Dual-mode probe for detecting hydrogen sulfide and use thereof
US-2024390529-A1 · Nov 28, 2024 · US
US9802963B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9802963-B2 |
| Application number | US-201415026356-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 2, 2014 |
| Priority date | Oct 2, 2013 |
| Publication date | Oct 31, 2017 |
| Grant date | Oct 31, 2017 |
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An object of the present invention is to enable the synthesis of various fluorine-containing compounds having an organic group at both terminals of their tetrafluoroethylene structure (—CF 2 —CF 2 —). The present invention provides a fluorine-containing complex compound including a fluorine-containing organic metal compound represented by formula (1a): R 1 —CF 2 —CF 2 -M 1 (1 a ) wherein M 1 is a metal selected from the group consisting of copper, zinc, nickel, iron, cobalt, and tin; and R 1 represents an organic group, and at least one ligand selected from the group consisting of pyridine ring-containing compounds and phosphines.
Opening claim text (preview).
The invention claimed is: 1. A fluorine-containing compound represented by formula (4-1): (R a1S —) ma1 R a1L —CF 2 —CF 2 —R a2L (—R a2S ) ma2 (4-1) wherein the moiety represented by formula:(R a1S —) ma1 R a1L indicates R a1L substituted with ma1 R a1S ; the moiety represented by formula: R a2L (—R a2S ) ma2 indicates R a2L substituted with ma2 R a2S ; R a1S and R a2S are the same or different, and each represents independently a moiety selected from the group consisting of (1) aldehyde, (2) alkenyl optionally substituted with at least one halogen atom, (3) alkynyl optionally substituted with at least one substituent selected from the group consisting of halogen and trimethylsilyl, (4) epoxy, (5) (meta)acryloyl optionally substituted with at least one halogen atom, and (6) alkyl and alkoxy each substituted with at least one substituent selected from the group consisting of: (a) cyano group, (b) aldehyde, (c) alkynyl optionally substituted with at least one halogen atom, (d) vinyl optionally substituted with at least one halogen atom, (e) epoxy, and (f) (meta)acryloyl optionally substituted with at least one halogen atom, ma1 and ma2 are independently 0 or 1, and the sum of ma1 and ma2 is 1 or 2 ; R a1L and R a2L are the same or different, and each represents a phenyl group optionally having, in addition to ma1 R a1S or ma2 R a2S , at least one substituent selected from the group consisting of fluoro group, perfluoro organic group, and pentafluorosulfanyl. 2. A fluorine-containing compound represented by formula (4-3): ( R a1S —) ma1 R a1L —CF 2 —CF 2 R a2L (—R a2S ) ma2 (4-3), wherein the moiety represented by (R a1S —) ma1 R a1L indicates R a1L substituted with ma1 R a1S ; p 1 the moiety represented by R a2L (—R a2S ) ma2 indicates R a2L substituted with ma2 R a2S ; R a1S represents 1, 3-dioxo- 1,3-dihydroisobenzofuran 5-yl R a2S represents (1) 1,3-dioxo-1,3-dihydroisobenzofuran 5-yl, (2) amino, (3) carboxy at para-position, or (4) halogenocarbonyl; ma1 is 1; ma2 is 0 or 1; and R a1L and R a2L are the same or different, and each represents (a) a phenyl group or a biphenyl group, or (b) a bond, with the proviso that when R a2S is (2) amino, (3) carboxy at para-position, or (4) halogenocarbonyl, R a2L is (a) a phenyl group or a biphenyl group. 3. The fluorine-containing compound according to claim 1 , wherein R a1S and R a2S are the same or different, and each represents independently a moiety selected from the group consisting of (1) cyano, (2) aldehyde, (3) alkenyl, (4) alkynyl optionally substituted with trimethylsilyl, (5) epoxy, (6) (meta)acryloyl optionally substituted with at least one halogen atom, and (7) alkoxy substituted with epoxy. 4. The fluorine-containing compound according to claim 1 , which is selected from the following compounds: 5. The fluorine-containing compound according to claim 2 , which is selected from the following compounds: 6. A method for producing the fluorine-containing compound according to claim 1 , the method comprising reacting a fluorine-containing complex compound comprising: a fluorine-containing organic metal compound represented by formula (1a): R 1 —CF 2 —CF 2 —M 1 (1a) wherein M 1 is a metal selected from the group consisting of copper, zinc, nickel, iron, cobalt, and tin; and R 1 represents ( R a1S —) ma1 R a1L as defined above, and at least one ligand selected from the group consisting of pyridine ring-containing compounds and phosphinesfluorine-containing complex compound, with a halogen compound represented by formula (5): X—R 2 (5) wherein R 2 represents R a2L (—R a2S ) ma2 as defined above; and X represents a halogen atom. 7. A method for producing the fluorine-containing compound according to claim 2 , the method comprising reacting a fluorine-containing complex compound comprising: a fluorine-containing organic metal compound represented by formula (1a): R 1 —CF 2 —CF 2 —M 1 (1a) wherein M 1 is a metal selected from the group consisting of copper, zinc, nickel, iron, cobalt, and tin; and R 1 represents (R a1S —) ma1 R a1L as defined above, and at least one ligand selected from the group consisting of pyridine ring-containing compounds and phosphinesfluorine-containing complex compound, with a halogen compound represented by formula (5): X—R 2 (5) wherein R 2 represents R a2L (—R a2S ) ma2 as defined above; and X represents a halogen atom.
Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages · CPC title
Boron compounds · CPC title
Copper compounds · CPC title
Radicals substituted by halogen atoms or nitro or nitroso radicals · CPC title
Benzo [c] furans; Hydrogenated benzo [c] furans · CPC title
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