RESUMEN
The C 1s X-ray absorption spectra of several isolated bundles of single-walled carbon nanotubes (SWCNT) have been measured using scanning transmission X-ray microscopy. First the C 1s and O 1s spectra of a purified but unfunctionalized SWCNT were measured. The C 1s --> pi* transition at 285 eV exhibited almost as strong a dichroic effect (spectral dependence on orientation) as that found in multiwalled carbon nanotubes (Najafi; et al. Small 2008, 7, 2279-2285). Second, purified SWCNT were functionalized with dodecyl and then investigated by STXM. Spectral evidence for the dodecyl functionalization is presented and discussed in comparison to the X-ray absorption spectra of aliphatic hydrocarbons. Both orientation and functionalization mapping of an individual SWCNT bundle is demonstrated.
Asunto(s)
Microscopía Electrónica de Rastreo/métodos , Nanotubos de Carbono/química , Oxígeno/química , Espectrometría Raman , Espectroscopía de Absorción de Rayos XRESUMEN
Single-walled carbon nanotubes (SWCNT) have been reduced with sodium naphthalide in THF. The reduced SWCNT are not only soluble in dimethylsulfoxide (DMSO) to form a stable solution/suspension, but also react spontaneously at room temperature with DMSO to evolve hydrocarbon gases and are converted into functionalized SWCNT. The degree of functionalization is about 2C% and the addends are mainly methyl and small oxygen-containing hydrocarbons. The functionalized SWCNT are apparently more soluble and stable in DMSO solution. It may open a new era for further processing and applications.
Asunto(s)
Cristalización/métodos , Dimetilsulfóxido/química , Nanotecnología/métodos , Nanotubos de Carbono/química , Nanotubos de Carbono/ultraestructura , Sustancias Macromoleculares/química , Ensayo de Materiales , Conformación Molecular , Oxidación-Reducción , Tamaño de la Partícula , Solubilidad , Propiedades de SuperficieRESUMEN
Infrared spectra of isolated unsaturated rhodium cluster-CO complexes in the region of the CO stretching vibration, nu(CO), are measured using a molecular beam depletion technique. These spectra provide benchmarks for interpreting values of nu(CO) that are found when CO is used to probe Rh surfaces and supported Rh nanoparticles. Supported nanoparticles have shifts of nu(CO) of as much as +100 cm-1 compared to the free clusters measured here, indicative of significant charge transfer to the support.
RESUMEN
An Al-cytosine association complex has been generated via laser ablation of a mixture of aluminum and cytosine powders that were pressed into a rod form. The ionization energy of the complex is found to be 5.16 +/- 0.01 eV. The photoionization efficiency spectrum of Al-cytosine has also been collected. DFT calculations indicate that binding of Al to cytosine manifests a significant weakening of the N-H bond, predicted to have a strength of 1.5 eV in the complex, and a significant stabilization of the oxo tautomeric form relative to the hydroxy forms. The predicted ionization energy of 5.2 eV agrees well with the experimental value. The threshold for dehydrogenation/ionization of Al-cytosine, forming (Al-cytosine-H)+, is found to occur at photoexcitation energies between 11.4 and 12.8 eV. This is a two-photon process that is proposed to occur via photoinduced electron transfer from Al to an antibonding (sigma) orbital localized on N-H. In the context of this mechanism, this work constitutes the first time charge transfer between a metal and DNA base has been photoinitiated in the gas phase.