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61.
Ellis WW Miedaner A Curtis CJ Gibson DH DuBois DL 《Journal of the American Chemical Society》2002,124(9):1926-1932
The hydride complex [Pt(dmpe)2H]+ (dmpe = 1,2-bis(dimethylphosphino)ethane) reversibly transfers H- to the rhenium carbonyl complex [CpRe(PMe3)(NO)(CO)]+, giving the formyl CpRe(PMe3)(NO)(CHO). From the equilibrium constant for the hydride transfer (16.2), the DeltaGdegrees for the reaction was determined (-1.6 kcal/mol), as was the hydride-donating ability of the formyl (44.1 kcal/mol). The hydride-donating ability, DeltaGdegrees(H-), is defined as the energy required to release the hydride ion into solution by the formyl complex [i.e. M(CHO) right arrow M(CO)+ + H-]. Subsequently, the hydride-donating ability of a series of formyl complexes was determined, ranging from 44 to 55 kcal/mol. With use of this information, two rhenium carbonyl complexes, [CpRe(NO)(CO)2]+ and [Cp*Re(NO)(CO)2]+, were hydrogenated to formyls, employing [Pt(dmpp)2]2+ and Proton-Sponge. Finally, the E(1/2)(I/0) values for five rhenium carbonyl complexes were measured by cyclic voltammetry. Combined with the known DeltaGdegrees(H-) values for the complexes, the hydrogen atom donating abilities could be determined. These values were all found to be approximately 50 kcal/mol. 相似文献
62.
The reactivity of the epoxy-fulvene 1 with various nucleophiles has been examined. It is a versatile Intermediate for the preparation of spiro[4.2]hepta-1,3-diene synthons via nucleophilic addition to the C6 position followed by intramolecular cyclization of the substituted cyclopentadiene anion generated in situ. 相似文献
63.
Electrochemical investigations of the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) have been conducted in a Ca2+-containing dimethyl sulfoxide electrolyte. While the ORR appears irreversible, the introduction of a tetrabutylammonium perchlorate (TBAClO4) co-salt in excess concentrations results in the gradual appearance of a quasi-reversible OER process. Combining the results of systematic cyclic voltammetry investigations, the degree of reversibility depends on the ion pair competition between Ca2+ and TBA+ cations to interact with generated superoxide (O2−). When TBA+ is in larger concentrations, and large reductive overpotentials are applied, a quasi-reversible OER peak emerges with repeated cycling (characteristic of formulations without Ca2+ cations). In situ Raman microscopy and rotating ring-disc electrode (RRDE) experiments revealed more about the nature of species formed at the electrode surface and indicated the progressive evolution of a charge storage mechanism based upon trapped interfacial redox. The first electrochemical step involves generation of O2−, followed primarily by partial passivation of the surface by CaxOy product formation (the dominant initial reaction). Once this product matrix develops, the subsequent formation of TBA+--O2− is contained within the CaxOy product interlayer at the electrode surface and, consequently, undergoes a facile oxidation reaction to regenerate O2.An interlayer product of oxygen reduction with Ca2+/TBA+ yields a quasi-reversible oxygen evolution reaction by inducing a trapped interfacial redox process. 相似文献
64.
The fragmentation reactions of deprotonated N-benzoyl peptides, specifically hippurylglycine, hippurylglyclyclycine, and hippurylphenylalanine (hippuryl = N-benzoylGly) have been studied using MS2 and MS3 experiments as well as deuterium labeling. A major fragment ion is observed at m/z 160 ([C9H6NO2]-) which, upon collisional activation, mainly eliminates CO2 indicating that the two oxygen atoms have become bonded to the same carbon. This observation is rationalized in terms of formation of deprotonated 2-phenyl-5-oxazolone. Various pathways to the deprotonated oxazolone have been elucidated through MS3 experiments. Fragmentation of deprotonated N-acetylalanylalanine gives a relatively weak signal at m/z 112 which, upon collisional activation, fragments, in part, by loss of CO2 leading to the conclusion that the m/z 112 ion is deprotonated 2,4-dimethyl-5-oxazolone. 相似文献
65.
The O?˙ chemical ionization mass spectrri of the C8H10 alkylbenzenes, o-, m-. andp -xylene and ethylbenzene, show formation of [M ? H + O]?, [M ? H]?, [M ? H2]?˙ and, for the xylenes, [M ? CH3 + O]? as primary reaction products; the relative importance of these products depends on the isomer. However, [OH]? is a primary product from reaction of O?˙ with both the C8H10 isomers and hydrogen-containing impurities; [OH]? reacts further with the alkylbenzenes to produce [M ? H]? with the result that the chemical ionization mass spectra depend on experimental conditions such as sample size and the presence of impurities. The collision-induced charge inversion mass spectra of the [M ? H + O]? and [M ? H]? products allow only distinction of ethylbenzene from the xylenes. However, the collision-induced charge inversion mass spectra of the [M ? H2]?˙ ions show differences which allow identification of each isomer. 相似文献
66.
The charge exchange mass spectra of a selection of C5-C7 ketones have been measured using [CS2]+˙, [COS]+˙ and [N2O]+. as reagent ions. The low energy charge exchange with [CS2]+˙ or [COS]+˙ provides simple primary ion mass spectra, which readily permit structure elucidation in contrast to metastable ion spectra. In several cases, isomer distinction is easier from the charge exchange mass spectra than from the electron impact mass spectra. The energy transfer from [N2O]+˙ is sufficiently high for complex spectra resembling electron impact mass spectra to be obtained. 相似文献
67.
