Journal of the American Chemical Society · 2019 · 110 citations · 51 references
We report O-H----S hydrogen-bond (H-bond) formation and its excited-state intramolecular H-bond on/off reaction unveiled by room-temperature phosphorescence (RTP). In this seminal work, this phenomenon is demonstrated with 7-hydroxy-2,2-dimethyl-2,3-dihydro-1 H-indene-1-thione (DM-7HIT), which possesses a strong polar (hydroxy)-dispersive (thione) type H-bond. Upon excitation, DM-7HIT exhibits anomalous dual RTP with maxima at 550 and 685 nm. This study found that the lowest lying excited state (S<sub>1</sub>) of DM-7HIT is a sulfur nonbonding (n) to π* transition, which undergoes O-H bond flipping from S<sub>1</sub>(nπ*) to the non-H-bonded S'<sub>1</sub>(nπ*) state, followed by intersystem crossing and internal conversion to populate the T'<sub>1</sub>(nπ*) state. Fast H-bond on/off switching then takes place between T'<sub>1</sub>(nπ*) and T<sub>1</sub>(nπ*), forming a pre-equilibrium that affords both the T'<sub>1</sub>(nπ*, 685 nm) and T<sub>1</sub>(nπ*, 550 nm) RTP. The generality of the sulfur H-bond on/off switching mechanism, dubbed a molecule wiper, was rigorously evaluated with a variety of other H-bonded thiones, and these results open a new chapter in the chemistry of hydrogen bonds.
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Mechanically robust, readily repairable polymers via tailored noncovalent cross-linking
Yu Yanagisawa, Yiling Nan, Kou Okuro et al. · Science · 2017 · 1K citations