Microwave-Assisted Synthesis and Spectroscopic Properties of 4 '-Substituted Rosamine Fluorophores and Naphthyl Analogues

• Tipo: Artigo em Revista Científica Internacional
• Data: 2012

Autores

Ines C S Cardoso (Autor) Outra; Ana L Amorim (Autor) Outra; Carla Queiros (Autor) Outra; Silvia C Lopes (Autor) FCUP; Paula Gameiro (Autor) FCUP; Baltazar de Castro (Autor) FCUP; Maria Rangel (Autor) ICBAS; Ana M G Silva (Autor) Outra

Revista

Título: European Journal of Organic Chemistry

Vol. 2012

Páginas: 5810-5817

ISSN: 1434-193X

Editora: Wiley-Blackwell

Indexação

ISI Web of Knowledge - 25 Citações

Scopus - 26 Citações

Classificação Científica

FOS: Ciências exactas e naturais > Química

Outras Informações

ID Authenticus: P-002-4VQ

DOI: 10.1002/ejoc.201200783

Abstract (EN): A series of rosamine fluorophores was obtained by reaction of the appropriate benzaldehyde and 3-(diethylamino)phenol followed by an oxidation step. Both conventional heating and microwave irradiation methods were utilized, and higher yields in a remarkably shorter period of time (10 min) were achieved by using the microwave irradiation protocol under closed vessel conditions (80 degrees C). The nitro-substituted rosamine was further converted into the corresponding amino derivative through Pd/C-catalysed hydrogenation. The synthetic protocol used for rosamines was also successfully employed to synthesise naphthyl analogues by using 1- and 2-naphthaldehyde. In the latter case, a novel hydroxy analogue was also obtained as a minor product. The photophysical behaviour of all the rosamines was studied in different solvents to rationalize the influence of the substituent groups on the electronic distribution, the effect of steric hindrance caused by the naphthyl ring, and the effect of the solvent. The results demonstrate that the introduction of different substituents in the periphery of the rosamine framework (in particular NO2 and NH2 groups) alters the fluorescence properties of the molecule such as emission wavelength and fluorescence quantum yield. All the rosamines are shown to be more fluorescent in dichloromethane than in more polar solvents such as ethanol. The spectroscopic properties of the 4'-carboxy-substituted rosamine, which is particularly attractive for labelling purposes, was also studied at physiological pH.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 8