School of Science, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China.
Shandong Province Key Laboratory of Medical Physics and Image Processing Technology, Institute of Materials and Clean Energy, School of Physics and Electronics, Shandong Normal University, Jinan 250014, China.
Spectrochim Acta A Mol Biomol Spectrosc. 2021 Apr 5;250:119244. doi: 10.1016/j.saa.2020.119244. Epub 2020 Nov 26.
Two-photon fluorescent probes with large two-photon absorption (TPA) cross sections have shown wide applications in biomedical domain. However, both the species and amounts of high efficient probes are far from meeting the requirements, one main reason is that the relationship between the molecular structures and the responsive mechanisms are not clear and theoretical framework in this field is not perfect. In this work, the photophysical properties including one- and two-photon absorption and emission of three newly synthesized fluorescent probes for hydrogen polysulfide (HS) detection are investigated by density functional theory and time-dependent density functional theory with the polarizable continuum model in different solvents. Results indicate that the enhanced fluorescent intensity and enlarged TPA cross section can be found when the probes reacted with HS. Moreover, the OPA intensity is largest and its fluorescent intensity is largely enhanced when detecting HS for Pro2, this verifies its superior performance in the detection of HS than Pro1 and Pro 3. Furthermore, the inner mechanism for the increase of TPA cross section is revealed, the responsive mechanisms for photo induced electron transfer (PET) and fluorescence resonance energy transfer (FRET) processes are revealed through analyzing the energies and distributions of frontier orbitals. Our calculations provide theoretical perspectives for experimental measurements and could sever as a useful reference for developing advanced probes in biomedical fields.
双光子荧光探针具有较大的双光子吸收(TPA)截面,在生物医学领域得到了广泛的应用。然而,高效探针的种类和数量远不能满足要求,一个主要原因是分子结构与响应机制之间的关系尚不清楚,该领域的理论框架也不完善。在这项工作中,通过含时密度泛函理论和极化连续模型,在不同溶剂中研究了三种新合成的用于检测氢多硫化物(HS)的荧光探针的光物理性质,包括单光子和双光子吸收和发射。结果表明,探针与 HS 反应时,可以发现荧光强度增强和 TPA 截面增大。此外,Pro2 对 OPA 的强度最大,其荧光强度也大大增强,这验证了其在 HS 检测方面优于 Pro1 和 Pro3。此外,揭示了 TPA 截面增大的内在机制,通过分析前沿轨道的能量和分布,揭示了光诱导电子转移(PET)和荧光共振能量转移(FRET)过程的响应机制。我们的计算为实验测量提供了理论视角,并可为开发生物医学领域的先进探针提供有益参考。