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Immobilization of a copper complex based on the tripodal ligand (2-aminoethyl)bis(2-pyridylmethyl)amine (uns-penp)

Titelangaben

Brückmann, Tim ; Becker, Jonathan ; Turke, Kevin ; Smarsly, Bernd M. ; Weiß, Morten ; Marschall, Roland ; Schindler, Siegfried:
Immobilization of a copper complex based on the tripodal ligand (2-aminoethyl)bis(2-pyridylmethyl)amine (uns-penp).
In: Zeitschrift für anorganische und allgemeine Chemie. Bd. 647 (2021) Heft 5 . - S. 560-571.
ISSN 1521-3749
DOI: https://doi.org/10.1002/zaac.202100022

Abstract

A new derivative of the ligand (2-aminoethyl)bis(2-pyridylmethyl)amine (uns-penp), capable for covalent immobilization on silica, was synthesized. Silica powder for column chromatography and mesoporous monoliths served as surface material. Functionalized silica was sufficiently characterized with reflectance UV/Vis and FTIR techniques. Copper(I) was successfully complexed with the immobilized ligand and exhibits reversible reactivity towards dioxygen at low temperatures. Suspending the oxygen species with toluene at low temperatures led to selective oxygenation to benzaldehyde, determined by GC-MS. Copper(I) complexes with the ligands Me-PTS-uns-penp and Me-Prop-uns-penp were prepared and characterized to model the reaction behavior towards dioxygen in solution. Additionally, solid copper peroxido complexes with these ligands were obtained by precipitation with the sterically demanding anion tetraphenylborate. Furthermore, these complexes could be obtained in a reversible reaction by treating corresponding copper(I) complexes with dioxygen. With all oxygenated copper complexes catalytic oxidation of toluene was observed.

Weitere Angaben

Publikationsform: Artikel in einer Zeitschrift
Begutachteter Beitrag: Ja
Keywords: immobilization; monolith; copper complex; tripodal ligands; superoxido complex
Institutionen der Universität: Fakultäten > Fakultät für Biologie, Chemie und Geowissenschaften > Fachgruppe Chemie
Fakultäten
Fakultäten > Fakultät für Biologie, Chemie und Geowissenschaften
Titel an der UBT entstanden: Nein
Themengebiete aus DDC: 500 Naturwissenschaften und Mathematik > 540 Chemie
Eingestellt am: 24 Sep 2021 06:51
Letzte Änderung: 07 Jun 2022 11:47
URI: https://eref.uni-bayreuth.de/id/eprint/67098