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Vibrational spectroscopy is a widely used technique for chemical characterizations across various analytical sciences. Its applications are increasingly extending to the analysis of complex samples such as biofluids, providing high‐throughput molecular profiling. While powerful, the technique suffers from an inherent limitation: The overlap of absorption information across different spectral domains hinders the capacity to identify individual molecular substances contributing to measured signals. Despite the awareness of this challenge, the difficulty of analyzing multi‐molecular spectra is often underestimated, leading to unsubstantiated molecular interpretations. Here, we examine the prevalent overreliance on spectral band assignment and illuminate the pitfalls of correlating spectral signals to discrete molecular entities or physiological states without rigorous validation. Focusing on blood‐based infrared spectroscopy, we provide examples illustrating how peak overlap among different substances, relative substance concentrations, and preprocessing steps can lead to erroneous interpretations. We advocate for a viewpoint shift towards a more careful understanding of complex spectra, which shall lead to either accepting their fingerprinting nature and leveraging machine learning analysis – or involving additional measurement modalities for robust molecular interpretations. Aiming to help translate and improve analytical practices within the field, we highlight the limitations of molecular interpretations and feature their viable applications. [ABSTRACT FROM AUTHOR]

A recent broadband rotational spectroscopic investigation of the cross-association mechanisms of CO2 with monoethanolamine (MEA) in molecular beams [F. Xie et al., Angew. Chem. Int. Ed., 2023, 62, e202218539] revealed an intriguing affinity of CO2 to the hydroxy group. These findings have triggered the present systematic vibrational spectroscopic exploration of weakly bound amine··CO2 and alcohol··CO2 van der Waals cluster molecules embedded in inert "quantum" matrices of neon at 4.2 K complemented by high-level quantum chemical conformational analyses. The non-covalent interactions formed between the amino and hydroxy groups and the electron-deficient carbon atom of CO2 are demonstrated to lift the degeneracy of the doubly degenerate intramolecular CO2-bending fundamental significantly with characteristic observed spectral splittings for the amine··CO2 (≈35–45 cm−1) and alcohol··CO2 (≈20–25 cm−1) interactions, respectively, despite the almost identically predicted total association energies (≈12–14 kJ·mol−1) for these van der Waals contacts, as revealed by benchmark Domain-based Local Pair Natural Orbital Coupled Cluster DLPNO-CCSD(T) theory. These high-level theoretical predictions reveal significantly higher "geometry preparation energies" for the amine··CO2 systems leading to a more severe distortion of the CO2 linearity upon complexation in agreement with the infrared spectroscopic findings. The systematic combined spectroscopic and quantum chemical evidences for cross-association between CO2 and amines/alcohols in the present work unambiguously confirm an intriguing binding preference of CO2 to the hydroxy group of the important carbon capture agent MEA, with an accurate vibrational zero-point energy corrected association energy (D0) of 13.5 kJ·mol−1 at the benchmark DLPNO-CCSD(T)/aug-cc-pV5Z level of theory. [ABSTRACT FROM AUTHOR]

Taurine is part of the cysteine cycle and is one of the few naturally occuring organosulfur‐based molecules in the human body. As implied by modern studies, protonated taurine is of biological impact. The first attempts to isolate its protonated species in the binary superacidic system HF/SbF5 were performed by Hopfinger, resulting in the isolation of monoprotonated taurine. Since the chosen conditions seemed rather harsh, investigations in less acidic systems were performed at room temperature to explore the involved protonated species. Herein, we present the structure of 2‐[dihydroxy(oxo)sulfanyliumyl]ethanaminium bis[hexafluoridoarsenate(V)], [H2O3SC2H4NH3][AsF6]2, the diprotonated form of 2‐aminoethanesulfonic acid (taurine). It was synthesized in the binary superacidic system HF/AsF5 and crystallizes as colourless needles. Diprotonated taurine was structurally characterized by single‐crystal X‐ray diffraction analysis, low‐temperature vibrational spectroscopy and NMR spectroscopy. [ABSTRACT FROM AUTHOR]

Vibrational spectroscopy allows the investigation of structural properties of pristine and doped poly(3-hexylthiophene-2,5-diyl) (P3HT) in highly anisotropic materials, such as electrospun micro- and nanofibers. Here, we compare several approaches for doping P3HT fibers. We have selected two different electron acceptor molecules as dopants, namely iodine and 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4TCNQ). In the case of iodine, we have explored the doping of the fibers according to several different procedures, i.e., by sequential doping both in vapors and in solution, and with a novel promising one-step method, which exploits the mixing of the dopant to the electrospinning feed solution. Polarized infrared (IR) spectroscopy experiments prove the orientation of P3HT chains, with the polymer backbone mainly running parallel to the fiber axis. After doping, P3HT fibers show very strong and polarized doping-induced IR active vibrations (IRAVs), which are the spectroscopic signature of the structure relaxation induced by the charged defects (polarons), thus providing an unambiguous proof of the effective doping. Raman spectroscopy complements the IR evidence: The Raman spectrum shows a clearly recognizable shift of the main band, the so-called effective conjugation coordinate band, in the doped samples. A simple protocol, which quantifies the evolution of the IRAV bands with time, allows monitoring of the doping stability over time and confirms that F4TCNQ is by far superior to iodine. [ABSTRACT FROM AUTHOR]

Lead–calcium phosphates are unusual compounds sometimes found in different kinds of cultural heritage objects. Structural and physicochemical properties of this family of materials, which fall into the hydroxypyromorphite–hydroxyapatite solid solution, or (Pb x Ca1− x )5(PO4)3OH, have received considerable attention during the last few decades for promising applications in different fields of environmental and material sciences, but their diagnostic implications in the cultural heritage context have been poorly explored. This paper aims to provide a clearer understanding of the relationship between compositional and structural properties of the peculiar series of (Pb x Ca1− x )5(PO4)3OH solid solutions and to determine key markers for their proper non-destructive and non-invasive identification in cultural heritage samples and objects. For this purpose, a systematic study of powders and paint mock-ups made up of commercial and in-house synthesized (Pb x Ca1− x )5(PO4)3OH compounds with a different Pb2+/Ca2+ ratio was carried out via a multi-technique approach based on scanning electron microscopy, synchrotron radiation-based X-ray techniques, i.e., X-ray powder diffraction and X-ray absorption near edge structure spectroscopy at the Ca K- and P K-edges, and vibrational spectroscopy methods, i.e., micro-Raman and Fourier transform infrared spectroscopy. The spectral modifications observed in the hydroxypyromorphite–hydroxyapatite solid solution series are discussed, by assessing the advantages and disadvantages of the proposed techniques and by providing reference data and optimized approaches for future non-destructive and non-invasive applications to study cultural heritage objects and samples. [ABSTRACT FROM AUTHOR]

