2015
DOI: 10.1016/j.chemphys.2015.07.004
|View full text |Cite
|
Sign up to set email alerts
|

Fluorescence and physical properties of the organic salt 2-chloro-4-nitrobenzoate–3-ammonium-phenol

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2016
2016
2022
2022

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 11 publications
(2 citation statements)
references
References 46 publications
0
2
0
Order By: Relevance
“…Such a characteristic peak appears to be sharper and shifts to 1645 cm –1 in the desorption sample (Figure b, green curve), which is assigned to the CO stretch of corresponding protonated free acid at pH 5.0. In the former case, proton transfer in ammonium–carboxylate ion pairs existing between SiO 2 –PEI NPs and CDs accounts for the diminished absorption and relatively low wavenumber. In the latter case, the breakup of such ionic hydrogen bonds due to protonation of carboxylic acid groups of CDs leads to a blue shift together with the increased absorption.…”
Section: Preparation and Characterization Of The Two Bbsmentioning
confidence: 99%
“…Such a characteristic peak appears to be sharper and shifts to 1645 cm –1 in the desorption sample (Figure b, green curve), which is assigned to the CO stretch of corresponding protonated free acid at pH 5.0. In the former case, proton transfer in ammonium–carboxylate ion pairs existing between SiO 2 –PEI NPs and CDs accounts for the diminished absorption and relatively low wavenumber. In the latter case, the breakup of such ionic hydrogen bonds due to protonation of carboxylic acid groups of CDs leads to a blue shift together with the increased absorption.…”
Section: Preparation and Characterization Of The Two Bbsmentioning
confidence: 99%
“…The vibrational changes in the functional groups that are involved in hydrogen bonding such as carboxylate and N-H in the benzimidazole can be identified in the FTIR and the Raman spectra. 41 The N-H stretching vibration of benzimidazolium appears at 3139 cm −1 in the FTIR spectrum. 42 In general, aromatic C-H stretching vibrations appear in the region of 3080-3010 cm −1 in the FTIR and Raman spectra.…”
Section: Vibrational Analysismentioning
confidence: 99%