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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Tuning the emissive triplet excited states of platinum(ii) Schiff base complexes with pyrene, and application for luminescent oxygen sensing and triplet-triplet-annihilation based upconversions
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Tuning the emissive triplet excited states of platinum(ii) Schiff base complexes with pyrene, and application for luminescent oxygen sensing and triplet-triplet-annihilation based upconversions

机译:用pyr调节铂(ii)Schiff碱配合物的发射三重态激发态,并应用于基于发光氧传感和三重态-三重态-灭的上转换

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Pt(ii) Schiff base complexes containing pyrene subunits were prepared using the chemistry-on-complex approach. This is the first time that supramolecular photochemical approach has been used to tune the photophysical properties of Schiff base Pt(ii) complexes, such as emission wavelength and lifetimes. The complexes show intense absorption in the visible region (ε = 13100 M ~(-1) cm~(-1) at 534 nm) and red phosphorescence at room temperature. Notably, much longer triplet excited state lifetimes (τ = 21.0 μs) were observed, compared to the model complexes (τ = 4.4 μs). The extension of triplet excited state lifetimes is attributed to the establishment of equilibrium between the metal-to-ligand charge-transfer (~3MLCT) state (coordination centre localized) and the intraligand (~3IL) state (pyrene localized), or population of the long-lived ~3IL triplet excited state. These assignments were fully rationalized by nanosecond time-resolved difference absorption spectra, 77 K emission spectra and density functional theory calculations. The complexes were used as triplet sensitizers for triplet-triplet-energy-tranfer (TTET) processes, i.e. luminescent O _2 sensing and triplet-triplet annihilation (TTA) based upconversion. The O_2 sensitivity (Stern-Volmer quenching constant) of the complexes was quantitatively evaluated in polymer films. The results show that the O _2 sensing sensitivity of the pyrene containing complex (K SV = 0.04623 Torr~(-1)) is 15-fold of the model complex (K_(SV) = 0.00313 Torr~(-1)). Furthermore, significant TTA upconversion (upconversion quantum yield ΦUC = 17.7% and the anti-Stokes shift is 0.77 eV) was observed with pyrene containing complexes being used as triplet sensitizers. Our approach to tune the triplet excited states of Pt(ii) Schiff base complexes will be useful for the design of phosphorescent transition metal complexes and their applications in light-harvesting, photovoltaics, luminescent O_2 sensing and upconversion, etc.
机译:含on亚基的Pt(ii)Schiff碱配合物是采用复杂化学方法制备的。这是第一次使用超分子光化学方法来调节席夫碱Pt(ii)配合物的光物理性质,例如发射波长和寿命。配合物在可见光区域(534 nm处的ε= 13100 M〜(-1)cm〜(-1))显示出强烈的吸收,并在室温下呈现红色磷光。值得注意的是,与模型络合物(τ= 4.4μs)相比,观察到更长的三重态激发态寿命(τ= 21.0μs)。三重态激发态寿命的延长归因于金属到配体的电荷转移(〜3MLCT)状态(配位中心局部化)和配体的内部(〜3IL)态(py位置局部化)之间的平衡或寿命长的〜3IL三重态激发态。这些分配已通过纳秒级时间分辨的吸收光谱,77 K发射光谱和密度泛函理论计算得到了充分的合理化。该络合物用作三重态-三重态能量转移(TTET)过程的三重态敏化剂,即基于发光的O _2传感和基于三重态-三重态an灭(TTA)的上转换。在聚合物薄膜中定量评估了配合物的O_2敏感性(Stern-Volmer猝灭常数)。结果表明,含complex配合物(K SV = 0.04623 Torr〜(-1))的O _2感测灵敏度是模型配合物(K_(SV)= 0.00313 Torr〜(-1))的15倍。此外,使用含pyr的配合物作为三重态敏化剂时,观察到显着的TTA上转换(上转换量子产率ΦUC= 17.7%,抗斯托克斯位移为0.77 eV)。我们调整Pt(ii)Schiff碱配合物三重激发态的方法将对磷光过渡金属配合物的设计及其在光收集,光伏,O_2发光感应和上转换等方面的应用很有用。

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