Multi-directional polydentate ligands for metal-organic hybrid structures
US-10562845-B2 · Feb 18, 2020 · US
US11465962B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11465962-B2 |
| Application number | US-201916500152-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 17, 2019 |
| Priority date | Jan 26, 2018 |
| Publication date | Oct 11, 2022 |
| Grant date | Oct 11, 2022 |
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A composition for detecting an acidic compound and a method using the same are discloses herein. In some embodiments, the method includes contacting a composition comprising a metal-organic hybrid structure formed by coordinate bond between a compound represented by the following Chemical Formula 1 or a salt thereof and a metal ion, with an acidic compound to be detected, wherein the composition is in the form of a metallogel prior to contact with the acidic compound, and detecting the acidic compound based on the transition of the composition from the form of a metallogel to a liquid phase. In some embodiments, detection of the acidic compound can be visually confirmed by phase transformation of the composition from a metallogel to a liquid phase.
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The invention claimed is: 1. A method of detecting an acidic compound, comprising: contacting a composition comprising a metal-organic hybrid structure formed by coordinate bond between a compound represented by the following Chemical Formula 1 or a salt thereof and a metal ion, with an acidic compound to be detected, wherein the composition is in the form of a metallogel prior to contact with the acidic compound; and detecting the acidic compound based on the transition of the composition from the form of a metallogel to a liquid phase: in Chemical Formula 1, each R is independently -R 1 , —NH—CO-R 2 , or —NH-R 2 , each R 1 is independently —OH, C 6-60 aryl, C 1-10 alkyl, or an amino acid residue, and R 2 is C 1-10 alkyl, C 6-60 aryl, or C 4-60 heteroaryl containing any one of N, O, and S. 2. The method according to claim 1 , wherein each R 1 is independently —OH, phenyl, naphthyl, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, tert-pentyl, neopentyl, isopentyl, sec-pentyl, 3-pentyl, or an amino acid residue selected from the group consisting of alanine, cysteine, aspartic acid, glutamic acid, phenylalanine, histidine, isoleucine, lysine, leucine, methionine, asparagine, pyrrolysine, glutamine, arginine, serine, threonine, selenocysteine, valine, tryptophan, and tyrosine. 3. The method according to claim 1 , wherein R 2 is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, tert-pentyl, neopentyl, isopentyl, sec-pentyl, 3-pentyl, hexyl, octyl, phenyl, naphthyl, or pyridinyl. 4. The method according to claim 1 , wherein the compound represented by Chemical Formula 1 are compounds represented by the following Chemical Formulas 1-1 to 1-5: 5. The method according to claim 1 , wherein the metal of the metal ion is Period 1 transition metal, Period 2 transition metal, Period 3 transition metal, or lanthanide metal. 6. The method according to claim 1 , wherein the metal of the metal ion is Ti, V, Mn, Fe, Co, Ni, Cu, Zn, Zr, Mo, Ru, Rh, Pd, Ag, Ir, Pt, Au, Tb, Eu, or Yb. 7. The method according to claim 1 , wherein the acidic compound is a liquid or a gas. 8. The method according to claim 1 , wherein the acidic compound is hydrogen chloride, hydrogen fluoride, hydrogen bromide, trifluoroacetic acid, acetic acid, nitrogen oxide, nitric acid, sulfur oxide or sulfuric acid. 9. The method according to claim 1 , wherein the composition further comprises: a solvent, wherein the solvent is trapped between spaces in the metal-organic hybrid structure.
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