Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 141, Issue 25, Pages 9885-9894Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jacs.9b02765
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- Ministry of Science and Technology, Taiwan [MOST 107-2628-M-002-017, MOST 107-2113-M-035-003, MOST 106-2113-M-003-010-MY3]
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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-dimethy1-2,3-dihydro-1H-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-1) of DM-7HIT is a sulfur nonbonding (n) to pi* transition, which undergoes O-H bond flipping from S-1 (n pi*) to the non-H-bonded S'(1)(n pi*) state, followed by intersystem crossing and internal conversion to populate the S-1(n pi*) state. Fast H-bond on/off switching then takes place between T'(1)(n pi*) and T-1 (n pi*), forming a pre-equilibrium that affords both the T'(1)(n pi*, 685 nm) and T-1(n pi*, 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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