Reversible stimuli-responsive luminescence of bimetallic cuprous complexes based on NH-deprotonated 3-(2′-pyridyl)pyrazole
Color regulation of solid-state luminescence is desirable and challenging. Herein, we report two new three- and four-coordinate bimetallic cuprous complexes 1 and 2 , which bear a NH-deprotonated 3-(2′-pyridyl)pyrazole adopting the monoanionic tridentate μ-η 1 (N)η 2 (N,N) bonding mode and exhibit r...
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Veröffentlicht in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2021-12, Vol.9 (46), p.16664-16671 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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Zusammenfassung: | Color regulation of solid-state luminescence is desirable and challenging. Herein, we report two new three- and four-coordinate bimetallic cuprous complexes
1
and
2
, which bear a NH-deprotonated 3-(2′-pyridyl)pyrazole adopting the monoanionic tridentate μ-η
1
(N)η
2
(N,N) bonding mode and exhibit reversible stimuli-responsive luminescence. It is revealed that the reversible stimuli-responsive luminescence for
1
and
2
is triggered by the destruction and restoration of orderly molecular stacking, along with the loss and recovery of the CH
2
Cl
2
solvent molecules for
1
. Virtually, this reversible stimuli-responsive luminescence originates from the breaking and rebuilding of various CH O hydrogen bonds around ClO
4
−
, as supported by X-ray single-crystal analysis, the
1
H NMR spectra, and the PXRD and FT-IR spectra in various forms. In addition, the possible applications of this reversible stimuli-responsive luminescence have also been investigated.
Reversible stimuli-responsive luminescence virtually stems from the breaking and rebuilding of various CH O hydrogen bonds around ClO
4
−
, as supported by single-crystal analysis, the
1
H NMR spectra, and the PXRD and FT-IR spectra in various forms. |
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ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/d1tc03864h |