Ring size matters: Supramolecular isomerism in self-assembled redox-active tetra- And hexaruthenium macrocycles

Fink D, Orth N, Linseis M, Ivanovic-Burmazovic I, Winter RF (2020)

Publication Type: Journal article

Publication year: 2020

Journal

Chemical Communications Royal Society of Chemistry

Book Volume: 56

Pages Range: 1062-1065

Journal Issue: 7

DOI: 10.1039/c9cc09307a

Abstract

Self-assembly of a divinylthiophene-bridged diruthenium complex with 2,5-furandicarboxylate leads to the formation of two macrocyclic structures that differ solely with regard to their respective nuclearities. Both supramolecular isomers were fully characterized and the conversion of the hexa- to the tetraruthenium macrocycle was followed by NMR monitoring.

Authors with CRIS profile

Nicole Orth Lehrstuhl für Bioanorganische Chemie Ivana Ivanovic-Burmazovic Lehrstuhl für Bioanorganische Chemie

Involved external institutions

Universität Konstanz DE Germany (DE)

How to cite

APA:

Fink, D., Orth, N., Linseis, M., Ivanovic-Burmazovic, I., & Winter, R.F. (2020). Ring size matters: Supramolecular isomerism in self-assembled redox-active tetra- And hexaruthenium macrocycles. Chemical Communications, 56(7), 1062-1065. https://doi.org/10.1039/c9cc09307a

MLA:

Fink, Daniel, et al. "Ring size matters: Supramolecular isomerism in self-assembled redox-active tetra- And hexaruthenium macrocycles." Chemical Communications 56.7 (2020): 1062-1065.

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