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We investigated IR spectra in the CH- and OH-stretching regions of size-selected methanol clusters, (CH(3)OH)(n) with n = 2-6, in a pulsed supersonic jet by using the IR-VUV (vacuum-ultraviolet) ionization technique. VUV emission at 118 nm served as the source of ionization in a time-of-flight mass spectrometer. The tunable IR laser emission served as a source of predissociation or excitation before ionization. The variations of intensity of protonated methanol cluster ions (CH(3)OH)(n)H(+) and CH(3)OH(+) and (CH(3)OH)(2)(+) were monitored as the IR laser light was tuned across the range 2650-3750 cm(-1). Careful processing of these action spectra based on photoionization efficiencies and the production and loss of each cluster due to photodissociation yielded IR spectra of the size-selected clusters. Spectra of methanol clusters in the OH region have been extensively investigated; our results are consistent with previous reports, except that the band near 3675 cm(-1) is identified as being associated with the proton acceptor of (CH(3)OH)(2). Spectra in the CH region are new. In the region 2800-3050 cm(-1), bands near 2845, 2956, and 3007 cm(-1) for CH(3)OH split into 2823, 2849, 2934, 2955, 2984, and 3006 cm(-1) for (CH(3)OH)(2) that correspond to proton donor and proton acceptor, indicating that the methanol dimer has a preferred open-chain structure. In contrast, for (CH(3)OH)(3), the splitting diminishes and the bands near 2837, 2954, and 2987 cm(-1) become narrower, indicating a preferred cyclic structure. Anharmonic vibrational wavenumbers predicted for the methanol open-chain dimer and the cyclic trimer with the B3LYP∕VPT2∕ANO1 level of theory are consistent with experimental results. For the tetramer and pentamer, the spectral pattern similar to that of the trimer but with greater widths was observed, indicating that the most stable structures are also cyclic.
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http://dx.doi.org/10.1063/1.3572225 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
Hefei National Research Center for Physical Sciences at the Microscale, School of Chemistry and Materials Science, State Key Laboratory of Precision and Intelligent Chemistry, National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui, 230026, China.
The construction of C─N bonds from simple precursors under ambient conditions is a fundamental challenge in green chemistry, especially when it comes to avoiding energy-intensive protocols. Here, we present a continuous flow photocatalytic platform that enables the efficient coupling of C─N bonds between methanol and ammonia at ambient temperature and pressure. By synergistically engineering a Pd clusters-decorated TiO photocatalyst (1Pd/TiO) and a mass transfer-enhanced gas-liquid-solid Taylor flow reactor, the system achieves a remarkable formamide productivity of 256.
View Article and Find Full Text PDFMolecules
August 2025
College of Biological Science, University of Guelph, Guelph, ON N1G 2W1, Canada.
Metabolite fingerprint profiling is a robust tool for verifying suppliers of authentic botanical ingredients. While comparative studies exist, few apply identical conditions across multiple species; this study utilized a cross-species comparison to identify versatile solvents despite biochemical variability. Multiple solvents were used for sample extraction prior to analysis by proton NMR and liquid chromatography-mass spectrometry (LC-MS) for multiple botanicals including , , , , , , , , and .
View Article and Find Full Text PDFJ Phys Chem A
September 2025
Department of Computer Science and the Institute of Technology, Resource and Energy-Efficient Engineering (TREE), University of Applied Sciences Bonn-Rhein-Sieg, Grantham-Allee 20, Sankt Augustin 53757, Germany.
The benzene···methanol dimer is one of the simplest systems that manifests an O-H···π nonbonded interaction. This interaction can be found in numerous systems, ranging from small-molecule clusters to biological systems, for example, phenyl-containing ligands bound within a protein's binding pocket. Herein, four gas-phase configurations are examined using quantum mechanics, which have O-H···π, CH···π and Bz-H···O interactions.
View Article and Find Full Text PDFJ Environ Sci (China)
December 2025
Guangdong Provincial Key Laboratory of Atmospheric Environment and Pollution Control, School of Environment and Energy, South China University of Technology, Guangzhou 510006, China; The Key Lab of Pollution Control and Ecosystem Restoration in Industry Clusters, Ministry of Education, South China U
The reduction of carbon emissions in the steel industry is a significant challenge, and utilizing CO from carbon intensive steel industry off-gases for methanol production is a promising strategy for decarbonization. However, steelwork off-gases typically contain various impurities, including HS, which can deactivate commercial methanol synthesis catalysts, Cu/ZnO/AlO (CZA). Reverse water-gas shift (RWGS) reaction is the predominant side reaction in CO hydrogenation to methanol which can occur at ambient pressure, enabling the decouple of RWGS from methanol production at high pressure.
View Article and Find Full Text PDFNat Commun
August 2025
School of Materials Science and Engineering, Guangdong Provincial Key Laboratory of Advanced Energy Storage Materials, South China University of Technology, Guangzhou, PR China.
The hydrolysis/methanolysis of silicon has received considerable attention to achieve efficient and on-demand hydrogen conversion. However, the intense covalent network and highly localized electrons in pure Si impede its reactivity with water (HO) or methanol (CHOH), thereby hindering the hydrogen release. In this work, we report the synthesis of Zintl phase alkalis-Si alloys via simple ball-milling or sintering, showing eminent performance in enhancement of HO/CHOH dissociation.
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