SN2 reaction | EPFL Graph Search

DISPLAYTITLE:SN2 reaction The SN2 reaction is a type of reaction mechanism that is common in organic chemistry. In this mechanism, one bond is broken and one bond is formed in a concerted way, i.e., in one step. The name SN2 refers to the Hughes-Ingold symbol of the mechanism: "SN" indicates that the reaction is a nucleophilic substitution, and "2" that it proceeds via a bi-molecular mechanism, which means both the reacting species are involved in the rate-determining step. The other major type of nucleophilic substitution is the SN1, but many other more specialized mechanisms describe substitution reactions. The SN2 reaction can be considered as an analogue of the associative substitution in the field of inorganic chemistry. Reaction mechanism The reaction most often occurs at an aliphatic sp3 carbon center with an electronegative, stable leaving group attached to it (often denoted X), which is frequently a halide atom. The breaking of the C–X bond and the formation of

Modelling oriented investigations of primary radiation damage in ultra high purity Fe and FeCr alloys

Anna Prokhodtseva

In the quest of the structural materials for the future fusion reactor, it has been shown that ferritic/martensitic (F/M) steels are very promising candidates, with a good radiation resistance in terms of damage accumulation in the microstructure relative to for example austenitic steels. However, our ability to predict their response to irradiation in such harsh conditions is still not satisfactory. In this view, there is a critical need for information on the primary damage occuring in this materials class, as input to the multiscale modelling of the irradiation effects, including the impact of He and H. Despite numerous studies in the last 50 years, there is still lack of knowledge in many areas of the irradiation response of the microstructure of ferritic steels. This is due to the complexity of these materials, for they contain numerous alloying elements, grains boundaries and precipitates. The strategy nowadays to identify basic mechanisms of primary damage is to investigate so-called model alloys of those, which allows parametric studies in simplified structures. In this work ultra high purity Fe and Fe(Cr) model alloys were investigated in a transmission electron microscope (TEM) under ion irradiation in an attempt to better understand the fundamental mechanisms of radiation damage starting from the lowest doses, and the dependence on Cr content. Attention is also paid to the effects of He and H. Radiation induced dislocation loops and cavities were quantified. This study provides data for validation of the modelling efforts. Single, dual and triple beam ion irradiations were performed in JANNuS facility located on two sites, in Orsay and in Saclay in France. In Orsay, electron transparent thin foils of UHP Fe, Fe -5, -10 and -14Cr were irradiated in situ in TEM as a single beam experiment with 500 keV Fe+ ions and as a dual beam experiment with 500 keV Fe+ and 10 keV He+ ion beams, to a dose of 1 dpa with and without 1000 appm/dpa He at room and liquid nitrogen temperatures in order to observe the very first defects, desirably before their thermal evolution. Effects of dose rate on the produced damage were assessed in UHP Fe. The impact of He and Cr on defect accumulation was scrutinized in terms of the number density, size and Burgers vector of the visible defects. Special care was taken in the analysis of the TEM micrographs, for which new techniques were developed, with a particular one to determine the Burgers vector of a dense dispersion of fine nanometric defects. Emphasis was put on the identification of the loops Burgers vector, which is considered to be either a0〈100〉 or 1/2 a0〈111〉 in ferritic materials. 