The quest of organic dyes presenting improved electronic features has been extremely active during the last decades, as new structures are necessary to build novel materials such as dye-sensitized solar cells, nonlinear optics commutators, or molecular photochromic switches. Cyanine derivatives occupy a key spot in that scene, as they present intense absorption bands and tunable colors, even when a relatively short pi-conjugated path is used. This behavior has often been interpreted as a consequence of a negligible bond length alternation. Recently, Thorley et al. have designed and characterized new cationic compounds that possess the cyanine electronic features, though presenting sizable bond length alternation (Angew. Chem. Int. Ed. 2008, 47, 7095-7098). In this contribution, I investigate, with quantum mechanical tools, the size dependence of these properties in model symmetric dyes displaying Thorley's patterns. Extended chains are simulated in order to obtain insights into the chain length convergence, and the results are compared to those obtained at the same level of theory for classical cyanine architectures. This theoretical work is a step toward the rational development of more efficient pi-conjugated compounds.