2-Iminopyrroles [H L, 4-tert-butyl phenyl(pyrrol-2-ylmethylene)amine] are non-fluorescent π systems. However, they display blue fluorescence after deprotonation with alkali metal bases in the solid state and in solution at room temperature. In the solid state, the alkali metal 2-imino pyrrolates, M( L), aggregate to dimers, [M( L)(NCR)] (M=Li, R=CH , CH(CH )CNH ), or polymers, [M( L)] (M=Na, K). In solution (solv=CH CN, DMSO, THF, and toluene), solvated, uncharged monomeric species M( L)(solv) with N,N'-chelated alkali metal ions are present. Due to the electron-rich pyrrolate and the electron-poor arylimino moiety, the M( L) chromophore possesses a low-energy intraligand charge-transfer (ILCT) excited state. The chelated alkali cations rigidify the chromophore, restricting intramolecular motions (RIM) by the chelation-enhanced fluorescence (CHEF) effect in solution and, consequently, switch-on a blue fluorescence emission.
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http://dx.doi.org/10.1002/chem.201806103 | DOI Listing |
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