Related Experiment Video
Updated: Jan 14, 2026

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
Panchromatic Gold Alkynyl Complexes with Pyrenyl-N-Heterocyclic Carbene Ligand Displaying Anti-Kasha Behavior
Yaping Cheng1, Lilith Ünal2, Geoffrey Gontard1
1Sorbonne Université-Faculté des Sciences et Ingénerie Campus Pierre et Marie Curie, CNRS, IPCM (UMR 8232), 4 place Jussieu, Paris cedex 05, 75252, France.
Abstract:
A unique family of alkynyl-gold(I)-complexes (1-6) containing pyrenyl-NHC chromophoric ligand (NHC = N-heterocyclic carbene) has been prepared and fully characterized. The complexes were engineered such that a pyrenyl ligand was introduced to one nitrogen center of the carbene unit while to the other nitrogen center we attached a methyl (1), n-butyl (2), or naphthyl (3-6) group in order to probe their effect on the photophysical properties of our Au-alkynyl complexes. For comparison purposes the cyanide-gold(I) complex (7) was prepared and fully characterized. The molecular structures of 3 and 4 and 7 were ascertained by X-ray diffraction study. In stark contrast to the alkynyl complexes, the cyano-Au complex 7 displayed only weak fluorescence highlighting the impact of the -C≡C─Ar unit on their emission properties. The alkynyl complexes displayed different behavior, for instance, complex 1 exhibited excimer emissions originated from the pyrene chromophore while compound 2-6 displayed remarkable multi-emissive properties, mainly 3-6 showing panchromatic behavior with emissions dependent on the excitation wavelengths suggesting anti-Kasha behavior. TD-DFT-calculations were carried out to support interpretation of the experimental results. These remarkable results have not been observed previously, making these molecules important candidates for a wide range of applications in the optical domain.
More Related Videos
Related Concept Videos
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
Basicity of Heterocyclic Aromatic Amines
Valence Bond Theory
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Five-Membered Heterocyclic Aromatic Compounds: Overview
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
![[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)
