Serveur d'exploration sur le cobalt au Maghreb

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Electron‐Sponge Behavior, Reactivity and Electronic Structures of Cobalt‐Centered Cubic Co9Te6(CO)8 Clusters (Eur. J. Inorg. Chem. 12/2008)

Identifieur interne : 000768 ( Main/Exploration ); précédent : 000767; suivant : 000769

Electron‐Sponge Behavior, Reactivity and Electronic Structures of Cobalt‐Centered Cubic Co9Te6(CO)8 Clusters (Eur. J. Inorg. Chem. 12/2008)

Auteurs : Mustapha Bencharif [Algérie] ; Olivier Cador [France] ; Hélène Cattey [France] ; Alexander Ebner [Allemagne] ; Jean-François Halet [France] ; Samia Kahlal [France] ; Walter Meier [Allemagne] ; Yves Mugnier [France] ; Jean-Yves Saillard [France] ; Patrick Schwarz [Allemagne] ; Fatima Zohra Trodi [Algérie, France] ; Joachim Wachter [Allemagne] ; Manfred Zabel [Allemagne]

Source :

RBID : ISTEX:856B23C0365D0A1A346E29FFB55A1D1CB7B9C7EE

Descripteurs français

English descriptors

Abstract

The cover picture shows an organometallic electron sponge and an elephant‐ear sponge in the background (photo by F. and J. Burek, National Marine Sanctuaries). The electronic flexibility of the cobalt‐centered cubic [Co9Te6(CO)8]n cluster ([3]n) in the central circle is expressed by differently charged states (n = 1+ to 5–). Starting from the upper left corner of our graphic in a clockwise direction, neutral [Co9Te6(CO)4(PPh3)4], structurally diverse networks of [Ph3PNPPh3][3] and [Ph3PNPPh3]2[3] salts and the core of the [Co9Te3{ν5‐Cp′2Nb(CO)Te}3(CO)8] cluster as a pseudo‐protonated representative of the [3]3– anion are shown. Details of the structural, electrochemical and theoretical properties of these compounds are described in the article by J. Wachter et al. on page 1959 ff.

Url:
DOI: 10.1002/ejic.200890029


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<div type="abstract">The cover picture shows an organometallic electron sponge and an elephant‐ear sponge in the background (photo by F. and J. Burek, National Marine Sanctuaries). The electronic flexibility of the cobalt‐centered cubic [Co9Te6(CO)8]n cluster ([3]n) in the central circle is expressed by differently charged states (n = 1+ to 5–). Starting from the upper left corner of our graphic in a clockwise direction, neutral [Co9Te6(CO)4(PPh3)4], structurally diverse networks of [Ph3PNPPh3][3] and [Ph3PNPPh3]2[3] salts and the core of the [Co9Te3{ν5‐Cp′2Nb(CO)Te}3(CO)8] cluster as a pseudo‐protonated representative of the [3]3– anion are shown. Details of the structural, electrochemical and theoretical properties of these compounds are described in the article by J. Wachter et al. on page 1959 ff.</div>
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