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Phenothiazine Scope: Steric Strain Induced Planarization and Excimer Formation
Authors:Deng‐Gao Chen  Yi Chen  Cheng‐Ham Wu  Yi‐An Chen  Meng‐Chi Chen  Jia‐An Lin  Chun‐Ying Huang  Jianhua Su  He Tian  Pi‐Tai Chou
Abstract:Phenothiazine derivatives based on the 10‐phenyl‐10H‐phenothiazine ( NAS ) chromophore, namely 7‐phenyl‐7H‐benzoc]phenothiazine ( NAS‐1 ) and 12‐phenyl‐12H‐benzoa]phenothiazine ( NAS‐2 ), were designed and synthesized. NAS‐1 and NAS‐2 are constitutional isomers with different steric strains imposed on the phenothiazine core moiety. In solution, the more‐strained NAS‐2 possesses a bent structure and undergoes photoinduced structural planarization (PISP). In the crystal, despite the absence of PISP, bent NAS‐2 exhibits prominent excimer emission as well as emission mechanochromism, which is not observed in the planar‐like NAS and NAS‐1 . This unconventional observation results from the bent core structure facilitating π–π stacking of the peripheral naphthalene moieties. Two‐photon‐coupled depth‐dependent emission shows spectral differences between the surface and kernel of the NAS‐2 crystal, and is believed to be a general phenomenon, at least in part, for materials exhibiting emission mechanochromism.
Keywords:Excimere  Heterocyclen  Konformationsanalyse  Ladungstransfer  Sterische Hinderung
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