2019
DOI: 10.1016/j.molliq.2019.04.110
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Solvent dependent spectroscopic properties of fingerprint reagent - 1,8-Diazafluoren-9-one

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Cited by 10 publications
(15 citation statements)
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“…However, the matrix remains chemically unmodified for all the samples and the effect of a potential significant polarity change of the whole matrix by only a concentration increase of DFO molecules seems rather unlikely. The location of the fluorescence peak of DFO by comparison to the fluorescence of DFO and other fluorenone-like molecules in liquid solutions [ 1 , 31 , 32 ] suggests that the TiO 2 matrix belongs to relatively nonpolar media. This is also in agreement with other results and discussions performed previously [ 25 , 26 , 33 ].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…However, the matrix remains chemically unmodified for all the samples and the effect of a potential significant polarity change of the whole matrix by only a concentration increase of DFO molecules seems rather unlikely. The location of the fluorescence peak of DFO by comparison to the fluorescence of DFO and other fluorenone-like molecules in liquid solutions [ 1 , 31 , 32 ] suggests that the TiO 2 matrix belongs to relatively nonpolar media. This is also in agreement with other results and discussions performed previously [ 25 , 26 , 33 ].…”
Section: Resultsmentioning
confidence: 99%
“…In our previous study, we investigated the solvation effects and the influence on the lowest singlet excited state of DFO. It was shown that, in protic environments, DFO forms a solute-solvent hydrogen bond complex in its ground and excited state [1].…”
Section: Introductionmentioning
confidence: 99%
“…Microcosmic electron aspect coordination of the ligand with the silver ion drew 1–11 nm distinction in UV‐Vis absorption between balk and nanoparticles of compound 1 , and dafo ligand, that is, the peaks shift towards blue region as the particle size is reduced [21] . Vibronic interplay between close‐lying n→π* and π→π* states in aromatic carbonyl and many nitrogen containing heterocyclic compounds result in a red shift of π→π* state and a blue shift of n→π* state [24] . As can be seen in Figure 2C and Table 2, the luminescence intensity of both bulk and nanosized analog of compound 1 obtained in anhydrous ethanol showed a blue shift by 2–10 nm.…”
Section: Resultsmentioning
confidence: 83%
“…[21] Vibronic interplay between closelying n!π* and π!π* states in aromatic carbonyl and many nitrogen containing heterocyclic compounds result in a red shift of π!π* state and a blue shift of n!π* state. [24] As can be seen in Figure 2C and Table 2, the luminescence intensity of both bulk and nanosized analog of compound 1 obtained in anhydrous ethanol showed a blue shift by 2-10 nm. The optical bandgap energy using the absorption edge of the UV-Vis spectra (λ max ) of bulk analog and nanoparticles of compound 1 was gained according to the value of αhν = A (hν -Eg) n equation (Tauc Plot relation) in which α = 2.303 (coefficient) log (T/d) (d = thickness of the sample and T = transmission), hν = photon energy ( Figure 2D and Table 2).…”
Section: Introductionmentioning
confidence: 77%
“…As it was mentioned, the positions of maxima and shape of the absorption and emission spectra reflect the nature of the solute-solvent interactions [60][61][62]. For this purpose, the multiple linear regression analysis proposed by Catalán was applied for each of the compounds dissolved in all 14 solvents.…”
Section: Multiparametric Linear Regression Analysis (Mlr)mentioning
confidence: 99%