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Two-photon absorption properties and 1O2 generation ability of Ir complexes: An unexpected large cross section of [Ir(CO)2Cl(4-(para-di-n-butylaminostyryl)pyridine)]

机译:Ir配合物的双光子吸收特性和 1 O 2 生成能力:[Ir(CO) 2 Cl( 4-(对-二-正丁基氨基苯乙烯基)吡啶)]

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摘要

The new complexes cis-[Ir(CO)(2)Cl(4-(para-di-n-butylaminostyryl)pyridine)] (1) and [Ir(cyclometallated-2-phenylpyridine) (2)(4,4'-(para-di-n-butylaminostyryl)-2,2'-bipyridine)][PF6] (3) were synthesized and fully characterized along with the known complex Ir(cyclometallated-2-phenylpyridine)(2)(5-Me-1,10-phenanthroline)][ PF6] (2). Remarkably, complex 1, with an Ir(I) centre, displays fluorescence - as opposed to the phosphorescence typical of many Ir(III) complexes -with a modestly high quantum yield in solution, opening a new route for the design of iridium-based emitters which should not be limited to the +3 oxidation state. It is also characterized by an unexpectedly large two-photon absorption (TPA) cross section, an order of magnitude higher than that previously reported for Ir(III) or Pt(II) complexes. The great potential of cyclometallated Ir(III) complexes for photodynamic therapy was confirmed, with 2 and 3 showing a good singlet oxygen generation ability, coupled with a modest TPA activity for 2.
机译:新的配合物顺式[[Ir(CO)(2)Cl(4-(对-二-正丁基氨基苯乙烯基)吡啶)](1)和[Ir(环金属化-2-苯基吡啶)(2)(4,4' -(对-二-正丁基氨基苯乙烯基)-2,2'-联吡啶)] [PF6](3)与已知的配合物Ir(环金属化-2-苯基吡啶)(2)(5-Me -1,10-菲咯啉)] [PF6](2)。值得注意的是,具有Ir(I)中心的配合物1显示出荧光-与许多Ir(III)配合物的典型磷光相反-在溶液中具有适度的高量子产率,这为铱基设计开辟了一条新途径发射极不应限于+3氧化态。它的特征还在于出乎意料的大双光子吸收(TPA)截面,其数量级比先前报道的Ir(III)或Pt(II)配合物高。证实了环金属化的Ir(III)配合物在光动力疗法方面的巨大潜力,其中2和3显示出良好的单线态氧生成能力,而2的TPA活性适中。

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