Theoretical study on photo-induced processes of 1-methyl-3-(N-(1, 8-naphthalimidyl)ethyl)imidazolium halide species: an application of constrained density functional theory. Issue 6 (15th December 2017)

• Record Type: Journal Article
• Authors: Otsuka, Takao; Sumita, Masato; Izawa, Hironori; Morihashi, Kenji
• Is Part Of: Physical chemistry chemical physics. Volume 20:Issue 6(2018)
• Page Start: 3911
• Page End: 3917
• Publication Date: 2017-12-15
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c7cp07877c
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Inter-molecular charge transfer (SET ) and intra-molecular charge transfer (SM1 ) excited states are involved in the photo-induced processes of 1-methyl-3-( N -(1, 8-naphthalimidyl)ethyl)imidazolium halide. Abstract : 1-Methyl-3-( N -(1, 8-naphthalimidyl)ethyl)imidazolium (MNEI) has potential as a versatile sensor that can measure the electronegativity of anions based on the fluorescence intensity upon irradiation. To clarify the factors that determine the fluorescence intensity, constrained density functional theory (CDFT) was applied to explore the electron transfer (ET) states of MNEI halide species (MNEI–X; X = F, Cl, Br, I). According to the CDFT potential energy surface, intra-molecular ET (SM1 ) states on MNEI are responsible for the intensity of absorption and fluorescence spectra. However, inter-molecular ET (SET ) states between MNEI and X are certainly responsible for fluorescence quenching. Hence, the energetic difference between the SM1 state and the SET state (Δ E M1_ET ) is a crucial factor that determines the fluorescence intensity in the spectra of MNEI–X complexes. Δ E M1_ET decreases as the electronegativity of X decreases ( i.e., F > Cl > Br > I). This explains the fluorescence intensity of MNEI–X.