Fron Eduard, Lor Marc, Pilot Roberto, Schweitzer Gerd, Dincalp Haluk, De Feyter Steven, Cremer Jens, Bauerle Peter, Mullen Klaus, Van der Auweraer Mark, De Schryver Frans C
Department of Chemistry, Katholieke Universiteit Leuven, Celestijnenlaan 200 F, 3001, Heverlee, Belgium.
Photochem Photobiol Sci. 2005 Jan;4(1):61-8. doi: 10.1039/b409346c. Epub 2004 Nov 9.
Based on femtosecond time-resolved spectroscopy and single photon timing experiments, intramolecular photoinduced charge transfer has been investigated in two systems containing a peryleneimide chromophore (P) and thiophene (T) groups. The first compound bearing a single thiophene ring (PT1) is used as model and shows a behavior similar to P, studied previously, while in the compound with two thiophene rings attached (PT2) electron transfer from the thiophene donor to the peryleneimide acceptor is observed in benzonitrile. Femtosecond fluorescence upconversion and femtosecond transient absorption experiments in benzonitrile indicate that this ion-pair state formation occurs in 19 ps. This ion-pair state then decays with two time constants of 1400 and 820 ps, probably corresponding to different conformations of the thiophene rings.
基于飞秒时间分辨光谱和单光子计时实验,对两个含有苝酰亚胺发色团(P)和噻吩(T)基团的体系中的分子内光致电荷转移进行了研究。第一个带有单个噻吩环的化合物(PT1)用作模型,表现出与之前研究的P类似的行为,而在连接有两个噻吩环的化合物(PT2)中,在苯甲腈中观察到了从噻吩供体到苝酰亚胺受体的电子转移。在苯甲腈中进行的飞秒荧光上转换和飞秒瞬态吸收实验表明,这种离子对状态的形成发生在19皮秒。然后,这种离子对状态以1400皮秒和820皮秒的两个时间常数衰减,这可能对应于噻吩环的不同构象。