Zirconium complexes of bipyrrolidine derived salan ligands for the isoselective polymerisation of rac-lactide.

Herein we report the synthesis and characterisation of a series of Zr(IV) 2,2'-bipyrrolidine-salan derived complexes and their exploitation for the ring opening polymerisation of rac-lactide to afford highly isotactically enriched polymers.

Heteroleptic titanium(IV) catecholato/piperazine systems and their anti-cancer properties.

In this paper we report the synthesis and full characterisation of a range of Ti(IV)-catecholato systems complexed to piperazine or homopiperazine salan ligands. The steric/electronic environment of the catecholate moiety has been varied and the effect this has on cytotoxicity discussed. It was observed that the 7-membered homopiperazine complexes are more stable to hydrolysis than their piperazine cousins in biological media.

Monomeric Ti(IV) homopiperazine complexes and their exploitation for the ring opening polymerisation of rac-lactide.

Background: The area of biodegradable/sustainable polymers is one of increasing importance in the 21st Century due to their positive environmental characteristics. Lewis acidic metal centres are currently one of the most popular choices for the initiator for the polymerisation. Thus, in this paper we report the synthesis and characterisation of a series of monometallic homopiperazine Ti(IV) complexes where we have systematically varied the sterics of the phenol moieties.

Aluminium salalen complexes based on 1,2-diaminocyclohexane and their exploitation for the polymerisation of rac-lactide.

In this paper nine various salalen ligands have been prepared and characterised. The steric and electronic effects of both the salen and salan fragments have been varied in a systematic fashion to ascertain how this affects the selectivity for the ROP of rac-lactide. These were complexed to AlMe3 to generate pseudo trigonal bypyramidal metal centred complexes.

Crystallographic characterisation of Ti(IV) piperazine complexes and their exploitation for the ring opening polymerisation of rac-lactide.

In this paper a series of eight Ti(IV) piperazine based complexes have been prepared and fully characterised in the solid-state by X-ray crystallography and in solution via NMR spectroscopy. In the solid-state either Ti(2)(L)(O(i)Pr)(6) or Ti(2)(L)(2)(O(i)Pr)(4) were observed depending upon the nature of the starting ligand. For complexes with less sterically demanding ligands (1H(2) and 2H(2)) an equilibrium was observed: 2 Ti(2)(L)(O(i)Pr)(6) ⇔ Ti(2)(L)(2)(O(i)Pr)(4) + 2 Ti(O(i)Pr)(4).