Turn-on solid state luminescence by solvent-induced modification of intermolecular interactions

被引:12
|
作者
Majumdar, Prabhat [1 ,2 ]
Ghora, Madhubrata [1 ,2 ]
Wannemacher, Reinhold [3 ]
Gierschner, Johannes [3 ]
Varghese, Shinto [1 ,2 ]
机构
[1] Indian Assoc Cultivat Sci, Tech Res Ctr, Kolkata 700032, India
[2] Indian Assoc Cultivat Sci, Sch Appl & Interdisciplinary Sci, Kolkata 700032, India
[3] Madrid Inst Adv Studies, IMDEA Nanosci, C Faraday 9,Ciudad Univ Cantoblanco, Madrid 28049, Spain
关键词
FLUORESCENCE QUANTUM YIELDS; MOLECULAR-CRYSTALS; PHOTOPHYSICS; BEHAVIORS; PACKING; VAPOCHROMISM; ENHANCEMENT; COCRYSTALS; ENERGIES; SURFACES;
D O I
10.1039/d0tc03645e
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Solid-state luminescent materials that are sensitive to external stimuli are of enormous importance due to their potential for application as smart responsive materials and devices. Here we report the changes in the photophysical properties of a novel benzimidazole-based chromophore upon the formation of an inclusion complex with DMSO molecules in the solid state, and the vapochromic properties of the co-assembly are explored. The chromophore is synthesised in a single step with a good yield. The compound is reasonably emissive in solution, however, it exhibits a red shift and quenching of emission in the solid state. Co-assembly with DMSO results in two distinctly emissive forms, with emission in the yellow (Y-form) and orange (O-form) regions of the visible spectrum. An enhanced emission is observed in the Y-form, while the O-form exhibits efficiency similar to the pristine solid. Various factors that stabilize the co-assembly and the basis of fluorescence enhancement are studied and substantiated by DFT investigations in a QM:MM framework. The crystalline co-assemblies can be reverted to a structure similar to the pristine form by vapours of polar protic solvents, which dramatically modify their photophysical properties. The new materials are therefore promising as vapochromic sensors for environmental monitoring.
引用
收藏
页码:15742 / 15750
页数:9
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