Nitric oxide adsorbed on zeolites: EPR studies

CW-EPR studies of NO adsorbed on sodium ion-exchanged zeolites were focused on the geometrical structure of NO monoradical and (NO)2 biradical formed on zeolites. The EPR spectrum of NO monoradical adsorbed on zeolite can be characterized by the three different g-tensor components and the resolved y-component hyperfine coupling with the 14N nucleus. Among the g-tensor components, the value of g(zz) is very sensitive to the local environment of zeolite and becomes a measure of the electrostatic field in zeolite. The temperature dependence of the g-tensor demonstrated the presence of two states of the Na-NO adduct, in rigid and rotational states. The EPR spectra of NO adsorbed on alkaline metal ion-exchanged zeolite and their temperature dependency are essentially the same as that on sodium ion-exchanged zeolite. On the other hand, for NO adsorbed on copper ion-exchanged zeolite it is known that the magnetic interaction between NO molecule and paramagnetic copper ion are observable in the spectra recorded at low temperature. The signals assigned to (NO)2 biradical were detected for EPR spectrum of NO adsorbed on Na-LTA. CW-EPR spectra as well as their theoretical calculation suggested that the two NO molecules are aligned along their N-O bond axes. A new procedure for automatical EPR simulation is described which makes it possible to analyze EPR spectrum easily. In the last part of this paper, some instances when other nitrogen oxides were used as a probe molecule to characterize the zeolite structure, chemical properties of zeolites, and dynamics of small molecules were described on the basis of selected literature data reported recently.     

Molecularly adsorbed oxygen on metals: electron spectroscopic studies

Oxygen is shown to adsorb molecularly on gold as well as on Ag and Pt. UV and X-ray photoelectron spectroscopy and Auger electron spectroscopy have been employed to investigate electron states of molecularly adsorbed oxygen.     

IR spectra of methane adsorbed on MgO

Methane adsorbed on MgO is activated to form CH₃ fragments stabilized on cations and OH groups.

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, MgO CH₃-, OH-.

     

Photodynamic action of amino substituted hypocrellins: EPR studies on the photogenerations of active oxygen and free radical species

A novel method has been employed to prepare 2-butylamino-2-demethoxy hypocrellin A (BADMHA) and 2-butylamino-2-demethoxy hypocrellin B (BADMHB). Both compounds exhibit stronger absorption at the phototherapeutic window (600-900 nm). The spin trapping and spin counteraction studies have shown that they are both efficient generators of the active oxygen (1O2, O2*-) in the aerobic condition. Under the anaerobic condition they generate non-oxygen free radical (semiquinone radical anion), and the active oxygen mechanism of photosensitization can be converted into non-oxygen free radical mechanism with the depletion of oxygen. The quantum yields of 1O2 generation of BADMHA and BADMHB are 0.46 and 0.44, respectively. Both are lower than those of their parent compounds HA and HB. But the productions of superoxide anion are enhanced significantly compared with HA and HB, indicating they are both favorable Type I phototherapeutic agents.     

ENDOR signal of hydrogen physically adsorbed on activated MgO

A matrix ENDOR signal has been observed for physisorbed molecular hydrogen interacting with trapped-hole surface paramagnetic centres on MgO. The localization of the physisorbed molecules is derived from the matrix ENDOR lineshape.     

EPR study on the photosensitized generation of reactive oxygen species by actinomycin D

Actinomycin D (AMD) is an anticancer antibiotic that can bind selectively to both double-stranded and single-stranded DNA, and this binding greatly enhances DNA photosensitization. Using electron paramagnetic resonance (EPR) in combination with spin trapping techniques, a systematic study was carried out on the reactive oxygen species generated in the photosensitization process of AMD. It was found that 1O2 and O2- are important reactive intermediates either insolution or in DNA complexes, and the generation of these species is in competition. This finding suggests that the photodynamic action of AMD proceeds via two pathways: energy transfer (type Ⅰ mechanism) and electron transfer (type Ⅱ mechanism). 1O2 is the main product formed via energy transfer reaction in solution while electron transfer between the excited states of AMD and DNA becomes the predominant pathway in DNA complexes.     

Density-functional model cluster studies of EPR g tensors of Fs+ centers on the surface of MgO

We report g tensors of surface color centers, so-called F(s) (+) centers, of MgO calculated with two density-functional approaches using accurately embedded cluster models. In line with recent UHV measurements on single-crystalline MgO film, we determined only small g-tensor anisotropies and negative shifts Deltag identical with g-g(e) for all F(s) (+) sites considered, namely, (001)-terrace, step, edge, and corner sites. The g values are very sensitive to the local structure of the defect: relaxation reverses the sign of Deltag. However, accounting for the spin-orbit interaction either self-consistently or perturbatively yields very similar results. In addition to the values of the tensor components, their direction with respect to the surface was determined. In contrast to edges, significant deviations from ideal C(2v) symmetry were found for F(s) (+) centers at steps. Recent data on single-crystalline thin films are reevaluated in the light of these results.     

Interaction of chromocene with MgO and reactivity of the adsorbed species towards CO: An IR study

The interaction of chromocene with partially and totally dehydroxylated MgO and the reactivity of the adsorbed species towards CO have been studied by IR spectroscopy. Cp₂Cr is weakly adsorbed on residual surface MgOH groups, forming hydrogen bonded species and, on the extended (100) faces, forming clustered (Cp₂Cr)_n species. A stronger interaction is observed with the highly unsaturated ions located on the edges and corners of the MgO microcrystals. Upon dosage of CO at room temperature, Cp₂CrCO complexes are formed which are stabilized by interaction with the Mg²⁺ and O²⁻ ions of the surface. The occurrence of an activated process leading to [Cp₂Cr]⁺ and [CpCr(CO)₃]⁻ charged reaction products is also observed.     

