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Sökning: WFRF:(Wells Jordann A. L.) > Sensitization Pathw...

Sensitization Pathways in NIR-Emitting Yb(III) Complexes Bearing 0, +1, +2, or +3 Charges

Mathieu, Emilie (författare)
Uppsala universitet,Institutionen för kemi - Ångström
Kiraev, Salauat R. (författare)
Uppsala universitet,Syntetisk molekylär kemi
Kovacs, Daniel (författare)
Uppsala universitet,Molekylär biomimetik
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Wells, Jordann A. L. (författare)
Uppsala universitet,Syntetisk molekylär kemi
Tomar, Monika (författare)
Uppsala universitet,Syntetisk molekylär kemi
Andres, Julien (författare)
Chemistry and Chemical Engineering Section, Ecole Polytechnique Fédérale de Lausanne (EPFL), BCH 3311, CH-1015 Lausanne, Switzerland
Borbas, K. Eszter (författare)
Uppsala universitet,Syntetisk molekylär kemi
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 (creator_code:org_t)
2022-11-08
2022
Engelska.
Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 144:46, s. 21056-21067
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Yb(III) complexes of macrocyclic ligands based on1,4,7,10-tetraazacyclododecane were synthesized. The ligands carried a carbostyril chromophore for Yb(III) sensitization, and carboxylate or carbamide donors for metal binding, forming complexes of 0, +1, +2, or +3 overall charge. The coordination geometry was little affected by the replacement of carboxylates with amides, as shown by paramagnetic 1H NMR spectroscopy. The Yb(III)/Yb(II) reduction potentials were dependent on the nature of the metal binding site, and the more positively charged complexes were easier to reduce. Carbostyril excitation resulted in Yb(III) luminescence in every complex. The residual carbostyril fluorescence quantum yields were smaller in complexes containing more reducible Yb(III) centers decreasing from 5.9% for uncharged complexes to 3.1−4.4% in +3 charged species, suggesting photoinduced electron transfer (PeT) from the antenna to the Yb(III). The relative Yb(III) luminescence quantum yields were identical within the experimental error, except for the +3 charged complex with fully methylated coordinating amides, which was the most intense Yb(III) emitter of the series in water. Quenching of the Yb(III) excited state by NH vibrations proved to limit Yb(III) emission. No clear improvement of the Yb(III) sensitization efficiency was shown upon faster PeT. This result can be explained by the concomitant sensitization of Yb(III) by phonon-assisted energy transfer (PAEnT) from the antenna triplet excited state, which was completely quenched in all of the Yb complexes. Depopulation of the triplet by PeT quenching of the donor singlet excited state would be compensated by the sensitizing nature of the PeT pathway, thus resulting in a constant overall sensitization efficiency across the series.

Ämnesord

NATURVETENSKAP  -- Kemi -- Oorganisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)
NATURVETENSKAP  -- Kemi -- Annan kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Other Chemistry Topics (hsv//eng)

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