2023
DOI: 10.1360/ssc-2023-0062
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A series of isopolymolybdate-viologen compounds: structures and photochromic, organic amine sensing, and double anti-counterfeiting properties

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Cited by 3 publications
(4 citation statements)
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“…The binding energy of N 1s moves from 398.80 eV (before irradiation) to 398.59 eV (after irradiation) (Figure S13c). Based on the above results, the O atoms are as electron donors, while the N atoms are as electron acceptors . So, the process of electron transfer is from O to N. Namely, electrons are transferred from O in POMs to N in organic ligands.…”
Section: Resultsmentioning
confidence: 88%
See 1 more Smart Citation
“…The binding energy of N 1s moves from 398.80 eV (before irradiation) to 398.59 eV (after irradiation) (Figure S13c). Based on the above results, the O atoms are as electron donors, while the N atoms are as electron acceptors . So, the process of electron transfer is from O to N. Namely, electrons are transferred from O in POMs to N in organic ligands.…”
Section: Resultsmentioning
confidence: 88%
“…Based on the above results, the O atoms are as electron donors, while the N atoms are as electron acceptors. 42 So, the process of electron transfer is from O to N. Namely, electrons are transferred from O in POMs to N in organic ligands.…”
Section: Crystal Structures Of [H(bypy)]•(bypy-2) 1/2 •(Pmo 12 O 40 )...mentioning
confidence: 99%
“…The peaks at 3062−3283, 772−947, and 1420−1650 cm −1 can be attributed to ν(C-H) and ν(C-N) [45]. The characteristic absorption peaks of the naphthalene ring are in the range of 1420−1650 cm −1 [46]. The PXRD pattern of 1 is provided in Fig.…”
Section: Ir and Powder X-ray Diffraction (Pxrd) Of Complexmentioning
confidence: 96%
“…In viologen organic ligands, the positively charged quaternary nitrogen facilitates the transfer of electrons through carbon to other atoms, creating a process analogous to redox reactions. 15,16 Simultaneously, the highly electronegative N and O atoms readily form hydrogen bonds, providing effective acceptors for constructing three-dimensional (3D) supramolecular frameworks. However, most viologen ligands are highly soluble in water and other solvents, which greatly hinders their practical application.…”
Section: Introductionmentioning
confidence: 99%