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Formaldoxim
ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
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Formaldoxim ist das Oxim des Formaldehyds. Es wird als Reagens zur fotometrischen Bestimmung von Mangan(II)-, Eisen(II)-, Nickel(II)-, Cer(IV)- und Vanadium(V)-Ionen eingesetzt.
Contents
β’ Eigenschaften
β’ Verwendung
β’ Einzelnachweise
ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
Gewinnung und Darstellung
Formaldoxim-LΓΆsung als Reagens fΓΌr fotometrische Messungen wird aus Formaldehyd und Hydroxylamin hergestellt.cite-ref-3[3]
H 2 C = O + H 2 N β β O H β β H 2 C = N O H + H 2 O . {\displaystyle \mathrm {H_{2}C{=}O+H_{2}N{-}OH\ \rightleftharpoons \ H_{2}C{=}NOH+H_{2}O.} }
Im festen Zustand liegt es trimer als 1,3,5-Trihydroxy-1,3,5-triazacyclohexan vor, dessen Hydrochlorid im Handel erhΓ€ltlich ist.
Eigenschaften
Formaldoxim bildet mit Mn3+ rot-braune und mit Fe2+ violette Komplexe.
3 H 2 C = N O H + M n 3 + β β [ ( H 2 C = N O ) 3 M n ] + 3 H + . {\displaystyle \mathrm {3H_{2}C{=}NOH+Mn^{3+}\ \rightleftharpoons \ [(H_{2}C{=}NO)_{3}Mn]+3H^{+}.} }
Verwendung
Formaldoxim-Reagens wird zur Bestimmung von Mangan(II) verwendet. Es kΓΆnnen auch Eisen(II), Nickel(II), Cer(IV) und Vanadium(V) bestimmt werden. Die durch Formaldoxim-Metall-Komplexe gefΓ€rbte LΓΆsung wird fotometrisch ausgemessen.
Einzelnachweise
cite-note-alfa-11. Datenblatt Formaldoxim (Trimerhydrochlorid) bei Alfa Aesar, abgerufen am 17. MΓ€rz 2010 (Seite nicht mehr abrufbar).
cite-note-sigma-22. Datenblatt Formaldoxime trimer hydrochloride bei Sigma-Aldrich, abgerufen am 2. April 2011 (PDF).
cite-note-33. β E. MΓΌller, O. Beyer, H. Meerwein, K. Ziegler (Hrsg.): Stickstoffverbindungen I (= Houben-Weyl Methods of Organic Chemistry. Band 10, Nr. 4). 4. Auflage. Georg Thieme Verlag, Stuttgart 1968, ISBN 978-3-13-210104-3, S. 58 (eingeschrΓ€nkte Vorschau in der Google-Buchsuche).