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Alternate cyclopolymer of diallylglutamic acid and sulfur dioxide
Zakariyah A. Jamiu,Shaikh A. Ali
RSC Advances Pub Date : 03/21/2016 00:00:00 , DOI:10.1039/C6RA03635J
Abstract

The monomer N,N-diallylglutamic acid hydrochloride [(CH2[double bond, length as m-dash]CH–CH2)2NH+CH(CO2H)CH2CH2CO2H·Cl] (I)/SO2, underwent cyclopolymerization to afford the alternate cationic polyelectrolyte (CPE) poly(I-alt-SO2) (II) in very good yields. Upon depletion of HCl during soaking in water, water-soluble triprotic (+) II was transformed to water-insoluble diprotic zwitterionic (±) III containing residues of glutamic acid in each repeating unit. Upon treatment with 1 and 2 equivalents of NaOH, polyzwitterions (±) III, was converted into water-soluble monoprotic poly(zwitterion-anion) (±−) IV and the fully deprotonated polydianion (=) V, respectively. Basicity strengths of the chelation centers of CO2 and nitrogen in (=) V have been determined. The polymer demonstrated its effectiveness as an antiscalant in the inhibition of CaSO4 scaling. Keeping in view the pH-dependent solubility of the polymers, a recyclable aqueous two-phase system (ATPS) comprising of (=) V and polyethylene glycol has been constructed for the potential purification of biomolecules. After its use, the ATPS can be recycled by precipitating the ionic polymer in the form of (±) III at a lower pH.

Graphical abstract: Alternate cyclopolymer of diallylglutamic acid and sulfur dioxide
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