In the present study, we have synthesized a polymerizable amphiphilic dendr
imer by attaching 10,12-pentacosadiynoic acid (PDA) to a third generation p
oly(amidoamine) (PAMAM) dendrimer core (PDA-PAMAM). This dendrimer was char
acterized by H-1 NMR and MALDI-TOF mass spectroscopy. The amphiphilic prope
rty of this dendrimer has been studied. Surface pressure and surface dipole
moment-area isotherm measurements have shown that PDA-PAMAM forms a stable
monolayer at the air-water interface with a limiting molecular area of 460
Angstrom(2) per molecule. The compressed monolayer can be readily polymeri
zed upon UV irradiation, as like other PDA derivatives. The topography of t
he monolayer was observed by Brewster angle microscopy (BAM) as well as by
the environmental scanning electron microscopy (ESEM). We found a good corr
elation between the size and shape of monolayer domains observed with the B
AM and ESEM techniques. To our knowledge, this is the first time wet mode E
SEM has been used to characterize L-B film. The wet mode ensures that L-B f
ilms remain intact without being damaged by the high vacuum system of tradi
tional SEM. As a preliminary study, we have found that this new dendrimer f
orms colloidal particles in chloroform solution and can be readily polymeri
zed by UV irradiation. (C) 2000 Elsevier Science B.V. All rights reserved.