Garain Swadhin, Garain Bidhan Chandra, Eswaramoorthy Muthusamy, Pati Swapan K, George Subi J
New Chemistry Unit and School of Advanced Material (SAMat), Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Jakkur, Bangalore, 560064, India.
Theoretical Science Unit, JNCASR, India.
Angew Chem Int Ed Engl. 2021 Sep 1;60(36):19720-19724. doi: 10.1002/anie.202107295. Epub 2021 Jul 28.
Solution phase room-temperature phosphorescence (RTP) from organic phosphors is seldom realized. Herein we report one of the highest quantum yield solution state RTP (ca. 41.8 %) in water, from a structurally simple phthalimide phosphor, by employing an organic-inorganic supramolecular scaffolding strategy. We further use these supramolecular hybrid phosphors as a light-harvesting scaffold to achieve delayed fluorescence from orthogonally anchored Sulforhodamine acceptor dyes via an efficient triplet to singlet Förster resonance energy transfer (TS-FRET), which is rarely achieved in solution. Electrostatic cross-linking of the inorganic scaffold at higher concentrations further facilitates the formation of self-standing hydrogels with efficient RTP and energy-transfer mediated long-lived fluorescence.
有机磷光体的溶液相室温磷光(RTP)很少能够实现。在此,我们报告了一种结构简单的邻苯二甲酰亚胺磷光体在水中实现的最高量子产率溶液态RTP(约41.8%)之一,这是通过采用有机-无机超分子支架策略实现的。我们进一步将这些超分子杂化磷光体用作光捕获支架,通过高效的三重态到单重态Förster共振能量转移(TS-FRET),实现正交锚定的磺基罗丹明受体染料的延迟荧光,这在溶液中很少能实现。在较高浓度下对无机支架进行静电交联,进一步促进了具有高效RTP和能量转移介导的长寿命荧光的自立水凝胶的形成。