Department of Chemistry, Indiana University, 800 East Kirkwood Avenue, Bloomington, Indiana 47405, United States.
J Am Chem Soc. 2020 Jul 15;142(28):12167-12180. doi: 10.1021/jacs.0c02450. Epub 2020 Jul 6.
Fluorophores are powerful tools for the study of chemistry, biology, and physics. However, fluorescence is severely impaired when concentrations climb above 5 μM as a result of effects like self-absorption and chromatic shifts in the emitted light. Herein, we report the creation of a charge-transfer (CT) fluorophore and the discovery that its emission color seen at low concentrations is unchanged even at 5 mM, some 3 orders of magnitude beyond typical limits. The fluorophore is composed of a triphenylamine-substituted cyanostar macrocycle, and it exhibits a remarkable Stokes shift of 15 000 cm to generate emission at 633 nm. Crucial to the performance of this fluorophore is the observation that its emission spectrum shows near-zero overlap with the absorption band at 325 nm. We propose that reducing the spectral overlap to zero is a key to achieving full fluorescence across all concentrations. The triphenylamine donor and five cyanostilbene acceptor units of the macrocycle generate an emissive CT state. Unlike closely related donor-acceptor control compounds showing dual emission, the cyanostar framework inhibited emission from the second state to create a zero-overlap fluorophore. We demonstrated the use of emission spectroscopy for characterization of host-guest complexation at millimolar concentrations, which are typically the exclusive domain of NMR spectroscopy. The binding of the PF anion generates a 2:1 sandwich complex with blue-shifted emission. Distinct from twisted intramolecular charge-transfer (TICT) states, experiment-supported density functional theory shows a 67° twist inside an acceptor unit in the CT state instead of displaying a twist between the donor and acceptor; it is TICT-like. Inspired by the findings, we uncovered similar concentration-independent behavior from a control compound, strongly suggesting this behavior may be latent to other large Stokes-shift fluorophores. We discuss strategies capable of generating zero-overlap fluorophores to enable accurate fluorescence characterization of processes across all practical concentrations.
荧光团是研究化学、生物学和物理学的有力工具。然而,由于自吸收和发射光的色移等效应,当浓度超过 5μM 时,荧光会严重受损。在此,我们报告了一种电荷转移(CT)荧光团的创建,并发现其在低浓度下观察到的发射颜色在 5mM 时保持不变,这比典型极限高出 3 个数量级。该荧光团由三苯胺取代的氰基星大环组成,它表现出显著的斯托克斯位移为 15000cm,在 633nm 处产生发射。这种荧光团的性能关键在于观察到其发射光谱与 325nm 处的吸收带几乎没有重叠。我们提出,将光谱重叠降低到零是实现所有浓度下完全荧光的关键。大环的三苯胺供体和五个氰基苯乙烯受体单元产生发射 CT 态。与表现出双发射的密切相关的供体-受体对照化合物不同,氰基星骨架抑制了第二态的发射,从而创造了一个零重叠荧光团。我们展示了使用发射光谱学来表征毫摩尔浓度下的主体-客体络合,这通常是 NMR 光谱学的专属领域。PF 阴离子的结合生成蓝色位移发射的 2:1 夹心配合物。与扭曲的分子内电荷转移(TICT)态不同,实验支持的密度泛函理论表明 CT 态中在一个受体单元内有 67°的扭曲,而不是在供体和受体之间显示扭曲;它类似于 TICT。受此发现的启发,我们从对照化合物中发现了类似的浓度独立行为,这强烈表明这种行为可能潜伏在其他大斯托克斯位移荧光团中。我们讨论了生成零重叠荧光团的策略,以实现所有实际浓度下过程的准确荧光特性。