2017
DOI: 10.1016/j.molstruc.2017.05.035
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FT-IR and NIR spectroscopic investigation of hydrogen bonding in indole-ether systems

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Cited by 21 publications
(12 citation statements)
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“…Moreover, the hydroxyl and carboxyl bands in the spectrum of MIL-125-CS-Pb were better defined than those in the spectrum of pure MIL-125-CS, which implied that Pb(II) was embedded through interactions with both the O–H and COO− units [ 24 ]. Reportedly, the stretching and torsional vibrations of these functional groups weaken with the increasing ionic volume, thus resulting in an altered adsorption maximal [ 25 ]. Through the aforementioned analysis, we concluded that Pb(II) reacted chemically with MIL-125-CS and caused changes in the infrared adsorption peaks, thereby demonstrating that Pb(II) was successfully adsorbed onto the surfaces of the MIL-125-CS beads.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, the hydroxyl and carboxyl bands in the spectrum of MIL-125-CS-Pb were better defined than those in the spectrum of pure MIL-125-CS, which implied that Pb(II) was embedded through interactions with both the O–H and COO− units [ 24 ]. Reportedly, the stretching and torsional vibrations of these functional groups weaken with the increasing ionic volume, thus resulting in an altered adsorption maximal [ 25 ]. Through the aforementioned analysis, we concluded that Pb(II) reacted chemically with MIL-125-CS and caused changes in the infrared adsorption peaks, thereby demonstrating that Pb(II) was successfully adsorbed onto the surfaces of the MIL-125-CS beads.…”
Section: Resultsmentioning
confidence: 99%
“…The indole ring is capable of various noncovalent interactions with other molecules by hydrogen bonding through the NH moiety and by π···π stacking, cation···π interactions, etc., through the aromatic moiety [17]. The study of indole inter-and intra-molecular interactions is essential for better understanding of its reactivity and mechanism of interactions in biological systems [18]. The noncovalent and weak interactions with the surrounding groups may also affect the binding properties and redox potential of the metal center in their complexes [19,[20][21][22].…”
Section: Introductionmentioning
confidence: 99%
“…8, the signal peak of the macromolecule ether bond appeared in the liquefied product with the HZSM-5 catalyst at 1040 cm -1 , but the addition of the catalyst liquefied infrared spectrum did not find the same signal peak. Instead, a small molecular ether bond signal peak appeared at 1061 cm -1 , indicating that the catalyst promoted the degradation of macromolecules (Kordić et al 2017).…”
Section: Ftir Analysis Of Liquefied Product Via Zn/hzsm-5 Catalystsmentioning
confidence: 99%