A new triazole-based N-heterocyclic cationic carbene iridium(I) complex with a tetra-fluorido-borate counter-anion, [Ir(CH)(CHN)(CHP)]BF, has been synthesized and structurally characterized. The Ir atom of the cationic complex has an expected square-planar coordination environment with unexceptional bond lengths. There are several close F⋯H contacts between the cations and the anions in the range 2.36-2.58 Å, stabilizing the orientation of the out-sphere [BF ] counter-anion. In the crystal, C-H⋯π(ring) inter-actions are observed that orient the phenyl rings of the tri-phenyl-phosphane ligands.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462289PMC
http://dx.doi.org/10.1107/S2414314621011421DOI Listing

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