The Ph.D. thesis deals with the preparation of highly hydraulic binders based on roman cement. Roman cement (natural cement) is recently not available on the market due to uneconomic production of such a specific binder. On the other hand there is a big lack of information on this hydraulic binder. These results in failure in meeting the basic principle of modern approaches to restoration of historical buildings or monuments made of such kind of materials, which is such, that the materials used for restoration should be compatible with original material. Recognition of the processes of roman cement preparation based on progressive methods of study can provide substantial information for more efficient raw material selection or even for nontraditional utilization, for example for artworks. This work hence is aimed at studying and selection of traditional natural as well as nontraditional raw materials such as clay. This work also studies the preparation of highly hydraulic binders based on roman cement and the kinetics of burning and hydration processes

Ce travail rapporte la synthèse et l'évaluation biologique des molécules hybrides de type isocombrétastatine A-4/belinostat. L'évaluation biologique de cette nouvelle série nous a permis d'identifier deux molécules inhibitrices de la polymérisation de la tubuline ainsi que de la HDAC8 possédant une puissante activité anti-proliférative dans la gamme du nanomolaire. De plus, nous démontrons que le système de catalyseur PtO2/PTSA-MeOH/H2O est très efficace pour convertir les alcynes internes et terminaux en cétones et qu’il est compatible avec une grande variété de groupes fonctionnels. / In this work, we report the synthesis and biological evaluation of isocombretastatin A-4/belinostat hybrid molecules. The biological evaluation of these new series has identified two molecules with potent anti-proliferative activity in the nanomolar range, which exhibit inhibitory activity on tubulin assembly and HDAC8. Second, we demonstrate that the PtO2/PTSA-MeOH/H2O catalyst system is very efficient in converting internal and terminal alkynes to ketones and that it is compatible with a wide variety of functional groups.

Membrane proteins are vital for cellular homeostasis. They maintain the electrochemical gradients that are essential for signaling and control the fine balance of trace elements. In order to fulfill these tasks, they need to undergo controlled conformational transitions within the lipid bilayer of a cell membrane. It is well-recognized that membrane protein structure and function depends on the lipid membrane. However, much less is known about the role of water re-partitioning at the protein–lipid interface and particularly within a membrane protein during functional transitions. Intra-membrane protein hydration is expected to be particularly important for ion transport processes, where the hydration shell of a solvated ion needs to be rearranged and partially removed in order to bind the ion within the transporter before it is re-solvated upon exiting the membrane protein. These processes are spatially and temporally organized in metal-transporting ATPases of the PIB-subtype of P-type ATPases. Here, the functional role of water entry into the transmembrane region of the copper-transporting PIB-type ATPase CopA from Legionella pneumophila (LpCopA) has been investigated. The recombinant protein was affinity-purified and functionally reconstituted into nanodiscs prepared with the extended scaffolding protein MSP1E3D1. Nanodiscs provide a planar native-like lipid bilayer in a water-soluble nanoparticle with advantageous optical properties for spectroscopy. The small polarity-sensitive fluorophore 6-bromoacetyl-2-dimethylaminonaphthalene (BADAN) was used as a probe for the molecular environment of the conserved copper-binding cysteine-proline-cysteine (CPC) motif which is located close to a wide “entry platform” for Cu+ to the transmembrane (TM) channel. The systematic study of proteins with mutated metal-binding motifs using steady-state and time-resolved fluorescence spectroscopy indicates that strong gradients of hydration and protein flexibility can exist across the narrow range of the CPC motif. The data suggest that Cu+ passes a “hydrophobic gate” at the more cytoplasmic C384 provided by rather stable TM helix packing before entering a more flexible and readily hydratable site in the interior of LpCopA around C382 where the polarity is strongly regulated by protein–lipid interactions. This flexibility could also be partly mediated by rearrangements of an adjacent amphipathic protein stretch that runs parallel to the membrane surface as a part of the cytoplasmic entry site. Using tryptophan fluorescence, circular dichroism, and Fourier-transform infrared absorption spectroscopy of a synthetic peptide derived from this segment, its lipid-dependent structural variability could be revealed. Depending on lipid-mediated helix packing interactions, the CPC motif has the potential to support a strong dielectric gradient with about ten units difference in permittivity across the CPC distance. This property may be crucial in establishing the directionality of ion transport by a non-symmetric re-solvation potential in the ion release channel of LpCopA. The experimental elucidation of these molecular details emphasizes not only the importance of intra-membrane protein water which has been hypothesized particularly for PIB-type ATPases. Moreover it is shown here, that the lateral pressure of a cell membrane may provide a force that restores a low hydration state from a transiently formed state of high internal water content at the distal side of the CPC motif. ATP-driven conformational changes that induce intra-membrane protein hydration of a conformational intermediate of the Post-Albers cycle could thus be set back efficiently by lateral pressure of the cell membrane at a later step of the cycle.

