Copper(0)-mediated radical polymerisation in a self-generating biphasic system

Herein, we demonstrate the synthesis of well-defined poly(n-alkyl acrylate)s via copper(0)-mediated radical polymerisation in a self-generating biphasic system. During the polymerisation of n-butyl acrylate in DMSO, the polymer phase separates to yield a polymer-rich layer with very low copper content (ICP-MS analysis: 0.016 wt%). The poly(n-butyl acrylate) has been characterized by a range of techniques, including GPC, NMR and MALDI-TOF, to confirm both the controlled character of the polymerisation and the end group fidelity. Moreover, we have successfully chain extended poly(n-butyl acrylate) in this biphasic system several times with n-butyl acrylate to high conversion without intermediate purification steps. A range of other alkyl acrylates have been investigated and the control over the polymerisation is lost as the hydrophobicity of the polymer increases due to the increase in alkyl chain length indicating that it is important for the monomer to be soluble in the polar solvent

Crystal Structure of Orthorhombic {bis-[(pyridin-2-yl)methyl](3,5,5,5-tetrachloropentyl)amine-κ\u3csup\u3e3\u3c/sup\u3e\u3cem\u3eN,N\u27,N\u27\u27\u3c/em\u3e}chloridocopper(II) Perchlorate

In the title compound, [CuCl(C17H19Cl4N3)]ClO4, the CuII ion adopts a distorted square-planar geometry defined by one chloride ligand and the three nitro­gen atoms from the bis­[(pyridin-2-yl)meth­yl](3,5,5,5-tetra­chloro­pent­yl)amine ligand. The perchlorate counter-ion is disordered over three sets of sites with refined occupancies 0.0634 (17), 0.221 (16) and 0.145 (7). In addition, the hetero-scorpionate arm of the bis­[(pyridin-2-yl)meth­yl](3,5,5,5-tetra­chloro­pent­yl)amine ligand is disordered over two sets of sites with refined occupancies 0.839 (2) and 0.161 (2). In the crystal, weak Cu⋯Cl inter­actions between symmetry-related mol­ecules create a dimerization with a chloride occupying the apical position of the square-pyramidal geometry typical of many copper(II) chloride hetero-scorpionate complexes

Towards the development of highly active copper catalysts for atom transfer radical addition (ATRA) and polymerization (ATRP)‡

Fundamentals of copper catalyzed atom transfer radical addition (ATRA) and mechanistically similar polymerization (ATRP) were discussed. Special emphasis was placed on structural characterization and electrochemical properties of copper complexes. Recent advances in the development of highly active copper complexes for both processes were also reviewed. It was found that electron-donating groups (methoxy and methyl in the 4 and 3,5 positions, respectively) of the pyridine rings in tris(2-pyridylmethyl)amine (TPMA) ligand, significantly increase the catalytic activity in copper mediated ATRA/ATRP.</jats:p