Interrelations between main chain and side chain packing are studied in a series of comb-like poly(1,4-phenylene-2,5-n-dialkyloxy terephthalate)s (PPAOTs) with C = 6-12 alkyl carbons per side chain by X-ray diffractometry. Two different polymorphic states, called modification A and modification B, are observed depending on thermal treatment and side chain length. For PPAOTs with short side chains (C ≤ 8), modification A is commonly observed. "As synthesized" (solution crystallized) PPAOTs with longer side chains (C ≥ 10) contain mostly modification B while modification A is growing during melt cooling. A solid-solid transition from modification B to modification A is observed above ≈70 °C for the decyl member (C = 10, PPDOT) while modification A converts under ambient conditions slowly to modification B. This indicates that modification B is thermodynamically stable at low temperature while modification A is stable at higher temperature. Crystallographic analysis shows that both modifications are characterized by an orthorhombic unit cell and a long-range ordered layered structure with alternating main chain and alkyl nanodomains. This is confirmed by 2D diffration data for shear oriented PPDOT fibers. The main difference between both modifications is the packing of the side chains which are in a crystalline state for modification B but disordered for modification A. This is concluded from values for the volume per CH unit V in alkyl nanodomains calculated without further assumptions from the obtained lattice parameters. Interestingly, the crystalline packing of the side chains in modification B leads to a significant increase (≈ 20%) in the application relevant π-π spacings within the main chain domains as compared to those for modification A. It is argued that the structure formation process and thermodynamic equilibrium in comb-like polymers might be strongly influenced by a competition of the individual packing tendencies of main and side chains.

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Placing artificial folding elements into precision polymers is an important strategy to systematically study structure formation in self‐assembly, particularly in the semicrystalline state. To this purpose, a series of precision polymers bearing either a N‐protected or N‐unprotected diaminopyridine (DAP) unit after every 16th, 18th, and 20th carbon as well as a urea unit after every 20th carbon along a polyethylene‐like polymer were synthesized via acyclic diene metathesis polymerization and subsequent hydrogenation. The polymers thus contain either H‐bonds (urea/DAP), π–π‐elements (DAP), or no H‐bonds (respective Nprotected urea/DAP‐units) in their main chain, able to consequently study the crystallization behavior under influence of such supramolecular moieties. Therefore, the thermal properties and crystallization behavior were analyzed via differential scanning calorimetry (DSC) as well as wide angle X‐ray diffraction. The obtained crystalline polymer is influenced by the different supramolecular interactions existing between adjacent polymer chains and the varying defect size exerted by the incorporated functional groups. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017, 55, 3736–3748