The reaction of copper salts with AlPO₄-5 or V^v-VAPO-5 under acidic (CuCl₂, pH adjusted to 2) but especially basic conditions (Cu(NH₃) ₄ ²⁺ , pH adjusted to 9) gives ion incorporations greater than expected by a simple ion exchange mechanism (both AlPO₄-5 and V^v-VAPO-5 could be expected to have no cation exchange capacity). Ion incorporation is proposed to occur initially at defect sites, and examination of the ESR spectrum of a dehydrated, evacuated CuCl₂-exchanged AlPO₄-5 shows that these defect sites give rise to a number of unique environments upon Cu^II incorporation. The CuCl₂-exchanged VAPO-5 retains a significant toluene accessibility to the V^v sites in the VAPO-5. However, the toluene accessibility in the Cu(NH₃) ₄ ²⁺ -exchanged VAPO-5 is significantly reduced and we propose this is due to a combination of the presence of crystalline CuO and structural collapse from reaction with base (NH₄OH). The ability of treatment with base (NH₄OH, pH 13) to restrict access of toluene to the V^v sites of the original VAPO-5 was verified in a separate experiment.