Oligophenylene 2,4,6-triarylpyridines and analogous diaza-p-terphenyls, diaza-p-quaterphenyls and diaza-p-quinquephenyls with luminiscent activity

1989 ◽  
Vol 54 (2) ◽  
pp. 462-472 ◽  
Author(s):  
Antonín Kurfürst ◽  
Pavel Lhoták ◽  
Miroslav Petrů ◽  
Josef Kuthan

Cyclocondensation of α,β-unsaturated aromatic ketones V and VIII with quaternary pyridinium salts VI in the presence of ammonium acetate gave 2,4,6-triarylpyridines I, aryl-substituted diaza-p-terphenyls IIa,b, diaza-p-quaterphenyls IIc,d and diaza-p-quinquephenyls IIe,f. All the new polyphenylene compounds exhibit characteristic luminiscence in the visible spectral region.

1992 ◽  
Vol 57 (2) ◽  
pp. 375-384 ◽  
Author(s):  
Richard Hrabal ◽  
Pavel Lhoták ◽  
Antonín Kurfürst

The reaction of 2-cinnamoylfluorene II with quaternary pyridinium salts IIIa, IIIb in the presence of ammonium acetate, gave 2-fluorenyl-2,6-diarylpyridines IV. The complete assignment of 1H and 13C resonances by 2D NMR methods is given.


1983 ◽  
Vol 48 (11) ◽  
pp. 3307-3314 ◽  
Author(s):  
Petr Nesvadba ◽  
Petr Štrop ◽  
Josef Kuthan

The quaternary pyridinium salts Ia-Ic react with alkaline solution of potassium ferricyanide to give the condensed heterocyclic derivatives IIIa, b, IV, whereas the salts Id-If give the pyrrole derivatives IIa-IIc under the same conditions. The diaza heterocycle IIIa reacts with methyl iodide to give methoiodide V, whereas by action of bromine it produces two monobromo derivatives VIa, b. The pyrrole derivatives IIa, b give monobromo derivatives IId, e on bromination. A probable mechanism of formation of the heterocyclic derivatives is discussed.


1996 ◽  
Vol 61 (1) ◽  
pp. 126-138 ◽  
Author(s):  
Richard Kubík ◽  
Stanislav Böhm ◽  
Iveta Ruppertová ◽  
Josef Kuthan

Substituted 1-(pyridin-2-yl)-2,4,6-triphenylpyridinium perchlorates 1b-1e were converted with potassium ferricyanide and potassium hydroxide to sterically crowded 2-phenyl-3-[(Z)-1,3-diphenyl-3-oxopropenyl]imidazo[1,2-a]pyridines 2b-2e accompanied by minor isomeric 2-benzoyl-3,5-diphenyl-1-(pyridin-2-yl)pyrroles 3c-3e. 4-Phenyl-2,6-di(4-substituted phenyl)-1-(pyridin-2-yl)pyridinium salts 4a, 4b gave exclusively corresponding imidazo[1,2-a]pyridines 5a, 5b while the ferricyanide oxidation of 1-(5-iodo- and 5-cyanopyridin-2-yl)-2,4,6-triphenylpyridinium perchlorates 6a, 6b led to mixtures of major imidazo[1,2-a]pyridines 7a-7c and minor pyrroles 8a-8c. Some mechanistic aspects of the oxidation procedure are discussed in connection with a resistance of 2,6-diphenyl-1,3,5-trimethylpyridinium perchlorate (9c) towards the oxidizing agents.


1981 ◽  
Vol 17 (4) ◽  
pp. 367-369 ◽  
Author(s):  
T. V. Stupnikova ◽  
A. I. Serdyuk ◽  
V. N. Kalafat ◽  
R. S. Sagitullin ◽  
V. P. Marshtupa

2014 ◽  
Vol 116 (4) ◽  
pp. 542-547 ◽  
Author(s):  
M. V. Zagidullin ◽  
M. I. Svistun ◽  
N. A. Khvatov ◽  
A. S. Insapov

1994 ◽  
Vol 49 (6) ◽  
pp. 849-851 ◽  
Author(s):  
G. C. Papavassiliou ◽  
I. B. Koutselas

The title compounds (natural low-dimensional semiconductors) show strong excitonic optical absorption bands in the UV-visible spectral region, because of the dielectric confinement of excitons. as in the cases of other similar systems based on PbX2-4, SnX2-4. PtI - X - PtIV-X , Cdx,Sy-clusters etc


Author(s):  
Rebeca Sola Llano ◽  
Edurne Avellanal Zaballa ◽  
Jorge Bañuelos ◽  
César Fernando Azael Gómez Durán ◽  
José Luis Belmonte Vázquez ◽  
...  

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