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Auteur Stefka Kaloyanova
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Faculty of chemistry - University of Sofia - Bulgarie
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Novel environmentally benign procedure for the synthesis of 2-aryl- and 2-hetaryl-4(3H)-quinazolinones / Todor Deligeorgiev in COLORATION TECHNOLOGY, Vol. 126, N° 1 (2010)
[article]
Titre : Novel environmentally benign procedure for the synthesis of 2-aryl- and 2-hetaryl-4(3H)-quinazolinones Type de document : texte imprimé Auteurs : Todor Deligeorgiev, Auteur ; Ana M. Cuadro, Auteur ; Julio Alvarez-Buila, Auteur ; Juan J. Vaquero, Auteur ; Aleksey Vasilev, Auteur ; Stefka Kaloyanova, Auteur Année de publication : 2010 Article en page(s) : p. 24-30 Note générale : Bibliogr. Langues : Anglais (eng) Index. décimale : 667.3 Teinture et impression des tissus Résumé : A novel environmentally benign procedure for the synthesis of 2-aryl- or 2-hetaryl-4(3H)-quinazolinones by condensation of anthranilamide with various aromatic aldehydes in polyethylene glycol under microwave irradiation has been developed. In contrast with other reported methods, this procedure provides the corresponding quinazolinones with good to high yields and purity, in very short reaction times and without the use of an oxidant. DOI : 10.1111/j.1478-4408.2010.00223.x En ligne : http://onlinelibrary.wiley.com/doi/10.1111/j.1478-4408.2010.00223.x/pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=8414
in COLORATION TECHNOLOGY > Vol. 126, N° 1 (2010) . - p. 24-30[article]Réservation
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Code-barres Cote Support Localisation Section Disponibilité 011984 - Périodique Bibliothèque principale Documentaires Disponible A novel general method for fast and easy preparation of cationic, neutral dimethinehemicyanine and dimethine dyes by uncatalysed Knoevenagel condensation / Todor Deligeorgiev in COLORATION TECHNOLOGY, Vol. 128, N° 6 (2012)
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Titre : A novel general method for fast and easy preparation of cationic, neutral dimethinehemicyanine and dimethine dyes by uncatalysed Knoevenagel condensation Type de document : texte imprimé Auteurs : Todor Deligeorgiev, Auteur ; Nikolay Gadjev, Auteur ; Stefka Kaloyanova, Auteur ; Nedyalko Lesev, Auteur ; Aleksey Vasilev, Auteur ; Alexi Alexiev, Auteur Année de publication : 2012 Article en page(s) : p. 417-424 Note générale : Bibliogr. Langues : Anglais (eng) Catégories : Absorption
Colorants -- Synthèse
Colorants cationiques
FluorescenceIndex. décimale : 667.3 Teinture et impression des tissus Résumé : Three novel general experimental procedures for preparation of cationic, neutral dimethinehemicyanine and dimethine dyes (eight of which are unpublished) by uncatalysed Knoevenagel condensation have been developed. The proposed methods are versatile as a variety of different starting materials can be used and they ensure good to very high yields, very short reaction times and high purity of the final dyes. Absorption and fluorescent properties of the novel dyes were investigated. DOI : 10.1111/j.1478-4408.2012.00408.x En ligne : http://onlinelibrary.wiley.com/doi/10.1111/j.1478-4408.2012.00408.x/pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=16442
in COLORATION TECHNOLOGY > Vol. 128, N° 6 (2012) . - p. 417-424[article]Réservation
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Code-barres Cote Support Localisation Section Disponibilité 14281 - Périodique Bibliothèque principale Documentaires Disponible Styryl dyes - synthesis and applications during the last 15 years / Todor Deligeorgiev in COLORATION TECHNOLOGY, Vol. 126, N° 2 (2010)
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Titre : Styryl dyes - synthesis and applications during the last 15 years Type de document : texte imprimé Auteurs : Todor Deligeorgiev, Auteur ; Aleksey Vasilev, Auteur ; Stefka Kaloyanova, Auteur ; Juan J. Vaquero, Auteur Année de publication : 2010 Article en page(s) : p. 55-80 Note générale : Bibliogr. Langues : Anglais (eng) Index. décimale : 667.3 Teinture et impression des tissus Résumé : One of the most widely used and important groups of functional dyes are the styryl dyes and a review of this functional dye class has not been published for more than 15 years. In this review article, we describe the new trends in the synthesis of a range of novel intermediates and styryl dyes and include the most interesting examples of their high-tech applications. However, this review is not intended to be comprehensive because of the large number of styryl dye studies that have been carried out in this time. Styryl cyanine dyes are widely used in optical recording media in laser discs, as flexible dyes, laser dyes, as optical sensitisers and in various other fields, for example dye-sensitised solar cells and dyes with non-linear optical properties. Additionally, the most important applications for these dyes are in bio-labelling and in medicinal analysis. DOI : 10.1111/j.1478-4408.2010.00235.x Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=9278
