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131.
On-surface synthesis is emerging as a highly rational bottom-up methodology for the synthesis of molecular structures that are unattainable or complex to obtain by wet chemistry. Here, oligomers of meta-polyaniline, a known ferromagnetic polymer, were synthesized from para-aminophenol building-blocks via an unexpected and highly specific on-surface formal 1,4 Michael-type addition at the meta position, driven by the reduction of the aminophenol molecule. We rationalize this dehydrogenation and coupling reaction mechanism with a combination of in situ scanning tunneling and non-contact atomic force microscopies, high-resolution synchrotron-based X-ray photoemission spectroscopy and first-principles calculations. This study demonstrates the capability of surfaces to selectively modify local molecular conditions to redirect well-established synthetic routes, such as Michael coupling, towards the rational synthesis of new covalent nanostructures.  相似文献   
132.
A theoretical mechanistic investigation of the cycloaddition reaction of quercetine with 3,5-di-tert-butyl-o-quinone has been carry out employing density functional calculations at M06-2X/6-31G(d,p) level of theory. This computational study was performed in order to gain insight in the energetic and structural parameters that rule the observed experimental selectivity in the synthetised cyclodimers obtained under classical heating and microwave irradiation conditions and the influence of the solvent on their chemical reactivity. The effect of the solvent in the selectivity was studied implicitly using the polarisable continuum model in absence and presence of one explicit solvent’s molecule. The theoretical results explain the main issues of the classical heating and the MWI reaction and suggest that thermal effects are directly responsible for the reaction selectivity observed. The comparison of the mechanistic pathway and the non-covalent interactions, shows that a dioxane assisted mechanism can explain the observed experimental selectivity of the two synthetised compounds, thus the dioxane molecule play a catalytic role on this hetero Diels–Alder reaction.  相似文献   
133.
2 , Ar) in a broad pressure range (10-7–1 mbar) are correlated to the plasma expansion dynamics. It is found that the deposited films present an excess of Ba in the intermediate pressure range (10-2<P<10-1 mbar) and a peaked distribution of Ba to Ti atoms ratio, that is not related to either the substrate temperature or the nature of the gas environment. The results are discussed in terms of the dependence of the plume length (LP) on the gas pressure and the existence of scattering processes for distances (d) from the target lower than LP and the diffusion of the ejected species for LP<d. Received: 7 November 1997/Accepted: 8 November 1997  相似文献   
134.
The optical behavior of a four-level tripod-type atomic system in a ring resonator driven by a cavity field and two external coherent fields is studied. It is shown that the atomic response exhibits an ultra-sensitive switch from high absorption to nearly transparency by changing the value of one of the control fields. The optical bistable response can be controlled by means of the external fields. The system can flip from the lower to the upper branch of the hysteresis curve without changing the incident probe. Switching and information storage of a light signal are predicted under appropriate triggering of the auxiliary external optical signals.  相似文献   
135.
The existence of an asymptotic average of linking numbers ofperiodic orbits of a basic set of an Axiom A flow in S3 or R3is proved.  相似文献   
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We give a formula for the rates of escape for Julia sets with preperiodic critical points and forC endomorphisms of the interval with non-flat pre-periodic critical points outside the basin of attracting periodic points.Research supported by CNPq, Brasil  相似文献   
140.
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