Transition metal complexes with sulfur ligands part CXXIX. Retention and reactivity of the [FeNHNHFe] chromophore in the iron sulfur diazene complex [μ-N2H2{Fe(PPr3)(‘S4’)}2] in exchange and oxidation processes. (‘S4’2− = 1,2-bis (2-mercaptophenylthio)ethane(2−))-Reference-Cited by-同舟云学术

Transition metal complexes with sulfur ligands part CXXIX. Retention and reactivity of the [FeNHNHFe] chromophore in the iron sulfur diazene complex [μ-N2H2{Fe(PPr3)(‘S4’)}2] in exchange and oxidation processes. (‘S4’2− = 1,2-bis (2-mercaptophenylthio)ethane(2−))

Published:1998-10 Issue:1-2 Volume:280 Page:39-49
ISSN:0020-1693
Container-title:Inorganica Chimica Acta
language:en
Short-container-title:Inorganica Chimica Acta

Author:

Sellmann Dieter,Hennige Andreas,Heinemann Frank W.

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry

Reference45 articles.

1. Heterolytic Activation of Dihydrogen at Transition-Metal Sulfur Sites in Coordinatively Unsaturated [rh(L)(“buS4”)]BF4 Complexes, Involving Neutral Hydrides, Thiol Hydrides, and Thiol–Hydride Proton Scrambling (L = CO, PCy3; “buS4”2- = 1,2-Bis[(2-mercapto-3,5-di-tert-butylphenylthio]ethane2-)

2. Übergangsmetallkomplexe mit Schwefelliganden, C*. Unerwartet einfache Bildung von Diazen-Komplexen und ein neuer Typ von Diastereomerie: [µ-N2H2{Fe(PPr3)('S4')}2] und analoge Komplexe mit [FeS]-Zentren. ( 'S4'2-= 1,2-Bis(2-mercaptophenylthio)ethan(2-)) / Transition Metal Complexes with Sulfur Ligands, C*. Unexpectedly Facile Formation of Diazene Complexes and a New Type of Diastereomerism: [µ-N2H2{Fe(PPr3)('S4')}2] and Analogous Complexes with [FeS]-Centers. ('S4'2- = 1,2-Bis(2-mercaptophenylthio)ethane(2-))

3. On the heat of formation of diimide

4. Diimide—Identification and Study by Mass Spectrometry

5. The Near-ultraviolet Absorption Spectrum of Diimide Vapor

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