Using specifically labelled compounds we have made a detailed study of the source of the hydrogen transferred in the elimination of C3H6 from the molecular ion of phenyln-propyl ether following electron impact ionization and from the protonated (and ethylated) molecule following chemical ionization. The migrating hydrogen originates from all three positions of the npropyl group but not in the ratio expected for randomization of the alkyl hydrogens prior to transfer. The source of the migrating hydrogen is similar for both electron impact ionization and chemical ionization, indicating that the factors governing the rearrangement are the same for both modes of ionization. From a comparison of the results for labelled 2,6-dimethyl phenyl n-propyl ethers with the results for the unsubstituted ether it is concluded that hydrogen transfer occurs only to the ether oxygen and not to the phenyl ring. A two-step mechanism involving a set of competing reversible hydrogen transfer reactions followed by C? O bond cleavage is proposed to explain the results. 相似文献
68.
Minimizing molecular mobility for desiccation preservation of biologics close to ambient temperature using trehalose glasses require quantitative characterization of their enthalpic relaxation at various end water contents. Differential scanning calorimetry (DSC) was used to characterize three different water contents: 0%, 1.5% and 10% over a wide range of aging temperatures. Results showed the characteristic time (τ) varies both with the water content and the aging temperature. τ increased with lowered aging temperature but showed a non-monotonous relationship as a function of water content. Fragility of trehalose glasses was analyzed using thermophysical parameters obtained from relaxation studies. The study showed trehalose to be a fragile glass former at all water contents, with 0% water samples showing a relatively stronger glass. A compromise between molecular mobility and glass fragility led to an optimal water content close to 1.5% and an aging temperature close to room temperature. This would ensure a τ value of 9000 h, which corresponds to a storage period of a year. 相似文献
69.
Temperature-programmed reaction spectroscopy (TPRS) and direct, isothermal reaction-rate measurements were employed to investigate the oxidation of CO on Pt(111) covered with high concentrations of atomic oxygen. The TPRS results show that oxygen atoms chemisorbed on Pt(111) at coverages just above 0.25 ML (monolayers) are reactive toward coadsorbed CO, producing CO(2) at about 295 K. The uptake of CO on Pt(111) is found to decrease with increasing oxygen coverage beyond 0.25 ML and becomes immeasurable at a surface temperature of 100 K when Pt(111) is partially covered with Pt oxide domains at oxygen coverages above 1.5 ML. The rate of CO oxidation measured as a function of CO beam exposure to the surface exhibits a nearly linear increase toward a maximum for initial oxygen coverages between 0.25 and 0.50 ML and constant surface temperatures between 300 and 500 K. At a fixed CO incident flux, the time required to reach the maximum reaction rate increases as the initial oxygen coverage is increased to 0.50 ML. A time lag prior to the reaction-rate maximum is also observed when Pt oxide domains are present on the surface, but the reaction rate increases more slowly with CO exposure and much longer time lags are observed, indicating that the oxide phase is less reactive toward CO than are chemisorbed oxygen atoms on Pt(111). On the partially oxidized surface, the CO exposure needed to reach the rate maximum increases significantly with increases in both the initial oxygen coverage and the surface temperature. A kinetic model is developed that reproduces the qualitative dependence of the CO oxidation rate on the atomic oxygen coverage and the surface temperature. The model assumes that CO chemisorption and reaction occur only on regions of the surface covered by chemisorbed oxygen atoms and describes the CO chemisorption probability as a decreasing function of the atomic oxygen coverage in the chemisorbed phase. The model also takes into account the migration of oxygen atoms from oxide domains to domains with chemisorbed oxygen atoms. According to the model, the reaction rate initially increases with the CO exposure because the rate of CO chemisorption is enhanced as the coverage of chemisorbed oxygen atoms decreases during reaction. Longer rate delays are predicted for the partially oxidized surface because oxygen migration from the oxide phase maintains high oxygen coverages in the coexisting chemisorbed oxygen phase that hinder CO chemisorption. It is shown that the time evolution of the CO oxidation rate is determined by the relative rates of CO chemisorption and oxygen migration, R(ad) and R(m), respectively, with an increase in the relative rate of oxygen migration acting to inhibit the reaction. We find that the time lag in the reaction rate increases nearly exponentially with the initial oxygen coverage [O](i) (tot) when [O](i) (tot) exceeds a critical value, which is defined as the coverage above which R(ad)R(m) is less than unity at fixed CO incident flux and surface temperature. These results demonstrate that the kinetics for CO oxidation on oxidized Pt(111) is governed by the sensitivity of CO binding and chemisorption on the atomic oxygen coverage and the distribution of surface oxygen phases. 相似文献
70.
Anthony Marshall Martin Tkaczyk Alex G. Harrison 《Journal of the American Society for Mass Spectrometry》1991,2(4):292-298
The negative ion chemical ionization mass spectra of twentyeight C4 to C7 carbonyl compounds were recorded using the oxide radical anion O?? as reagent ion. As noted earlier, the reactions occurring include H+ abstraction, H 2 +? abstraction, H? atom displacement, and alkyl radical displacement. In addition, the [M?2H]? ions fragment further by alkyl radical elimination. The relative importance of these reactions depends strongly on molecular structure, with the result that isomer distinction frequently is possible. Where this is not possible, as for isomeric aldehydes, the collisional charge inversion mass spectra of common product ions provides isomer distinction. The H 2 +? abstraction reaction is shown to involve abstraction not only of two hydrogens from the same α-carbon but also, in part, abstraction of one hydrogen from each α-carbon. 相似文献