2 In order to study the effect of the free surfaces of the electron transparent thin specimens on the irradiation induced microstructure, the results obtained for TEM thin foils were compared to bulk samples that were irradiated ex situ in Saclay in single beam experiments with 24 MeV Fe8+ ions, and dual beam ones with 24 MeV Fe8+ to 1 dpa and 2 MeV He+ ions 1000 appm/dpa He at RT. To study synergistic effects of He and H a triple beam bulk irradiation with 24 MeV Fe8+, 2 MeV He+ and 0.6 MeV H+ ions, to 1 dpa, 1000 appm/dpa He and 4000 appm/dpa H at room temperature was preformed. From the bulk specimens thin lamellae were extracted by focused ion beam, which allowed the TEM observation of the damage through the whole implanted range of about 3.5 μm. In this way, the effect of irradiation with and without He and synergistic effects of simultaneous He and H implantation on the produced defects were assessed. In addition, radiation induced hardening was assessed by nano-indentation and related to the radiation induced microstructure. The analysis shows that in thin foils of UHP Fe the defect population is dominated by a0〈100〉 defects, while in presence of He it is dominated by 1/2 a0〈111〉 loops after irradiation to 1 dpa. It indicates that helium stabilizes mobile 1/2 a0〈111〉 loops, which in thin foils otherwise escape to 2 the free surfaces. Irradiation to the lowest dose of 0.05 dpa resulted in the production of either increased ratio of 1/2 a0〈111〉 loops, compared to the highest dose, or in the entire population of 2 1/2 a0〈111〉 loops in all materials in single and dual beam. In bulk UHP Fe and Fr(Cr) samples 2 after single and dual beam irradiation mainly 1/2 a0〈111〉 loops and few a0〈100〉 loops were 2 observed, but of smaller size than in thin foils, emphasizing the effects of free surfaces on the type of produced loops. It is thus inferred that 1/2 a0〈111〉 loops dominate the early loop 2 2 population and visible a0〈100〉 loops observed in UHP Fe and Fe(Cr) thin foils stem from addition and/or absorption reactions between 1/2 a0〈111〉 loops. It follows that these reactions 2 are reduced by the presence of He, which may eventually impede the formation of a0〈100〉 loops, leaving a loop population dominated by 1/2 a0〈111〉 loops. The same type of reactions 2 are valid for Fe(Cr) alloys, but the reduction in mobility of 1/2 a0〈111〉 loops by Cr in the single 2 beam case and the synergistic effects of He and Cr after dual beam irradiation result in a mixed population of 1/2 a0〈111〉 and a0〈100〉 type loops. This confirms the idea that the formation of 2 visible a0〈100〉 loops is promoted by the presence of free surfaces. Irradiation of UHP Fe thin foil at liquid nitrogen temperature confirmed the assumption of initial 1/2 a0〈111〉 loops. These then escape to the free surfaces after warming to RT, the more so 2 in the thinnest regions of the sample leaving a loop population dominated by a0〈100〉 loops. In single beam irradiated UHP Fe no dependence of the total density of defects or their Burgers vector on the rate of irradiation was observed. However, in the presence of He, only 1/2 a0〈111〉 2 loops formed under higher dose/implantation rates, while at the lowest dose rate results were similar to the single beam. This observation is attributed to the local increase of the effective He/defect ratio in the case of the high dose rate due to the increased temporal overlap of displacement cascades. Regarding mechanical properties, it appears that hardness of the as received materials increases with increasing Cr content. Following irradiation there is a significant hardening, which is not monotonous with Cr content, and which increases for all materials when irradiated together with He, and the more so when irradiated simultaneously with He and H. Hardening relates well to the observed microstructure and is the largest for Fe-5Cr.

EPFL2013

Understanding the anomalous behavior of Vegard's law in Ce1-xMxO2 (M = Sn and Ti; 0 < x

