The thermochromic behavior of diacetylene-containing hydrogen-bonding
thermotropic Liquid crystalline monomers and a semirigid main chain th
ermotropic poly(ester-diacetylene) were examined. These materials were
successfully designed to undergo dramatic, first-order thermochromic
transitions at the onset of their characteristic mesogenic transitions
, as exhibited by changes in the shapes and locations of their polydia
cetylene absorption bands and the corresponding visually observed colo
r changes. Two different types of chromic response have been observed:
one case, the diacid monomer 5,7-DODBA, in which the polydiacetylene
chain responds to the liquid crystalline transitions of its host monom
eric lattice, and two cases, the 10,12-DHDP monomer and 10,12-DHDP/TC
polyester, in which the side chains covalently bonded to the polydiace
tylene chain undergo mesogenic transitions that drive the thermochromi
c transition. It was found that the thermochromic transition is not re
versible beyond the melting points of the partially polymerized monome
rs, whereas the poly(ester-diacetylene) exhibited partial reversibilit
y above the polyester melting point. In all cases, a new absorption cu
rve at higher energies represented the liquid crystalline phase above
the mesogenic melt transition.