Das American Concrete Institute (ACI) definiert Hochleistungsbeton (High performance concrete, HPC) als einen Beton, der spezielle Leistungs- und Gleichförmigkeitsanforderungen erfüllt. Die Anforderungen schließen vereinfachtes Ausbringen, verbesserte Frühfestigkeiten und mechanische Langzeiteigenschaften, Härte, Volumenstabilität und Belastbarkeit unter besonderen Umweltbedingungen ein. Diesen Anforderungen kann für gewöhnlich nicht mit klassischen Rohstoffen, normalen Misch- und Abbindeprozeduren entsprochen werden. Daher wurde in dieser Studie in Übereinstimmung mit der Literatur die Einfachheit des Ausbringens beziehungsweise die Selbstverdichtung als Kriterium für Hochleistungseigenschaften genommen. Während einer bautechnischen Begutachtung eines brandgeschädigten Gebäudes in Lahore deutete sich an, dass die Schäden zum größten Teil durch mangelhafte Kenntnis der Materialeigenschaften und mangelhafte Verarbeitung verursacht wurden. Dies war unter anderem Anlass für die Durchführung der vorliegenden Untersuchungen. Die Arbeiten über Hochleistungsbetone begannen mit der Auswahl von alternativen Rohstoffen (secondary raw materials, SRM) entsprechend den Ergebnissen des Literaturstudiums. Die Verwendung von Reisasche (Rice husk ash, RHA) in selbstverdichtenden Betonen (Self compacting concrete, SCC) ist eine neue Idee, die bislang nicht veröffentlicht wurde. Deshalb wurden vergleichende Untersuchungen mit Mikrosilika (Silica fume, SF), amorpher und kristalliner Reisasche (RHA bzw. RHAP) durchgeführt. In vielen Entwicklungsländern ist Mikrosilika guter Qualität auf absehbare Zeit kaum zu vernünftigen Preisen verfügbar, während Reisasche in reisanbauenden Ländern wie Pakistan hochverfügbar ist. Bei entsprechenden Ergebnissen soll mit dieser Studie die Verwendung von RHA alternativ zu SF in SCC empfohlen werden. Das Literaturstudium zeigte ferner, dass die Verwendung von Flugasche in Kombination mit anderen puzzolanischen Materialien wie Mikrosilika in Deutschland nicht üblich ist, während dies in Skandinavien erfolgreich getan wird. Deshalb ist ein weiterer Aspekt der vorliegenden Arbeit die Untersuchung der Rolle binärer und ternärer Binder in SCC. Als SRM wurden Kalksteinmehl, Flugasche, Mikrosilika sowie RHA (aus USA) und RHAP (aus Pakistan) ausgewählt. Die Studie beschäftigt sich mit Fließverhalten, Festigkeit, Mikrostruktur und Volumenstabilität (gemessen als frühes Schwinden) von SCC. Die durch binäre und ternäre Binder bewirkte Erhöhung der Gesamtfestigkeit soll möglichst einfach berechnet werden können. Die ist von großem Wert für Bauingenieure, da sie