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锌萘酞菁-次萘酞菁自组装二聚体的电子转移反应:光谱、电化学、计算和光化学研究。

Electron transfer reaction of light harvesting zinc naphthalocyanine-subphthalocyanine self-assembled dyad: spectroscopic, electrochemical, computational, and photochemical studies.

机构信息

Department of Chemistry, Faculty of Science, Kafr El-Sheikh University, Kafr El-Sheikh University, Egypt.

出版信息

Phys Chem Chem Phys. 2010 Oct 21;12(39):12746-52. doi: 10.1039/c0cp00612b. Epub 2010 Aug 27.

Abstract

Electron transfer reaction of a self-assembled donor-acceptor dyad formed by axial coordination of zinc naphthalocyanine, ZnNc, and subphthalocyanine appended with pyridine coordinating ligand, SubPc(py), was investigated in the present study. The SubPc(Py) : ZnNc self-assembled dyad absorbs the light in a wide section of the UV/Vis/NIR spectra. The formation constant of SubPc(py) : ZnNc in o-dichlorobenzene was found to be 1.2 × 10(5) M(-1) from the steady-state absorption and emission measurements, suggesting stable complex formation. The geometric and electronic calculations by using ab initio B3LYP/6-311G methods showed the majority of the highest occupied frontier molecular orbital (HOMO) on the zinc naphthalocyanine entity, while the lowest unoccupied molecular orbital (LUMO) was on the subphthalocyanine entity, suggesting that the charge-separated state of the supramolecular complex is (SubPc(py))˙(-) : ZnNc˙(+). The electrochemical results suggest the exothermic charge-separation process via the singlet states of both SubPc(py) and ZnNc entities. Upon coordination the pyridine appended subphthalocyanine to ZnNc; the main quenching pathway involved charge separation via the singlet excited states of ZnNc and SubPc(py). A clear evidence of the intramolecular electron transfer from the singlet state of ZnNc to SubPc(py) was monitored by femtosecond laser photolysis in o-dichlorobenzene by observing the characteristic absorption band of the ZnNc radical cation in the NIR region at 960 nm. The rate of charge-separation process was found to be 1.3 × 10(10) s(-1), indicating fast and efficient charge separation. The rate of charge recombination and the lifetime of the charge-separated state were found to be 1.0 × 10(9) s(-1) and 1 ns, respectively. The absorption in a wide section of the solar spectrum and high charge-separation/charge-recombination ratio suggests the usefulness of self-assembled SubPc(Py) : ZnNc for being a photosynthetic model.

摘要

本研究考察了轴向配位锌萘酞菁(ZnNc)和吡啶配位配体取代次酞菁(SubPc(py))形成的自组装给体-受体偶联物的电子转移反应。SubPc(Py):ZnNc 自组装偶联物在紫外/可见/近红外光谱的宽波段吸收光。从稳态吸收和发射测量中发现,SubPc(py):ZnNc 在邻二氯苯中的形成常数为 1.2×10(5) M(-1),表明稳定的配合物形成。使用从头算 B3LYP/6-311G 方法进行的几何和电子计算表明,最高占据前线分子轨道(HOMO)的大部分位于锌萘酞菁实体上,而最低未占据分子轨道(LUMO)位于次酞菁实体上,表明超分子复合物的电荷分离态为(SubPc(py))˙(-):ZnNc˙(+)。电化学结果表明,通过 SubPc(py) 和 ZnNc 实体的单重态发生放热电荷分离过程。吡啶取代的次酞菁与 ZnNc 配位后,主要的猝灭途径涉及通过 ZnNc 和 SubPc(py) 的单重激发态进行电荷分离。通过在邻二氯苯中观察到 960nm 处的 NIR 区域的 ZnNc 自由基阳离子的特征吸收带,在飞秒激光光解中监测到从 ZnNc 的单重态到 SubPc(py) 的分子内电子转移的明确证据。发现电荷分离过程的速率为 1.3×10(10) s(-1),表明快速有效的电荷分离。电荷复合速率和电荷分离态的寿命分别为 1.0×10(9) s(-1)和 1ns。自组装 SubPc(Py):ZnNc 在宽光谱段吸收和高电荷分离/复合比表明其在作为光合模型方面的有用性。

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