Separating agent
US-2015343420-A1 · Dec 3, 2015 · US
US10940425B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10940425-B2 |
| Application number | US-201616064797-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 23, 2016 |
| Priority date | Dec 24, 2015 |
| Publication date | Mar 9, 2021 |
| Grant date | Mar 9, 2021 |
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A subject of the present invention is the use of a compound having the general formula (I): (I) wherein V, W, X 4 , X 5 , X 6 , X 7 , X′ 4 , X′ 5 , X′ 6 , X′ 7 , Y, Y′, R 3 , R′ 3 , R 4 and R′ 4 are as defined in any one of claims 1 to 11 , for the detection, capture and/or separation of polluting gases, in particular those selected from the group comprising carbon dioxide, methane, sulfur dioxide, nitrogen oxides, carbon monoxide, linear hydrocarbons, linear mono-olefins and their mixtures, and preferably carbon dioxide. Another subject of the invention is a compound of formula (I) wherein V, W, X 4 , X 5 , X 6 , X 7 , X′ 4 , X′ 5 , X′ 6 , X′ 7 , Y, Y′, R 3 , R′ 3 , R 4 and R′ 4 are as defined in any one of claims 12 to 21 .
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The invention claimed is: 1. A method for the detection, capture and/or separation of polluting gases, comprising capture and/or separation into/by a compound having general formula (I) wherein V represents: W has the same meaning as V or W is absent, and when W is absent then R 4 and R′ 4 are also absent, X 1 , X 2 , X 3 , X′ 1 , X′ 2 , X′ 3 , X 4 , X 5 , X 6 , X 7 , X′ 4 , X′ 5 , X′ 6 , X′ 7 , X 8 and X 9 are each independently N or a CH group, when W has the same meaning as V, then Y and Y′ are each a carbon atom, when W is absent, then Y and Y′ are each independently N or a CR group, with R representing H, R a , NR a R b , OR a , SR a , CO 2 R a , COR a , CONHR a , CONR a R b , NHCOR a , SO 2 R a , SO 2 NHR a , SO 2 NR a R b , PR a R b , P(O)R a R b , P(O)(OR a )(OR b ), CH 2 PO(OR a )(OR b ), COCH 2 COR a , CSOR a , CSR a , CSNHR a , CSNR a R b , NHCSR a , P(S)R a R b , CSCH 2 CSR a , NHCONHR a , NHCSNHR a or a five or six-membered aromatic or heteroaromatic compound chosen from benzene, pyridine, diazine, triazine, tetrazine, pyrrole, thiophene, furan, azole, triazole or tetrazole, with R a and R b being each independently H, OH; an alkyl radical having from 1 to 10 carbon atoms (alkyl C 1 -C 10 ); a five or six-membered carbocycle chosen from cyclohexane, piperidine, piperazine, tetrahydrothiophene, tetrahydropyrrole or dihydroazole; or an aromatic or heteroaromatic compound chosen from