Abstract

AbstractWe describe the preparation of helically chiral gold(I) complexes bearing a [5]helicenic‐N‐heterocyclic carbene ligand. They were successfully obtained as enantiopure compounds by semi‐preparative chiral HPLC and their structural, chiroptical, and photophysical properties were subsequently investigated. Notably, strong electronic circular dichroism, dual emission from singlet and triplet states, with the timescale of the latter up to the millisecond range at room temperature, and moderate circularly phosphorescence were observed. The σ‐donating and π‐accepting properties of the constituent helical ortho‐fused π‐conjugated carbene were investigated by classical quantitative analysis of the IR stretching frequencies and NMR characteristics of the corresponding Ir(CO)2Cl complex and selenourea.

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