2020
DOI: 10.1016/j.molstruc.2020.128746
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Structure investigation of β-D-fructose crystal under high pressure: Raman scattering, IR absorption, and synchrotron X-ray diffraction

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Cited by 6 publications
(3 citation statements)
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“…The fructose molecule is selected because it has a considerably smaller Raman cross-section than those of other model molecules frequently used in conventional Raman experiments and does not form covalent bonds with Au. As shown in Figure d, e, a distinctive Raman transition of fructose at 1250 cm –1 , assigned to the twisting of CH 2 , is clearly observed only for the AuNR with tip-selectively grown SiO 2 -on-Au film, whereas no Raman transition is observed for the other substrates.…”
Section: Results and Discussionmentioning
confidence: 99%
“…The fructose molecule is selected because it has a considerably smaller Raman cross-section than those of other model molecules frequently used in conventional Raman experiments and does not form covalent bonds with Au. As shown in Figure d, e, a distinctive Raman transition of fructose at 1250 cm –1 , assigned to the twisting of CH 2 , is clearly observed only for the AuNR with tip-selectively grown SiO 2 -on-Au film, whereas no Raman transition is observed for the other substrates.…”
Section: Results and Discussionmentioning
confidence: 99%
“…A higher oxygen flow rate to the APPJ can remove surface-adsorbed species [25] and even etch the polystyrene polymer thin films due to its high reactivity induced by the reactive species [36,37] The evolution of the surface species located at 1900-1000 cm −1 is also provided in figure 4(c). During the ignition of CH 4 /O 2 /Ar plasma, absorption bands at 1590 cm −1 (carboxylate [38,39]), 1420 cm −1 (C-O-H group [40] or CH 2 [41]), and 1280 cm −1 (carbonate [42]) emerged, as the reaction took place. Upon the ignition of O 2 /Ar plasma, the 1590 cm −1 and 1420 cm −1 bands decreased and the 1280 cm −1 band did not show obvious changes due to exposure to the O 2 /Ar plasma.…”
Section: Investigation Of the Catalyst Activationmentioning
confidence: 99%
“…Hydrogen bonds and intermolecular contacts can considerably change under pressure, which can affect the strength and nature of interactions Tomkowiak & Katrusiak, 2019;Resnati et al, 2015;Bhatt et al, 2016). Structural phase transitions induced by pressure were described for d-sucrose (Patyk et al, 2012), -d-glucose , -d-mannose (Patyk-Kaźmierczak et al, 2016) and -d-fructose (Yao et al, 2020). It was concluded that small voids present in the ambient-pressure structures of these crystals collapse under sufficiently high pressure, which triggers transformations of the O-HÁ Á ÁO hydrogen-bonding patterns.…”
Section: Introductionmentioning
confidence: 99%