pyridine, diazine, triazine, tetrazine, pyrrole, thiophene, furan, azole, triazole, tetrazole, benzoazole, benzotriazole or indole, R 1 represents O, S, SO 2 , SO, CO, a NR a , SiR a R b , SnR a R b , BR a or a PR a group, R a and R b being as defined above, R 2 and R′ 2 are each independently COOR a , NO 2 , CONR a R b , SO 2 R a , SO 3 H, OSO 3 H, COR a , PO 3 H 2 , OPO 3 H 2 or CN, R a and R b being as defined above, R 3 , R′ 3 , R 4 and R′ 4 are each independently S, NR a , P, Se or Te, R a being as defined above. 2. A method according to claim 1 , wherein in the compound of formula (I): V represents: X 4 , X 5 , X 6 , X 7 , X′ 4 , X′ 5 , X′ 6 and X′ 7 are each independently N or CH, when W has the same meaning as V, then Y and Y′ are each a carbon atom, when W is absent, then Y and Y′ are each independently N or a CR group, R being H, NR a R b , CO 2 R a , P(O)(OR a )(OR b ), CH 2 PO(OR a )(OR b ), R 1 represents S, SO 2 , NR a or O, R 2 and R′ 2 are each independently NO 2 , COOR a , COR a or CONR a R b , R 3 , R′3, R 4 and R′ 4 are each independently S or NR a , with R a and R b are each independently H or an alkyl C 1 -C 10 . 3. A method according to claim 1 , wherein in the compound of formula (I): W, R 4 and R′ 4 are absent, V represents: 4. A method according to claim 3 , wherein compound of formula (I) is selected from the group consisting of: Y═Y′═CNH 2 , R 1 ═SO 2 , R 2 ═R′ 2 ═NO 2 and R 3 ═R′ 3 ═S (1), Y═Y′═CNH 2 , R 1 ═SO 2 , R 2 ═R′ 2 ═NO 2 and R 3 ═R′ 3 ═NH (2), Y═Y′═N, R 1 ═SO 2 , R 2 ═R′ 2 ═NO 2 and R 3 ═R′ 3 ═S (3), Y═Y′═N, R 1 ═SO 2 , R 2 ═R′ 2 ═NO 2 and R 3 ═R′ 3 ═NH (4), Y═Y′═N, R 1 ═SO 2 , R 2 ═R′ 2 ═COOR a and R 3 ═R′ 3 ═NH (5), Y═Y′═N, R 1 ═SO 2 , R 2 ═R′ 2 ═COOR a and R 3 ═R′ 3 ═S (6), Y═Y′═N, R 1 ═5, R 2 ═R′ 2 ═COOR a and R 3 ═R′ 3 ═S (7), Y═Y′═N, R 1 ═5, R 2 ═R′ 2 ═COOR a and R 3 ═R′ 3 ═NH (8), Y═Y′═CNH 2 , R 1 ═S, R 2 ═R′ 2 ═COOR a and R 3 ═R′ 3 ═NH (9), Y═Y′═CNH 2 , R 1 ═S, R 2 ═R′ 2 ═COOR a and R 3 ═R′ 3 ═S (10), Y═Y′═CNH 2 , R 1 ═S, R 2 ═R′ 2 ═CONR a R b and R 3 ═R′ 3 ═S (11), Y═Y′═CNH 2 , R 1 ═S, R 2 ═R′ 2 ═CONR a R b and R 3 ═R′ 3 ═NH (12), Y═Y′═CNH 2 , R 1 ═SO 2 , R 2 ═R′ 2 ═CONR a R b and R 3 ═R′ 3 ═NH (13), Y═Y′═CNH 2 , R 1 ═SO 2 , R 2 ═R′ 2 ═CONR a R b and R 3 ═R′ 3 ═S (14), Y═Y′═N, R 1 ═SO 2 , R 2 ═R′ 2 ═CONR a R b and R 3 ═R′ 3 ═S (15), Y═Y′═N, R 1 ═SO 2 , R 2 ═R′ 2 ═CONR a R b and R 3 ═R′ 3 ═NH (16), Y═Y′═CCOOH, R 1 ═SO 2 , R 2 ═R′ 2 ═NO 2 and R 3 ═R′ 3 ═S (17), Y═Y′═CCH 2 PO(OC 2 H 5 ) 2 , R 1 ═SO 2 , R 2 ═R′ 2 ═NO 2 and R 3 ═R′ 3 ═NH (18), and in each compound (1) to (18): X 1 ═X 2 ═X 3 ═X′ 1 ═X′ 2 ═X′ 3 ═X 4 ═X 5 ═X 6 ═X 7 ═X′ 4 ═X′ 5 ═X′ 6 ═X′ 7 ═CH, R a and R b are each independently H or an alkyl C 1 -C 10 . 