Volatile organic compounds (VOCs) are widespread in our daily life and greatly harmful to human health, as well as to the environment. To date, it remains a formidable challenge to develop a highly sensitive visual system for selective detection of VOCs. Herein, we report on a metal-free organic molecule of 2,4-di(10 H-phenothiazin-10-yl)-1,3,5-triazine (TDP) with ultralong organic phosphorescence (UOP) feature as a visible chemical probe for chloroform detection. In the pristine solid state, this phosphor shows a green UOP with a lifetime of 56 ms after the removal of excitation light source; however, the UOP greatly diminishes when fumed with chloroform, which is ascribed to the variation in both radiative and nonradiative transitions in crystal with embedded chloroform. Remarkably, TDP materials demonstrate great potential as a visual chemical probe for chloroform, showing high sensitivity, excellent selectivity, and good repeatability. The limitation for chloroform detection is as low as 5 ppm. Combining experimental data and theoretical calculations, it is reasoned that the space confinement via intermolecular interactions between chloroform and TDP molecules play a vital role for high selectivity of chloroform detection. These results pave the way toward expanding the scope of organic luminogens with UOP as well as their applications.
Keywords: H-aggregation; chloroform detection; crystal engineering; organic persistent luminescence; ultralong organic phosphorescence; volatile organic compounds.