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F?rster Resonance Energy Transfer Sensitized Singlet Fission in BODIPY-Pentacene Dimer Conjugates

机译:BODIPY-五苯二聚体偶联物中的F?rster共振能量转移敏化单线态裂变

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摘要

In the present work, the energy donor 4,4-difluoro-4-bora-3a,4a-diaza-sindacene(BODIPY) is used for the first time in combination with a pentacenedimer (Pnc_2) to provide the conjugate BODIPYPnc_2 that features absorptionthroughout a large part of the solar spectrum. Upon photoexcitation, thesinglet excited state energy of BODIPY is transferred to the pentacene dimervia intramolecular F?rster resonance energy transfer (FRET). Subsequently,the pentacene dimer undergoes intramolecular singlet fission. In this process,a singlet correlated triplet pair is generated from the first singlet excited statevia coupling to an intermediate state. The results show that solvent polarityhas an influence on the system, with the largest FRET rate (i.e., 7.46 × 10~(11)s~(?1)) being obtained in the most polar solvent (namely, benzonitrile) alongwith the largest triplet quantum yield (i.e., 207 ± 20).
机译:在本工作中,能量供体4,4-二氟-4-硼-3a,4a-二氮杂-sindacene(BODIPY)首次与五苯二聚体(Pnc_2)结合使用,以提供在太阳光谱的大部分中具有吸收特征的共轭BODIPYPnc_2。光激发后,BODIPY的单线态激发态能量通过分子内F?rster共振能量转移(FRET)转移到五酮二聚体。随后,五苯二聚体发生分子内单线态裂变。在此过程中,从第一单线态激发态通过耦合到中间态产生单线态相关三重态对。结果表明,溶剂极性对体系有影响,在极性最强的溶剂(即苯甲腈)中FRET速率最大(即7.46×10~(11)s~(?1)),三重态量子产率最大(即207±20%)。

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