RESUMEN
We present the synthesis and characterization of a series of photolabile phenacyl derivative polymers and their subsequent thin film preparation. These systems are composed of up to three methacrylate units: a photolabile component including a p-methoxyphenacyl moiety which after selective irradiation (UV/laser) can provide free carboxylic groups in specific areas for further modification; an anchoring unit, trimethoxysiloxane or glycidyl methacrylate derivative, which allows the covalent attachment of the polymer to the substrate; and a spacer, methyl methacrylate or styrene, which in the appropriate proportion ensures the formation of films with good quality. Structural and thermal properties of these materials have been analyzed by means of NMR, FTIR, elemental analysis, UV, gel permeation chromatography, differental scanning calorimetry, and thermogravimetric analysis. The polymers have been subsequently processed by spin coating to render ultrathin films (<50 nm). Topographic and structural characterization studies of the films have been carried out with atomic force microscopy, contact angle measurements, and X-ray photoelectron spectroscopy. The extent of the substrate attachment of the polymers depending on the nature of the anchoring groups have been studied by ellipsometry and FTIR.
RESUMEN
The surface properties of films made of p-methoxyphenacyl derivative terpolymers, associated with photocleavage by UV irradiation, and their optical patterning are investigated. The deprotection reaction has been monitored by UV and FTIR spectroscopy, contact angle measurements, and X-ray photoelectron spectroscopy, revealing the photoremoval of the protecting p-methoxyphenacyl group in high yields under mild conditions. Parallel and serial patterning of the films has been performed by selective irradiation through optical masks and by laser irradiation via fiber tips of a scanning near-field optical microscope, respectively. By irradiation of photolabile protected functional groups, free carboxylic groups become exposed to the surface with which fluorescent dyes and proteins can be associated specifically.
Asunto(s)
Ácidos Carboxílicos/química , Polímeros/química , Microscopía de Fuerza Atómica , Estructura Molecular , Fotoquímica , Espectrofotometría , Propiedades de Superficie , Agua/químicaRESUMEN
Pulsed light-induced recording in azobenzene polymers has recently been studied due to its potential use in optical storage applications. In this paper we study the photoinduced birefringence (Deltan) and holographic grating recording in an azobenzene side chain liquid-crystalline polymethacrylate irradiating with a single 4 ns light pulse at 532 nm. For some irradiation conditions, Deltan grows in less than 50 ns reaching an essentially stable value of about 10(-2). Holographic gratings have been registered using intensity and polarization patterns. Fast response and stability, similar to those of Deltan, was observed in the holographic recording process. Both light-induced anisotropy and relief contributions have been found in the case of gratings recorded using intensity patterns, relief being the dominant contribution at high recording energies. Polarization gratings have been recorded using two orthogonally circularly polarized beams. The resultant gratings showed stable efficiencies up to 0.8% (measured at 633 nm in 1-mum-thick films) and no measurable relief was observed.