A new bicyclic oxazaborines with a bridged nitrogen atom, their thermic rearrangement and fluorescence properties

Cyclic β-enaminones bearing secondary amino group react with 4-substituted benzenediazonium tetraphenylborates in dichloromethane to form substituted bicyclic [1,3,2λ4]oxazaborines The oxazaborines rearrange, on heating to 200°C in the absence of solvent or in DMF or DMSO, to isomeric 2H-[1,2,4,3λ4]...

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Published inJournal of organometallic chemistry Vol. 699; pp. 75 - 81
Main Authors Josefík, František, Svobodová, Markéta, Bertolasi, Valerio, Šimůnek, Petr, Macháček, Vladimír, Almonasy, Numan, Černošková, Eva
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LanguageEnglish
Published LAUSANNE Elsevier B.V 15.02.2012
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Abstract Cyclic β-enaminones bearing secondary amino group react with 4-substituted benzenediazonium tetraphenylborates in dichloromethane to form substituted bicyclic [1,3,2λ4]oxazaborines The oxazaborines rearrange, on heating to 200°C in the absence of solvent or in DMF or DMSO, to isomeric 2H-[1,2,4,3λ4]triazaborines. Previously prepared [1,3,2λ4]oxazaborines derived from acyclic β-enaminones bearing secondary amino group either did not undergo the rearrangement or with a lot of difficulties and with negligible yield. The fluorescence behaviour of the prepared triazaborines was observed. These compounds fluoresce in 2-methyltetrahydrofurane and in solid state under low temperatures. The enaminones bearing cyclic amino group react with 4-substituted benzenediazonium tetraphenylborate to form new condensed heterocycles – oxazaborines. The condensed triazaborines, showing fluorescence both in 2-methyl THF and in solid state at low temperatures, have been prepared from these oxazaborines. [Display omitted] ►A novel bicyclic [1,3,2λ4]oxazaborines were prepared. ►The oxazaborines rearrange to the triazaborines under various conditions. ►All the boron heterocycles were characterized by means of NMR and also by X-ray. ►Fluorescence properties were studied in various solvents and in the solid state.
AbstractList Cyclic β-enaminones bearing secondary amino group react with 4-substituted benzenediazonium tetraphenylborates in dichloromethane to form substituted bicyclic [1,3,2λ4]oxazaborines The oxazaborines rearrange, on heating to 200°C in the absence of solvent or in DMF or DMSO, to isomeric 2H-[1,2,4,3λ4]triazaborines. Previously prepared [1,3,2λ4]oxazaborines derived from acyclic β-enaminones bearing secondary amino group either did not undergo the rearrangement or with a lot of difficulties and with negligible yield. The fluorescence behaviour of the prepared triazaborines was observed. These compounds fluoresce in 2-methyltetrahydrofurane and in solid state under low temperatures. The enaminones bearing cyclic amino group react with 4-substituted benzenediazonium tetraphenylborate to form new condensed heterocycles – oxazaborines. The condensed triazaborines, showing fluorescence both in 2-methyl THF and in solid state at low temperatures, have been prepared from these oxazaborines. [Display omitted] ►A novel bicyclic [1,3,2λ4]oxazaborines were prepared. ►The oxazaborines rearrange to the triazaborines under various conditions. ►All the boron heterocycles were characterized by means of NMR and also by X-ray. ►Fluorescence properties were studied in various solvents and in the solid state.
Cyclic beta-enaminones bearing secondary amino group react with 4-substituted benzenediazonium tetraphenylborates in dichloromethane to form substituted bicyclic [1,3,2 lambda(4)] oxazaborines The oxazaborines rearrange, on heating to 200 degrees C in the absence of solvent or in DMF or DMSO, to isomeric 2H-[1,2,4,3 lambda(4)] triazaborines. Previously prepared [1,3,2 lambda(4)] oxazaborines derived from acyclic beta-enaminones bearing secondary amino group either did not undergo the rearrangement or with a lot of difficulties and with negligible yield. The fluorescence behaviour of the prepared triazaborines was observed. These compounds fluoresce in 2-methyltetrahydrofurane and in solid state under low temperatures. (C) 2011 Elsevier B.V. All rights reserved.
Author Josefík, František
Svobodová, Markéta
Almonasy, Numan
Šimůnek, Petr
Černošková, Eva
Bertolasi, Valerio
Macháček, Vladimír
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Keywords [1,3,2λ4]Oxazaborines
Fluorescence
2H-[1,2,4,3λ4]triazaborines
β-Enaminones
Diazonium tetraphenylborates
ORGANOBORON COMPOUNDS
BORON COMPLEXES
[1,3,2 lambda]Oxazaborines
beta-Enaminones
2H-[1,2,4,3 lambda]triazaborines
ELECTROLUMINESCENCE
DIPHENYLBORON
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0000-0002-7572-3532
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Elsevier
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SSID ssj0001308
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Snippet Cyclic β-enaminones bearing secondary amino group react with 4-substituted benzenediazonium tetraphenylborates in dichloromethane to form substituted bicyclic...
Cyclic beta-enaminones bearing secondary amino group react with 4-substituted benzenediazonium tetraphenylborates in dichloromethane to form substituted...
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SubjectTerms 2H-[1,2,4,3λ4]triazaborines
[1,3,2λ4]Oxazaborines
Chemistry
Chemistry, Inorganic & Nuclear
Chemistry, Organic
Diazonium tetraphenylborates
Fluorescence
Physical Sciences
Science & Technology
β-Enaminones
Title A new bicyclic oxazaborines with a bridged nitrogen atom, their thermic rearrangement and fluorescence properties
URI https://dx.doi.org/10.1016/j.jorganchem.2011.11.004
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