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Well-characterized templates of polymer-forming ligands and their ruthenium tris(α,α′-diimine) initiators were utilized to divergently ring open an ε-caprolactone monomer. The same polymers were also obtained through the synthesis of quinoline and bipyridine diimine ligands incorporating poly(ε-caprolactone) (PCL) chains. These polymers contain vacant molecular recognition sites, enabling subsequent chelation of these macroligands to metal precursors. Both methods provided telechelic (ε-caprolactone) ruthenium(II)-centered polyesters of various hierarchy. Solution properties and thermal behaviour of such polyesters are described.
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Farah et al. (2004) studied this question.
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