Carbon dioxide activation by surface excess electrons: an EPR study of the CO2- radical ion adsorbed on the surface of MgO

The CO2- radical anion has been generated at the surface of MgO by direct electron transfer from surface trapped excess electrons and characterized by electron paramagnetic resonance spectroscopy. Both 13C and 17O hyperfine structures have been resolved for the first time, leading to a detailed mapping of the unpaired electron spin density distribution over the entire radical anion. The magnetic equivalence of the two O nuclei has been ascertained allowing a side-on adsorption structure at low-coordinate Mg2+ ions to be proposed for the surface stabilized radical.     

Low-temperature heat capacity of TMS monolayers adsorbed on graphite and MgO+

The heat capacity obtained below 30 K for the tetramethylsilane monolayers, which are adsorbed either on graphite or on the (100) surface of MgO, is analyzed to investigate the vibrational properties. The 2-D Debye temperatures are approximately 60% of the Debye temperature of the bulk solid (γ -phase), reflecting the dimensionality of lattice vibrations. The contributions from the vibrations perpendicular to the surface as well as the librational motions are determined by fitting the experimental heat capacities. All the results are consistent with those obtained from the incoherent inelastic neutron scattering and the molecular dynamics simulation. This revised version was published online in August 2006 with corrections to the Cover Date.     

The role of the cation in the oxygen isotopic exchange in crystalline sulfate salt hydrates

The oxygen isotopic exchange during dehydration and decomposition of five sulfate salt hydrates (CoSO₄·6H₂O, NiSO₄·7H₂O, ZnSO₄·7H₂O, CaSO₄·2H₂O, Li₂SO₄·H₂O) was studied in detail by temperature programmed desorption mass spectrometry (TPD-MS) in a supersonic molecular beam (SMB) inlet mode. Crystals of the ¹⁸O-enriched salts were grown and the detailed desorption steps of the various gaseous products released during dehydration and decomposition of these compounds were recorded. The desorption patterns confirmed the known characteristic stepwise dehydration of these salts, where regardless of the crystalline structure and composition, in all the salts (excluding the Li and Ca sulfates) a major group of n ? 1 loosely bounded water of crystallization molecules (out of total of n molecules in the fully hydrated form) are released at adjacent temperatures in a typical low temperature range (<200 °C), while the last, most strongly bounded water molecule, consistently desorbs at relatively higher temperatures (240 < T < 440 °C). Interestingly, it is established that the oxygen isotopic exchange occurs exclusively between that latter, most strongly bound water molecule, and the salt anion. Remarkably, the results point out that the exchange process is mostly of solid-solid nature. Finally, the results point out that the probability of the isotopic exchange increases with the increment in the desorption temperature of the last dehydration step, i.e. with the bond strength in the monohydrate, between the last water molecule of crystallization and the cation.     

The determination of the oxygen consumption in autoxidation studies by means of EPR spectroscopy

Stable paramagnetic species give rise in the presence of oxygen to EPR spectra characterized by broad lines due to Heisenberg spin exchange. This property can be conveniently used to determine the amount of oxygen present in the system under investigation. In the present paper we describe the use for this purpose of two radical probes: one is the stable aliphatic nitroxide 2,2,6,6-tetramethyl-l-piperidinyloxyl (TEMPO) which is employed as a homogeneous probe and the other is fusinite, a derivative of coal used as a finely grinded black powder totally insoluble both in water and in organic solvents. Both have been employed to follow the autoxidation reaction of three representative oxidizable substrates, i.e. cumene, styrene and methyl linoleate, in solution of chlorobenzene or of tert-butyl alcohol. The advantages of this technique with respect to traditional methods are emphasized.     

Isotopic exchange of CO adsorbed on Pt(111)

The isotopic exchange of CO adsorbed on Pt(111) was studied using polarization modulation IR reflection absorption spectroscopy (PM-IRRAS) and temperature programmed desorption. It was found that the rate constants for the exchange reaction are much higher than would be expected from previous investigations of CO adsorbed on Pt nanoparticles. The adsorption of CO on Pt(111) under elevated pressures of CO and H(2) was also studied using PM-IRRAS. It was seen that CO pressures above 1 mbar lead to a shift in the absorption peak arising from CO adsorbed on a bridge site from 1850 to 1875 cm(-1). Exposing the CO-covered Pt(111) surface to 1000 mbar H(2) did not lead to any significant desorption of CO at room temperature, whereas at 363 K H(2) exposure did lead to a significant desorption of CO, due to the increased chemical potential of H(2). In a mixture of CO and H(2) with partial pressures of 0.01 mbar and 1000 mbar, respectively, no significant effect of H(2) on the PM-IRRAS spectrum was seen at temperatures below 423 K.     

Synthesis and characterization of antimony mixed-valence compounds in view of solid state isotopic exchange studies

Several attempts have been made to synthesize mixed-valence compound of antimony at low temperature in view of studying the isotopic exchange in solids. The experimental procedure for the synthesis, at 263 K of Cs₄(Sb^IIICl₆)(Sb^VCl₆) has been established. This compound seems very promising for isotopic exchange studies in the solid state.     

STM studies on adsorbed liquid crystal on HOPG

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