Various α,β-unsaturated (E)-alkenylphosphonamidates were prepared in excellent stereo- and regioselectivties via the electrophilic hydrophosphonylation of cyclic and acyclic imines with alkylphosphonochloridates in the presence of base. For unsaturated imines, only...
A NIR‐II fluorescent probe (Et‐1080) for H2S detection was fabricated based on the intramolecular charge transfer blocking mechanism. The enhanced electron density of the indole donor further drove the Et‐1080′s absorption and emission to the NIR‐II region with a high molar absorption coefficient and acceptable fluorescence quantum yield. The C=N double bond of electron‐deficient indole can react with H2S rapidly via a nucleophilic addition mechanism, resulting in the destruction of conjugated structure and fluorescence quenching of the Et‐1080 molecule. The probe showed high selectivity and sensitivity to H2S, which could realize the rapid detection of H2S in NIR‐II band and showed great potential in the further disease diagnosis associated with H2S.
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