Hoang Hao Minh, Pham Van Thi Bich, Grampp Günter, Kattnig Daniel R
Ho Chi Minh City University of Technology and Education, Vo Van Ngan 01, Linh Chieu Ward, Thu Duc District, Ho Chi Minh City 700000, Vietnam.
Institute of Physical and Theoretical Chemistry, Graz University of Technology, Stremayrgasse 9/I, A-8010 Graz, Austria.
ACS Omega. 2018 Aug 31;3(8):10296-10305. doi: 10.1021/acsomega.8b01232.
Donor-acceptor systems forming exciplexes are versatile models for the study of magnetic field effects (MFEs) on charge recombination reactions. The MFEs originate from singlet-triplet interconversion within transient radical ion pairs (RIPs), which exist in a dynamic equilibrium with the exciplexes. Here, we describe the synthesis and MFEs of the chain-linked ,-dimethylaniline (DMA)/9-methylanthracene (MAnt) donor-acceptor system MAnt-(CH) --CH-CH-DMA for = 6, 8, 10, and 16. The MFEs are found to increase with increasing chain length. Effects as large as 37.5% have been observed for the long-chain compound with = 16. The solvent dependence of the MFEs at magnetic field intensity 75 mT is reported. For the range of solvent static dielectric constants ε = 6.0-36.0, the MFEs go through a maximum for intermediate polarities, for which the direct formation of RIPs prevails and their dissociation and reencounter are balanced. Field-resolved measurements (MARY spectra) are reported for solutions in butyronitrile. The MARY spectra reveal that for = 8, 10, 16, the average exchange interaction is negligible during the coherent lifetime of the radical pair. However, singlet-triplet dephasing broadens the lineshape; the shorter the linker, the more pronounced this effect is. For = 6, a dip in the fluorescence intensity reveals a nonzero average exchange coupling of the order of ±5 mT. We discuss the field-dependence in the framework of the semiclassical theory taking spin-selective recombination, singlet-triplet dephasing, and exchange coupling into account. Singlet recombination rates of the order of 0.1 ns and various degrees of singlet-triplet dephasing govern the spin dynamics. In addition, because of a small free energy gap between the exciplex and the locally excited fluorophore quencher pair, a fully reversible interconversion between the RIP, exciplex, and locally excited fluorophore is revealed by spectrally resolved MFE measurements for the long-chain systems ( = 10, 16).
形成激基复合物的供体-受体体系是研究磁场对电荷复合反应影响(MFE)的通用模型。MFE源于瞬态自由基离子对(RIP)内的单重态-三重态相互转换,RIP与激基复合物处于动态平衡。在此,我们描述了链联的N,N-二甲基苯胺(DMA)/9-甲基蒽(MAnt)供体-受体体系MAnt-(CH₂)ₙ--CH₂-CH₂-DMA(n = 6、8、10和16)的合成及MFE。发现MFE随链长增加而增大。对于n = 16的长链化合物,观察到高达37.5%的效应。报道了在磁场强度75 mT下MFE的溶剂依赖性。对于溶剂静态介电常数ε = 6.0 - 36.0的范围,MFE在中等极性时达到最大值,此时RIP的直接形成占主导,其解离和再相遇达到平衡。报道了丁腈溶液的场分辨测量(MARY光谱)。MARY光谱表明,对于n = 8、10、16,在自由基对的相干寿命期间平均交换相互作用可忽略不计。然而,单重态-三重态退相使线形变宽;连接链越短,这种效应越明显。对于n = 6,荧光强度的下降揭示了约±5 mT量级的非零平均交换耦合。我们在半经典理论框架内讨论场依赖性,考虑了自旋选择性复合、单重态-三重态退相和交换耦合。约0.1 ns量级的单重态复合速率和不同程度的单重态-三重态退相支配着自旋动力学。此外,由于激基复合物与局部激发的荧光猝灭剂对之间的自由能差较小,通过长链体系(n = 10、16)的光谱分辨MFE测量揭示了RIP、激基复合物和局部激发的荧光团之间完全可逆的相互转换。