Thiol-functionalized nanobuilding blocks (NBBs) were synthesized from 3-mercaptopropyltrimethoxysilane by using the in situ water production (ISWP) process in which the water needed to hydrolyze the precursor was provided by means of an esterification reaction. In the present study the reaction between 1-propanol and chloroacetic acid was used. Whereas the growth of the Si oligomers was followed at room temperature and 100°C using 1D 29 Si and 2D 1 H-29 Si heteronuclear single quantum correlation (HSQC) NMR spectroscopic experiments, the amount of water delivered along the process was followed by means of 1 H NMR spectroscopy. The results show a good correlation between the evolution of the degree [a]

Detailed crystallographic information provided by X-ray diffraction (XRD) is complementary to molecular information provided by Raman spectroscopy. Accordingly, the combined use of these techniques allows the identification of an unknown compound without ambiguity. However, a full combination of Raman and XRD results requires an appropriate and reliable reference database with complete information. This is already available for XRD. The main objective of this paper is to introduce and describe the recently developed Raman Open Database (ROD, http://solsa.crystallography.net/rod). It comprises a collection of high-quality uncorrected Raman spectra. The novelty of this database is its interconnectedness with other open databases like the Crystallography Open Database (http://www.crystallography.net/cod and Theoretical Crystallography Open Database (http://www.crystallography.net/tcod/). The syntax adopted to format entries in the ROD is based on the worldwide recognized and used CIF format, which offers a simple way for data exchange, writing and description. ROD also uses JCAMP-DX files as an alternative format for submitted spectra. JCAMP-DX files are compatible to varying degrees with most commercial Raman software and can be read and edited using standard text editors.

The first transparent silicon oxycarbide aerogel has been obtained through H2decarbonzation at 800 °C starting from an alkylene-bridged silicon alkoxide precursor.

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The identification of mineralogical phases in drill cores is one of the most challenging tasks in the mining activity in view of an efficient metal extraction. This process requires the analytical characterization of large volumes of material to obtain a complete set of data in a minimum of time. None of the commonly used methods in mineralogical analyses, such as IR‐based techniques, X‐rays fluorescence, and hyperspectral imaging, is capable to provide a fully satisfactory response for several reasons, the main one being the complexity of the ores. Moreover, the characterization is often conducted in remote laboratories and only on selected samples to limit the time waste. A possible alternative solution requires a multianalytical approach exploiting on‐field techniques. This strategy is currently being developed within SOLSA, a joint EU H2020 project, and consists of an automatic expert system coupling sonic drilling, imaging, profilometer, hyperspectral cameras, and a combination of Raman spectroscopy, X‐rays fluorescence, and X‐rays diffraction. In this work, the principles on which this cooperative approach is based are discussed, with application to two specific test samples, showing the potential and novelty of the method. In particular, a case is considered in which the sample characterization by the separate use of a single technique fails, whereas the combination of the three analyses (Raman spectroscopy, X‐rays fluorescence, and X‐rays diffraction) works even if the system is very complex.

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Thiol-functionalized oligosilsesquioxanes have been synthesized by sol-gel chemistry via the in-situ water production (ISWP) approach, exploiting the esterification reaction of chloro-acetic acid and 1-propanol. The extent of hydrolysis-condensation of 3-Mercaptopropyltrimethoxysilane (McPTMS) has been studied by FT-IR and NMR spectroscopy, gel permeation chromatography (GPC) and MALDI-TOF techniques. The esterification reaction plays a key role in ruling out the oligomer structural development. In this work, we have investigated the influence of the theoretical amount of water available for the organosilane hydrolysis, defined by the ratio of chloro-acetic acid to McPTMS in the reaction mixture, and the role of different catalysts like trifluoroacetic acid (TFA) and dibutyldilauryltin (DBTL). The behavior of the catalyst is complex since, according to its nature, it may improve the kinetics of the sol-gel reactions and the esterification reaction as well. Comparing the reactions carried out with under-stoichiometric water content, the degree of condensation of the silsesquioxanes is higher if the reaction is catalyzed by TFA than by DBTL, because TFA may improve the kinetics of both hydrolysis-condensation and esterification reactions. The use of DBTL in under-stoichiometric and stoichiometric hydrolytic conditions raises the yield in ladder-like structures. The degree of condensation generally increases increasing the hydrolysis ratio as well as the yield in cage-like structures. However, when an over-stoichiometric amount of water is provided for the sol-gel reaction, condensation degree and ratio among cages and ladder-like structures appear unaffected by the employed catalyst.

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