Papers Published

1. Aspin, Ian P. and Barros, Ana M. and Hodge, Philip and Towns, Carl R. and Ali-Adib, Ziad, Langmuir and Langmuir-Blodgett films of derivatives of α-olefin-maleic anhydride alternating copolymers prepared from olefins containing hydrophilic groups, Polymer, vol. 36 no. 8 (1995), pp. 1707 - 1714 [0032-3861(95)99017-O] .
   (last updated on 2007/04/08)

   Abstract:
   A range of long chain α-olefins were prepared which contained amide(four examples) or ester (five examples) linkages. The olefins were copolymerized with maleic anhydride and the alternating copolymers produced were subjected to ring-opening reactions at the anhydride residues to give polymers containing acid-ester, acid-acid or acid-amide head groups. Monolayers of these polymers on water were studied and, in favourable cases, thick Langmuir-Blodgett multilayers were prepared. The latter were studied by X-ray reflectivity. The results obtained were compared with those obtained from analogous polymers prepared starting from the simple α-olefins undecene, octadecene and tricosene. The polymers prepared from the α-olefins containing amide linkages generally gave poor monolayers and in only one case could a Langmuir-Blodgett multilayer be prepared. The polymers prepared from the α-olefins containing ester linkages generally gave better monolayers, especially if the ester group was shielded from solvation either by being surrounded with lipophilic chains or by virtue of being a t-butyl ester or an ester of an aromatic acid, or because the ester was linked to a mesogenic group. Several of the latter polymers gave excellent Langmuir-Blodgett films. In general polymers with acid-acid head groups gave better films than the analogues with acid-methyl ester head groups.

   Keywords:
   Langmuir Blodgett films;Derivatives;Olefins;Copolymerization;Monolayers;Multilayers;Organic acids;