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首页> 外文期刊>Chemical science >On–off switch of charge-separated states of pyridine-vinylene-linked porphyrin–C60 conjugates detected by EPR
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On–off switch of charge-separated states of pyridine-vinylene-linked porphyrin–C60 conjugates detected by EPR

机译:通过EPR检测到的吡啶 - 乙烯基连接的吡啶 - 乙烯基连接的卟啉 - 乙烯基连接的卟啉-c 60 缀合物的接通开关

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The design, synthesis, and electronic properties of a new series of D–π–A conjugates consisting of free base (H2P) and zinc porphyrins (ZnP) as electron donors and a fullerene (C60) as electron acceptor, in which the two electroactive entities are covalently linked through pyridine-vinylene spacers of different lengths, are described. Electronic interactions in the ground state were characterized by electrochemical and absorption measurements, which were further supported with theoretical calculations. Most importantly, charge-transfer bands were observed in the absorption spectra, indicating a strong pushpull behavior. In the excited states, electronic interactions were detected by selective photoexcitation under steady-state conditions, by time-resolved fluorescence investigations, and by pump probe experiments on the femto-, pico-, and nanosecond time scales. Porphyrin fluorescence is quenched for the different D–π–A conjugates, from which we conclude that the deactivation mechanisms of the excited singlet states are based on photoinduced energy- and/or electron transfer processes between H2P/ZnP and C60, mediated through the molecular spacers. The fluorescence intensity decreases and the fluorescence lifetimes shorten as the spacer length decreases and as the spacer substitution changes. With the help of transient absorption spectroscopy, the formation of charge-separated states involving oxidized H2P/ZnP and reduced C60 was confirmed. Lifetimes of the corresponding charge-separated states, which ranged from ~400 picoseconds to 165 nanoseconds, depend on the spacer length, the spacer substitution, and the solvent polarity. Interestingly, D–π–A conjugates containing the longest linkers did not necessarily exhibit the longest charge-separated state lifetimes. The distances between the electron donors and the acceptors were calculated by molecular modelling. The longest charge-separated state lifetime corresponded to the D–π–A conjugate with the longest electron donor–acceptor distance. Likewise, EPR measurements in frozen media revealed charge separated states in all the D–π–A conjugates investigated. A sharp peak with g values ~2.000 was assigned to reduced C60, while a broader, less intense signal (g ~ 2.003) was assigned to oxidized H2P/ZnP. On–off switching of the formation and decay of the charge-separated states was detected by EPR at 77 K by repeatedly turning the irradiation source on and off.
机译:新系列D-π-A缀合物的设计,合成和电子性质由自由碱(H 2 p)和锌卟啉(ZnP)为电子作为电子受体的供体和富勒烯(C <小> <亚> 60 ),其中描述了两个电活性实体通过不同长度的吡啶 - 乙烯基间隔物共价连接。地面状态的电子相互作用的特征在于电化学和吸收测量,其进一步支持理论计算。最重要的是,在吸收光谱中观察到电荷转移带,表示强推动 - 拉出行为。在激发的状态下,通过稳态条件下的选择性光筛选检测电子相互作用,通过时间分辨的荧光研究,并通过泵探针对毫微微,微微和纳秒和纳秒的时间尺度进行泵浦实验。卟啉荧光被猝灭,用于不同的D-π-a缀合物,我们得出结论,激发态单位的失活机制基于H 2之间的光突出能量和/或电子转移过程。亚> P / ZNP和C <小> <亚> 60 ,通过分子间隔物介导。荧光强度降低,随着间隔长度的减小并且随着间隔物的取代而变化,荧光寿命缩短。在瞬态吸收光谱的帮助下,涉及氧化H <少> 2 P / ZnP的致电分离状态的形成,并减少C 60 确认。相应的电荷分离状态的寿命范围为〜400 picoSeconds至165纳秒,取决于间隔长度,间隔物替代和溶剂极性。有趣的是,含有最长接头的D-π-缀合物不一定表现出最长的电荷分离状态寿命。通过分子建模计算电子给体和受体之间的距离。最长的电荷分离状态寿命对应于具有最长的电子供体 - 受体距离的D-π-A缀合物。同样地,冷冻介质中的EPR测量显示在所研究的所有D-π-A缀合物中的电荷分离状态。具有 G 值〜2.000的锐峰被分配给减少C 60 ,而更广泛的强烈的信号( G 〜2.003)分配给氧化H <少> <亚> 2 P / ZnP。通过反复打开和关闭辐照源,通过EPR在77K处检测到电荷分离状态的形成和衰减的开关切换。

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