization.

## Abstract

Reticular frameworks are promising candidates for chiral
environments,
yet most rely on static stereogenic units, overlooking adaptive host–guest
interactions in enantioselective recognition. We report a modular
postsynthetic click strategy to install amino acid-derived peptidic
moieties into UiO-68 frameworks without compromising crystallinity.
Only the histidine-functionalized material exhibits high enantioselectivity
for cetirizine. Simulations reveal adaptive interaction pockets, emphasizing
the importance of local pore reorganization in chiral molecular recognition.

## Linked entities

- **Chemicals:** cetirizine (PubChem CID 2678)

## Full-text entities

- **Chemicals:** amino acid (MESH:D000596), cetirizine (MESH:D017332), histidine (MESH:D006639), UiO-68 (-)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12833797/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12833797/full.md

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Source: https://tomesphere.com/paper/PMC12833797