Isomeric Distribution and Catalyzed Isomerization of Cobalt(III) Complexes with Pentadentate Macrocyclic Ligands. Importance of Hydrogen Bonding

• Published in: Inorganic chemistry Vol. 45; no. 21; pp. 8551 - 8562
• Main Authors: Aullón, Gabriel, Bernhardt, Paul V, Bozoglián, Fernando, Font-Bardía, Mercè, Macpherson, Brendan P, Martínez, Manuel, Rodríguez, Carlos, Solans, Xavier
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 16-10-2006
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/ic060720s

We have investigated the isomeric distribution and rearrangement of complexes of the type [CoXL n ]2+,3+ (where X = Cl-, OH-, H2O, and L n represents a pentadentate 13-, 14-, and 15-membered tetraaza or diaza−dithia (N4 or N2S2) macrocycle bearing a pendant primary amine). The preparative procedures for chloro complexes produced almost exclusively kinetically preferred cis isomers (where the pendant primary amine is cis to the chloro ligand) that can be separated by careful cation-exchange chromatography. For L13 and L14 the so-called cis-V isomer is isolated as the kinetic product, and for L15 the cis-VI form (an N-based diastereomer) is the preferred, while for the L14 S complex both cis-V and trans-I forms are obtained. All these complexes rearrange to form stable trans isomers in which the pendent primary amine is trans to the monodentate aqua or hydroxo ligand, depending on pH and the workup procedure. In total 11 different complexes have been studied. From these, two different trans isomers of [CoClL14 S]2+ have been characterized crystallographically for the first time in addition to a new structure of cis-V-[CoClL14 S]2+; all were isolated as their chloride perchlorate salts. Two additional isomers have been identified and characterized by NMR as reaction intermediates. The remaining seven forms correspond to the complexes already known, produced in preparative procedures. The kinetic, thermal, and baric activation parameters for all the isomerization reactions have been determined and involve large activation enthalpies and positive volumes of activation. Activation entropies indicate a very important degree of hydrogen bonding in the reactivity of the complexes, confirmed by density functional theory studies on the stability of the different isomeric forms. The isomerization processes are not simple and even some unstable intermediates have been detected and characterized as part of the above-mentioned 11 forms of the complexes. A common reaction mechanism for the isomerization reactions has been proposed for all the complexes derived from the observed kinetic and solution behavior.