Eng Mattias P, Mårtensson Jerker, Albinsson Bo
Department of Chemical and Biological Engineering, Physical and Organic Chemistry, Chalmers University of Technology, Kemivägen 10, S-412 96, Sweden.
Chemistry. 2008;14(9):2819-26. doi: 10.1002/chem.200701477.
A series of donor-bridge-acceptor (D-B-A) systems with varying donor-acceptor distances has been studied with respect to the temperature dependence of the triplet excitation energy transfer (TEET) rates. The donor and acceptor, zinc(II) and free-base porphyrin, respectively, were separated by oligo-p-phenyleneethynylene (OPE) bridges, where the number of phenyleneethynylene groups was varied between two and five, giving rise to edge-to-edge separations ranging between 12.7 and 33.4 A. The study was performed in 2-MTHF between room temperature and 80 K. It was found that the distance dependence was exponential, in line with the McConnell model, and the attenuation factor, beta, was temperature dependent. The experimentally determined temperature dependence of beta was evaluated by using a previously derived model for the conformational dependence of the electronic coupling based on results from extensive quantum chemical, DFT and time-dependent DFT (TD-DFT), calculations. Two regimes in the temperature interval could be identified: one high-temperature, low-viscosity regime, and one low-temperature, high-viscosity regime. In the first regime, the temperature dependence of beta was, according to the model, well described by a Boltzmann conformational distribution. In the latter, the molecular motions that govern the electronic coupling are slowed down to the same order of magnitude as the TEET rates. This, in effect, leads to a distortion of the conformational distribution. In the high-temperature regime the model could reproduce the temperature dependence of beta, and the extracted rotational barrier between two neighboring phenyl units of the bridge structure, E(i)=1.1 kJ mol(-1), was in line with previous experimental and theoretical studies. After inclusion of parameters that take the viscosity of the medium into account, successful modeling of the experimentally observed temperature dependence of the distance dependence was achieved over the whole temperature interval.
研究了一系列供体-桥-受体(D-B-A)体系,这些体系中供体-受体距离各不相同,研究内容为三重态激发能量转移(TEET)速率的温度依赖性。供体和受体分别为锌(II)和游离碱卟啉,它们由寡聚对苯撑乙炔(OPE)桥隔开,其中苯撑乙炔基团的数量在2到5之间变化,导致边缘到边缘的间距在12.7至33.4埃之间。该研究在2-甲基四氢呋喃中于室温至80K之间进行。发现距离依赖性是指数型的,符合麦康奈尔模型,且衰减因子β与温度有关。基于广泛的量子化学、密度泛函理论(DFT)和含时密度泛函理论(TD-DFT)计算结果,通过使用先前推导的电子耦合构象依赖性模型,对实验测定的β的温度依赖性进行了评估。在温度区间内可识别出两种状态:一种是高温、低粘度状态,另一种是低温、高粘度状态。在第一种状态下,根据模型,β的温度依赖性可用玻尔兹曼构象分布很好地描述。在第二种状态下,控制电子耦合的分子运动减慢到与TEET速率相同的数量级。这实际上导致了构象分布的扭曲。在高温状态下,该模型可以再现β的温度依赖性,并且提取的桥结构中两个相邻苯基单元之间的旋转势垒E(i)=1.1 kJ mol(-1),与先前的实验和理论研究一致。在纳入考虑介质粘度的参数后,在整个温度区间内成功地对实验观察到的距离依赖性的温度依赖性进行了建模。