Wrigley Liam, Hwang Doyk, Pios Sebastian V, Schlenker Cody W
Department of Chemistry, University of Washington, Seattle, Washington 98195, United States.
Zhejiang Laboratory, Hangzhou 311100, China.
ACS Phys Chem Au. 2024 Jul 5;4(6):598-604. doi: 10.1021/acsphyschemau.4c00030. eCollection 2024 Nov 27.
Using trianisole heptazine (TAHz) as a monomeric analogue for carbon nitride, we performed ultrafast pump-photolysis-probe transient absorption (TA) spectroscopy on the intermediate TAHzH heptazinyl radical produced from an excited state PCET reaction with 4-methoxyphenol (MeOPhOH). Our results demonstrate an optically gated photolysis that releases H and regenerates ground state TAHz. The TAHzH radical signature at 520 nm had a lifetime of 7.0 ps, and its photodissociation by the photolysis pulse is clearly demonstrated by the ground state bleach recovery of the closed-shell neutral TAHz. This behavior has been previously predicted as evidence of a dissociative πσ* state. For the first time, we experimentally demonstrate photolysis of the TAHzH heptazinyl radical through a repulsive πσ* state. This is a critical feature of the proposed reaction mechanisms involving water oxidation and CO reduction.
我们使用三苯甲醚七嗪(TAHz)作为氮化碳的单体类似物,对由激发态质子耦合电子转移(PCET)反应与4-甲氧基苯酚(MeOPhOH)产生的中间产物TAHzH七嗪基自由基进行了超快泵浦-光解-探测瞬态吸收(TA)光谱研究。我们的结果表明存在一种光门控光解过程,该过程释放出氢并使基态TAHz再生。520 nm处TAHzH自由基的特征寿命为7.0皮秒,通过闭壳中性TAHz的基态漂白恢复清楚地证明了其被光解脉冲光解离。这种行为先前已被预测为解离性πσ态的证据。我们首次通过排斥性πσ态实验证明了TAHzH七嗪基自由基的光解。这是所提出的涉及水氧化和CO还原的反应机制的一个关键特征。