首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Ultrafast intersystem crossing and spin dynamics of zinc meso-tetraphenylporphyrin covalently bound to stable radicals
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Ultrafast intersystem crossing and spin dynamics of zinc meso-tetraphenylporphyrin covalently bound to stable radicals

机译:共价键合于稳定基团的介孔四苯基锌卟啉锌的超快体系间穿越和自旋动力学

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摘要

Tert-Butylphenylnitroxide (BPNO?) and α,γ- bisdiphenylene-β-phenylallyl (BDPA?) stable radicals are each attached to zinc meso-tetraphenylporphyrin (ZnTPP) at a fixed distance using one of the ZnTPP phenyl groups. BPNO? and BDPA ? are oriented para (1 and 3, respectively) or meta (2 and 4, respectively) relative to the porphyrin macrocycle. Following photoexcitation of 1-4, transient optical absorption spectroscopy is used to observe excited state quenching of ~1ZnTPP by the radicals and time-resolved electron paramagnetic resonance (TREPR) spectroscopy is used to monitor the spin dynamics of the paramagnetic product states. The presence of BPNO? or BDPA? accelerates the intersystem crossing rate of ~1ZnTPP about 10- to 500-fold in 1-4 depending on the structure compared to that of ~1ZnTPP itself. In addition, the lifetime of ~3ZnTPP in 1 is shorter than that of ~3ZnTPP itself as a result of enhanced intersystem crossing (EISC) from ~3ZnTPP to the ground state. The TREPR spectra of the three unpaired spins produced within 1 and 2 show spin-polarized excited doublet (D_1) and quartet (Q) states and subsequent formation of a spin-polarized ground state radical (D _0). All three signals are absorptive for 1 and emissive for 2. Polarization inversion of the Q state is observed on a tens of nanoseconds time scale in 2, while no polarization inversion is observed for 1. The lack of polarization inversion in 1 is attributed to the short lifetime of the doublet-quartet manifold as a result of the very large exchange interaction. The TREPR spectra of 3 and 4 show ground state radical polarization at X-band (9.5 GHz) at room temperature, but not at 85 K, and similarly no polarization is observed at W-band (94 GHz). No evidence of excited doublet or quartet states is observed, indicating that the exchange interaction is both weak and temperature dependent. These results show that although ultrafast EISC produces ~3ZnTPP within 1-4, the magnitude of the exchange interactions between the three relevant spins in the resulting ~3ZnTPP-BPNO ? and ~3ZnTPP-BDPA? systems dramatically alters their spin dynamics.
机译:叔丁基苯基硝基氧(BPNO 3)和α,γ-双二亚苯基-β-苯基烯丙基(BDPA 2)稳定基团使用ZnTPP苯基之一固定间隔地连接到内消旋四苯基卟啉锌(ZnTPP)上。 BPNO?和BDPA?相对于卟啉大环是对位的(分别为1和3)或间位的(分别为2和4)。 1-4的光激发后,使用瞬态光吸收光谱观察自由基对〜1ZnTPP的激发态猝灭,并使用时间分辨电子顺磁共振(TREPR)光谱监测顺磁性产物状态的自旋动力学。 BPNO的存在吗?还是BDPA?与〜1ZnTPP本身的结构相比,取决于结构,它会加速1-4〜1ZnTPP的系统间交叉速率约10到500倍。另外,〜3ZnTPP在1中的寿命比〜3ZnTPP本身的寿命短,这是由于从〜3ZnTPP到基态的增强的系统间穿越(EISC)。在1和2内产生的三个不成对的自旋的TREPR光谱显示自旋极化的激发双峰(D_1)和四重态(Q)态,以及随后形成的自旋极化基态自由基(D _0)。这三个信号均对1吸收,对2发射。在2的数十纳秒时间尺度上观察到Q状态的极化反转,而对于1则未观察到极化反转。在1中没有极化反转的原因是由于非常大的交换相互作用,导致双重态四联体歧管的寿命很短。 3和4的TREPR光谱在室温下在X波段(9.5 GHz)处显示基态自由基极化,但在85 K时则没有,并且在W波段(94 GHz)上也未观察到极化。没有观察到激发的二重态或四重态的迹象,表明交换相互作用既弱又取决于温度。这些结果表明,尽管超快EISC在1-4之内产生〜3ZnTPP,但在〜3ZnTPP-BPNOβ中三个相关自旋之间的交换相互作用的幅度却很大。和〜3ZnTPP-BDPA?系统会极大地改变其自旋动力学。

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