We report on the impact on the equatorial and meridional orientation in hairy-rod poly͓9,9-bis͑2-ethylhexyl͒-fluorene-2,7-diyl͔ thin films when blended with tris-cyclometalated oligo-fluorenylpyridine iridium͑III͒ complex. The presence of this transition-metal complex does not alter the underlying helical motif of the polymer chain or the hexagonal unit-cell intermolecular packing. However, systematic changes in the resulting texture patterning of the crystallites are observed. Crystallites with two preferred a-b orientations, so called type I and II and differing by 30 degrees, are superimposed on an isotropic background that is designated as type III. The extent of meridional alignment for all three is found to be similar. DOI: 10.1103/PhysRevB.74.214203 PACS number͑s͒: 61.10.Ϫi, 82.35.Lr, 81.07.Bc, 81.16.Dn Manipulating and controlling the molecular-level structure of functionalized polymers in bulk and at surfaces is central to the science and applications of these materials. Hairy-rod polymers 1 are one important example and, among those with -conjugated backbones 2 ͓e.g., poly͑p-phenylenes͒, 3 polyfluorenes ͑PFs͒, 4 and ladder derivatives 5 ͔, the nature of the main chain conformation and interchain packing are crucial factors in ultimately determining optical and transport properties. The structural characteristics at larger length scales are equally as important, and this has been the main emphasis in a number of recent studies. A classic example is the poly͑3-alkylthiophene͒ family 6 in which the extent of structural isomorphism or regioregularity strongly affects the internal crystallite structure 7 and the subsequent structural evolution when intercalated or doped. 8 Among PFs, important blue emitting polymers, even small differences in the molecular structure can influence the charge carrier mobility 9 and fluorescence. 10 Poly͓9,9-bis͑2-ethylhexyl͒-9H-fluorene-2,7-diyl͔ ͑or PF2/6͒ ͑Ref. 11͒ is a well-known helical PF polymer functionalized with branched alkyl side chains. PF2/6's optical properties 12 are relatively insensitive to either changes in the molecular weight ͑MW͒ or processing history, and so it is an excellent model system for studies of intermolecular self-organization. 13 However, this intermolecular assembly is affected by changes in the MW ͑or number averaged MW, M n ͒. In PF2/6, there is a threshold MW, M n * , at which there is a crossover in the phase behavior. 14 Low MW samples exhibit only a single nematic liquid crystal phase ͑n-LC and M n Ͻ M n * ͒ while high MW samples ͑M n Ͼ M n * ͒ include a distinctive thermotropic transition between this n-LC phase and a hexagonal crystalline phase. This threshold MW also marks sharp changes in both meridional alignment 15 and surface morphology. 16 In aligned films on rubbed polyimide ͑PI͒, the rigid PF2/6 lies on the substrate with the helical axes pointing along the rubbing direction ͑denoted z here͒. Consequently, meridional alignment leads to a large absorption and dispersion of the refractive index in the ͑xy0͒ plane along the z...