Abstract
New bis-pyrazole complexes [Pt(C^C*)(RpzH)2 ]X, containing a cyclometalated N-heterocyclic carbene ligand (HC^C*=1-(4-(ethoxycarbonyl)phenyl)-3-methyl-1H-imidazol-2-ylidene) were prepared as chloride (X=Cl- , RpzH: 3,5-Me2 pzH 1 a, 4-MepzH 2 a, pzH 3 a), perchlorate (X=ClO4- , 1 b-3 b), or hexafluorophosphate (X=PF6- , RpzH: 3,5-Me2 pzH 1 c) salts. The X-ray structure of 1 a showed that the Cl- anion is trapped by the cation through two N-H⋅⋅⋅Cl bonds. In solution of methanol, acetone and THF at RT, 1 a-3 a coexist in equilibrium with the corresponding [PtCl(C^C*)(RpzH)] (B) and RpzH species. In CH2 Cl2 , this equilibrium takes place just for 2 a and 3 a, but it is completely shifted to the left at 243 and 223 K for 2 a and 3 a, respectively. The low-lying absorption and emission bands were assigned to intraligand (ILCT) charge transfer on the NHC group. Quantum yield measurements in PMMA films revealed that 1 b, 2 b and 1 c are amongst the most efficient blue-light emitters, with values up to 100 %. Proton abstraction from the coordinated 3,5-Me2 pzH in 1 b by NEt3 and replacement by Ag+ afforded a neutral [Pt2 Ag2 ] cluster containing Pt→Ag dative bonds.
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