üblicherweise nur an der Gesamtfestigkeit des zementären Systems und nicht an den Festigkeitsanteilen chemischer oder physischer Komponenten interessiert sind. Es wird vorgeschlagen, das vergleichsweise inerte Material für andere puzzolanische Binder und deren Kombinationen als Ausgangspunkt zur einfachen Quantifizierung der Festigkeit zu nehmen. Es ist in der Praxis nicht üblich, die frühe Gesamtschwindung mit deren einzelnen Teilprozessen zu beschreiben. Deshalb wurde die Volumenstabilität als lineare Gesamtschwindung ermittelt. Die Arbeiten begannen mit selbstverdichtenden Pasten (High performance self compacting pastes, HP SCP), die zu selbstverdichtenden Mörteln (High performance self compacting mortars, HP SCM) und selbstverdichtenden Betonen (High performance self compacting concretes, HP SCC) weiterentwickelt wurden. Die Ergebnisse dieser Arbeiten können als anwendungsfreundlicher angesehen werden, als Ergebnisse von Arbeiten durchgeführt ausschließlich an SCC. Darüber hinaus wurden ausgehend von Laborergebnissen einige Versuche an einem Beton-Mischwerk und anschließend während des Einbringens in einen Versuchsstollen des Lehrbergwerks durchgeführt. Zur Abschätzung von Wasserbedarf, Fließverhalten und Festigkeit von HP SCC werden verschiedene einfache Methoden und Konzepte vorgeschlagen. Die Erfindung von Verflüssigern in Deutschland und Japan Anfang der 80er Jahre ermöglichte zusammen mit geeigneten Zuschlägen das Erreichen hoher Festigkeiten und Dauerhaftigkeiten. Es wird eine Methode zur indirekten Berechnung des Wasserbedarfs für jeden Zuschlag, der in geeigneten Mengen mit Zement gemischt wird. Weiterhin schlägt der Autor die Messung der T 25 cm Fließzeit für HP SCM/SCP-Systeme (das Verhältnis zwischen T 25 cm Ausbreitmaß und dem Kegelbodendurchmesser) in Analogie zur Ermittlung des 50cm-Ausbreitmaßes mittels Abrams-Kegel bei SCC vor. Dies wäre ein brauchbarer indirekter Indikator der rheologischen Eigenschaften von SCC-Systemen. Der Durchmesser des Abramskegels ist 20 cm und das besprochene Verhältnis ist 2,5. Ausgehend von den Ergebnissen lässt sich feststellen, dass sicher amorphe RHA als Ersatz für SF in SCC genommen werden kann. Dies gilt selbst bei RHA mittlerer puzzolanischer Aktivität, wie sie von Kraftwerken mit Reistrohfeuerung erhältlich ist. Die Verbesserung von Leistung und Dauerhaftigkeit konnte sowohl für binäre als auch für ternäre Binder in SCC-Systemen festgestellt werden. Für gute Dauerhaftigkeit wie auch aus ökonomischen Gründen wird vorgeschlagen, dass die Menge des zuzumischenden Wassers in etwa dem Wasserbedarf entspricht.

