Reversible Concerted Ligand Substitution at Alternating Metal Sites in an Extended Solid

We report a synthetic material, [Co₂(bipy)₃(SO₄)₂(H₂O)₂](bipy) (CH₃OH), (1, where bipy = 4,4'-bipyridyl) that contains discrete reactive and inert structural motifs that undergo a reversible substitution reaction involving the concerted and spatially controlled introduction of bipyridine and me...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 2007-02, Vol.315 (5814), p.977-980
Hauptverfasser: Bradshaw, Darren, Warren, John E, Rosseinsky, Matthew J
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container_title Science (American Association for the Advancement of Science)
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creator Bradshaw, Darren
Warren, John E
Rosseinsky, Matthew J
description We report a synthetic material, [Co₂(bipy)₃(SO₄)₂(H₂O)₂](bipy) (CH₃OH), (1, where bipy = 4,4'-bipyridyl) that contains discrete reactive and inert structural motifs that undergo a reversible substitution reaction involving the concerted and spatially controlled introduction of bipyridine and methanol molecules at the reactive sites. This reaction defines the pore geometry of the resulting open-framework structure and controls the manner in which this structure sorbs small molecules. The molecules involved in the reaction are positioned by an array of well-defined interactions during their path to binding to the metal centers.
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source JSTOR Archive Collection A-Z Listing; American Association for the Advancement of Science
subjects Analytical chemistry
Anions
Arrays
Atoms
Binding
Chemistry
Colloidal state and disperse state
Control equipment
Coordination numbers
Crystal structure
Crystals
Exact sciences and technology
General and physical chemistry
Hydrogen
Inert
Ligands
Metals
Methyl alcohol
Molecular chains
Molecular interactions
Molecular structure
Molecules
Porosity
Porous materials
Substitution reactions
Surface physical chemistry
title Reversible Concerted Ligand Substitution at Alternating Metal Sites in an Extended Solid
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