Langmuir-Blodgett mono- and multilayers of (di)alkoxy-substituted poly(p-phenylenevinylene) precursor polymers. 2. Stability, transfer, and multilayer structure of (di)alkoxy-substituted precursor PPVs

Citation
Jc. Hagting et al., Langmuir-Blodgett mono- and multilayers of (di)alkoxy-substituted poly(p-phenylenevinylene) precursor polymers. 2. Stability, transfer, and multilayer structure of (di)alkoxy-substituted precursor PPVs, MACROMOLEC, 32(12), 1999, pp. 3939-3945
Citations number
31
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
MACROMOLECULES
ISSN journal
00249297 → ACNP
Volume
32
Issue
12
Year of publication
1999
Pages
3939 - 3945
Database
ISI
SICI code
0024-9297(19990615)32:12<3939:LMAMO(>2.0.ZU;2-K
Abstract
The Langmuir monolayer stability and transfer properties of (di)alkoxy-subs tituted precursor PPVs were studied. All polymers formed stable monolayers, but the packing of the monomeric units in the monolayer depended strongly on the substituents. The less closely packed monolayers can be transferred with the Langmuir-Blodgett technique, while the closely packed monolayers, with strong pi-pi interaction between the aromatic rings, can only be trans ferred with the Langmuir-Schaefer technique due to the stiffness of the mon olayers. Transmission and grazing incidence reflection FT-IR spectroscopy i n combination with IR spectra computer simulations revealed that in many in stances the orientation of the precursor at the water interface is largely preserved after transfer of the monolayer. The roughness and the thickness of the multilayers were determined by small-angle X-ray reflection.