An optimized procedure was designed for the preparation of the microporous metal–organic framework (MOF) [Cu3(btc)2] (BTC=benzene‐1,3,5‐tricarboxylate). The crystalline material was characterized by X‐ray diffraction, optical microscopy, SEM, X‐ray photoelectron spectroscopy, N2 sorption, thermogravimetry, and IR spectroscopy of adsorbed CO. CO adsorbs on a small number of Cu2O impurities, and particularly on the free CuII coordination sites in the framework. [Cu3(btc)2] is a highly selective Lewis acid catalyst for the isomerization of terpene derivatives, such as the rearrangement of α‐pinene oxide to campholenic aldehyde and the cyclization of citronellal to isopulegol. By using the ethylene ketal of 2‐bromopropiophenone as a test substrate, it was demonstrated that the active sites in [Cu3(btc)2] are hard Lewis acids. Catalyst stability, re‐usability, and heterogeneity are critically assessed.
This review addresses the most relevant aspects of vibrational spectroscopies (IR, Raman and INS) applied to zeolites and zeotype materials. Surface Brønsted and Lewis acidity and surface basicity are treated in detail. The role of probe molecules and the relevance of tuning both the proton affinity and the steric hindrance of the probe to fully understand and map the complex site population present inside microporous materials are critically discussed. A detailed description of the methods needed to precisely determine the IR absorption coefficients is given, making IR a quantitative technique. The thermodynamic parameters of the adsorption process that can be extracted from a variable-temperature IR study are described. Finally, cutting-edge space- and time-resolved experiments are reviewed. All aspects are discussed by reporting relevant examples. When available, the theoretical literature related to the reviewed experimental results is reported to support the interpretation of the vibrational spectra on an atomic level.
IR spectroscopy is a technique particularly adapted for understanding the mechanism of catalytic reactions, being able to probe the surface mechanisms at the molecular level. In this critical review the main advances in the field are presented, both under the aspects of the in situ and operando approaches. A broad view of the most authoritative literature of the domain is given, based largely on the experience built up at the LCS laboratory in the last decades. After having presented the general methodology to observe a potential active site directly or by probe molecule adsorption, several examples illustrate the qualitative and quantitative analysis of the physical-chemical properties of the surface entities. The last part of the review is dedicated to the discrimination of the role of the active site and its links with the catalytic steps; the hot problem of the reaction intermediates and their visibility via spectroscopic techniques is critically addressed (138 references).
This study presents a detailed methodology, which combines high-precision thermogravimetry and FTIR spectroscopy, aiming to establish the most accurate and reliable means of measuring the molar absorption coefficients of adsorbed species. As the integrated molar absorption coefficients of Py complexes with Brønsted and Lewis acid sites, ɛ(Py-B) and ɛ(Py-L), are determined and the validity of the Beer-Lambert-Bouguer law for IR characterisation of solid acids is demonstrated, this work is setting a benchmark for the quantitative acidity measurements in zeolites and related materials. The following values of ɛ(Py-B) have been obtained at 150°C (band at ~1545 cm-1): 1.09±0.08 cm µmol-1 for ZSM-5; 1.12±0.16 cm µmol-1 for BEA; 1.29±0.04 cm µmol-1 for MOR and 1.54±0.15 cm µmol-1 for FAU. The value of ɛ(Py-L) (band at ~1455 cm-1 , which refers to different cations) measured at the same temperature is 1.71±0.1 cm µmol-1. Values of ɛ(Py-B) depend on the zeolite structure, in contrast to that for ɛ(Py-L). Clear correlations are presented between the temperature of the FTIR measurements and ɛ values for Py complexes and other species, which decrease by ~10% as the temperature increases by 100 o C. In addition, the effects of key experimental procedures, instrumentation design and sample preparation are established and quantified.
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