Some aspects of the orientational order distribution of flexible chains in a diblock mesophase
- Institut de Chimie et des Matériaux Paris-Est, UMR 7182 CNRS/Université Paris-Est Créteil, 2-8 rue Henri Dunant, 94320 Thiais (France)
- Laboratoire de Physique des Solides, UMR 8502 CNRS/Université Paris-Sud XI, Bâtiment 510 - Université Paris-Sud XI, 91405 Orsay (France)
The segmental motions of flexible chains in the lamellar structure of a strongly segregated poly(styrene)-poly(dimethylsiloxane) (PS-PDMS) diblock were investigated over a time scale of a few tens of microseconds. {sup 2}H NMR experiments were performed on the PDMS block, selectively perdeuterated. Transverse relaxation measurements show that the main part of the PDMS repeat units display anisotropic reorientational motions within the diblock lamellae and such a segmental ordering essentially results from interchain steric repulsions. {sup 2}H double quantum-based experiments evidenced a non-uniform local stretching of PDMS chains and enabled the underlying distribution of the orientational order parameter to be determined quantitatively. Besides, a fraction of the PDMS chain segments, about 14%, were found to display isotropic – or nearly isotropic – reorientations, which could be assigned to repeat units located within a thin sublayer (about 1–2 nm) at the lamellae midplane, but also deeper in the lamellae, close to folded parts of the chains. These experimental results were confronted to theoretical descriptions of opposing polymer brushes and, in particular, to the strong-stretching theory (SST) including the entropic contribution of free chain ends.
- OSTI ID:
- 22253823
- Journal Information:
- Journal of Chemical Physics, Vol. 139, Issue 22; Other Information: (c) 2013 AIP Publishing LLC; Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-9606
- Country of Publication:
- United States
- Language:
- English
Similar Records
A Quantitative Study of Tethered Chains in Various Solution Conditions Using Langmuir Diblock Copolymer Monolayers
Crystallization in Ordered Polydisperse Polyolefin Diblock Copolymers