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• W3090261112 endingPage "129401" @default.
• W3090261112 startingPage "129401" @default.
• W3090261112 abstract "The properties of phosphole-based π-conjugated compounds could be well tuned via simple chemical modification. Four π-conjugated groups with different electronic nature including naphthalen-2-yl, 4-methoxyphenyl, 4-Methyl benzoate, and 4-benzonitrile were introduced to the C8 position of 5-phenylbenzo[b]phosphindole 5-oxide (PhBPO) to reveal the relationship between structures and properties. Density functional theory (DFT) calculations were carried out to comparatively study the ground state geometries, orbital energy gaps, infrared (IR) spectra, UV–vis spectra, and fluorescence (FL) spectra of the five PhBPO derivatives. Good correspondences between the simulated and experimental IR and UV–vis spectral properties were found, proving the feasibility of the DFT method. The IR and Uv-vis spectra were assigned and explained in detail on the basis of the calculation results and the substituional effect of different substituents on the structure and spectral properties was revealed. The large FL oscillator strengths indicate these PhBPO derivatives are good candidates for fluorescent materials. PhBPO derivatives possess easy-to-modify sites and thus can be further utilized as functional materials." @default.
• W3090261112 created "2020-10-08" @default.
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• W3090261112 date "2021-02-01" @default.
• W3090261112 modified "2023-09-26" @default.
• W3090261112 title "Structures and spectral properties of 5-phenyl-5H-benzo[b]phosphindole 5-oxide and its substituted derivatives: The substitutional effect study based on density functional theory calculations" @default.
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• W3090261112 doi "https://doi.org/10.1016/j.molstruc.2020.129401" @default.
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