Photochemistry Channels of Merocyanine Encapsulated in Sol-Gel Glasses

1994 ◽  
Vol 346 ◽  
Author(s):  
A. M. Mahloudji ◽  
L. B. Meuret ◽  
C. T. Lin

ABSTRACTPhotophysical properties of l-Docosyl-4-(4-hydroxystyryl)pyridiniurn bromide (SB), a merocyanine dye in solution and encapsulated in sol-gel derived glass are investigated at 298 and 77 K. In solution, the absorption spectra of SB display an equilibrium between the quinolinium and benzoid forms. The equilibrium can be shifted to either quinolinium or benzoid form under an acidic or basic condition, respectively. The emission spectra of SB, on the other hand, give not only the quinolinium and benzoid forms but also the quinoid form which emits at 500 nm. The existence of excited state quinoid form of SB is also evident in the excitation spectrum while the emission at 500 nm is monitored. Both in solution and in xerogel, the quinoid form of SB is shown to be photochemically unstable as compared to the benzoid form. It is proposed that the photoexcited quinolinium form of SB is a proton dissociative species which transforms readily to become the quinoid form. The results indicate that photochemistry channels of SB are originated from the quinoid form. Moreover, the benzoid form of SB (photochemically stable) exhibits large hyperpolarizability due to its charge-transfer characteristic, and is a desired molecular form for nonlinear optical (NLO) applications. The material processing techniques for stabilizing the benzoid form of SB in optically transparent sol-gel glasses are illustrated for the first time.

2011 ◽  
Vol 239-242 ◽  
pp. 1006-1009
Author(s):  
Yun Long Deng ◽  
Yun Hui Sun ◽  
Du Xia Cao ◽  
Ying Chen ◽  
Zhi Qiang Liu

A D-π-D type of organic dye 2,7-di[4-(N,N-diphenylamino)styryl]-9-n-pentyl-9H- carbazole (DPSPC) with diphenylamine as donor group and styrene-carbazole-styrene as conjugation bridge has been synthesized. The photophysical properties of the dye in different solvents and poly methyl methacrylate/organic modified sol-gel glasses are researched. The results indicate that the fluorescence properties of the organic dye in composite glass increase relative to that in solvents and there are no fluorescence quenching in high doped concentration in composite glass matrixes. The dye has higher stability in the composite glass than that in solution.


2021 ◽  
Author(s):  
Mahmoud Sakr ◽  
Maram T. H. Abou Kana ◽  
Ahmed H.M. Elwahy ◽  
Samy A. El-Daly A. El-Daly ◽  
El-Zeiny M. Ebeid

Abstract This paper deals the optical and photophysical properties of dihydrophenanthro [9,10-e] [1,2,4] triazine fluorescent derivative dyes doped in Silicate based sol–gel, homo-poly methyl methacrylate (PMMA). Solid hosts effect on the optical and photophysical parameters such as molar absorptivity, cross sections of singlet–singlet electronic absorption and emission spectra, excited state lifetime, quantum yield of fluorescence. Also the dipole moment of electronic transition, the length of attenuation and Oscillator strength of electronic transition from So →S1 have been detected. The dyes with different pumping power were pumped by 3rd harmonic Nd:YAG pulsed laser 8ns pulse duration, with a repetition rate at (10Hz). Good Photo stability of compound 1 and 2 were obtained that was decreased to 49%, 54% and 46%, 40% of the initial ASE of dyes in sol gel and PMMA respectively, after 55000 pumping pulses at (10 mJ/pulse). The dyes in sol-gel show improved Photo stability compared with those in organic polymeric matrices.


Coatings ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1255
Author(s):  
Alina Raditoiu ◽  
Valentin Raditoiu ◽  
Florentina Monica Raduly ◽  
Georgiana Cornelia Ispas ◽  
Violeta Purcar ◽  
...  

Fluorescent film-forming materials were obtained by embedding salicylaldazine (SAA) in silica hybrids generated by sol–gel processes from different silane precursors in acid catalysis. Tuned local environments for the fluorophore were generated in the hosting network by modifying silica sols with organic groups through the co-condensation of tetraethylortosilicate (TEOS) and different alkoxysilanes hydrolysis products. The photophysical properties of the luminescent hybrid films were studied in direct relationship with structural, textural, and surface properties and based on interactions between SAA species and the silica hosting network. Film-forming materials were studied in order to determine differences in absorption and fluorescence emission due to the environments around the fluorophore. The variations recorded in the fluorescence emission spectra of the hybrid films were related to interactions established between the fluorophore species and their sterically hindered surroundings of the host hybrid silica, where free molecular motions are restricted. The influence of the type and amount of network modifier and of the fluorophore loading on the transparency of the films and fluorescence intensity was also investigated. The study carried out led to the elucidation of the necessary conditions for obtaining luminescent film-forming materials with high luminescence intensity and transparency useful for the design of new light concentrators.


2018 ◽  
Vol 5 (2) ◽  
pp. 171719 ◽  
Author(s):  
Muhammad Farooq Saleem Khan ◽  
Jing Wu ◽  
Bo Liu ◽  
Cheng Cheng ◽  
Mona Akbar ◽  
...  

