Structure and photoluminescent features of di-amide cross-linked alkylene-siloxane hybrids

• Autor(a) principal: Nunes, Sílvia
• Data de Publicação: 2005
• Outros Autores: Zea Bermudez, V. de, Cybinska, J., Ferreira, R. A. Sá, Carlos, Luís, Silva, Maria Manuela, Smith, Michael John, Ostrovskii, David, Rocha, João
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/1822/5482
• topic: Sol-gel synthesis; Thermal stability; Science & Technology

Novel amide cross-linked alkylene/siloxane hybrid materials (di-amidosils) synthesized by the sol-gel process have been investigated. Two samples identified by the notation d-A(x) with x = 4 and 8 (where x is the number of methylene groups of the alkylene chain) have been produced as transparent, amorphous, rigid monoliths, thermally stable up to about 381 and 400 ºC, respectively. In the d-A(8) hybrid the siliceous framework is composed of [(SiO)3Si(CH2)-] and [(SiO)2(HO)Si(CH2)-] substructures. Structural unit distances of 4.1 and 4.2 Å and average interparticle distances of 12 and 17 Å have been determined for d-A(4) and d-A(8), respectively. In these compounds the alkyl chains are disordered and adopt gauche conformations. While a negligible proportion of the amide linkages remain non-bonded, the great majority of these groups belong to highly disordered strong hydrogen-bonded amide-amide associations. The hybrids introduced are room temperature white light emitters, presenting an emission large, broad band in the blue/purplish-blue spectral region. The origin of such band have been ascribed to the convolution of donor-acceptor pair (D-A) recombinations that occur in the NH groups of the urea linkages and in the siliceous nanodomains. The maximum quantum yield value of the d-A(8) di-amidosil is 5.4 %.