This study presents the calculation of stretching vibrational frequencies for the triatomic molecule dichlorine monoxide (Cl2 O), explicitly focusing on the fourth, fifth, and sixth overtones. Using a Lie algebraic framework, a detailed mathematical modeling approach is provided to predict these higher overtone frequencies accurately. The results demonstrate the effectiveness of the Lie algebraic method in capturing the complex vibrational behavior of Cl2 O, offering valuable insights into its vibrational spectra. [ABSTRACT FROM AUTHOR]

This study aimed at the geographical origin discrimination of Jatropha mollissima saps using mid- and near-infrared spectroscopies (MIR and NIR, respectively) and Linear Discriminant Analysis (LDA). For this purpose, a total of 108 sap samples were collected in 3 different geographical regions over 12 months, and their content of total polyphenols, flavonoids, and tannins were quantified. Overall, samples from region C had consistently lower levels of these secondary metabolites throughout most of the months studied. In contrast, samples from regions A and B displayed relatively stable metabolite concentrations over the collection period. Since raw sap samples are subject to deterioration during storage, lyophilization was employed to remove moisture and consequently increase their shelf-life. Thus, MIR spectroscopy was applied to both raw and lyophilized sap samples, while NIR spectroscopy was only applied to lyophilized samples. Then, Principal Component Analysis from the secondary metabolites and spectral data indicated a trend of separation between the region C (located in Sertão) and the regions A and B (located in Agreste). Next, the Successive Projection Algorithm (SPA), Genetic Algorithm (GA), and Ant Colony Optimization (ACO) were used for variable selection in LDA. As a result, all constructed models achieved a sensitivity, specificity, and accuracy of 100 %, or very close to it, in both the training and test sets. However, the SPA-LDA models were more parsimonious, selecting fewer variables and presenting reproductive results as it is a deterministic technique. Hence, the proposed analytical methodologies align with the principles of Green Chemistry by requiring a simple sample preparation, avoiding the use of reagents and solvents, and reducing waste generation. Moreover, special attention can be given to NIR spectroscopy, as it offers a cost-effective analytical tool that can be explored in situ using a portable miniaturized device in the future. [Display omitted] • Performance of NIR and MIR was evaluated to distinguish Jatropha mollisima saps from three different geographical origins. • Discriminant power of LDA with selected variables from the AOC, GA, and SPA algorithms were evaluated and showed high sensitivity and specificity. • Evaluated techniques achieved classification errors of less than 5 %. • Methods developed are fast, quick, and efficient in solving the proposed problem. [ABSTRACT FROM AUTHOR]

Vibrational spectroscopic techniques have gained significant attention in recent years for their potential in the rapid and efficient analysis of virgin olive oils, offering a distinct advantage over traditional methods. These techniques are particularly valuable for detecting and quantifying bio-active compounds that contribute to the nutritional and health benefits of virgin olive oils. This comprehensive review explores the latest advancements in vibrational spectroscopic techniques applied to virgin olive oils, focusing on the detection and measurement of key bio-active compounds such as unsaturated fatty acids, phenolic compounds, and other antioxidant compounds. The review highlights the improvements in vibrational spectroscopy, data processing, and chemometric techniques that have significantly enhanced the ability to accurately identify these compounds compared to conventional analytical methods. Additionally, it addresses current challenges, including the need for standardized methodologies and the potential for integrating vibrational spectroscopy with other analytical techniques to improve accuracy and reliability. Finally, findings over the last two decades, in which vibrational spectroscopy techniques were effectively used for the detailed characterization of bio-active compounds in virgin olive oils, are discussed. [ABSTRACT FROM AUTHOR]

A Raman and IR study of AlCl3-based ethereal solutions is here presented and aims at identifying the [AlCl2]+ cation, which has been so far unambiguously characterized by 27Al NMR spectrometry. To do that, experimental–theoretical vibrational spectroscopy was so employed, and the data are interpreted successfully. As a known amount of water is added to the tetrahydrofuran (THF)-containing electrolyte, a Raman band at 271 cm−1 has its intensity increased along with the most intense band of [AlCl4]−, and such behavior is also seen for a band at 405 cm−1 in the IR spectra. New bands at around 420 and 400 cm−1 are observed in both Raman and IR spectra for the tetraglyme (G4)-based systems. The [AlCl2(THF)4]+ complex, in the cis and trans forms, is present in the cyclic ether, while the cis-[AlCl2(G4)]+ isomer is identified in the acyclic one. [ABSTRACT FROM AUTHOR]

Sr4Ba3(BO3)3.83H2.5, as the second compound to combine borate and hydride ions, has been synthesized by a mechanochemical synthesis route. The structure has been elucidated by synchrotron X‐ray and neutron diffraction and determined to crystallize in the non‐centrosymmetric space group P63mc (186) with the cell parameters a=10.87762(15) Å and c=6.98061(11) Å. A detailed investigation of the compound by vibrational spectroscopy in combination with Density Functional Theory calculations reveals the disordered nature of the structure and proves the presence of both borate and hydride ions. Electronic band structure calculations predict a large band gap of 7.1 eV. Hydride states are predicted at the topmost valence band, which agrees well with earlier reported heteroanionic hydrides. We hereby were able to successfully apply previously synthetic and analytical schemes to introduce another member of the rare compounds that contain complex oxoanions simultaneously with hydride ions. [ABSTRACT FROM AUTHOR]

Sr4Ba3(BO3)3.83H2.5, as the second compound to combine borate and hydride ions, has been synthesized by a mechanochemical synthesis route. The structure has been elucidated by synchrotron X‐ray and neutron diffraction and determined to crystallize in the non‐centrosymmetric space group P63mc (186) with the cell parameters a=10.87762(15) Å and c=6.98061(11) Å. A detailed investigation of the compound by vibrational spectroscopy in combination with Density Functional Theory calculations reveals the disordered nature of the structure and proves the presence of both borate and hydride ions. Electronic band structure calculations predict a large band gap of 7.1 eV. Hydride states are predicted at the topmost valence band, which agrees well with earlier reported heteroanionic hydrides. We hereby were able to successfully apply previously synthetic and analytical schemes to introduce another member of the rare compounds that contain complex oxoanions simultaneously with hydride ions. [ABSTRACT FROM AUTHOR]

