Different mechanisms of ultrafast excited state deactivation of coumarin 500 in dioxane and methanol solvents: experimental and theoretical study. Issue 2 (2nd December 2014)

• Record Type: Journal Article
• Authors: Cong, Lin; Yin, Hang; Shi, Ying; Jin, Mingxing; Ding, Dajun
• Is Part Of: RSC advances. Volume 5:Issue 2(2015)
• Page Start: 1205
• Page End: 1212
• Publication Date: 2014-12-02
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c4ra09773d
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : The effect of hydrogen bonding on the intermolecular photoinduced ICT and TICT processes for coumarin 500 has been demonstrated, and a reliable mechanism has been revealed to explain the unusual behavior of C500 in dioxane and methanol. Abstract : Solute–solvent intermolecular photoinduced intramolecular charge transfer (ICT) and twisted intramolecular charge transfer (TICT) states are proposed to account for the unusual properties of coumarin 500 (C500) in 1, 4-dioxane (Diox) and methanol (MeOH) solvents. Our femtosecond transient absorption experiment on C500 shows that in Diox, there exists a single exponential component with a time constant of τ 1 ∼ 1.4 ps, however in MeOH two exponential components with lifetimes of τ 1 ∼ 0.5 ps and τ 2 ∼ 8.0 ps are observed. DFT and TDDFT methods were used to optimize the geometries of complexes C500–Diox and C500–(MeOH)3 in the ground and excited states, respectively. They show that the rapid decay time could be due to ICT and ICT → TICT could be responsible for the slow decay time. Strengthening of the hydrogen bond N–H⋯O–H and the weakening of the hydrogen bond N⋯H–O in the excited state of the C500–(MeOH)3 complex could facilitate the process of ICT from the 7-NHEt group to the CF3 group and induce the formation of the TICT state in hydrogen bonding with MeOH. Together, the experimental and theoretical results reveal that C500 exhibits unusual deactivation mechanisms in Diox and MeOH solvents.