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Sigma-Aldrich

Cobalt(II) oxo pivalate

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Synonyme(s) :

Basic cobalt(II) pivalate, Cobalt, hexakis[μ-(2,2-dimethylpropanoato-κO:κO′)]hexakis[μ3-(2,2-dimethylpropanoato-κO:κO:κO′)]di-μ4-oxoocta-, Tetrameric Co cluster

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About This Item

Formule empirique (notation de Hill):
C60H108Co8O26
Numéro CAS:
301663-94-5
Poids moléculaire :
1716.95
Numéro MDL:
MFCD22200509
Code UNSPSC :
26111700
ID de substance PubChem :
329765968
Nomenclature NACRES :
NA.23

Forme

powder

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Chaîne SMILES 

CC(C)(C)C(=O)O[Co-]1O[Co-](O\C(=[O+]/[Co-](OC(=O)C(C)(C)C)O\C(=[O+]/[Co-](OC(=O)C(C)(C)C)OC(=O)C(C)(C)C)C(C)(C)C)C(C)(C)C)[O+]=C(O[Co-]2O[Co-](O\C(=[O+]\1)C(C)(C)C)\[O+]=C(\O[Co-](OC(=O)C(C)(C)C)\[O+]=C(\O[Co]OC(=[O+]2)C(C)(C)C)C(C)(C)C)C(C)(C)C)C(C)(C)C

InChI

1S/12C5H10O2.8Co.2O/c12*1-5(2,3)4(6)7;;;;;;;;;;/h12*1-3H3,(H,6,7);;;;;;;;;;/q;;;;;;;;;;;;4*+1;4*+2;;/p-12

Clé InChI

PBKALLJUIAKYSI-UHFFFAOYSA-B

Description générale

Cobalt(II) oxo pivalate is a dinuclear complex that is typically formed by the direct reaction of cobalt carbonate with pivalic acid, followed by crystallization from MeCN. Its structure has two Co(II) sites bridged by two 2,11-carboxylates (Harris notation) and an oxygen atom.
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Application

Synthesis of trinuclear complex [Co3(Piv)2L12L22] by reacting cobalt(II)pivalate with spin labeled Schiff base has been reported in a study.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Redox-Induced Change in the Ligand Coordination Mode.
Ovcharenko V, et al.
Inorganic Chemistry, 53(19), 10033-10035 (2014)
Synthetic and structural studies of cobalt-pivalate complexes
Aromi G, et al.
Chemistry?A European Journal , 9(20), 5142-5161 (2003)
Steffen Hausdorf et al.
Dalton transactions (Cambridge, England : 2003), 7(7), 1107-1113 (2009-03-27)
An ethynylene diisophthalic acid linker molecule was synthesized and used to form a zinc carboxylate-based metal organic framework (MOF) with very large pores and unit cell volume resulting from the unusual combination of structurally different inorganic units forming the secondary
Steffen Hausdorf et al.
The journal of physical chemistry. A, 112(33), 7567-7576 (2008-07-26)
The contributions of terephthalic acid and Zn(2+)-coordinated water in N,N-diethylformamide (DEF) to the overall proton activity in the synthesis of MOF-5 (Zn4O(BDC)3, BDC = 1,4-benzenedicarboxylate) were quantitatively determined by combined electrochemical and UV-vis spectroscopic measurements. Structural transformations of zinc carboxylate-based
Steffen Hausdorf et al.
Journal of the American Chemical Society, 132(32), 10978-10981 (2010-08-12)
A simple two-component procedure was developed to synthesize not only classical zinc-based IRMOFs represented by MOF-5 but also the cobalt and beryllium homologues of this most prominent MOF. The procedure is the first manifestation of mirroring the IRMOF series with

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