A recent work by Marks et al. on the formation of carbamic acid in NH 3‐CO 2 interstellar ices pointed out its stability in the gas phase and the concomitant production of its dimer. Prompted by these results and the lack of information on these species, we have performed an accurate structural, energetic and spectroscopic investigation of carbamic acid and its dimer. For the former, the structural and spectroscopic characterization employed composite schemes based on coupled cluster (CC) calculations that account for the extrapolation to the complete basis set limit and core correlation effects. A first important outcome is the definitive confirmation of the nonplanarity of carbamic acid, then followed by an accurate estimate of its rotational and vibrational spectroscopy parameters. As far as the carbamic acid dimer is concerned, the investigation started from the identification of its most stable forms. For them, structure and vibrational properties have been evaluated using density functional theory, while a composite scheme rooted in CC theory has been employed for the energetic characterization. Our results allowed us to provide a better interpretation of the feature observed in the recent experiment mentioned above. [ABSTRACT FROM AUTHOR]

Cosmetics such as makeup or other personal products are widely used and easily transferred upon physical contact. As such, they may be used as trace evidence to link people to each other or to places in criminal investigations. To maximize their probative value, it is important to understand the variability among representative market products and the way in which they transfer to, or persist on various surfaces. Additionally, it is required that analysis techniques be non‐destructive, readily available and relatively inexpensive. Raman spectroscopy and attenuated total reflectance—Fourier transform infrared (ATR‐FTIR) are powerful tools for probing the chemistry of trace cosmetics. As well as fitting the criteria above, they offer the capability of studying a wide range of sample types with minimal prior preparation. The complementary information derived from these techniques can help analysts to understand and visualize spectral variability, potentially enabling discrimination between samples. However, the move from academic research toward forensic casework is not without challenges. In this article, we provide a focused exploration of the current state‐of‐the‐art in forensic cosmetic research; providing context for how we may begin to address these challenges to more effectively exploit cosmetic traces for criminal investigation. This article is categorized under:Forensic Chemistry and Trace Evidence > Emerging Technologies and MethodsForensic Chemistry and Trace Evidence > Trace Evidence [ABSTRACT FROM AUTHOR]

This study aims to improve our understanding of some differences in odd and even chain-length alkanethiol self-assembled monolayers (SAMs) using infrared reflection absorption spectroscopy (IRRAS) and density functional theory (DFT). Xe, Kr, CH2Cl2, CD2Cl2, and CDCl3 were used experimentally to perturb the CH2 and CH3 stretches arising from the tail region of the SAM films and changes in position and intensity were monitored in the infrared. Using DFT methods, noble gases and CH2Cl2 were added to models of the SAM monolayers, and energies and vibrational spectra were calculated. It was observed that perturbing species affected the CH3 symmetric and asymmetric stretches on hexadecanethiol SAMs (an "even" SAM with a 16-carbon backbone) while on pentadecanethiol SAMs (an "odd" SAM with a 15-carbon backbone) both CH2 and CH3 symmetric and asymmetric stretches were affected. Films formed with shorter chain-length species, hexanethiol (even) and pentanethiol (odd), had less consistent results, likely due to more disorder in the alkanethiol chains from weaker van der Waals interactions. Adsorption energies for different perturbing species on the monolayers were higher for the hexanethiol than the pentanethiol. The vibrational spectrum of pentanethiol monolayers with adsorbed species mainly showed shifts to higher frequencies for CH2 and CH3 stretches; for hexanethiol, shifts to lower frequencies for CH2 stretches and higher frequencies for CH3 stretches were observed. Thus, the odd and even alkanethiol SAMs were affected differently by the perturbing species as observed both experimentally and computationally. [ABSTRACT FROM AUTHOR]

AbstractVibrational spectroscopy is a nondestructive analysis technique that depends on the periodic variations in dipole moments and polarizabilities resulting from the molecular vibrations of molecules/atoms. These methods have important advantages over conventional analytical techniques, including (a) their simplicity in terms of implementation and operation, (b) their adaptability to on-line and on-farm applications, (c) making measurement in a few minutes, and (d) the absence of dangerous solvents throughout sample preparation or measurement. Food safety is a concept that requires the assurance that food is free from any physical, chemical, or biological hazards at all stages, from farm to fork. Continuous monitoring should be provided in order to guarantee the safety of the food. Regarding their advantages, vibrational spectroscopic methods, such as Fourier-transform infrared (FTIR), near-infrared (NIR), and Raman spectroscopy, are considered reliable and rapid techniques to track food safety- and food authenticity-related issues throughout the food chain. Furthermore, coupling spectral data with chemometric approaches also enables the discrimination of samples with different kinds of food safety-related hazards. This review deals with the recent application of vibrational spectroscopic techniques to monitor various hazards related to various foods, including crops, fruits, vegetables, milk, dairy products, meat, seafood, and poultry, throughout harvesting, transportation, processing, distribution, and storage. [ABSTRACT FROM AUTHOR]

Fingernails can act as important forensic evidence as they can be a source of DNA that may link the victim or accused to the crime scene and may also contain traces of drugs such as cocaine and heroin, in regular users. Moreover, previous studies have shown that analyzing fingernails with various techniques can reveal important information, such as age and sex. In this work, ATR-FTIR spectroscopy with chemometric tools has been used to estimate the age and sex from fingernails by analyzing 140 fingernail samples (70 males, and 70 females) collected from volunteers aged between 10 and 70 years old. The amide bands obtained from spectra confirmed the presence of keratin proteins in the samples. PCA and PLS-R were used for the classification of samples. For sex estimation, samples were divided into four categories based on age groups, followed by the differentiation of sex in each group. Similarly, for age estimation, all samples were divided into two sets based on male and female followed by differentiation of age groups in each set. The result showed that PLS-R was able to differentiate fingernail samples based on sex in groups G1, G2, G3, and G4 with R-square values of 0.972, 0.993, 0.991, and 0.996, respectively, and based on age in females, and males with R-square values of 0.93 and 0.97, respectively. External validation and blind tests were also performed which showed results with 100% accuracy. This approach has proved to be effective for the estimation of sex and age from fingernail samples. Highlights: • Estimation of age and sex using fingernails via ATR-FTIR and chemometrics. • PLS-R successfully estimated age and sex using fingernails with high R-square values. • Blind and external validation tests illustrated 100% accuracy. • The present approach is quick, and non-destructive with minimal or no sample preparation. [ABSTRACT FROM AUTHOR]

Due to the high mortality rate, more effective non-invasive diagnostic methods are still needed for lung cancer, the most common cause of cancer-related death worldwide. In this study, the integration of Raman and Fourier-transform infrared spectroscopy with advanced data-fusion techniques is investigated to improve the detection of lung cancer from human blood plasma samples. A high statistical significance was found for important protein-related oscillations, which are crucial for differentiating between lung cancer patients and healthy controls. The use of low-level data fusion and feature selection significantly improved model accuracy and emphasizes the importance of structural protein changes in cancer detection. Although other biomolecules such as carbohydrates and nucleic acids also contributed, proteins proved to be the decisive markers found using this technique. This research highlights the power of these combined spectroscopic methods to develop a non-invasive diagnostic tool for discriminating lung cancer from healthy state, with the potential to extend such studies to a variety of other diseases. [ABSTRACT FROM AUTHOR]