5. A method according to claim 1 , wherein in the compound of formula (I): W has the same meaning as V, V represents: 6. A method according to claim 5 , wherein compound of formula (I) is selected from the group consisting of: R 1 ═SO 2 , R 2 ═R′ 2 ═NO 2 , R 3 ═R′ 3 ═R 4 ═R′ 4 ═NH (19), R 1 ═SO 2 , R 2 ═R′ 2 ═NO 2 , R 3 ═R 4 ═NH, R′ 3 ═R′ 4 ═S (20), R 1 ═S, R 2 ═R′ 2 ═NO 2 , R 3 ═R′ 3 ═R 4 ═R′ 4 ═NH (21), R 1 ═S, R 2 ═R′ 2 ═NO 2 , R 3 ═R 4 ═NH, R′ 3 ═11′ 4 ═S (22), R 1 ═SO 2 , R 2 ═R′ 2 ═NO 2 , R 3 ═R′ 3 ═S, R 4 ═R′ 4 ═NH (23), R 1 ═S, R 2 ═R′ 2 ═NO 2 , R 3 ═R′ 3 ═S, R 4 ═R′ 4 ═NH (24), and in each compound (19) to (24): X 1 ═X 2 ═X 3 ═X′i═X′ 2 ═X′ 3 ═X 4 ═X 5 ═X 6 ═X 7 ═X′ 4 ═X′ 5 ═X′ 6 ═X′ 7 ═CH. 7. A method according to claim 1 , wherein in the compound of formula (I): W, R 4 and R′ 4 are absent, V represents: 8. A method according to claim 7 , wherein compound of formula (I) is selected from the group consisting of: Y═Y′═N, R 2 ═R′ 2 ═NO 2 and R 3 ═R′ 3 ═S (25), Y═Y′═CPO(OH) 2 , R 2 ═R′ 2 ═NO 2 and R 3 ═R′ 3 ═NH (26), Y═Y′═CCH 2 PO(OC 2 H 5 ) 2 , R 2 ═R′ 2 ═NO 2 , R 3 ═R′ 3 ═NH (27), Y═Y′═CCOOH, R 2 ═R′ 2 ═NO 2 , R 3 ═R′ 3 ═S (28), Y═Y′═CNH 2 , R 2 ═R′ 2 ═CO 2 Et, R 3 ═R′ 3 ═S (29), Y═Y′═CCOOH, R 2 ═R′ 2 ═CO 2 Et, R 3 ═R′ 3 ═S (30), and in each compound (25) to (30): X 4 ═X 5 ═X 6 ═X 7 ═X′ 4 ═X′ 5 ═X′ 6 ═X′ 7 ═X 8 ═X 9 ═CH. 9. A method according to claim 1 wherein in the compound of formula (I): W has the same meaning as V, V represents: 10. A method according to claim 9 , wherein compound of formula (I) is selected from the group consisting of: R 2 ═R′ 2 ═NO 2 , R 3 ═R′ 3 ═R 4 ═11′ 4 ═NH (31), R 2 ═R′ 2 ═NO 2 , R 3 ═R′ 3 ═R 4 ═R′ 4 ═S (32), R 2 ═R′ 2 ═CO 2 Et, R 3 ═R′ 3 ═R 4 ═11′ 4 ═S (33), R 2 ═R′ 2 ═NO 2 , R 3 ═R′ 3 ═S, R 4 ═R′ 4 ═NH (34), and in each compound (31) to (34): X 4 ═X 5 ═X 6 ═X 7 ═R 4 ═X′ 5 ═X′ 6 ═X′ 7 ═X 8 ═X 9 ═CH. 11. A method according to claim 1 for the depollution of the air and/or toxic exhaust fumes. 12. Compound having the general formula (I): wherein V represents: W has the same meaning as V or W is absent, and when W is absent then R 4 and R′ 4 are also absent, X 1 , X 2 , X 3 , X′ 1 , X′ 2 , X′ 3 , X 4 , X 5 , X 6 , X 7 , X′ 4 , X′ 5 , X′ 6 , X′ 7 , X 8 and X 9 are each independently N or a CH group,
Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00 · CPC title
comprising organic material · CPC title
condensed with carbocyclic rings or ring systems · CPC title
condensed with carbocyclic rings or ring systems · CPC title
Sulfur atoms · CPC title
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