A series of end-functionalised polyethylene materials (PE-X) has been prepared via the catalysed chain growth (CCG) reaction of diethyl zinc with ethylene, catalysed by a bis(imino)pyridine iron catalyst activated by MAO. This CCG catalyst system enables the in situ formation of long alkyl chain zinc species Zn(PE)2, which are subsequently quenched to form PE-X. Quenching with oxygen results in PE-OH, but the functionalisation appears to be limited to approximately 80% due to the formation of mixed [ZnR(OR)]n clusters. Functionalisation with sulfur leads to polysulfides, PE-Sk-PE, whereby k is affected by temperature. Functionalisation with iodine leads to PE-I with high conversion, but the degree of functionalisation appears to be chain length dependant. PE-I has been blended with LDPE, either through solution mixing or via melt blending to give PE-I/LDPE blends with different chain lengths. Characterisation of the PE-I/LDPE blends has been carried by IR spectroscopy and thermal analysis (DSC). Surface analysis by FIB-SEM and EDX analysis up to 6 μm into the surface has shown a uniform distribution of PE-I within the LDPE matrix. The propensity of alkyl iodides to undergo photolytic cleavage makes these PE-I/LDPE materials interesting candidates for degradable PE.