Lipid analysis is an integral part of food authentication and quality control which provides consumers with the necessary information to make an informed decision about their lipid intake. Recent advancement in lipid analysis and lipidome scope represents great opportunities for food science. In this review we provide a comprehensive overview of available tools for extraction, analysis and interpretation of data related to dietary fats analyses. Different analytical platforms are discussed including GC, MS, NMR, IR and UV with emphasis on their merits and limitations alongside complementary tools such as chemometric models and lipid-targeted online databases. Applications presented here include quality control, authentication of organic and delicacy food, tracing dietary fat source and investigating the effect of heat/storage on lipids. A multitude of analytical methods with different sensitivity, affordability, reproducibility and ease of operation are now available to comprehensively analyze dietary fats. Application of these methods range from studies which favor the use of large data generating platforms such as MS-based methods, to routine quality control which demands easy to use affordable equipment as TLC and IR. Hence, this review provides a navigation tool for food scientists to help develop an optimal protocol for their future lipid analysis quest. [ABSTRACT FROM AUTHOR]

Propiolamide and cellocidin were investigated in superacidic media. In both acetylenic amides, the amide moiety is immediately monoprotonated in anhydrous HF, HF/SbF5 and HF/BF3. An increase of SbF5 does not lead to a more highly protonated species. The salts were characterized by low-temperature Raman, NMR and room temperature IR spectroscopy, as well as by single-crystal X-ray diffraction. The experimental data are discussed together with results of quantum-chemical calculations on the M06-2X/aug-cc-pVTZ level of theory, which are consistent with the observation of pure monoprotonation. The second protonation of the amide moiety or the triple bond is not observed due to the high positive charge caused by the monoprotonation. [ABSTRACT FROM AUTHOR]

The crystal structure, thermal behavior, and vibrational spectra of the anthropogenic analogue of boussingaultite, (NH4)2Mg(SO4)2·6H2O, and its dehydrated counterpart efremovite, (NH4)2Mg2(SO4)3, were studied in detail. The sample from the Chelyabinsk burning coal dumps has the composition of (NH4)1.92(Mg1.02Mn0.01Fe0.01)∑1.04(SO4)2·6H2O and crystallizes in the space group P21/a, with a = 9.3183(4), b = 12.6070(4), c = 6.2054(3) Å, β = 107.115(5)°, V = 696.70(5) Å3 (at 20 °C), Z = 2. The thermal evolution steps are as follows: boussingaultite (NH4)2Mg(SO4)2·6H2O (25–90 °C) → X-ray amorphous phase (100–150 °C) → efremovite (NH4)2Mg2(SO4)3 (160–340 °C) → MgSO4 Cmcm + Pbnm (340–580 °C) → MgSO4 Pbnm (580–700 °C). Thermal expansion is anisotropic, with the coefficients (×106 °C−1) α11 = 52(2), α22 = 68(2), α33 = –89(3), and αv = 31(3) at T = –123 °C; and α11 = 53(2), α22 = 67(2), α33 = 15(1), and αv = 136(3) at T = 60 °C. The maximal thermal expansion is along the b-axis and is due to straightening of corrugated pseudolayers (within the ab plane) of Mg(H2O)6 octahedra and SO4 tetrahedra with NH4 groups in the interlayer space. Vibrational spectroscopy outlines the general trend of dehydration and deammonization as the difference in the temperature intervals of these transformation steps allows separation of O–H and N–H vibrations in the process of dehydration by infrared and Raman spectroscopy. The intermediate partially dehydrated modification of boussingaultite was detected by in situ Raman spectroscopy at 110 °C that may correspond to ammonium leonite. [ABSTRACT FROM AUTHOR]

Bostrycoidin is one of the pigments produced by the Fusarium genus of fungi. On the one hand, it has significant pharmacological importance, while on the other hand, it serves as a presence marker of Fusarium infection in useful grain crops, fruits, and soils. In this regard, the structural and optical properties of the bostrycoidin molecule were studied in the framework of density functional theory (DFT). The most stable geometry as well as higher-energy conformers and tautomers were investigated. The lowest-energy tautomer was found to be about 3 kcal/mol higher in energy than the most stable structure, resulting in relatively low population of this state. The obtained conformational rotamers associated with the rotation of the OMe group possess similar energy. The vibrational spectrum was modeled for the most stable conformer, and the most active peaks in the IR absorbance spectrum were assigned. Moreover, the electronic absorption spectrum was simulated within the time-dependent DFT approach. The obtained theoretical spectrum is in good agreement with the experimental data and the theoretically calculated longest-wavelength transition (HOMO–LUMO) was about 498 nm. [ABSTRACT FROM AUTHOR]

Small‐molecule receptors are increasingly employed to probe various functional groups for (bio)chemical analysis. However, differentiation of polyfunctional analogs sharing multiple functional groups remains challenging for conventional mono‐ and bidentate receptors because their insufficient number of binding sites limits interactions with the least reactive yet property‐determining functional group. Herein, we introduce 6‐thioguanine (TG) as a supramolecular receptor for unique tridentate receptor‐analyte complexation, achieving ≥97 % identification accuracy among 16 polyfunctional analogs across three classes: glycerol derivatives, disubstituted propane, and vicinal diols. Crucially, we demonstrate distinct spectral changes induced by the tridentate interaction between TG's three anchoring points and all the analyte's functional groups, even the least reactive ones. Notably, hydrogen bond (H‐bond) networks formed in the TG‐analyte complexes demonstrate additive effects in binding strength originating from good bond linearity, cooperativity, and resonance, thus strengthening complexation events and amplifying the differences in spectral changes induced among analytes. It also enhances spectral consistency by selectively forming a sole configuration that is stronger than the respective analyte‐analyte interaction. Finally, we achieve 95.4 % accuracy for multiplex identification of a mixture consisting of multiple polyfunctional analogs. We envisage that extension to other multidentate non‐covalent interactions enables the development of interference‐free small molecule‐based sensors for various (bio)chemical analysis applications. [ABSTRACT FROM AUTHOR]

Viewing interfacial molecular environments is of great importance to develop novel functional materials and to understand atmospheric, catalytic, and electrochemical reactions. Due to development in the lasing instruments and optical techniques in the past 20 years, the interface-specific vibrational spectroscopy, i.e., sum-frequency generation spectroscopy (SFG), has become a power tool to access such interfacial molecular structures. Here, I illustrate that heterodyne-detected SFG can provide quantitative interfacial property and molecular picture, and also can identify interfacial species from the interfacial waters' structure with recent examples. [ABSTRACT FROM AUTHOR]

