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1.
Chemphyschem ; 20(5): 665-671, 2019 03 04.
Artigo em Inglês | MEDLINE | ID: mdl-30645049

RESUMO

A blue-light emitting material based on a boron complex containing heteroaromatic phosphonate ligand is synthesized and characterized. The Phospho-Fries rearrangement is used in the synthesis route of the ligand as a convenient method of introducing phosphonate groups into phenols. Structural, thermal and photophysical properties of the resulting oxazaborinin phosphonate compound have been characterized. DFT geometry optimizations were studied as well as the spatial position and symmetry of the HOMO and LUMO. Good thermal stability up to 250 °C enables vacuum deposition methods next to solution processing. Combining the work function with the optical band gap from UV-Vis measurements shows that band alignment is possible with standard contact materials. Photoluminescence reveals an emission peak at 428 nm, which is suitable for a blue light-emitter.

2.
Org Biomol Chem ; 9(24): 8228-32, 2011 Dec 21.
Artigo em Inglês | MEDLINE | ID: mdl-22011698

RESUMO

Acetylenephosphonates carrying the XCF(2) group have been studied in a base-mediated heterocyclization reaction with selected 2-amino-3-formylchromones to give 2-difluoromethyl azaxanth-3-ylphosphonates. The presence of the fluorinated substituent determined the regioselectivity as well as the reactivity of this process.


Assuntos
Alcinos/química , Fluorocarbonos/química , Organofosfonatos/química , Piridinas/síntese química , Xantonas/síntese química , Ciclização , Estrutura Molecular , Piridinas/química , Estereoisomerismo , Xantonas/química
3.
J Org Chem ; 76(1): 71-9, 2011 Jan 07.
Artigo em Inglês | MEDLINE | ID: mdl-21121658

RESUMO

An efficient synthesis of 2-perfluoroalkyl 4H-chromen-3-ylphosphonates 4a-i (R(F) = CF(3)) and 5a-i (R(F) = C(2)F(5)) has been accomplished via regioselective cycloaddition of 2-hydroxybenzaldehydes to diethyl 3,3,3-trifluoropropyn-1-yl- and diethyl 3,3,4,4,4-pentafluorobutyn-1-ylphosphonate, using trialkyl amines or phosphines as mediators. 2H-Chromen-3-ylphosphonates 6a-i were regioselectively obtained in the presence of triphenylphosphine. A convenient method for the isomerization of 4H-chromen-3-ylphosphonates into 2H-chromen-3-ylphosphonates 6a-i (R(F) = CF(3)) and 7a-i (R(F) = C(2)F(5)) was established.


Assuntos
Aldeídos/química , Aminas/química , Benzopiranos/química , Benzopiranos/síntese química , Fluorocarbonos/química , Fluorocarbonos/síntese química , Fosfinas/química , Ciclização , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Estereoisomerismo
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