Among the most impressive developments observed in the last 20 years, the improvement of the installation methods of monolithic refractories is certainly to be taken into account. However, this evolution, from vibratable castables to shotcrete and drycrete was not applied to materials based on magnesia, which are still mostly commercialized as ramming mixes, or as pouring castables with poor properties due to excessive water use. The major issues associated to this lack of technology is the scarcity of submicrometric powders compatible to magnesian systems, and the expansion followed by hydration of the magnesia, which is a disruptive reaction. By a thorough research on the literature, some potential additives were identified to be tested as anti-hydration additives. Hydration tests of powders in autoclave, complemented by pH and rheological measurements on magnesia pastes have identified five possible additives which can be used to inhibit the hydration: tartaric acid, citric acid, boric acid, magnesium fluoride and microsilica. Salts from the organic acids can also be successfully used. Of these, microsilica also presented the advantage of providing the submicrometric particles necessary to improve the flow of the castable, and to improve the bond of the castable. The three acids are very effective in inhibiting the formation of magnesium hydroxide, but affect negatively flow properties and mechanical resistance after cure. Microsilica prevented hydration cracks due to the reaction between the silicic acid generated under basic environment with the newly formed brucite, leading to the precipitation of a magnesium-silica-hydrated phase of poor crystallinity between the magnesia grains. This phase does not promote volumetric change, and also enable water release at a wider temperature range. Due to its nature close to serpentine minerals, it forms forsterite and enstatite at low temperatures, thus generating suitable strength between room temperature and at least 1400 °C. Magnesium fluoride changed the nature of this magnesium-silica-hydrated phase, by being incorporated to it and forming a phase more similar to the humite minerals. These minerals present higher MgO:SiO2 molar ratio than serpentine, and their formation requires a lower content of microsilica for a same effect against hydration, which is beneficial for the overall properties of the castable. The properties of the castable, as well as the influence of a number of other variables (for instance, refractoriness under load, creep, cold crushing strength, cold modulus of rupture, bulk density and apparent porosity) were also studied and hereby reported. It is believed that this technology can be further developed for industrial use, provided that some issues regarding the properties at high temperatures are solved. Not only had the study and comprehension of the nature of the bond between microsilica and magnesia, and the role of magnesium fluoride been pioneered by this work, but also the methodology used to evaluate the hydration after the drying process of castings, which was close to real refractory components.

Les ciments sulfoalumineux sont des liants hydrauliques qui, jusqu’aujourd’hui ne sont pas normalisés et ne possèdent donc pas une composition fixe. La teneur en ye’elimite – la phase principale de ce ciment- peut varier de 5 à 70 %. Or la composition du ciment sulfoalumineux (la composition du clinker ainsi que le pourcentage de gypse ajouté) est un paramètre critique qui contrôle sa réactivité, ses performances mécaniques, ainsi que sa durabilité. L’objectif principal de cette thèse est donc l’étude de l’influence de la composition des ciments sulfoalumineux sur leurs propriétés techniques, telles que les performances mécaniques et durabilité. Trois axes principaux ont été abordés. Tout d’abord une étude de l’influence de la composition du ciment sulfoalumineux (25-75 % en masse de ye’elimite) sur ses propriétés hydrauliques et mécaniques ainsi que sur la valeur limite en élément trace (Zn) a été menée. Dans ce but trois ciment sulfoalumineux (25, 50 et 75 % en masse de ye’elimite) ont été synthétisés. Ensuite l’effet de la variabilité de ce ciment sur sa durabilité dans l’eau pure et sulfatée a été investigué par rapport à un ciment sulfoalumineux commercial. Enfin, une étude des potentialités du ciment sulfoalumineux commercial à inhiber la réaction alcali silice dans les mortiers, lors de l’utilisation d’un granulat réactif (Silex), a été conduite. Il en résulte de cette étude qu’une augmentation de taux de ye’elimite dans le ciment sulfoalumineux engendre une augmentation des performances mécaniques. La valeur limite en Zn est de 0,3 % indépendamment de la composition du ciment sulfoalumineux. Par contre cette dernière influence la durabilité de ces ciments. Les résultats révèlent que même si la formulation contenant 75 % en ye’elimite confère les meilleures performances mécaniques, sa durabilité était la plus faible due à l’absence de stratlingite dans sa matrice cimentaire. Enfin, l’utilisation du ciment sulfoalumineux présente des bonnes potentialités à inhiber la réaction alcali silice. / Sulfoaluminate cements are hydraulic binders that, until today, are not standardized and therefore do not have a fixed composition. The content of ye'elimite - the main compound of this cement - can vary from 5 to 70 %. However, the composition of sulfoaluminate cement (clinker composition as well as the percentage of added gypsum) is a critical parameter that controls its reactivity, mechanical performance, as well as its durability. The main objective of this thesis is to study the influence of sulfoaluminate cements composition on their technical properties, such as mechanical performances and durability. Three main axes were discussed in this work. First, the influence of the sulfoaluminate cement composition (25-75 wt. % of ye'elimite) on its hydraulic and mechanical properties, as well as on the threshold limit of Zn, was studied. For this purpose three sulfoaluminate cements (25, 50 and 75 wt. % of ye'elimite) were synthesized. Then the effect of the variability of this cement on its durability in pure and sulphated water was investigated compared to a commercial sulfoaluminate cement. Finally, a study of the potentialities of commercial sulfoaluminate cement to inhibit the alkali silica reaction in mortars, when using a reactive aggregate (flint), was conducted. This study reveals that an increase in ye'elimite content in the sulfoaluminate cement increases the mechanical performance. The threshold limit of Zn is 0.3 % independently of the sulfoaluminate cement composition. Contrariwise, the sulfoaluminate cement composition influences the durability of these cements. Although the formulation containing 75 % of ye’elimite gives the best mechanical performances, its durability was lowest due to the absence of stratlingite in its cement matrix. Finally, the use of sulfoaluminate cement has good potential towards the inhibition of the alkali silica reaction.