[Display omitted] Switchable emulsifiers are commonly studied at the macroscopic scale without significant insight into the molecular properties and processes underpinning their behaviour. This work aims to investigate on the molecular scale a switchable emulsifier comprising poly(methacrylic acid) (PMAA) and poly(ethylene glycol) methacrylate (PEGMA). This emulsifier forms stable oil/water emulsions at pH > 10, but the emulsion becomes unstable at pH < 3 due to droplet aggregation. It has been suggested that H-bonding between the MAA (methacrylic acid) and EG (ethylene glycol) groups is central for the switching behaviour. However, no detailed molecular understanding of the surface of the emulsifier coated droplets has been developed so far. Using sum frequency generation spectroscopy, we compared the spectra of the PMAA/PEGMA polymer deposited on a water surface under acidic (pH 2.5) and basic (pH 11.5) conditions. We found that at pH 2.5, both MAA-EG H-bonds and MAA = MAA cyclic dimers contribute to droplet aggregation in the emulsion. In contrast, at pH 11.5 deprotonation and solvation of the PMAA component lead to a polymer restructuring. As a result, the PMAA chains form a negative shell around the droplets, electrostatically stabilising the emulsion in alkaline conditions. [ABSTRACT FROM AUTHOR]

Solvent molecules interact with a solute through various intermolecular forces. Here we employed a potential energy surface (PES) analysis to interpret the solvent‐induced variations in the strengths of dative (Me3NBH3) and ionic (LiCl) bonds, which possess both ionic and covalent (neutral) characteristics. The change of a bond is driven by the gradient (force) of the solvent‐solute interaction energy with respect to the focused bond length. Positive force shortens the bond length and increases the bond force constant, leading to a blue‐shift of the bond stretching vibrational frequency upon solvation. Conversely, negative force elongates the bond, resulting in a reduced bond force constant and red‐shift of the stretching vibrational frequency. The different responses of Me3NBH3 and LiCl to solvation are studied with valence bond (VB) theory, as Me3NBH3 and LiCl are dominated by the neutral covalent VB structure and the ionic VB structure, respectively. The dipole moment of an ionic VB structure increases along the increasing bond distance, while the dipole moment of a neutral covalent VB structure increases with the decreasing bond distance. The roles of the dominating VB structures are further examined by the geometry optimizations and frequency calculations with the block‐localized wavefunction (BLW) method. [ABSTRACT FROM AUTHOR]

During the past few decades, Raman spectroscopy has progressed and captivated added attention in the field of science. However, the application of Raman spectroscopy is not limited to the field of forensic science and analytical chemistry; it is one of the emerging spectroscopic techniques, utilized in the field of forensic science which in turn could be a supporting tool in the law and justice system. The advantage of Raman spectroscopy over the other conventional techniques is that it is rapid, reliable, and non-destructive in nature with minimal or no sample preparation. The quantitative and qualitative analysis of evidence from biological and non-biological origins could easily be performed by using Raman spectroscopy. The forensic domain is highly complex with multidisciplinary branches, and therefore a plethora of techniques are utilized for the detection, identification, and differentiation of innumerable pieces of evidence for the purpose of law and justice. Herein, a systematic review is carried out on the application of Raman spectroscopy in the realm of forensic biology and serology considering its usefulness in practical perspectives. This review paper highlights the significance of modern techniques, including micro-Raman spectroscopy, confocal Raman spectroscopy, surface-enhanced Raman spectroscopy, and paper-based surface-enhanced Raman spectroscopy, in the field of Raman spectroscopy. These techniques have demonstrated notable advancements in terms of their applications and capabilities. Furthermore, to comprehensively capture the progress in the development of Raman spectroscopy, all the published papers which could be retrieved from the available databases from the year 2007 to 2022 were incorporated. [ABSTRACT FROM AUTHOR]

We have approached the construction of an artificial enzyme by employing a robust protein scaffold, lactococcal multidrug resistance regulator, LmrR, providing a structured secondary and outer coordination spheres around a molecular rhodium complex, [RhI(PEt2NglyPEt2)2]−. Previously, we demonstrated a 2–3 fold increase in activity for one Rh-LmrR construct by introducing positive charge in the secondary coordination sphere. In this study, a series of variants was made through site-directed mutagenesis where the negative charge is located in the secondary sphere or outer coordination sphere, with additional variants made with increasingly negative charge in the outer coordination sphere while keeping a positive charge in the secondary sphere. Placing a negative charge in the secondary or outer coordination sphere demonstrates decreased activity by a factor of two compared to the wild-type Rh-LmrR. Interestingly, addition of positive charge in the secondary sphere, with the negatively charged outer coordination sphere restores activity. Vibrational and NMR spectroscopy suggest minimal changes to the electronic density at the rhodium center, regardless of inclusion of a negative or positive charge in the secondary sphere, suggesting another mechanism is impacting catalytic activity, explored in the discussion. [ABSTRACT FROM AUTHOR]

In this article, we propose an approach to reconstruct the timing of human activity at Points Cave, an Upper Paleolithic rock art site located in the middle of the Ardèche River Gorge (Rhône valley, France), based on the dating and characterisation of a stalagmite containing soot. Points Cave ('Grotte aux Points' in French), also called the 'little sister of Chauvet Cave', is famous for its parietal art including a series of dots made of palm prints. A large number of stalagmites formed in the cave during the last 500 ka. However, quarrying of the cave floors during historic times led to the partial destruction of the sedimentary deposits, and many of the stalagmites were found lying on the floor. In particular, one of them (STM‐18‐04) showed the presence of at least four dark layers in cross‐section, which appeared as possible remnants of fire‐related activities in the cave. Despite being present at the same site, no other specific link between STM‐18‐04 and the rock art has been documented. This stalagmite, however, allows us to identify phases of human presence, located at the cave entrance. To do so, we performed a series of analyses to determine its period of growth and the nature of the dark layers that it contains. Scanning electron microscopy and Raman microspectroscopy confirmed that the dark layers include soot, and uranium‐series dating indicated that the fire events occurred, respectively, around 14,200–14,100 and 12,500 years ago, in agreement with the radiocarbon ages of charcoal specimens recovered from the excavation areas nearby. We thus highlighted phases of human activity at the site during the Upper Magdalenian and/or beginning of the Epipaleolithic. By comparing our results with the regional paleoclimatic record, the soot layers trapped in the stalagmite appear to be synchronous with two cold periods, likely the Older Dryas and the Younger Dryas. [ABSTRACT FROM AUTHOR]

