POLY[BIS(ETHYLGLYCOXYPROPYL)SILYLENE]S AND POLY[N-ALKYL(ETHYLGLYCOXY)SILYLENE]S AND THEIR HIGHER HOMOLOGS, 2 - AMPHIPHILICITY AND MOLECULARORDERING IN THE SOLID-STATE
La. Schwegler et al., POLY[BIS(ETHYLGLYCOXYPROPYL)SILYLENE]S AND POLY[N-ALKYL(ETHYLGLYCOXY)SILYLENE]S AND THEIR HIGHER HOMOLOGS, 2 - AMPHIPHILICITY AND MOLECULARORDERING IN THE SOLID-STATE, Macromolecular chemistry and physics, 199(9), 1998, pp. 1865-1871
A series of polyglycol substituted polysilylenes containing up to thre
e ethoxy units in one or both substituents of the silicon atoms were i
nvestigated for their bulk and solution properties. In comparison to t
he analogous nonpolar poly(di-n-alkylsilylenes), these ether functiona
lized polysilylenes show improved solubility in alcohols and a distinc
t amphiphilic character depending on the length of side chains and num
ber of oxygen atoms incorporated. Spreading experiments on water/air i
nterfaces demonstrated the formation of stable monolayers. Polysilylen
e samples with -CH2(CH2-CH2-O)(n)-CH2-CH3; n=1, 2 substituents exhibit
thermochromism which was correlated to a first order endotherm found
by calorimetric measurements. Specimen containing two ethylglycoxyprop
yl substituents per silicon atom or ethyldiglycoxypropyl side chains s
howed no temperature or solvent dependence of the UV absorption.