Gegenstand der Arbeit ist die Untersuchung der kollektiven Diffusion von Wasser und Ionen in wässrigen Elektrolytlösungen. Dabei wird insbesondere die Dynamik der Wassermoleküle innerhalb der Hydratationshüllen der Ionen und der Einfluss poröser Materialien untersucht. Nach einer Einführung zur Dynamik der Hydratationshülle folgen Grundlagen der NMR-Diffusometrie, welche genutzt wurde um die Selbstdiffusionskoefifizienten der Wassermoleküle und der Ionen der Lösungen zu messen. Daraus wurden die dynamischen Hydratationszahlen der Ionen bestimmt, welche die Anzahl an Wassermolekülen angeben, die durch die Diffusion des Ions in ihrer translatorischen Bewegung beeinflusst sind. Der Einfluss poröser Materialien auf die Dynamik wird am Beispiel nanoporöser Glasmonolithe und mikroporöser Li-LSX Kristalle untersucht.

The number of people suffering from neurodegenerative diseases, such as Alzheimer`s disease, increased dramatically over the past centuries and is expected to increase even further within the next years. Based on predictions of the World Health Organization and Alzheimer`s Disease International, 115 million people will suffer from dementia by the year 2050. An additionally increase in other age related neurodegenerative diseases is also forecasted. Quite naturally, neurodegenerative diseases became a focus of attention of governments and health insurances, trying to control the uprising financial burden. Early detection and treatment of neurodegenerative diseases could be an important component in containing this problem. In particular, researchers focused on automatic methods to analyze patients’ imaging data. One way to detect structural changes in magnetic resonance images (MRI) is the voxel-based method approach. It was specifically implemented for various imaging modalities, e.g. T1-weighted images or diffusion tensor imaging (DTI). Voxel-based morphometry (VBM), a method specifically designed to analyze T1-weighted images, has become very popular over the last decade. Investigations using VBM revealed numerous structural brain changes related to, e.g. neurodegeneration, learning induced structural changes or aging. Although voxel-based methods are designed to be robust and reliable structural change detection methods, it is known that they can be influenced by physical and physiological factors. Dehydration, for example, can affect the volume of brain structures and possibly induce a confound in morphometric studies. Therefore, three-dimensional T1-weighted images were acquired of six young and healthy subjects during different states of hydration. Measurements during normal hydration, hyperhydration, and dehydration made it possible to assess consequential volume changes in gray matter (GM), white matter (WM), and cerebrospinal fluid (CSF). The datasets were analyzed using VBM, FreeSurfer and SIENA. A significant decrease of GM and WM volume, associated with dehydration, was found in various brain regions. The most prominent effects were found in temporal and parietal areas, in the left inferior orbito-frontal region, and in the extra-nuclear region. Moreover, we found consistent increases in CSF, an expansion around 6% of the ventricular system affecting both lateral ventricles, i.e. the third and fourth ventricle. Similar degrees of shrinkage in WM volume and increase of the ventricular system have been reported in studies of Alzheimer’s disease during disease progression and in its prestage mild cognitive impairment. Based on these findings, a potential confound in GM and WM or CSF studies due to the subjects’ hydration state cannot be excluded and should be appropriately addressed. These results underline the sensitivity of VBM and might also concern other voxel-based methods, such as Tract-Based Spatial Statistics (TBSS). TBSS was specifically designed for WM analyses and its sensitivity might be helpful for revealing the spatial relation of structural WM changes and related blood serum biomarkers. Two common brain related biomarkers are the glial protein S100B, a plasticity inducing neuro- and gliotrophin, and neuron-specific enolase (NSE), a marker for neuronal damage. However, the spatial specificity of these biomarkers for brain region has not been investigated in vivo until now. Therefore, we acquired two MRI parameters – T1- weighted and DTI - sensitive to changes in GM and WM, and obtained serum S100B and NSE levels of 41 healthy subjects. Additionally, the gene expression of S100B on the whole brain level in a male cohort of three subjects from the Allen Brain Database was analyzed. Furthermore, a female post mortal brain was investigated using double immunofluorescence labeling with oligodendrocyte markers. It could be shown that S100B is