Intramolecular cyclization reactions in haloalkyl-cobalt complexes with macrocyclic equatorial ligands

Summary: Organocobalt complexes containing axial haloalkyl groups afford metallacycles of different size by N or O alkylation of the macrocyclic equatorial ligands. The reaction mechanism involves the intra-molecular nucleophilic attack of a negatively charged atom of the equatorial ligand on the ax...

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Permalink: http://skupni.nsk.hr/Record/nsk.NSK01000734645/Details
Matična publikacija: Croatica chemica acta
82 (2009), 2 ; str. 455-461
Glavni autor: Dreos, Renata (-)
Ostali autori: Randaccio, Lucio (-), Siega, Patrizia, Vrdoljak, Višnja
Vrsta građe: Članak
Jezik: eng
Predmet:
Online pristup: Croatica Chemica Acta
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245 1 0 |a Intramolecular cyclization reactions in haloalkyl-cobalt complexes with macrocyclic equatorial ligands /  |c Renata Dreos, Lucio Randaccio, Patrizia Siega, and Višnja Vrdoljak. 
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504 |a Bibliografija: 32 jed 
520 8 |a Summary: Organocobalt complexes containing axial haloalkyl groups afford metallacycles of different size by N or O alkylation of the macrocyclic equatorial ligands. The reaction mechanism involves the intra-molecular nucleophilic attack of a negatively charged atom of the equatorial ligand on the axial XCH2 haloalkyl group with simultaneous detachment of a halide ion, X−. In imino/oxime and amino/oxime derivatives, the generation of the negatively charged nitrogen requires the abstraction of a proton and the reaction occurs only in alkaline medium. In bis(dimethylglioximato) and Schiff base complexes, a negatively charged oxygen is present in the equatorial ligand and the reaction occurs even in neutral medium. Three-, six- and seven- membered metallacycles are obtained, with the common feature that the Co–C bond is shorter and more resistant toward homolysis than in parent complexes or in closely related derivatives 
653 0 |a Makrociklički ekvatorijalni ligand  |a Kobalt  |a Ciklizacija 
700 1 |a Randaccio, Lucio 
700 1 |a Siega, Patrizia 
700 1 |a Vrdoljak, Višnja 
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