ArticleAngewandte Chemie (International ed. in English)2021
Isoreticular Crystallization of Highly Porous Cubic Covalent Organic Cage Compounds*.
Article in Angewandte Chemie (International ed. in English), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
11 citing papers in PubMed.
- Ion-Permselective Porous Organic Cage Membranes.Angewandte Chemie (International ed. in English) · 2026Review
- Dynamic Covalent Radical Recombination for the Assembly of Tuneable Responsive Porous Organic Cages.Angewandte Chemie (International ed. in English) · 2026Article
- A robust boronic acid-integrated olefin-linked covalent organic framework for high-performance enrichment of glycopeptides and determination in laryngeal cancer serum.Mikrochimica acta · 2026Article
- Structural control of dynamic covalent cages: kineticChemical science · 2025Article
- A Water-Stable Boronate Ester Cage.Journal of the American Chemical Society · 2024Article
- COChemistry (Weinheim an der Bergstrasse, Germany) · 2022Article
- Purely Covalent Molecular Cages and Containers for Guest Encapsulation.Chemical reviews · 2022Review
- Enantioselective assembly and recognition of heterochiral porous organic cages deduced from binary chiral components.Chemical science · 2022Article
- Chiral proline-substituted porous organic cages in asymmetric organocatalysis.Chemical science · 2022Article
- Water-stable hydrazone-linked porous organic cages.Chemical science · 2021Article
- Isoreticular Crystallization of Highly Porous Cubic Covalent Organic Cage Compounds*.Angewandte Chemie (International ed. in English) · 2021Article
Corrections and comments
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Authors and funding
7 authors.
Funding
Abstract
Modular frameworks featuring well-defined pore structures in microscale domains establish tailor-made porous materials. For open molecular solids however, maintaining long-range order after desolvation is inherently challenging, since packing is usually governed by only a few supramolecular interactions. Here we report on two series of nanocubes obtained by co-condensation of two different hexahydroxy tribenzotriquinacenes (TBTQs) and benzene-1,4-diboronic acids (BDBAs) with varying linear alkyl chains in 2,5-position. n-Butyl groups at the apical position of the TBTQ vertices yielded soluble model compounds, which were analyzed by mass spectrometry and NMR spectroscopy. In contrast, methyl-substituted cages spontaneously crystallized as isostructural and highly porous solids with BET surface areas and pore volumes of up to 3426 m
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Registered trials
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