2008
DOI: 10.1080/02678290802120323
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis, optical properties and thermal behaviour of 1,3,4‐oxadiazole‐based twin dimers

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
18
0
1

Year Published

2008
2008
2015
2015

Publication Types

Select...
8

Relationship

2
6

Authors

Journals

citations
Cited by 58 publications
(20 citation statements)
references
References 12 publications
1
18
0
1
Order By: Relevance
“…The emission peak at l = 515 nm (2.40 eV) with a large Stokes shift of the order of 165 nm (1.15 eV) was attributed to the formation of intermolecular excimer. The Stokes shift, which reflects the structural relaxation of the excited molecule and is significantly larger than the reported push-pull systems exhibiting LC behavior, [30][31][32][33][34] confirmed the molecular conformational changes upon excitation. The plot of the fluorescence spectra at different concentrations shows that the relative intensity of the peak at l = 515 nm diminishes gradually with dilution, indicating the tendency of these molecules to form excimers in concentrated solution ( Figure 6).…”
Section: Photophysics and Photophysical Properties In Solutionsmentioning
confidence: 76%
“…The emission peak at l = 515 nm (2.40 eV) with a large Stokes shift of the order of 165 nm (1.15 eV) was attributed to the formation of intermolecular excimer. The Stokes shift, which reflects the structural relaxation of the excited molecule and is significantly larger than the reported push-pull systems exhibiting LC behavior, [30][31][32][33][34] confirmed the molecular conformational changes upon excitation. The plot of the fluorescence spectra at different concentrations shows that the relative intensity of the peak at l = 515 nm diminishes gradually with dilution, indicating the tendency of these molecules to form excimers in concentrated solution ( Figure 6).…”
Section: Photophysics and Photophysical Properties In Solutionsmentioning
confidence: 76%
“…b) a nitração da acetanilida para obtenção da p-nitroacetanilida (2). Aqui a reação forma majoritariamente o produto de substituição para em relação ao orto (64:36 por CG), sendo este último eliminado na recristalização com etanol, devido a sua maior solubilidade neste 13 Esta reação em meio heterogêneo (cetona e carbonato) tem a desvantagem de necessitar de agitação constante, contudo, mostrou-se mais eficiente quando comparado ao método empregando meio homogêneo (metanol e hidróxido de potássio). O refluxo foi realizado usando uma chapa de aquecimento com agitação magnética, de forma muito eficaz.…”
Section: Resultsunclassified
“…The foregoing observations for such compounds are particularly noteworthy, and we have already devoted efforts in synthesizing and characterizing thermally stable luminescent liquid crystals possessing 1,2,3-triazole [17], 2,1,3-benzothiadiazole [18], isoxazole [19], and 1,2,4-or 1,3,4-oxadiazole moiety in their molecular frameworks [20][21][22][23].…”
Section: Introductionmentioning
confidence: 95%