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Cobalt supramolecular structure

Some related examples with BR2 monocapped ligands are also known [181] and one of these molecules, 129, assembles to an interesting supramolecular structure, in which the cobalt(III) ions in a methylcobaloxime unit are coordinated to the pyridine residues of the bridging B(py)(OMe) group (Fig. 34). The dinuclear complex forms a large rectangular cage that is limited by the two pyridine residues and the cobaloxime moieties. The two pyridine... [Pg.36]

Fig. 34. Compound 129 assembles to a supramolecular structure through coordinative bonds between the cobalt(III) ions and the pyridine residues of the bridging B(py)(OMe) group... Fig. 34. Compound 129 assembles to a supramolecular structure through coordinative bonds between the cobalt(III) ions and the pyridine residues of the bridging B(py)(OMe) group...
The lead(II) derivative of a cobalt cluster carboxylate, [Pb (CO)9Co3-(/43-CC00) 2], has an unusual supramolecular structure. It is made up of chains,... [Pg.261]

Fig. 7.15 Proposed structure of the supramolecular structure formed by complexation of meso-tetraMs((4-pyridyl)porphyrinato)cobalt (CoPCpy) ) with [Ru(NH3)3(H20)3] on a graphite electrode... Fig. 7.15 Proposed structure of the supramolecular structure formed by complexation of meso-tetraMs((4-pyridyl)porphyrinato)cobalt (CoPCpy) ) with [Ru(NH3)3(H20)3] on a graphite electrode...
The complexation of coordination compounds may make it possible to control their photochemical behaviour via the structure of the supramolecular species formed. For instance, the binding of cobalt(m) hexacyanide by macrocyclic polyammonium receptors markedly affects their photoaquation quantum yield in a structure-dependent manner [8.73-8.77]. It thus appears possible to orient the photosubstitution reactions of transition-metal complexes by using appropriate receptor molecules. Such effects may be general, applying to complex cations as well as to complex anions [2.114]. [Pg.100]

A second important focus of our work is the development of suitable analytical methods for the solid state and in solution. The physical characterization of metallo-supramolecular systems has mainly relied on crystal structure determination. Studies have also been performed on surface layers 40-42). The classical analytical methods (like FAB mass spectrometry) or most polymer methods (like light scattering, vapor pressure osmometry or membrane osmometry) can not be used. In solution, ESI mass spectrometry (43-45) and NMR (27,46) have been succesfully applied. We have explored whether MALDI-TOF mass spectrometry in the solid state (Schubert, U. S. Lehn, J.-M. Weidl, C. H. Spickermann, J. Goix, L. Rader, J. Mullen, K., unpublished data.) and sedimentation equilibrium analysis in the analytical ultracentrifuge for solutions may be employed. Grid-like cobalt coordination arrays ([2 X 2] Co(n)-Grid) were used as model systems in the analytical ultracentrifuge (47). [Pg.250]

Amouri H, Desmarets C, Bettoschi A, Rager MN, Boubekeur K, Rabu P, Drillon M (2007) Supramolecular cobalt cages and coordination polymers templated by anion guests self-assembly, structures, and magnetic properties. Chem Eur J 13 5401-5407... [Pg.418]


See other pages where Cobalt supramolecular structure is mentioned: [Pg.60]    [Pg.27]    [Pg.1147]    [Pg.350]    [Pg.376]    [Pg.91]    [Pg.143]    [Pg.15]    [Pg.425]    [Pg.1080]    [Pg.35]    [Pg.425]    [Pg.257]    [Pg.343]    [Pg.344]    [Pg.181]    [Pg.525]    [Pg.63]    [Pg.68]   
See also in sourсe #XX -- [ Pg.22 ]




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