In this work we have reported the pKa values for straight chain (without branches) oligomers of Acrylic acid using CBS-QB3 gas phase energies with solvation free energies from CPCM/HF 6-31G(d) and SMD/B3LYP (2df,p). We have found that the negative log of the first acid dissociation constant decreases with the chain length. Within a chain, the microscopic pKa for the COOH groups present at the end of the chain is maximum and minimum for centrally located COOH groups.
Cite
@article{arxiv.2007.13070,
title = {Trends in pKa Values for polyprotic carboxylic acids},
author = {Shivam Parashar and Prateek K. Jha},
journal= {arXiv preprint arXiv:2007.13070},
year = {2020}
}