Chemistry | 2019
Heat-Resistant Properties in the Phosphorescence of trans-Bis[β-(iminomethyl)aryloxy]platinum(II) Complexes: Effect of Aromaticity on d-π Conjugation Platforms.
Abstract
The heat-resistant properties towards thermal emission quenching of trans-bis[(β-iminomethyl)aryloxy]platinum(II) complexes bearing 3-iminomethyl-2-naphtholato- (1), 1-iminomethyl-2-naphtholato- (2), 2-iminomethyl-1-naphtholato- (3), and 2-iminomethyl-1-phenolato (4) moieties, and a mechanistic rationale of these properties, are described in this report. Complex 1\u2009a, with N,N -dipentyl groups, exhibits intense red emission in 2-methyl-2,3,4,5-tetrahydrofuran (2-MeTHF) at 298\u2005K, whereas the analogues 2\u2009a-4\u2009a are less or non-emissive under the same measurement conditions. All four complexes are highly emissive at 77\u2005K. The heat-resistant properties toward thermal emission quenching (Φ298\u2005K /Φ77\u2005K ) increase in the order 1\u2009a (0.52)>2\u2009a (0.09)>3\u2009a (0.02)>>4\u2009a (0.00). We investigated the emission decay and thermal-deactivation processes using density functional theory (DFT), time-dependent (TD) DFT, and double-hybrid density functional theory (DHDF) calculations of N,N -diethyl forms 1\u2009b-4\u2009b, and discuss the results with a focus on the energy levels, molecular structures, and electronic configurations in the triplet excited states. The energy differences between the triplet metal-ligand charge transfer (3 MLCT) state and minimum-energy crossing point between the lowest triplet state and singlet ground state (MECP) increase in the order 1\u2009a>2\u2009a,\u20093\u2009a>4\u2009a, consistent with the experimental results for the heat-resistant properties of these complexes. The origin of the present structure dependence of the 3 MLCT-MECP energy gap is ascribed to the ease or difficulty of the high-lying dσ* orbital participating in the MECP upon thermal structural distortion. The structure dependence in energy gaps between the π* and dσ* orbitals, which is key for facilitating the thermal deactivation process, is rationally correlated with the extent of aromaticity on the coordination platforms (1\u2009b>(2\u2009b,\u20093\u2009b)>4\u2009b).