BE577371A - - Google Patents
Info
- Publication number
- BE577371A BE577371A BE577371DA BE577371A BE 577371 A BE577371 A BE 577371A BE 577371D A BE577371D A BE 577371DA BE 577371 A BE577371 A BE 577371A
- Authority
- BE
- Belgium
- Prior art keywords
- metal
- ligands
- borohydrides
- amine
- complex
- Prior art date
Links
- 150000001412 amines Chemical class 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 229910052751 metal Inorganic materials 0.000 claims description 12
- 239000002184 metal Substances 0.000 claims description 12
- 239000003446 ligand Substances 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 3
- 238000006073 displacement reaction Methods 0.000 claims description 3
- -1 nitrogenous boron compounds Chemical class 0.000 claims description 3
- 229910052723 transition metal Inorganic materials 0.000 claims description 2
- 150000003624 transition metals Chemical class 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- JBANFLSTOJPTFW-UHFFFAOYSA-N azane;boron Chemical compound [B].N JBANFLSTOJPTFW-UHFFFAOYSA-N 0.000 description 4
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 230000001376 precipitating effect Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910017464 nitrogen compound Inorganic materials 0.000 description 2
- 150000002830 nitrogen compounds Chemical class 0.000 description 2
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- ZGSDJMADBJCNPN-UHFFFAOYSA-N [S-][NH3+] Chemical class [S-][NH3+] ZGSDJMADBJCNPN-UHFFFAOYSA-N 0.000 description 1
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical compound CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- VDQVEACBQKUUSU-UHFFFAOYSA-M disodium;sulfanide Chemical compound [Na+].[Na+].[SH-] VDQVEACBQKUUSU-UHFFFAOYSA-M 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 210000001747 pupil Anatomy 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE577371A true BE577371A (enrdf_load_stackoverflow) | 1900-01-01 |
Family
ID=190908
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE577371D BE577371A (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE577371A (enrdf_load_stackoverflow) |
-
0
- BE BE577371D patent/BE577371A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Pedersen | Crystalline salt complexes of macrocyclic polyethers | |
EP3830073A1 (fr) | Procédé de préparation monotope de composés organo-iodés intermédiaires à la synthèse du ioversol | |
EP0331556A2 (fr) | Nouveau procédé de préparation de l'acide éthylène-diamine-N-N'-bis (ortho-hydroxyphénylacétique) et de dérivés de celui-ci | |
BE577371A (enrdf_load_stackoverflow) | ||
CH616918A5 (enrdf_load_stackoverflow) | ||
Reinheimer et al. | Intermediates from ring-opening reactions. Reactions of 2-chloro-5-nitropyridine and 2-chloro-3-nitropyridine with deuteroxide ion in selected solvents | |
FR2480767A1 (fr) | Procede de preparation de colorants oxaziniques basiques | |
CA1099292A (fr) | Preparation du nitro-2 methyl-2 propanol-1 | |
EP0168296B1 (fr) | Procédé de préparation de l'amino-3 triazole-1,2,4 | |
CH405264A (fr) | Procédé de préparation des mercapto-succinates de bases azotées | |
EP1136476B1 (en) | Process for the preparation of 5,5'-bi-1H-Tetrazolediammonium salts using hydrazine hydrate and dicyan as starting materials | |
US20020058820A1 (en) | Process for the preparation of highly pure 5,5' -bi-1H-tetrazolediammonium salts | |
Rây | XI.—Mercury mercaptide nitrites and their reaction with the alkyl iodides. Part III. Chain compounds of sulphur | |
Chattaway et al. | LXII.—Hydrolysis of perthiocyanic acid | |
RU2307793C2 (ru) | Способ получения гексагидрата сульфата цинка-аммония | |
SU1657054A3 (ru) | Способ получени солей 4,4 @ -динитростильбен-2,2 @ -дисульфокислоты | |
DE1468398C (de) | Verfahren zur Herstellung von symmet Tischen N,N disubstituierten Harnstoffen | |
CH617674A5 (enrdf_load_stackoverflow) | ||
JPH04506520A (ja) | 低級アルカンスルホン酸をそのアルカリ金属塩から製造する方法 | |
US4626423A (en) | Process for the production of alkalithiocyanate | |
US1802073A (en) | 2-hydroxy-3-aminopyridine-5-arsonic acid and the process of making it | |
US1104149A (en) | Auric compounds from cantharidylethylenediamin and process of making same. | |
BE413785A (enrdf_load_stackoverflow) | ||
JPS62178560A (ja) | 2,3−ジシアノ−1,4−ジヒドロキシナフタレン誘導体の製造方法 | |
Henderson et al. | The Action of Sulfurous Acid upon the Sulfides of Iron, Zinc and Manganese. |