specifically related to white matter structures, namely the corpus callosum, anterior forceps and superior longitudinal fasciculus in female subjects. This effect was observed in fractional anisotropy and radial diffusivity – the latest an indicator of myelin changes. Histological data confirmed a co-localization of S100B with oligodendrocyte markers in the human corpus callosum. S100B was most abundantly expressed in the corpus callosum according to the whole genome Allen Human Brain Atlas. In addition, NSE was related to gray matter structures, namely the amygdala. This effect was detected across sexes. The data demonstrates a very high S100B expression in white matter tracts, in particular in human corpus callosum. This was the first in vivo study validating the specificity of the glial marker S100B for the human brain, and supporting the assumption that radial diffusivity represents a myelin marker. The results open a new perspective for future studies investigating major neuropsychiatric disorders. All above mentioned studies are mainly dependent on the sensitivity and accuracy of soft and hardware parameters. In particular, technical developments have improved acquisition accuracy in the field of MRI. Interestingly, very little is known about the confounding effects of variations due to hardware parameters and their possible impact on reliability and sensitivity of VBM. Recent studies have shown that different acquisition parameters may influence VBM results. Therefore age-related GM changes were investigated with VBM in 36 healthy volunteers grouped into 12 young, 12 middle-aged and 12 elderly subject. Six T1-weighted datasets were acquired per subject with a 12-channel matrix coil, as well as a 32-channel array, MP-RAGE and MP2RAGE, and with isotropic resolutions of 0.8 and 1 mm. DARTEL-VBM was applied on all images and GM, WM and CSF segments were statistically analyzed.. Paired t-tests and statistical interaction tests revealed significant effects of acquisition parameters on the estimated gray-matter-density (GMD) in various cortical and subcortical brain regions. MP2RAGE seemed slightly less prone to false positive results when comparing data acquired with different RF coils and yielded superior segmentation of deep GM structures. With the 12-channel coil, MP-RAGE was superior in detecting age-related changes, especially in cortical structures. Most differences between both sequences became insignificant with the 32-channel coil, indicating that the MP2RAGE images benefited more from the improved signal-to-noise ratio and improved parallel-imaging reconstruction). A possible explanation might be an overestimation of the GM compartment on the MP-RAGE images. In view of substantial effects obtained for all parameters, careful standardization of the acquisition protocol is advocated. While the current investigation focused on aging effects, similar results are expected for other VBM studies, like on plasticity or neurodegenerative diseases. This work has shown that voxel-based methods are sensitive to subtle structural brain changes, independent of imaging modality and scanning parameters. In particular, the studies investigated and discussed the analysis of T1- and diffusion weighted images with VBM and TBSS in the context of dehydration, blood serum sensitive biomarkers and aging were discussed. The major goal of these studies was the investigation of the sensitivity of voxel-based methods. In conclusion, sensitivity and accuracy of voxelbased methods is already high, but it can be increased significantly, using optimal hardand software parameters. It is of note, though, that these optimizations and the concomitant increase of detection sensitivity could also introduce additional confounding factors in the imaging data and interfere with the latter preprocessing and statistical computations. To avoid an interference e.g. originating from physiological parameters, a very careful selection and monitoring of biological parameters of each volunteer throughout the whole study is recommended. A potential impact of scanning parameters can be minimized by strict adherence to the imaging protocol for each study subjectwithin a study. A general increase in detection sensitivity due to optimized parameters selection in hard- and/or can not be concluded by the above mentioned studies. Although the present work addressed some of those issues, the topic of optimal selection of parameters for morphometric studies is still very complex and controversial and has to be individually decided. Further investigations are needed to define more general scanning and preprocessing standards to increase detection sensitivity without the concomitant amplification of confounding factors.

