Trinuclear complexes and coordination polymers of redox-cctive guanidino-functionalized aromatic (GFA) compounds with a triphenylene core

Herein, we report on the synthesis, redox activity, and coordination chemistry of 2,3,6,7,10,11-hexakis(tetramethylguanidino)triphenylene. CV measurements indicated that the new compound could be oxidized in three separate reversible two-electron oxidation events. The HOMO and LUMO energies were est...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Lebkücher, Anna (VerfasserIn) , Wagner, Christoph (VerfasserIn) , Hübner, Olaf (VerfasserIn) , Kaifer, Elisabeth (VerfasserIn) , Himmel, Hans-Jörg (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: September 4, 2014
In: Inorganic chemistry
Year: 2014, Jahrgang: 53, Heft: 18, Pages: 9876-9896
ISSN:1520-510X
DOI:10.1021/ic501482u
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/ic501482u
Volltext
Verfasserangaben:Anna Lebkücher, Christoph Wagner, Olaf Hübner, Elisabeth Kaifer, and Hans-Jörg Himmel
Beschreibung
Zusammenfassung:Herein, we report on the synthesis, redox activity, and coordination chemistry of 2,3,6,7,10,11-hexakis(tetramethylguanidino)triphenylene. CV measurements indicated that the new compound could be oxidized in three separate reversible two-electron oxidation events. The HOMO and LUMO energies were estimated from the oxidation wave and the onset of absorption in the UV/vis spectrum. Our discussion also includes the related new compound 2,3,6,7,10,11-hexakis(N,N′-dimethylethyleneguanidino)triphenylene. Then trinuclear CuI and CuII complexes of the new triphenylene ligands were characterized, and their electronic properties are discussed. In contrast to previously studied redox-active GFA ligands, oxidation of trinuclear copper(I) iodide complexes with I2 leads to copper instead of ligand oxidation. In the tetra-coordinated CuII complexes, the coordination mode is intermediate between tetrahedral and square planar. The optical properties of the complexes were studied, and low-energy electronic transitions were assigned to ligand-to-metal charge-transfer (LMCT) excitations. We then extended our analysis to trinuclear NiII and CoII complexes. The magnetic coupling mediated through the triphenylene ligand in the trinuclear CuII and CoII complexes was studied by SQUID magnetometry, revealing ferromagnetic coupling of the spin centers and different degrees of spin delocalization into the guanidino groups. Finally, we show that the GFA ligands could be linked to one- or two-dimensional coordination polymers and porous materials with a layer structure by reaction with silver halides.
Beschreibung:Gesehen am 07.08.2020
Beschreibung:Online Resource
ISSN:1520-510X
DOI:10.1021/ic501482u