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A designed and potentially decadentate ligand for use in lanthanide(III) catalysed biomass transformations: targeting diastereoselective trans-4,5-diaminocyclopentenone derivatives

Peewasan, Krisana 1; Merkel, Marcel P. 2; Fuhr, Olaf ORCID iD icon 2,3; Powell, Annie K. 2,4
1 Karlsruher Institut für Technologie (KIT)
2 Institut für Nanotechnologie (INT), Karlsruher Institut für Technologie (KIT)
3 Karlsruhe Nano Micro Facility (KNMF), Karlsruher Institut für Technologie (KIT)
4 Institut für Anorganische Chemie (AOC), Karlsruher Institut für Technologie (KIT)

Abstract:

The goal of this study was to design a ligand system which can accommodate single lanthanide(III)-ions and investigate the properties of the resulting complexes. The complexes of all the accesible lanthanides and yttrium with the new ligand LH6 = N,N′-dimethyl-N,N′-ethylene-bis(5-bromo-3-(1H-benzimidazol-2-yl)hydrazineylidene)-2-hydroxybenzylamine) were obtained in high yield at room temperature under aerobic reaction conditions. The corresponding compounds were characterised using X-ray diffraction, FT-IR, elemental analysis and the optical properties of all complexes were investigated using UV-vis and fluorescence spectroscopy. The air stable complexes efficiently transform biomass furfural to trans-4,5-cyclopentenones in high yield.


Verlagsausgabe §
DOI: 10.5445/IR/1000117607
Veröffentlicht am 09.03.2020
Originalveröffentlichung
DOI: 10.1039/D0DT00183J
Scopus
Zitationen: 9
Dimensions
Zitationen: 8
Cover der Publikation
Zugehörige Institution(en) am KIT Institut für Anorganische Chemie (AOC)
Institut für Nanotechnologie (INT)
Karlsruhe Nano Micro Facility (KNMF)
Publikationstyp Zeitschriftenaufsatz
Publikationsjahr 2020
Sprache Englisch
Identifikator ISSN: 1477-9226, 1477-9234
KITopen-ID: 1000117607
HGF-Programm 43.21.04 (POF III, LK 01) Molecular Engineering
Erschienen in Dalton transactions
Verlag Royal Society of Chemistry (RSC)
Band 49
Heft 7
Seiten 2331–2336
Schlagwörter 2014-013-004854 SCXD
Nachgewiesen in Scopus
Dimensions
Web of Science
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