Spontaneous Raman spectroscopy is a well‐established diagnostic tool, allowing for the identification of all Raman active species with a single measurement. Yet, it may suffer from low‐signal intensity and fluorescent background. In contrast, coherent anti‐Stokes Raman scattering (CARS) offers laser‐like signals, but the traditional approach lacks the multiplex capability of spontaneous Raman spectroscopy. We present an ultrabroadband CARS setup which aims at exciting the full spectrum (300–3700 cm−1) of biological molecules. A dual‐output optical parametric amplifier provides a ~7 fs pump/Stokes and a ~700 fs probe pulse. CARS spectra of DMSO, ethanol, and methanol show great agreement with spontaneous Raman spectroscopy and superiority in fluorescent environments. The spectral resolution proves sufficient to differentiate between the complex spectra of L‐proline and hydroxyproline. Moreover, decay constants in the sub picosecond range are determined for individual Raman transitions, providing an additional approach for sample characterization. [ABSTRACT FROM AUTHOR]

While protein aggregation is a hallmark of many neurodegenerative diseases, acquiring structural information on protein aggregates inside live cells remains challenging. Traditional microscopy does not provide structural information on protein systems. Routinely used fluorescent protein tags, such as Green Fluorescent Protein (GFP), might perturb native structures. Here, we report a counter‐propagating mid‐infrared photothermal imaging approach enabling mapping of secondary structure of protein aggregates in live cells modeling Huntington's disease. By comparing mid‐infrared photothermal spectra of label‐free and GFP‐tagged huntingtin inclusions, we demonstrate that GFP fusions indeed perturb the secondary structure of aggregates. By implementing spectra with small spatial step for dissecting spectral features within sub‐micrometer distances, we reveal that huntingtin inclusions partition into a β‐sheet‐rich core and a ɑ‐helix‐rich shell. We further demonstrate that this structural partition exists only in cells with the [RNQ+] prion state, while [rnq−] cells only carry smaller β‐rich non‐toxic aggregates. Collectively, our methodology has the potential to unveil detailed structural information on protein assemblies in live cells, enabling high‐throughput structural screenings of macromolecular assemblies. [ABSTRACT FROM AUTHOR]

Advanced vibrational spectroscopic experiments have reached a level of sophistication that can only be matched by numerical simulations in order to provide an unequivocal analysis, a crucial step to understand the structure‐function relationship of biomolecules. While density functional theory (DFT) has become the standard method when targeting medium‐size or larger systems, the problem of its reliability and accuracy are well‐known and have been abundantly documented. To establish a reliable computational protocol, especially when accuracy is critical, a tailored benchmark is usually required. This is generally done over a short list of known candidates, with the basis set often fixed a priori. In this work, we present a systematic study of the performance of DFT‐based hybrid and double‐hybrid functionals in the prediction of vibrational energies and infrared intensities at the harmonic level and beyond, considering anharmonic effects through vibrational perturbation theory at the second order. The study is performed for the six‐lowest energy glycine conformers, utilizing available "state‐of‐the‐art" accurate theoretical and experimental data as reference. Focusing on the most intense fundamental vibrations in the mid‐infrared range of glycine conformers, the role of the basis sets is also investigated considering the balance between computational cost and accuracy. Targeting larger systems, a broad range of hybrid schemes with different computational costs is also tested. [ABSTRACT FROM AUTHOR]

The development of new methods of identification of active pharmaceutical ingredients (API) is a subject of paramount importance for research centers, the pharmaceutical industry, and law enforcement agencies. Here, a system for identifying and classifying pharmaceutical tablets containing acetaminophen (AAP) by brand has been developed. In total, 15 tablets of 11 brands for a total of 165 samples were analyzed. Mid-infrared vibrational spectroscopy with multivariate analysis was employed. Quantum cascade lasers (QCLs) were used as mid-infrared sources. IR spectra in the spectral range 980–1600 cm−1 were recorded. Five different classification methods were used. First, a spectral search through correlation indices. Second, machine learning algorithms such as principal component analysis (PCA), support vector classification (SVC), decision tree classifier (DTC), and artificial neural network (ANN) were employed to classify tablets by brands. SNV and first derivative were used as preprocessing to improve the spectral information. Precision, recall, specificity, F1-score, and accuracy were used as criteria to evaluate the best SVC, DEE, and ANN classification models obtained. The IR spectra of the tablets show characteristic vibrational signals of AAP and other APIs present. Spectral classification by spectral search and PCA showed limitations in differentiating between brands, particularly for tablets containing AAP as the only API. Machine learning models, specifically SVC, achieved high accuracy in classifying AAP tablets according to their brand, even for brands containing only AAP. [ABSTRACT FROM AUTHOR]

In contrast to the traditional analysis of molecules using local mode behavior, where the degree of locality is given through a function in terms of Morse potential parameters, new criteria for locality/normality (LN) suitable for application to any molecular system are proposed. The approach is based on analysis of the connection between the algebraic normal and local mode representations. It is shown that both descriptions are equivalent as long as the polyad (total number of quanta) in the local representation is not conserved. The constraint of a local polyad conservation naturally provides a criterion for assigning an LN degree in quantitative form, without an analogue in configuration space. The correlation between the different parameters reveals the physical properties of molecules. A clear connection between the LN degree (based on the fundamentals) and spectroscopic properties is also presented, suggesting a promising approach for identifying mixtures of isotopologues. [ABSTRACT FROM AUTHOR]

The potential energy surfaces and photoelectron spectra of the interstellar molecule H2S and its cation H2S+ were calculated using ab initio methods based on the MOLPRO software package. First, the potential energy surfaces of H2S expanded along the normal coordinates were obtained at the（U）CCSD/cc-pVQZ level of theory. The potential energy surfaces visually describe the effect of different vibrational modes coupling on the molecular energy change, and the combined effect of the asymmetric stretching vibration of the S-H bond and the in-plane bending vibration makes the potential energy change range of the system significantly larger. The vibrational multi-reference configuration interaction method was used to calculate the anharmonic vibrational frequencies and vibrational spectrum, and the calculations showed that strong Fermi resonances appear between the overtones and combination bands, resulting in a significant enhancement of the infrared intensity at the corresponding bands. Finally, the photoelectron spectrum of H2S X¹A1→ H2S+ X²B1 was calculated for the first time using the Raman wave function and the contracted invariant Krylov subspaces method. This study will help to further understand the internal structure of interstellar molecules and provide a reference for experimental studies and interstellar observations. [ABSTRACT FROM AUTHOR]

