2007
DOI: 10.1080/00268970601146856
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Fourier transform infrared spectral study of N,N′-dimethylformamide-water-rhodamine 6G mixture

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Cited by 34 publications
(10 citation statements)
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“…The shift at 2931 cm -1 is due to symmetric methyl C-H bond stretching in membrane with DMF [46]. It is attributed to the presence of residual solvent [47]. While the peaks in the region of 2839 and 2931 cm -1 of membranes with cosolvent system are due to the presence of C-H stretching vibrations of THF [48].…”
Section: Resultsmentioning
confidence: 93%
“…The shift at 2931 cm -1 is due to symmetric methyl C-H bond stretching in membrane with DMF [46]. It is attributed to the presence of residual solvent [47]. While the peaks in the region of 2839 and 2931 cm -1 of membranes with cosolvent system are due to the presence of C-H stretching vibrations of THF [48].…”
Section: Resultsmentioning
confidence: 93%
“…Likewise, the peaks located near 816, 746, and 653 cm −1 confirmed Zn-O stretching modes. IR bands at 1502, 1294, and 653 cm −1 indicated a random dimethyl formamide (DMF) distribution in the MOF-5 framework structure 44 . The band located at 3607 cm −1 indicated adsorbed water molecules.…”
Section: Resultsmentioning
confidence: 99%
“…54 Raman spectra were recorded with a Bruker MultiRAM spectrometer equipped with a Nd:YAG laser (1064 nm) and an InGaAs detector (4000–70 cm −1 ). 55 Band assignments for 1 were made using the IR spectra of DMF 56 and metal trifluoroacetates, 57 for 2 additionally of trifluoroacetic acid 35 and trifluoroacetic acid esters 58 and for 3 of pentafluoropropionic acid 59 and some of its esters. 60…”
Section: Methodsmentioning
confidence: 99%