We report here a case of apparent failure of the size exclusion chromatography/matrix-assisted laser desorption/ionization (SEC/MALDI) method to provide polymer fractions with narrow molar mass distribution, showing that intermolecular chain association is responsible for this phenomenon. Poly(bisphenol A carbonate) (PC) chains terminated with hydroxyl groups undergo self-association by hydrogen bonding, providing macromolecular aggregates with higher hydrodynamic volume. These aggregates are eluted through SEC columns at the same volume as higher molar mass chains, which remain non-associated. Thus, self-association affects negatively the SEC fractionation experiments, and even the sharpest SEC fractions contain a heterogeneous mixture of PC chains of different size. When the off-line SEC/MALDI procedure is applied, the SEC fraction is diluted in the matrix which, being a dissociating medium (carboxylic acid) for hydrogen-bonded aggregates, suppresses the chains' self-association. Therefore, the MALDI spectra of these PC fractions indicate a polydisperse character, with irregular bimodal distributions of peaks. As a consequence, in the presence of chain association, the SEC/MALDI method for the calculation of molar masses of polymers cannot be directly applied. In the present case we have found that, under opportune experimental conditions, self-association in polycarbonates can be avoided, so that nearly monodisperse SEC fractions can be obtained and the SEC/MALDI method can be applied. Our results also show that MALDI is a very sensitive technique for the detection of association of polymers in dilute solutions.

Analysis of poly(bisphenol A carbonate) by size exclusion chromatography/matrix-assisted laser desorption/ionization. 2. Self-association due to phenol end groups

Concetto Puglisi;Filippo Samperi;Sabrina Carroccio;
1999

Abstract

We report here a case of apparent failure of the size exclusion chromatography/matrix-assisted laser desorption/ionization (SEC/MALDI) method to provide polymer fractions with narrow molar mass distribution, showing that intermolecular chain association is responsible for this phenomenon. Poly(bisphenol A carbonate) (PC) chains terminated with hydroxyl groups undergo self-association by hydrogen bonding, providing macromolecular aggregates with higher hydrodynamic volume. These aggregates are eluted through SEC columns at the same volume as higher molar mass chains, which remain non-associated. Thus, self-association affects negatively the SEC fractionation experiments, and even the sharpest SEC fractions contain a heterogeneous mixture of PC chains of different size. When the off-line SEC/MALDI procedure is applied, the SEC fraction is diluted in the matrix which, being a dissociating medium (carboxylic acid) for hydrogen-bonded aggregates, suppresses the chains' self-association. Therefore, the MALDI spectra of these PC fractions indicate a polydisperse character, with irregular bimodal distributions of peaks. As a consequence, in the presence of chain association, the SEC/MALDI method for the calculation of molar masses of polymers cannot be directly applied. In the present case we have found that, under opportune experimental conditions, self-association in polycarbonates can be avoided, so that nearly monodisperse SEC fractions can be obtained and the SEC/MALDI method can be applied. Our results also show that MALDI is a very sensitive technique for the detection of association of polymers in dilute solutions.
1999
CHIMICA E TECNOLOGIA DEI POLIMERI
Istituto per i Polimeri, Compositi e Biomateriali - IPCB
Polycarbonate
SEC
MALDI
Mass Spectrometry
Association
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/196040
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