Stepwise Formation of Iridium(III) Complexes with Monocyclometalating and Dicyclometalating Phosphorus Chelates

作者：Lin Cheng Huei; Lin Chih Yuan; Hung Jui Yi; Chang Yao Yuan; Chi Yun^*; Chung Min Wen; Chang Yuh Chia; Liu Chun; Pan Hsiao An; Lee Gene Hsiang; Chou Pi Tai

来源：Inorganic Chemistry, 2012, 51(3): 1785-1795.

DOI：10.1021/ic202090j

With the motivation of assembling cyclometalated complexes without nitrogen-containing heterocycle, we report here the design and systematic synthesis of a class of Ir(III) metal complexes functionalized with facially coordinated phosphite (or phosphonite) dicyclometalate tripod, together with a variety of phosphine, chelating diphosphine, or even monocyclometalate phosphite ancillaries. Thus, treatment of [IrCl3(tht)(3)] with stoichiometric amount of triphenylphosphite (or diphenyl phenylphosphonite), two equiv of PPh3, and in presence of NaOAc as cyclometalation promoter, gives formation of respective tripodal dicyclometalating complexes [Ir(tpit)(PPh3)(2)Cl] (2a), [Ir(dppit)(PPh3)(2)Cl] (2b), and [Ir(dppit)(PMe2Ph)(2)Cl] (2c) in high yields, where tpitH(2) = triphenylphosphite and dppitH(2) = diphenyl phenylphosphonite. The reaction sequence that afforded these complexes is established. Of particular interest is isolation of an intermediate [Ir(tpitH)(PPh3)(2)Cl-2] (1a) with monocyclometalated phosphite, together with the formation of [Ir(tpit)(tpitH)(PPh3)] (3a) with all tripodal, bidentate, and monodentate phosphorus donors coexisting on the coordination sphere, upon treatment of 2a with a second equiv of triphenylphosphite. Spectroscopic studies were performed to explore the photophysical properties. For all titled Ir(III) complexes, virtually no emission can be observed in either solution at room temperature or 77 K CH2Cl2 matrix. Time-dependent DFT calculation indicates that the lowest energy triplet manifold involves substantial amount of metal centered (MC)-M-3 dd contribution. Due to its repulsive potential energy surface (PES) that touches the PES of ground state, the (MC)-M-3 dd state executes predominant nonradiative deactivation process.

• 出版日期2012-2-6
• 单位清华大学