Anhydrit II (AII) wird industriell hauptsächlich als Bindemittel bei der Fußbodenestrich-Herstellung eingesetzt. Zur Beschleunigung der Abbindereaktion und der daraus resultierenden schnelleren Verfestigung des Fußbodens wird Kaliumsulfat als Additiv verwendet. Im Rahmen dieser Arbeit wurden anorganische Salze (Sulfate und Chloride) im Vergleich zu Kaliumsulfat hinsichtlich ihrer beschleunigenden Wirkung auf die Abbindereaktion von AII untersucht, um eine mögliche Alternative und einen Mechanismus für die Wirkungsweise der Additive angeben zu können. Unter den verwendeten Salz-Additiven wurde keine Alternative zu K2SO4 für die industrielle Anwendung gefunden. Als Ursache für die beschleunigende Wirkung von K2SO4 wird die Bildung des Doppelsalzes Syngenit auf der Anhydrit-Oberfläche angenommen. Durch epitaktische Beziehungen von Kristallflächen oder den Zerfall des Syngenits wird die heterogene Gips-Keimbildung begünstigt und die Abbindereaktion beschleunigt.

La spectroscopie de dissociation par absorption de photons infrarouges (IRPD) permet d’obtenir les signatures vibrationnelles d’espèces chargées en phase gazeuse, telles que de petits peptides ou des ions hydratés dans des agrégats d’eau. L’attribution des modes de vibration pour établir une relation entre le spectre expérimental et une structure moléculaire est une tâche délicate et nécessite le recours à la modélisation moléculaire.Ce manuscrit présente un ensemble d’outils théoriques pour le calcul et l’attribution de spectres vibrationnels, basée principalement sur la dynamique moléculaire classique et le champ de forces polarisable AMOEBA, ainsi que son application à des ions gazeux de tailles diverses. Les ions hydratés dans des agrégats d’eau M(H2O)n (n allant de 6 à 100) sont caractérisés par une dynamique importante, et leur spectre expérimental ne peut pas être décrit par une seule structure. La signature des peptides évolue avec la température et les effets d’anharmonicité dynamique. Ils peuvent également être le siège de mécanismes de transfert de proton, présentant une signature vibrationnelle très caractéristique.La surface d’énergie potentielle de ces systèmes est explorée par la dynamique moléculaire classique en trajectoires individuelles ou avec échange de répliques, afin d’engendrer des structures énergétiquement stables. Pour les plus petits systèmes, les méthodes quantiques DFT et post-HF sont utilisées pour confirmer les structures de plus basse énergie, calculer leurs spectres IR statiques et proposer des attributions des modes de vibration. Pour les plus systèmes de plus grandes tailles, c’est-à-dire les ions dans des gouttes d’eau de plusieurs dizaines de molécules, la simulation des spectres IR à température finie est basée sur la transformée de Fourier de la fonction d’autocorrélation du moment dipolaire (DACF), calculée pour une trajectoire de dynamique moléculaire classique. Cette méthode n’offrant pas d’accès direct aux modes normaux de vibration, nous avons implémenté une méthode d’attribution dynamique, basée sur la Driven Molecular Dynamics (DMD) et couplée au DACF. La combinaison AMOEBA/DACF/DMD a été utilisée pour reproduire et attribuer le spectre du dipeptide Ace-Phe-Ala-NH2, et ceux d’ions hydratés dans des agrégats d’eau.Enfin, la signature vibrationnelle d’un transfert de proton ne peut être décrite, ni par des méthodes statiques quantiques, ni par la dynamique classique. Sa modélisation a nécessité le développement d’un modèle Empirical Valence Bond (EVB) à deux états, couplé au champ de forces polarisable AMOEBA. Le modèle EVB a été implémenté dans la suite logicielle Tinker. Il permet de reproduire le comportement dynamique du transfert de proton au sein de petits peptides et de diacides déprotonés, ainsi que la signature