Post‐Assembly Modification of Homochiral Titanium–Organic Cages for Recognition and Separation of Molecular Isomers
A chiral metal–organic cage (MOC) was extended and fixed into a porous framework using a post‐assembly modification strategy, which made it easier to study the host–guest chemistry of the solid‐state MOC using a single‐crystal diffraction technique. Anionic Ti4L6 (L=embonate) cage can be used as a 4...
Saved in:
Published in | Angewandte Chemie International Edition Vol. 62; no. 16; pp. e202300726 - n/a |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
11.04.2023
|
Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | A chiral metal–organic cage (MOC) was extended and fixed into a porous framework using a post‐assembly modification strategy, which made it easier to study the host–guest chemistry of the solid‐state MOC using a single‐crystal diffraction technique. Anionic Ti4L6 (L=embonate) cage can be used as a 4‐connecting crystal engineering tecton, and its optical resolution was achieved, thus homochiral ΔΔΔΔ‐ and ΛΛΛΛ‐[Ti4L6] cages were obtained. Accordingly, a pair of homochiral cage‐based microporous frameworks (PTC‐236(Δ) and PTC‐236(Λ)) were easily prepared by a post‐assembly reaction. PTC‐236 has rich recognition sites provided by the Ti4L6 moieties, chiral channels and high framework stability, affording a single‐crystal‐to‐single‐crystal transformation for guest structure analyses. Thus it was successfully utilized for the recognition and separation of isomeric molecules. This study provides a new approach for the orderly combination of well‐defined MOCs into functional porous frameworks.
A chiral metal–organic cage has been extended and introduced into a porous framework by using a post‐assembly modification strategy. The microporous frameworks were successfully utilized for the recognition and separation of isomeric molecules, including aromatic compounds, nitriles, and chiral aromatic alcohols. |
---|---|
Bibliography: | These authors contributed equally to this work. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1433-7851 1521-3773 1521-3773 |
DOI: | 10.1002/anie.202300726 |