首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Theoretical Insights into the Phosphorescence Quantum Yields of Cyclometalated (C boolean AND C*) Platinum(II) NHC Complexes: pi-Conjugation Controls the Radiative and Nonradiative Decay Processes
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Theoretical Insights into the Phosphorescence Quantum Yields of Cyclometalated (C boolean AND C*) Platinum(II) NHC Complexes: pi-Conjugation Controls the Radiative and Nonradiative Decay Processes

机译:环金属化(C布尔和C *)铂(II)NHC配合物的磷光量子产率的理论见解:π共轭控制辐射和非辐射衰变过程。

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In this article, the radiative and nonradiative decay processes of four cyclometalated (C<^>C*) platinum(II) N-heterocyclic carbene (NHC) complexes were unveiled via density functional theory and time-dependent density functional theory. In order to explore the influence of pi-conjugation on quantum yields of (NHC)Pt(acac) (NHC=N-heterocyclic carbene, acac = acetylacetonate) complexes, the factors that determine the radiative process, including singlet triplet splitting energies, transition dipole moments, and spin orbit coupling (SOC) matrix elements between the lowest triplet states and singlet excited states were calculated. In addition, the SOC matrix elements between the lowest triplet state and the ground state as well as Huang-Rhys factors were also computed to describe the temperature independent nonradiative decay processes. Also, the triplet potential energy surfaces were investigated to elucidate the temperature-dependent nonradiative decay processes. The results indicate that complex Pt-1 has higher radiative decay rate than complexes Pt-2-4 due to the larger SOC matrix elements between the lowest triplet states and singlet excited states. However, complexes Pt-2-4 have smaller Huang-Rhys factors, smaller SOC matrix elements between the lowest triplet and the ground states, and higher active energy barriers than complex Pt-1, indicating that complexes Pt-2-4 have smaller nonradiative decay rate constants. According to these results, one may discern why complex Pt-2 has higher phosphorescence quantum efficiency than complex Pt-1; meanwhile, it can be inferred that the nonradiative decay process plays an important role in the whole photodeactivation process. In addition, on the basis of complex Pt-2, Pt-5 was designed to investigate the influence of substitution group on the photodeactivation process of rigid (NHC)Pt(acac) complex.
机译:在本文中,通过密度泛函理论和时变密度泛函理论揭示了四种环金属化的(C ^ C *)铂(II)N-杂环卡宾(NHC)配合物的辐射和非辐射衰变过程。为了探索π共轭对(NHC)Pt(acac)(NHC = N-杂环卡宾,acac =乙酰丙酮)络合物的量子产率的影响,决定辐射过程的因素包括单重态三重态分裂能,跃迁计算了最低三重态和单重态激发态之间的偶极矩和自旋轨道耦合(SOC)矩阵元素。此外,还计算了最低三重态与基态之间的SOC矩阵元素以及Huang-Rhys因子,以描述与温度无关的非辐射衰变过程。此外,研究了三重态势能表面,以阐明与温度有关的非辐射衰变过程。结果表明,由于最低三重态与单重激发态之间较大的SOC矩阵元素,复合物Pt-1具有比复合物Pt-2-4更高的辐射衰减率。然而,复合物Pt-2-4具有较小的Huang-Rhys因子,在最低的三重态与基态之间的SOC矩阵元素较小,并且与复合物Pt-1相比具有更高的活性能垒,这表明复合物Pt-2-4具有较小的非辐射衰减率常数。根据这些结果,可以看出为什么复合物Pt-2具有比复合物Pt-1更高的磷光量子效率。同时,可以推断出非辐射衰变过程在整个光灭活过程中起着重要作用。此外,在配合物Pt-2的基础上,设计了Pt-5来研究取代基对刚性(NHC)Pt(acac)配合物光致失活过程的影响。

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