spectroscopique observée expérimentalement.Une partie importante des applications de ces développements concerne des ions simples hydratés dans des nano-gouttelettes, et en particulier l’ion sulfate de grande importance environnementale. Nous avons pu reproduire de façon satisfaisante, pour la première fois, les spectres d’agrégats contenant jusqu’à 100 molécules d’eau. Le principal contributeur à cette spectroscopie expérimentale est l’équipe d’E. Williams à l’université de Californie à Berkeley. Nous avons établi avec eux une collaboration pour compléter ce travail en modélisant les spectres IR d’ions sulfates hydratés [SO4(H2O)n=9-36]2-, dont ils ont obtenu les signatures expérimentales. / Spectroscopy dissociation by absorption of infrared photons (IRPD) provides vibrational signatures of charged species in the gas phase, such as small peptides or hydrated ions in water clusters. The vibrational normal modes assignment to establish a relationship between the experimental spectrum and molecular structure is a delicate task and requires the use of molecular modeling.This manuscript presents a set of theoretical tools for calculation and assignment of vibrational spectra, based mainly on classical molecular dynamics and polarizable AMOEBA force field, and its application to gaseous ions of various sizes. Hydrated ions in water clusters M(H2O)n (n in 6-100 range) are characterized by a dynamic behavior, and their experimental spectrum can not be described by a single structure. The signature of peptides changes with temperature and dynamic anharmonicity effects. They can also be the site of proton transfer mechanisms, with a very characteristic vibrational signature.The potential energy surface of these systems is explored by classical molecular dynamics in individual trajectories or replica exchange to generate energetically stable structures. For smaller systems, quantum methods, as DFT and post-HF, are used to confirm the lowest energy structures, calculate their static IR and propose normal modes assignments. For larger systems, i.e ions in water drops of several tens of molecules, the simulation of IR spectra at finite temperature is based on the Fourier transform of the autocorrelation function of the dipole moment (DACF), calculated during a classical molecular dynamics trajectory. As this method does not allow direct access to the vibrational normal modes, we implemented a method of dynamic assigments, based on the Driven Molecular Dynamics (DMD) and coupled to the DACF. The combination AMOEBA /DACF / DMD was used to reproduce and assign the spectrum of the dipeptide Ace-Phe-Ala-NH2, and those of hydrated ions in water clusters.Finally, the vibrational signature of a proton transfer can not be described by quantum static methods or by classical dynamics. Its modeling required the development of a two states Empirical Valence Bond Model (EVB), coupled with AMOEBA polarizable force field. The two states EVB model was implemented in the software TINKER. It can reproduce the dynamic behavior of proton transfer in small peptides and deprotonated acids, as well as the spectroscopic signatures observed experimentally.An important part of the applications of these developments relates simple hydrated ions in nano-droplets, and in particular the sulfate ion of great environmental importance. We were able to reproduce satisfactorily, for the first time, the spectra of clusters containing up to 100 water molecules. The main contributor to this experimental spectroscopy is the team of E. Williams from the University of California of Berkeley. We have established cooperation with them to complete this work by modeling the IR spectra of hydrated sulfates ions [SO4(H2O) n=9-36]2-, for which they obtained experimental signatures.