Olga Safonova

The dependence of the lattice parameter on dopant concentration in Ce1-xMxO2 (M = Sn and Ti) solid solutions is not linear. A change towards a steeper slope is observed around x similar to 0.35, though the fluorite structure (space group Fm3m) is preserved up to x = 0.5. This phenomenon has not been observed for Ce1-xZrxO2 solid solutions showing a perfectly linear decrease of the lattice parameter up to x = 0.5. In order to understand this behavior, the oxidation state of the metal ions, the disorder in the oxygen substructure and the nature of metal-oxygen bonds have been analyzed by XPS, Sn-119 Mossbauer spectroscopy and X-ray absorption spectroscopy. It is observed that the first Sn-O coordination shell in Ce1-xSnxO2 is more compact and less flexible than that of Ce-O. The Sn coordination remains symmetric with eight equivalent, shorter Sn-O bonds, while Ce-O coordination gradually splits into a range of eight non-equivalent bonds compensating for the difference in the ionic radii of Ce4+ and Sn4+. Thus, a long-range effect of Sn doping is hardly extended throughout the lattice in Ce1-xSnxO2. In contrast, for Ce1-xZrxO2 solid solutions, both Ce and Zr have similar local coordination creating similar rearrangement of the oxygen substructure and showing a linear lattice parameter decrease up to 50% Zr substitution. We suggest that the localized effect of Sn substitution due to its higher electronegativity may be responsible for the deviation from Vegard's law in Ce1-xSnxO2 solid solutions.

Royal Soc Chemistry2016

Ring-Opening Reactions of Aminocyclopropanes and Aminocyclobutanes

Mingming Wang

Nitrogen-containing compounds are an important class of molecules in medicinal chemistry, chemical biology, biochemistry, material sciences or environmental sciences. Organic nitrogen occurs in many forms, ranging from small building blocks such as urea, amino acids, nucleotides, to complex natural products, drug molecules, proteins, nucleic acids, among others. The transformation of easily-accessed nitrogen-containing building blocks into more complex nitrogen-containing structures is therefore important for the synthesis of bioactive compounds or functional materials. Interested in donor-acceptor aminocyclopropanes and aminocyclobutanes, we first developed a Lewis-acid catalyzed formal [4+1] cycloaddition of donor-acceptor aminocyclobutanes with isocyanides, which resulted in the formation of cyclopentene-1,2-diamines. We then attempted to develop a formal [3+2] cycloaddition of donor-acceptor aminocyclopropanes with electron-deficient alkenes, which was mechanistically inspired by the Morita-Baylis-Hillman reaction. Apart from the donor-acceptor system, we were also attracted by simple aminocyclopropanes without electron-withdrawing group at vicinal position. We anticipated that the incorporation of cyclopropylamine into carboxylic-containing compounds followed by ring opening functionalization reactions could be used for the synthesis of more complex products. Therefore, we first disclosed an oxidative ring-opening strategy to transform acyl, sulfonyl or carbamate protected aminocyclopropanes into 1,3-dielectrophilic carbon intermediates bearing a halide atom (Br, I) and a N,O-acetal. Replacing the alkoxy group of the N,O-acetal was achieved under acidic conditions via an elimination-addition pathway, while substitution of the halides by nucleophiles was done under basic conditions via a SN2 pathway, generating a wide range of 1,3-difunctionalized propylamines. Based on the transformation described above, we further discovered an efficient synthesis of 4-amino thiochromans starting from simple aminocyclopropanes and thiophenols through a formal [3+3] annulation reaction. Next, we developed an oxidative ring-opening strategy to transform cyclopropylamides and cyclobutylamides into fluorinated imines. The imines can be isolated in their more stable hemiaminal form, with the fluorine atom installed selectively at the terminal position. Both cheap benzophenone with UV A light or organic and inorganic dyes with blue light could be used as photoredox catalysts to promote this process. Various fluorinated amines were then obtained by nucleophilic attack on the hemiaminals in one pot, giving access to a broad range of useful building blocks for medicinal chemistry. Finally, we turned our attention to the synthesis of diamines, which are essential building blocks for the synthesis of agrochemicals, drugs and organic materials, yet their synthesis remains challenging, as both nitrogen moieties need to be differentiated and diverse substitution patterns (1,2-, 1,3 or 1,4) are required. We described a new strategy giving access to 1,2-, 1,3- and 1,4- amido azides as orthogonally protected diamines based on the nitrogen-directed diazidation of alkenes, cyclopropanes and cyclobutanes.Other unsuccessful efforts over the last four years have also been described, together with some preliminary results of ring-opening cyanation and arylation reactions.