How does chiral self-sorting take place in the formation of homochiral Pd6L8 capsules consisting of cyclotriveratrylene-based chiral tritopic ligands?
Author:
Affiliation:
1. Department of Basic Science
2. Graduate School of Arts and Sciences
3. The University of Tokyo
4. Tokyo 153-8902
5. Japan
6. School of Chemistry
7. University of Leeds
8. Leeds LS2 9JT
9. UK
Abstract
The chiral self-sorting in the formation of homochiral Pd6L8 capsules consisting of cyclotriveratrylene (CTV)-based chiral tritopic ligands and Pd(ii) ions takes place through the initial formation of heterochiral Pd6L8X2 (X indicates a leaving ligand) immature capsules (ICs) followed by the correction of chirality in the ICs assisted by the free tritopic ligands to lead to the homochiral capsules.
Funder
Japan Society for the Promotion of Science
Asahi Glass Foundation
Leverhulme Trust
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/SC/C8SC01062E
Reference20 articles.
1. Making a Right or Left Choice: Chiral Self-Sorting as a Tool for the Formation of Discrete Complex Structures
2. Chiral metallosupramolecular architectures
3. Supramolecular Chirality in Self-Assembled Systems
4. Exciton approach to the optical activity of C3-cyclotriveratrylene derivatives
5. Optical activity due to isotopic substitution. Synthesis, stereochemistry, and circular dichroism of (+)- and (-)-[2,7,12-2H3]cyclotribenzylene
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