The single crystals of the title compound (1) were grown from a water solution. The compound crystallizes in the centrosymmetric space group P21/c of the monoclinic system with eight molecules per unit cell. Multiple recrystallizations of the crystals from heavy water gives deuterated analogue 1d. The asymmetric unit of 1 contains two salt molecules. Both independent cations interact with anions via N−H...O hydrogen bonds with R22(8) and R21(6) graphs forming 1:1 salt molecules. Both salt molecules are linked by additional N−H...O and O−H...O hydrogen bonds with a graph R22(9). The oppositely charged components of the crystals, i.e., 1-(diaminomethylene)thiouron-1-ium cations and 2,3-pyridine-dicarboxylate anions, interact each other forming three-dimensional supramolecular hydrogen bonded network. The interactions between the components as well as between the 1:1 salt molecules were analysed using the Hirshfeld surface. The compound was also characterized by vibrational spectroscopy. The vibrational bands were interpreted based on the optimized structure and force field calculations of normal coordinates based on the density functional theory (DFT) with the base set 6-31G(d,p). Isotopic frequency shift and potential energy distribution (PED) were used to assign the bands. The electronic absorption spectra of 1 in the gas phase, as well as in polar and non-polar solvents, were calculated. [ABSTRACT FROM AUTHOR]

Three hybrid compounds based on decavanadates, i.e., (NH4)2[Co(H2O)5(β-HAla)]2[V10O28]·4H2O (1), (NH4)2[Ni(H2O)5(β-HAla)]2[V10O28]·4H2O (2), and (NH4)2[Cd(H2O)5(β-HAla)]2[V10O28]·2H2O (3), (where β-Hala = zwitterionic form of β-alanine) were prepared by reactions in mildly acidic conditions (pH ~ 4) at room temperature. These compounds crystallise in two structure types, both crystallising in monoclinic P21/n space group but with dissimilar cell packing, i.e., as tetrahydrates (1 and 2) and as a dihydrate (3). An influence of crystal radii and spin state of the central atom in [M(H2O)5(β-HAla)]2+ complex cations on the crystal packing leading to the formation of different crystallohydrate forms was investigated together with previously prepared (NH4)2[Zn(H2O)5(β-HAla)]2[V10O28]·4H2O (4) and (NH4)2[Mn(H2O)5(β-HAla)]2[V10O28]·2H2O (5) and spin states of [M(H2O)5(β-HAla)]2+ (M = Co2+, Ni2+, and Mn2+) cations in solution were confirmed by 1H-NMR paramagnetic effects. FT-IR and FT-Raman spectra for 1–5 are in agreement with the X-ray structure analysis results. [ABSTRACT FROM AUTHOR]

Although interfacial solvation plays an important role in determining carbon dioxide reduction (CO2R) kinetics, present understanding of the potential dependent properties of the electrochemical double layer under conditions relevant for CO2R remains limited. This article summarizes the development and recent applications of plasmon‐enhanced vibrational sum frequency generation (VSFG) spectroscopy to study the effects of cation hydration and interfacial solvation on CO2R using CO as a vibrational Stark reporter. Results show that electrolyte cations retain their entire solvation shell upon adsorption to inactive sites, while active sites retain only a single water layer between the gold surface and the cation. Measurements also show that the total interfacial electric field can be separated into two contributions: one from the electrochemical double layer (Stern field) and another from the polar solvation environment (Onsager field). Surprisingly, correlating VSFG spectra with reaction kinetics reveals that it is the solvation‐mediated Onsager field that governs the chemical reactivity at the electrode/electrolyte interface. Measuring the interfacial water spectra during electrocatalysis also provides evidence for the proton source during H2 evolution, which competes with CO2R in aqueous electrolyte. These findings highlight the importance of directly probing cation hydration and interfacial solvation, which mediates reaction kinetics at electrochemical interfaces. [ABSTRACT FROM AUTHOR]

Aluminium is one of the most abundant metals in the universe and impacts the evolution of various astrophysical environments. Currently detected Al‐bearing molecules represent only a small fraction of the aluminium budget, suggesting that aluminium may reside in other species. AlO and AlOH molecules are abundant in the oxygen‐rich supergiant stars such as VY Canis Majoris, a stellar molecular factory with 60+ molecules including the prebiotic NC‐bearing species. Additional Al‐bearing molecules with N, C, O, and H may form in O‐rich environments with radiation‐accelerated chemistry. Here, we present spectroscopic identification of novel aluminium‐bearing molecules composed of [Al, N, C, O, H] and [Al, N, C, O] from the reactions of Al atoms and HNCO in solid argon matrix, which are potential Al‐bearing molecules in space. Photoinduced transformations among six [Al, N, C, O, H] isomers and three [Al, N, C, O] isomers, along with their dissociation reactions forming the known interstellar species, have been disclosed. These results provide new insight into the chemical network of astronomically detected Al‐bearing species in space. [ABSTRACT FROM AUTHOR]

Supercritical water provides distinctly different solvation properties compared to what is known from liquid water. Despite its prevalence deep in the Earth's crust and its role in chemosynthetic ecosystems in the vicinity of hydrothermal vents, molecular insights into its solvation mechanisms are still very scarce compared to what is known for liquid water. Recently, neutral metal particles have been detected in hydrothermal fluids and proposed to explain the transport of gold species to ore deposits on Earth. Using ab initio molecular dynamics, we elucidate the solvation properties of small gold species at supercritical conditions. The neutral metal clusters themselves contribute enormous THz intensity not because of their intramolecular vibrations, but due to their pronounced electronic polarization coupling to the dynamical supercritical solvent, leading to a continuum absorption up to about 1000 cm−1. On top, long‐lived interactions between the gold clusters and solvation water leads at these supercritical conditions to a sharp THz resonance that happens to be close to the one due to H‐bonding in liquid water at ambient conditions. The resulting distinct resonances can be used to analyse the solvation properties of neutral metal particles in supercritical aqueous solutions. [ABSTRACT FROM AUTHOR]

The gallium(III) complex of warfarin was synthesized, and its structure was determined by means of theoretical, analytical, and spectral analyses. Significant differences in the IR and Raman spectra of the complex were observed as compared to the spectra of the ligand and confirmed the suggested metal-ligand binding mode. The theoretical study of the Ga(III) complex of warfarin has been done to elucidate the structure-activity relation, inter- and intra-molecular interactions, and frontier molecular orbital energy analysis based on DFT computations. A molecular docking study has been performed to predict the biological activity of the molecule. In this paper, we report preliminary results about the cytotoxicity of the investigated compounds. The cytotoxic effects of the ligand and its Ga(III) complex were determined using the MTT method on different tumor cell lines. The screening performed revealed that the tested compounds exerted cytotoxic activity on the evaluated cell lines. [ABSTRACT FROM AUTHOR]

