Bertran Arnau, Ciuti Susanna, Panariti Daniele, Rogers Ciarán J, Wang Haiqing, Zhao Jianzhang, Timmel Christiane R, Gobbo Marina, Barbon Antonio, Di Valentin Marilena, Bowen Alice M
Centre for Advanced Electron Spin Resonance and Inorganic Chemistry Laboratory, University of Oxford, South Parks Road, Oxford OX1 3QR, UK.
Department of Chemical Sciences, University of Padova, Via Marzolo 1, Padova 35131, Italy.
Phys Chem Chem Phys. 2024 Nov 20;26(45):28398-28405. doi: 10.1039/d4cp02297a.
Electron paramagnetic resonance (EPR) pulsed dipolar spectroscopy (PDS) using triplet states of organic molecules is a growing area of research due to the favourable properties that these transient states may afford over stable spin centers, such as switchability, increased signal intensity when the triplet is formed in a non-Boltzmann distribution and the triplet signal is used for detection, and high orientation selection, when the triplet signal is probed by microwave pulses. This arises due to the large spectral width at low fields, a result of the large zero field splitting, and limited bandwidth of microwave pulses used. Here we propose the triplet state of a substituted BODIPY moiety as a spin label in light induced PDS, coupled to a nitroxide, in a model peptide with a rigid structure. Orientation selection allows information on the relative position of the centres of the two labels to be obtained with respect to the nitroxide reference frame. Additionally, magnetophotoselection effects are employed to introduce optical selection and additional constraints for the determination of the relative orientation of the spin labels considering the reference frame of the triplet state.
利用有机分子三重态的电子顺磁共振(EPR)脉冲偶极光谱(PDS)是一个不断发展的研究领域,这是因为这些瞬态相较于稳定自旋中心可能具有一些有利特性,比如可切换性、当三重态以非玻尔兹曼分布形成且三重态信号用于检测时信号强度增加,以及当用微波脉冲探测三重态信号时具有高取向选择性。这是由于低场下的大光谱宽度,这是大零场分裂的结果,以及所使用微波脉冲的有限带宽。在此,我们提出在具有刚性结构的模型肽中,将取代的BODIPY部分的三重态作为光诱导PDS中的自旋标记,与氮氧自由基耦合。取向选择性使得能够相对于氮氧自由基参考系获得关于两个标记中心相对位置的信息。此外,利用磁光选择效应引入光学选择以及额外的约束条件,以便在考虑三重态参考系的情况下确定自旋标记的相对取向。