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Code-barres Cote Support Localisation Section Disponibilité 012133 - Périodique Bibliothèque principale Documentaires Disponible Synthesis of novel 3-hetaryl-substituted 6- and 8-hydroxybenzo[f]coumarin derivatives / Todor Deligeorgiev in COLORATION TECHNOLOGY, Vol. 126, N° 4 (2010)
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Titre : Synthesis of novel 3-hetaryl-substituted 6- and 8-hydroxybenzo[f]coumarin derivatives Type de document : texte imprimé Auteurs : Todor Deligeorgiev, Auteur ; Teodora Tsvetkova, Auteur ; Stefka Kaloyanova, Auteur ; Diana Ivanova, Auteur ; Iliana Timtcheva, Auteur Année de publication : 2010 Article en page(s) : p. 209-214 Note générale : Bibliogr. Langues : Anglais (eng) Index. décimale : 667.3 Teinture et impression des tissus Résumé : Eight novel 3-hetaryl-substituted 6- and 8-hydroxybenzo[f]iminocoumarin compounds were synthesised by the reaction of 2,5-dihydroxynaphthaldehydes or 2,7-dihydroxynaphthaldehydes with 2-cyanomethylbenzo-thiazole, 2-cyanomethylbenzoimidazole, 1-methyl-2-cyanomethylbenzoimidazole and 2-cyanomethyl-4-phenylthiazole. The iminocompounds obtained were hydrolysed with hydrochloric acid to the benzo[f]coumarins. Becaue of the high reactivity of the iminocoumarins, only mixtures which also contained the corresponding coumarin compounds were isolated. The absorption and steady-state fluorescence characteristics of the benzo[f]coumarins (benzo[f]chromen-2-ones) synthesised were studied in ethanol and in toluene. Note de contenu : EXPERIMENTAL : Synthesis of 3-hetarylbenzo[f]iminocoumarin compounds - Synthesis of 3-hetarylbenzo[f]coumarin.
RESULTS AND DISCUSSION : Synthetic procedure of 3-hetaryl-6- and 8-hydroxybenzo[f]coumarins - Absorption and fluorescent properties of 3-hetaryl-6- and _-hydroxybenzo[f]coumarins.DOI : 10.1111/j.1478-4408.2010.00249.x En ligne : http://onlinelibrary.wiley.com/doi/10.1111/j.1478-4408.2010.00249.x/pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=9873
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Code-barres Cote Support Localisation Section Disponibilité 012370 - Périodique Bibliothèque principale Documentaires Disponible Synthesis of novel tetracationic asymmetric monomeric monomethine cyanine dyes – highly fluorescent dsDNA probes / Aleksey Vasilev in COLORATION TECHNOLOGY, Vol. 127, N° 1 (2011)
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Titre : Synthesis of novel tetracationic asymmetric monomeric monomethine cyanine dyes – highly fluorescent dsDNA probes Type de document : texte imprimé Auteurs : Aleksey Vasilev, Auteur ; Todor Deligeorgiev, Auteur ; Stefka Kaloyanova, Auteur ; Stanimir Stoyanov, Auteur ; Vera Maximova, Auteur ; Juan J. Vaquero, Auteur ; Julio Alvarez-Buila, Auteur Année de publication : 2011 Article en page(s) : p. 69-74 Note générale : Bibliogr. Langues : Anglais (eng) Catégories : ADN
Cyanines monométhines
Fluorescence
Lumière -- Absorption
Pigments à effets spéciaux -- Effets de la lumièreIndex. décimale : 667.3 Teinture et impression des tissus Résumé : Quaternisation of monomethine cyanine dyes bearing haloalkyl chains, with the appropriate monoquaternised 1,4-diazabicyclo[2.2.2]octane derivatives, yielded novel tetracationic asymmetric monomeric monomethine cyanine dyes belonging to the thiazole orange family. The optimal conditions for this reaction were investigated. The longest wavelength absorption maxima of the studied dyes are in the region 504–507 nm. The molar absorptivities of the target dyes are high, with values between 70 500 and 99 500 l mol?1 cm?1. The fluorescence intensity and the fluorescence quantum yields of the free dyes in solution or in the presence of double-stranded DNA were determined using thiazole orange for comparison. The dyes are suitable for nucleic acid detection and have a high binding affinity, attributable to their four positive charges. DOI : 10.1111/j.1478-4408.2010.00280.x En ligne : http://onlinelibrary.wiley.com/doi/10.1111/j.1478-4408.2010.00280.x/pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=10906
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Code-barres Cote Support Localisation Section Disponibilité 012843 - Périodique Bibliothèque principale Documentaires Disponible 013134 - Périodique Bibliothèque principale Documentaires Disponible