School of Physical, Environmental and Mathematical Sciences, UNSW Australia, Australian Defence Force Academy, Canberra, Australia.
Analyst. 2018 Jan 15;143(2):519-527. doi: 10.1039/c7an01632h.
Iridium(iii) cyclometalated complexes in aqueous solution often display relatively weak luminescence. It has been shown in previous work that this emission can be significantly enhanced (by up to two orders of magnitude) by encapsulation in cucurbit[10]uril (Q[10]). Luminescence lifetime measurements suggest a dynamic self-quenching mechanism is active, possibly due to displacement of an excited guest complex via collision with an unbound complex. We devise a model for the association of a group of iridium(iii) cyclometalated complexes with Q[10]. The model parameters are then fitted to steady-state emission titration curves. The excellent agreement of experimental data with the model provides valuable mechanistic information relating to the way this class of metal complexes interact and associate with the Q[10] host.
铱(III)环金属配合物在水溶液中通常显示出相对较弱的发光。以前的工作表明,通过葫芦脲[10](Q[10])的包封可以显著增强这种发射(高达两个数量级)。荧光寿命测量表明存在动态自猝灭机制,可能是由于通过与未结合的配合物碰撞而置换激发的客体配合物。我们设计了一组铱(III)环金属配合物与 Q[10]的缔合模型。然后将模型参数拟合到稳态发射滴定曲线。实验数据与模型的极好一致性提供了与这类金属配合物与 Q[10]主体相互作用和缔合方式相关的有价值的机制信息。