Gr. Schulz et al., MICELLES FORMED FROM PHOTOCHEMICALLY ACTIVE AMPHIPHILES - STRUCTURAL CHARACTERIZATION BY SMALL-ANGLE NEUTRON-SCATTERING, Journal of molecular structure, 383(1-3), 1996, pp. 191-196
A novel class of photochemically active amphiphiles has been synthesiz
ed containing a ketone moiety as a biradical or radical pair precursor
on the hydrophobic tail of sodium sulfate surfactants. Alteration of
the molecular structure of each ketone-containing surfactant allows fo
r the systematic and predictable manipulation of the micellar size and
shape, both of which are important in determining the coupling betwee
n the unpaired electrons confined within the micelle and the intraradi
cal dynamics. The structure of the resulting aggregates has been analy
zed by small-angle neutron scattering (SANS). The results show that th
e amphiphiles form ellipsoidal micelles with aggregation numbers betwe
en 30 and 150 that depend on the balance between monomer dimensions an
d steric effects caused by the atomic spatial arrangement within the h
ydrophobic tail of the different surfactants.