A thorough analysis of the photophysical properties involved in electronic transitions in excitation–emission spectra of xylene isomers has been carried out using the time-dependent density functional theory (PBEPBE/6-31 + G(d,p)) method. For the first time a structural and spectroscopic investigation to distinguish isomers of xylene, a widespread priority pollutant, was conducted experimentally and theoretically. The fluorescence properties of xylene isomers (sole and mixture (binary and ternary)) in water were studied. The fluorescence peak intensities of xylenes were linearly correlated to concentration, in the order of p -xylene >  o -xylene >  m -xylene at an excitation/emission wavelength (ex/em) of 260 nm/285 nm for o -, m -xylene and ex/em 265 nm/290 nm for p -xylene at the same concentration. The theoretical excitation/emission wavelengths were at ex/em 247 nm/267 nm, 248 nm/269 nm and 251 nm/307 nm for o -, m - and p -xylene, respectively. The vertical excitation and emission state energies of p -xylene (ex/em 4.94 eV/4.03 eV) were lower and the internal conversion energy difference (0.90 eV) was higher than those of m -xylene (ex/em 5.00 eV/4.60 eV) (0.4 eV) and o -xylene (ex/em 5.02 eV/4.64 eV) (0.377 eV). The order of theoretical emission and oscillator strength (0.0187 > 0.0175 > 0.0339) for p -xylene >  o -xylene >  m -xylene was observed to be in agreement with the experimental fluorescence intensities. These findings provide a novel fast method to distinguish isomers based on their photophysical properties.


1990 ◽  
Vol 189 ◽  
Author(s):  
Srinivas Surapanani ◽  
Michael E. Mullins ◽  
B.C. Cornilsen

ABSTRACTMicrowave processing was carried out on SiO2 -B2O3 solutions and gels prepared by sol-gel methods. Monolithic gels were prepared from alcoholic solutions of trimethylborate and tetraethylorthosilicate using a two-step hydrolysis process. A novel technique of Liquid State Processing (LSP) was employed for the first time, and it was found to be faster and more effective than the conventional processing techniques. The structural evolution of the dried products was followed using FTIR. The effect of processing was examined via surface area analysis (BET), electron microscopy, and FTIR. The microwave drying has been compared with conventional oven drying and vacuum drying techniques. Shorter processing times, improved microstructures, and unique properties have been obtained.


Author(s):  
George C. Ruben ◽  
Merrill W. Shafer

Traditionally ceramics have been shaped from powders and densified at temperatures close to their liquid point. New processing methods using various types of sols, gels, and organometallic precursors at low temperature which enable densificatlon at elevated temperatures well below their liquidus, hold the promise of producing ceramics and glasses of controlled and reproducible properties that are highly reliable for electronic, structural, space or medical applications. Ultrastructure processing of silicon alkoxides in acid medium and mixtures of Ludox HS-40 (120Å spheres from DuPont) and Kasil (38% K2O &62% SiO2) in basic medium have been aimed at producing materials with a range of well defined pore sizes (∼20-400Å) to study physical phenomena and materials behavior in well characterized confined geometries. We have studied Pt/C surface replicas of some of these porous sol-gels prepared at temperatures below their glass transition point.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Azam Marjani ◽  
Reza Khan Mohammadi

AbstractHg(II) has been identified to be one of the extremely toxic heavy metals because of its hazardous effects and this fact that it is even more hazardous to animals than other pollutants such as Ag, Au, Cd, Ni, Pb, Co, Cu, and Zn. Accordingly, for the first time, tetrasulfide-functionalized fibrous silica KCC-1 (TS-KCC-1) spheres were synthesized by a facile, conventional ultrasonic-assisted, sol–gel-hydrothermal preparation approach to adsorb Hg(II) from aqueous solution. Tetrasulfide groups (–S–S–S–S–) were chosen as binding sites due to the strong and effective interaction of mercury ions (Hg(II)) with sulfur atoms. Hg(II) uptake onto TS-KCC-1 in a batch system has been carried out. Isotherm and kinetic results showed a very agreed agreement with Langmuir and pseudo-first-order models, respectively, with a Langmuir maximum uptake capacity of 132.55 mg g–1 (volume of the solution = 20.0 mL; adsorbent dose = 5.0 mg; pH = 5.0; temperature: 198 K; contact time = 40 min; shaking speed = 180 rpm). TS-KCC-1was shown to be a promising functional nanoporous material for the uptake of Hg(II) cations from aqueous media. To the best of our knowledge, there has been no report on the uptake of toxic Hg(II) cations by tetrasulfide-functionalized KCC-1 prepared by a conventional ultrasonic-assisted sol–gel-hydrothermal synthesis method.


2021 ◽  
Author(s):  
Y. Kitamoto ◽  
K. Oda ◽  
K. Ogino ◽  
K. Hiyama ◽  
H. Kita ◽  
...  

An azadioxa-planar triphenylborane was synthesized for the first time and it was found that bridging groups have a critical role in changing its molecular properties.


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