Английская Википедия:Cupferron

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Версия от 21:20, 22 февраля 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{chembox | Watchedfields = changed | verifiedrevid = 420653113 | Name = Cupferron | ImageFile = cupferron.png | ImageName = Cupferron | OtherNames = cupferron<br /> ammonium ''N''-nitrosophenylhydroxylamine |Section1={{Chembox Identifiers | SMILES = O=NN([O-])c1ccccc1.[NH4+] | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 2006262 | PubChem = 2724103 | EC_nu...»)
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Шаблон:Chembox

Cupferron is jargon for the ammonium salt of the conjugate base derived from N-nitroso-N-phenylhydroxylamine. It once was a common reagent for the complexation of metal ions, being of interest in the area of qualitative inorganic analysis. Its formula is NH4[C6H5N(O)NO]. The anion binds to metal cations through the two oxygen atoms, forming five-membered chelate rings.

Synthesis and complexes

Файл:Fe(CU)3.svg
Structure of ferric cupferron complex.

Cupferron is prepared from phenylhydroxylamine and an NO+ source:[1]

C6H5NHOH + C4H9ONO + NH3 → NH4[C6H5N(O)NO] + C4H9OH

Being a bidentate mono-anionic ligand, CU forms complexes analogous to those produced with acetylacetonate. Illustrative complexes include Cu(CU)2, Fe(CU)3, and Zr(CU)4.[2][3][4]

References

Шаблон:Ammonium salts


Шаблон:Aromatic-stub