Catalytic ring-¿opening copolymn. of limonene oxide with phthalic anhydride was performed applying metal t-¿Bu-¿salophen complexes (t-¿Bu-¿salophen)¿MX; M = Cr, X = Cl (1)¿, M = Al, X = Cl (2)¿, M = Co, X = OAc (3)¿, M = Mn, X = Cl (4)¿, t-¿Bu-¿salophen = N,¿N-¿bis(3,¿5-¿di-¿tert-¿butylsalicylidene)¿diimine. The chromium and aluminum catalysts performed best, and catalyst 1 was selected for further studies. Investigating the effect of different cocatalysts in the copolymn. of limonene oxide and phthalic anhydride revealed that the onium salt PPN+Cl-¿ showed the best activity while phosphines and N-¿heterocyclic-¿based amines showed a somewhat lower activity. 1H NMR and MALDI-¿ToF-¿MS spectra of the copolymers formed confirmed the alternating microstructure. Applying various mono-¿, di-¿, and trifunctional chain transfer agents (CTA)¿s such as water, (poly)¿alcs., acids, and diamines in all cases resulted in a decrease in mol. wt. while the PDI remained low, characteristic for an immortal system. Catalyst 1 proved to be robust in the presence of these CTAs not showing any drop of catalytic activity, which allows the formation of polyesters with tunable mol. wts. and narrow PDIs and varying nos. of functionalities.