The self-association mechanisms of phenol have represented long-standing challenges to quantum chemical methodologies owing to the competition between strongly directional intermolecular hydrogen bonding, weaker non-directional London dispersion forces and C–H· · · π interactions between the aromatic rings. The present work explores these subtle self-association mechanisms of relevance for biological molecular recognition processes via spectroscopic observations of large-amplitude hydrogen bond librational modes of phenol cluster molecules embedded in inert neon “quantum” matrices complemented by domain-based local pair natural orbital-coupled cluster DLPNO-CCSD(T) theory. The spectral signatures confirm a primarily intermolecular O-H· · · H hydrogen-bonded structure of the phenol dimer strengthened further by cooperative contributions from inter-ring London dispersion forces as supported by DLPNO-based local energy decomposition (LED) predictions. In the same way, the hydrogen bond librational bands observed for the trimeric cluster molecule confirm a pseudo-C3 symmetric cyclic cooperative hydrogen-bonded barrel-like potential energy minimum structure. This structure is vastly different from the sterically favored “chair” conformations observed for aliphatic alcohol cluster molecules of the same size owing to the additional stabilizing London dispersion forces and C–H· · · π interactions between the aromatic rings. The hydrogen bond librational transition observed for the phenol monohydrate finally confirms that phenol acts as a hydrogen bond donor to water in contrast to the hydrogen bond acceptor role observed for aliphatic alcohols. [ABSTRACT FROM AUTHOR]

Understanding the structure‐function relationships of the green fluorescent protein (GFP) chromophore is important in rationally developing new molecular tools for biological imaging and beyond. Herein, we systematically modified the GFP chromophore structure with electron‐withdrawing and ‐donating groups (EWGs and EDGs) to investigate the substituent effects on the excited‐state proton transfer (ESPT) and twisting dynamics of the cationic chromophore in solution. With key insights gained from femtosecond transient absorption and stimulated Raman spectroscopy, we reveal that the EWG substitution by –F increases photoacidity in an additive manner and leads to an ultrafast barrierless ESPT by difluorination, while the EDG substitution by –OCH3 also results in ultrafast ESPT despite the weak photoacidity as estimated by the Förster equation. We ascribe the unusually fast kinetics in methoxylated derivatives to the occurrence of a pre‐existing chromophore‐solvent complex that sets up the acceptor site for ESPT. Furthermore, the kinetic competition between ESPT and twisting pathways is crucial for the observation of ESPT in action, particularly for molecules undergoing efficient nonradiative decay in the excited state through torsional motions. Such flexible and highly engineerable molecules can enable more versatile photoswitches and sensors. [ABSTRACT FROM AUTHOR]

A novel 0D organic–inorganic hybrid antimony-based halide [((R)-C8H12N)4](Sb2Cl10) was achieved through a slow evaporation method at room temperature. Single crystal X-ray diffraction analysis revealed that the compound crystallizes in the monoclinic system, within the P21 space group. The structure consists of(R)-1-phenylethylammonium (C8H12N)+cations and [Sb2Cl10]4− dimers, formed by edge-sharing distorted octahedra. The cohesion of the structure were ensured by N-H…Cl hydrogen bonds. Hirshfeld surface analysis indicated H…H interactions as the dominant intermolecular interaction contacts (42.4 %). Infrared and Raman spectroscopy confirmed the presence of organic cations and inorganic components. The thermogravimetric analysis demonstrated that the compound exhibits thermal stability up to 180 °C. Finally, Optical studies further suggest that this material holds significant promise for optical and optoelectronic applications.

This study investigates the effects of silicon ion bombardment on the phononic properties of Si/Si+Ge and SiO2/SiO2+Ge superlattices to enhance neutron superreflector technology. Through precise ion implantation and Fourier Transform Infrared Spectroscopy (FTIR), we observed significant alterations in transverse and longitudinal optical phonon modes. The Si/Si+Ge system exhibited notable blueshifts and intensity changes, while SiO2/SiO2+Ge showed increased lattice disorder and peak broadening. These findings highlight ion bombardment's potential to optimize phononic landscapes for improved nuclear reactor safety and efficiency via advanced phonon engineering.

Abstract Bulk composition of kidney stones, often analyzed with infrared spectroscopy, plays an essential role in determining the course of treatment for kidney stone disease. Though bulk analysis of kidney stones can hint at the general causes of stone formation, it is necessary to understand kidney stone microstructure to further advance potential treatments that rely on in vivo dissolution of stones rather than surgery. The utility of Raman microscopy is demonstrated for the purpose of studying kidney stone microstructure with chemical maps at ≤ 1 µm scales collected for calcium oxalate, calcium phosphate, uric acid, and struvite stones. Observed microstructures are discussed with respect to kidney stone growth and dissolution with emphasis placed on

Hard X-ray absorption spectroscopy is a valuable in situ probe for non-destructive diagnostics of metal sites. The low-energy interval of a spectrum (XANES) contains information about the metal oxidation state, ligand type, symmetry and distances in the first coordination shell but shows almost no dependency on the bridged metal–metal bond length. The higher-energy interval (EXAFS), on the contrary, is more sensitive to the coordination numbers and can decouple the contribution from distances in different coordination shells. Supervised machine-learning methods can combine information from different intervals of a spectrum; however, computational approaches for the near-edge region of the spectrum and higher energies are different. This work aims to keep all benefits of XANES and extend its sensitivity towards the interatomic distances in the first and second coordination shells. Using a binuclear bridged copper complex as a case study and cross-validation analysis as a quantitative tool it is shown that the first 170 eV above the edge are already sufficient to balance the contributions of Cu–O/N scattering and Cu–Cu scattering. As a more general outcome this work highlights the trivial but often overlooked importance of using `longer' energy intervals of XANES for structural refinement and machine-learning predictions. The first 200 eV above the absorption edge still do not require parametrization of Debye–Waller damping and can be calculated within full multiple scattering or finite difference approximations with only moderately increased computational costs.

Nowadays one of the main challenge in the effective application of a plastic circular economy and overall energy and raw material recovery is the capability of doing selective sorting. The sorting process is the first and important step to obtain homogeneous fluxes of waste materials, which can be utilized as feedstock for raw material recovery, oil based material generation or for energy production. There are many activities for solving the challenges of sorting complex objects in a general waste stream; in this study we used Vibrational Spectroscopy and the most recent NIR technologies to demonstrate the sortability of multilayered samples containing PVDC layers. The NIR results find scientific baseline in the fundamental normal modes observed in IR and Raman spectroscopy and the relative discussion and assignments. The on field success of the sorting tests open the way for advancement in the technologies aimed at achieving a sustainable and economically viable approach to polymer production.