Fink D, Orth N, Ebel V, Gogesch FS, Staiger A, Linseis M, Ivanovic-Burmazovic I, Winter RF (2020)
Publication Type: Journal article
Publication year: 2020
DOI: 10.1021/acs.organomet.0c00116
We report on five tetranuclear metallamacrocycles with particularly large inner voids of up to 19.4 × 18.9 Å. The macrocyclic complexes were obtained by the self-assembly of spatially extended organic dicarboxylate linkers with two different dinuclear bis(alkenyl) diruthenium precursors. The five complexes include one pair of constitutional isomers, complexes 2-NB and 2-BN, which differ with respect to whether the incorporated triarylamine functionality is part of the "conductive" π-conjugated (2-NB) or the insulating dicarboxylate linkers (2-BN). All macrocyclic complexes were characterized by NMR spectroscopy, UHR ESI mass spectrometry, cyclic and square wave voltammetry, and in two instances by X-ray diffraction studies on single crystals. We also investigated the properties of their various oxidized forms via IR/NIR and UV/vis/NIR spectroelectrochemistry as well as by EPR spectroscopy. DFT studies provide further insight into the structural and electronic properties of these compounds.
APA:
Fink, D., Orth, N., Ebel, V., Gogesch, F.S., Staiger, A., Linseis, M.,... Winter, R.F. (2020). Self-Assembled Redox-Active Tetraruthenium Macrocycles with Large Intracyclic Cavities. Organometallics. https://dx.doi.org/10.1021/acs.organomet.0c00116
MLA:
Fink, Daniel, et al. "Self-Assembled Redox-Active Tetraruthenium Macrocycles with Large Intracyclic Cavities." Organometallics (2020).
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