A series of six fully aromatic ionomers with precisely sequenced sulfonated sites along the polymer chains have been designed, prepared, and characterized as proton-exchange membranes. Two straightforward and efficient synthetic strategies based on Ullmann ether reactions and a Baeyer-Villiger rearrangement were devised to obtain bisphenol monomers with four or six phenylene units linked exclusively by ether bridges to avoid transetherification reactions. Polycondensations of these bisphenol monomers with mono- or disulfonated dihalide monomers gave high molecular weight poly(arylene ether), poly(arylene ether sulfone), and poly(arylene ether ketone) homopolymers having microblock-like structures with sulfonated moieties separated by monodisperse nonsulfonated oligo(ether) spacers. The nanoscale morphology and properties of solvent cast membranes were closely related to the nature of the oligo(ether) spacers. Small angle X-ray scattering (SAXS) measurements showed intense scattering and very narrow ionomer peaks with second-order features for the polymers with the six-ring spacers. This clearly indicated that the controlled ionic sequencing enabled self-assembly of ionic aggregates with a much higher degree of organization in relation to a corresponding aromatic ionomer with a statistical distribution of the sulfonate groups. At an identical ionic content, the ionomers containing meta ether linkages had lower glass transition temperatures than the all-para materials, leading to a higher water uptake and proton conductivity of the former ionomers. A membrane with an ion exchange capacity (IEC) of 2.05 mequiv g(-1) and containing exclusively para linkages reached the same level of proton conductivity as Nafion at 100% relative humidity (RH), and also had an excellent dimensional stability in boiling water. Under reduced RH, the conductivity of this membrane greatly exceeded that of a membrane based on a statistical copolymer analogue with a similar ionic content.