A quantum chemical model for a series of self-assembled nanocages: the origin of stability behind the coordination-driven formation of transition metal complexes up to [M12L24]24+
Author:
Affiliation:
1. Department of Molecular Engineering
2. Graduate School of Engineering
3. Kyoto University
4. Kyoto 615-8510
5. Japan
6. Graduate School of Informatics
7. Nagoya University
8. Nagoya 464-8601
Abstract
We present a systematic computational model to study the electronic states and free energies of a self-assembled multi-metal complex series.
Funder
Japan Society for the Promotion of Science
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2021/CP/D0CP04755D
Reference73 articles.
1. Self-Assembled M 24 L 48 Polyhedra and Their Sharp Structural Switch upon Subtle Ligand Variation
2. Self-Assembly of M24L48 Polyhedra Based on Empirical Prediction
3. Self-Assembly of M 30 L 60 Icosidodecahedron
4. Self-assembly of tetravalent Goldberg polyhedra from 144 small components
5. Geometrically Restricted Intermediates in the Self‐Assembly of an M 12 L 24 Cuboctahedral Complex
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