DE673874C - Process for the preparation of antimony complex compounds - Google Patents

Process for the preparation of antimony complex compounds

Info

Publication number
DE673874C
DE673874C DET40162D DET0040162D DE673874C DE 673874 C DE673874 C DE 673874C DE T40162 D DET40162 D DE T40162D DE T0040162 D DET0040162 D DE T0040162D DE 673874 C DE673874 C DE 673874C
Authority
DE
Germany
Prior art keywords
antimony
salts
complex compounds
preparation
solution
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
DET40162D
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German (de)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
FRITZ KUHBIER DR
Original Assignee
FRITZ KUHBIER DR
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by FRITZ KUHBIER DR filed Critical FRITZ KUHBIER DR
Priority to DET40162D priority Critical patent/DE673874C/en
Priority to DE1930627838D priority patent/DE627838C/en
Priority claimed from DET40140D external-priority patent/DE646703C/en
Application granted granted Critical
Publication of DE673874C publication Critical patent/DE673874C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H23/00Compounds containing boron, silicon, or a metal, e.g. chelates, vitamin B12
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • C07C51/412Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic System
    • C07F5/06Aluminium compounds
    • C07F5/069Aluminium compounds without C-aluminium linkages
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/90Antimony compounds
    • C07F9/902Compounds without antimony-carbon linkages

Description

Verfahren zur Herstellun, von Antimonkomplexverbindungen Gegenstand des Patents 627 838 ist ein Verfahren zur Herstellung von Komplexverbindungen des Wismuts, Antimons, Aluminiums und Chroms. Dieses Verfahren besteht darin, daß man die Salze oder Oxyde des Wismuts, Antimons, Aluminiums -oder Chroms mit deiner aliphatischen Polyoxyverbindung in wässerig alkalischer Lösung behandelt, die dabei @entstehenden Komplexverbindungen durch Zusatz von Barium-, Calcium- oder Strontiumsalzen in Form der entsprechenden Erdalkalisalze abscheidet und die letzteren, gegebenenfalls durch doppelte Umsetzung, in die wasserlösliche Alkalisalze überführt.Process for the preparation of antimony complex compounds of patent 627 838 is a process for the preparation of complex compounds of the Bismuth, antimony, aluminum and chromium. This procedure consists in that one the salts or oxides of bismuth, antimony, aluminum or chromium with your aliphatic Treated polyoxy compound in an aqueous alkaline solution, the resulting @ Complex compounds by adding barium, calcium or strontium salts in the form the corresponding alkaline earth metal salts are deposited and the latter, optionally through double conversion into which water-soluble alkali salts are converted.

Bei der weiteren Bearbeitung wurde nun gefunden, daß man unmittelbar wasserlösliche Komplexsalze des Antimons gewinnen kann, wenn man das Oxyd, Hydroxyd oder Salze des 3wertigen Antimons mit Hexiten in wässerigen Lösungen von Alkali-oder Erdalkalihydroxyden umsetzt und die so erhaltenen Metallkomplexsalze in an sich b.ek.annter Weise durch Zusatz von wasserlöslichen organischen Lösungsmitteln oder durch Einengen der Lösung abscheidet.In further processing it has now been found that one immediately Water-soluble complex salts of antimony can be obtained by using the oxide, hydroxide or salts of trivalent antimony with hexites in aqueous solutions of alkali or Alkaline earth hydroxides and the resulting metal complex salts in itself b.ek. as known by adding water-soluble organic solvents or separates by concentrating the solution.

