Excitation‐Dependent Luminescent Properties with Wide Range of Color Changes Using a Liquescent Cationic Gold(I) Complex

The solid form of a bis(trifluoromethanesulfonyl)imide ion salt of a cationic gold(I) complex ligated with cyclohexylisocyanide and an N ‐heterocyclic carbene is found to exhibit excitation‐dependent luminescent properties. The solid form, prepared by maintaining the liquid phase of the complex at 90 °C for 7 days followed by cooling to 25 °C, displays bluish‐purple, purple, orange, and red emissions under excitations at 340, 360, 370, and 380 nm, respectively. Excitation‐dependent emission spectra reveal that the observed color changes result from varying intensity ratios of two emission bands centered at 430 and 652 nm. Control experiments suggest that these excitation‐dependent luminescent properties originate from the coexistence of gold(I)–π aggregates and gold(I)–gold(I)‐interacted oligomers, which exhibit higher and lower bandgap energies, respectively.

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Publication Details

Journal
ChemPhotoChem
Published
2025-04-24
DOI
https://doi.org/10.1002/cptc.202500035
Primary Topic
Organic Light-Emitting Diodes Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Excitation‐Dependent Luminescent Properties with Wide Range of Color Changes Using a Liquescent Cationic Gold(I) Complex

Soichiro Kawamorita, Naoki Ando, Takeshi Naota, Daiki Hishikawa et al.
ChemPhotoChem
Organic Light-Emitting Diodes Research
article

Excitation‐Dependent Luminescent Properties with Wide Range of Color Changes Using a Liquescent Cationic Gold(I) Complex

Soichiro Kawamorita, Naoki Ando, Takeshi Naota, Daiki Hishikawa, Shuichi Suzuki
article en

Abstract

The solid form of a bis(trifluoromethanesulfonyl)imide ion salt of a cationic gold(I) complex ligated with cyclohexylisocyanide and an N ‐heterocyclic carbene is found to exhibit excitation‐dependent luminescent properties. The solid form, prepared by maintaining the liquid phase of the complex at 90 °C for 7 days followed by cooling to 25 °C, displays bluish‐purple, purple, orange, and red emissions under excitations at 340, 360, 370, and 380 nm, respectively. Excitation‐dependent emission spectra reveal that the observed color changes result from varying intensity ratios of two emission bands centered at 430 and 652 nm. Control experiments suggest that these excitation‐dependent luminescent properties originate from the coexistence of gold(I)–π aggregates and gold(I)–gold(I)‐interacted oligomers, which exhibit higher and lower bandgap energies, respectively.

ChemPhotoChemVol. 9(7)
The University of Osaka (JP)
Mazda Foundation, Amano Institute of Technology
Openalex Percentile: Top 93%
Organic Light-Emitting Diodes Research
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