ArticleAngewandte Chemie (International ed. in English)2021
Chiral Self-sorting of Giant Cubic [8+12] Salicylimine 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 28 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
28 citing papers in PubMed.
- Ion-Permselective Porous Organic Cage Membranes.Angewandte Chemie (International ed. in English) · 2026Review
- From triangles to squares - chiral, overcrowded polyimine macrocycles of significant chiroptical response enable the capture of chlorinated solvents.Scientific reports · 2026Article
- Intermolecular Stacking-Instructed Chiral Preference in Covalent 2 + 2 Macrocyclization.JACS Au · 2026Article
- Structural control of dynamic covalent cages: kineticChemical science · 2025Article
- Homochiral Self-Sorting During Macrocycle Formation and their Chiroptical Properties.ChemistryOpen · 2025Article
- Chiral covalent organic cages: Construction and chiral functions.Smart molecules : open access · 2025Review
- Engineering a Surfactant Trap via Postassembly Modification of an Imine Cage.Chemistry of materials : a publication of the American Chemical Society · 2024Article
- Social Self-Sorting of Quasi-Racemates: A Unique Approach for Dual-Pore Molecular Crystals.Journal of the American Chemical Society · 2024Article
- Triamine and Tetramine Edge-Length Matching Drives Heteroleptic Triangular and Tetragonal Prism Assembly.Journal of the American Chemical Society · 2024Article
- Smart touchless human-machine interaction based on crystalline porous cages.Nature communications · 2024Article
- Stereocontrolled Self-Assembly of a Helicate-Bridged CuJournal of the American Chemical Society · 2024Article
- Self-similar chiral organic molecular cages.Nature communications · 2024Article
- The sharp structural switch of covalent cages mediated by subtle variation of directing groups.Nature communications · 2023Article
- Dynamic covalent self-assembly and self-sorting processes in the formation of imine-based macrocycles and macrobicyclic cages.Chemical science · 2023Article
- Purely Covalent Molecular Cages and Containers for Guest Encapsulation.Chemical reviews · 2022Review
- Heterochiral Diastereomer-Discriminative Diphanes That Form Hierarchical Superstructures with Nonlinear Optical Properties.JACS Au · 2022Article
- Chiral self-sorting and guest recognition of porous aromatic cages.Nature communications · 2022Article
- Enantioselective assembly and recognition of heterochiral porous organic cages deduced from binary chiral components.Chemical science · 2022Article
- Article
- Chiral proline-substituted porous organic cages in asymmetric organocatalysis.Chemical science · 2022Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
Chiral self-sorting is intricately connected to the complicated chiral processes observed in nature and no artificial systems of comparably complexity have been generated by chemists. However, only a few examples of purely organic molecules have been reported so far, where the self-sorting process could be controlled. Herein, we describe the chiral self-sorting of large cubic [8+12] salicylimine cage compounds based on a chiral TBTQ precursor. Out of 23 possible cage isomers only the enantiopure and a meso cage were observed to be formed, which have been unambiguously characterized by single crystal X-ray diffraction. Furthermore, by careful choice of solvent the formation of meso cage could be controlled. With internal diameters of d
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.