So löst z. B. eine Auflösung von Mannit in Natronlauge oder Barytwasser erhebliche Mengen von Antim:ontrioxyd auf. Aus der Lösung kann man die Komplexverbindung, die z. B. im Falle der Verwendung von Barytwasser die Zusammensetzung (C12 H26 01,3 Sb)2 Ba hesitzt, durch Zusatz von Alkoholoder durch Eindunsten gewinnen. An Stelle des Oxyds lassen sich auch Salze, im besonderen die Halogenide ioder Oxyhalogenide, z. B. Antimonoxychloridoder Antim-onchlorid, für die Gewinnung der Metallkomplexsalze verwenden. Beispiel i Man löst 1,8 Teile Sorbit in 5 Teilen einer 4%igen Natronlauge und trägt in der Hitze 0,7 Teile Antimonoxyd ein, wobei Lösung eintritt. Den entstandenen Natrium-Antimon-Sorbit gewinnt man am besten in der Weise, daß man die Lösung mit Alkohol fällt, wobei er als farbloser, in Wasser spielend leicht löslicher Niederschlag erhalten wird. Die neue Komplexverbindung ist nach der Formel C12 H26 013 Sb Na zusammengesetzt. Beispiel 2 Man löst 3,6 Teile Mannit in 12 Teilen warmen Barytwass@ers, @en;haltendetwa 7 bis 8% Bariumhydroxyd, und fügt zu der im Sieden gehaltenen Flüssigkeit 44 Teile Antimontrioxyd, welches sich fast restlos in der Flüssigkeit auflöst. Versetzt man die klare, wieder abgekühlte Lösung mit Alkohol, so fällt der Barium-Antimon-Mannit als fein kristalliner Niederschlag aus. Man kann die Verbindung auch durch Einengen gewinnen. Die Komplexverbindung, die in wenig Wasser klar löslich ist, enthält nach der Analyse g Moleküle Mannit, z Grammatome Antimon und i Grammatom Barium. Beispiel 3 In einer Lithiumhydroxydlösung, welche etwa q. bis 5 Mol Lithiumhydroxyd :enthält, werden z Mol Mannit aufgelöst. Zu der Lösung wird dann i Mol Antimontrichlörid hinzugefügt. Durch Erwärmen wird die Auflösung des gefällten Antimonhydroxyds beschleunigt. Dann wird gegebenenfalls vom Ungelösten abfiltriert und der Lithium-Antimon-Mannit durch Zusatz von Methyl- -oder Äthylalkohol ausgefällt.So z. B. a dissolution of mannitol in caustic soda or barite water on considerable amounts of antimony trioxide. From the solution you can the complex compound, which z. B. in the case of using barite water, the composition (C12 H26 01.3 Sb) 2 Ba hesitz, gain by adding alcohol or by evaporation. Instead of the oxide, it is also possible to use salts, in particular the halides or oxyhalides, e.g. B. antimony oxychloride or antimony chloride, use for the extraction of the metal complex salts. EXAMPLE i 1.8 parts of sorbitol are dissolved in 5 parts of a 4% strength sodium hydroxide solution and 0.7 part of antimony oxide is introduced in the heat, during which time solution occurs. The resulting sodium-antimony-sorbitol is best obtained by precipitating the solution with alcohol, whereby it is obtained as a colorless precipitate which is easily soluble in water. The new complex compound is composed according to the formula C12 H26 013 Sb Na. EXAMPLE 2 3.6 parts of mannitol are dissolved in 12 parts of warm barium water, containing approximately 7 to 8% barium hydroxide, and 44 parts of antimony trioxide are added to the boiling liquid, which dissolves almost completely in the liquid. If the clear, re-cooled solution is mixed with alcohol, the barium-antimony-mannitol precipitates out as a finely crystalline precipitate. The connection can also be made by narrowing it down. The complex compound, which is clearly soluble in a little water, contains, according to analysis, g molecules of mannitol, z gram atoms of antimony and 1 gram atom of barium. Example 3 In a lithium hydroxide solution, which is about q. contains up to 5 moles of lithium hydroxide: z moles of mannitol are dissolved. One mole of antimony trichloride is then added to the solution. The dissolution of the precipitated antimony hydroxide is accelerated by heating. If necessary, the undissolved material is then filtered off and the lithium antimony mannitol is precipitated by adding methyl or ethyl alcohol.

Claims (1)

PATENTANSPRUCH: Weitere Ausbildung des Verfahrens nach Patent 627 838 zur Herstellung von Amtimonkomplexverbindungen, dadurch gekennzeichnet, daß man das Oxyd, Hydroxyd ioder Salze des 3wertigen Antimons mit Hexiten in wässerigen Lösungen von Alkali- oder Erdalkalihydroxyden umsetzt und die so erhaltenen Metallkomplexsalze in an sich bekannter Weise durch Zusatz von wasserlöslichen organischen Lösungsmitteln oder durch Einengen der Lösung abscheidet.PATENT CLAIM: Further development of the process according to Patent 627 838 for the production of amimon complex compounds, characterized in that the oxide, hydroxide or salts of trivalent antimony are reacted with hexites in aqueous solutions of alkali or alkaline earth metal hydroxides and the metal complex salts thus obtained are reacted in a manner known per se deposited by adding water-soluble organic solvents or by concentrating the solution.
DET40162D 1930-12-16 1930-12-16 Process for the preparation of antimony complex compounds Expired DE673874C (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
DET40162D DE673874C (en) 1930-12-16 1930-12-16 Process for the preparation of antimony complex compounds
DE1930627838D DE627838C (en) 1930-12-16 1930-12-16 Process for the production of complex compounds of bismuth, antimony, aluminum and chromium

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DET40162D DE673874C (en) 1930-12-16 1930-12-16 Process for the preparation of antimony complex compounds
DET40140D DE646703C (en) 1932-01-30 1932-01-30 Process for the production of metal complex compounds

Publications (1)

Publication Number Publication Date
DE673874C true DE673874C (en) 1939-03-30

Family

ID=33030701

Family Applications (2)

Application Number Title Priority Date Filing Date
DE1930627838D Expired DE627838C (en) 1930-12-16 1930-12-16 Process for the production of complex compounds of bismuth, antimony, aluminum and chromium
DET40162D Expired DE673874C (en) 1930-12-16 1930-12-16 Process for the preparation of antimony complex compounds

Family Applications Before (1)

Application Number Title Priority Date Filing Date
DE1930627838D Expired DE627838C (en) 1930-12-16 1930-12-16 Process for the production of complex compounds of bismuth, antimony, aluminum and chromium

Country Status (1)

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DE (2) DE627838C (en)

Also Published As

Publication number Publication date
DE627838C (en) 1936-03-24

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