Rodríguez Riego, RafaelQuiñoá Cabana, EmilioRiguera Vega, RicardoFreire Iribarne, Félix Manuel2019-06-172020-02-202019-02-20Rodríguez, R., Quiñoá, E., Riguera, R., Freire, F., Small 2019, 15, 1805413. https://doi.org/10.1002/smll.2018054131613-6810http://hdl.handle.net/10347/18882This is the peer reviewed version of the following article: Rodríguez, R., Quiñoá, E., Riguera, R., Freire, F., Small 2019, 15, 1805413. https://doi.org/10.1002/smll.201805413, which has been published in final form at https://doi.org/10.1002/smll.201805413. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived VersionsInterconversion between extended and bent structures at the pendant groups of a chiral polyene framework [poly(phenylacetylene) with (R)‐(2‐methoxy‐2‐phenylacetyl)glycine residues linked to 4‐vinylanilines] allows the reversible colorimetric transformation from stretched to compressed helical cis‐transoid polyenic structures through manipulation of the flexible spacer. This transformation generates either organogels (stretched helical form) or nanoparticles (compressed helical form) under the control of polar/low polar stimuli respectively and opens the way to the development of new sensors and stimuli‐sensitive materials based on these conceptseng© 2019 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived VersionsHelical polymerGelColorimetric sensorSelf-assemblyPoly(phenylacetylene)Stimuli‐Directed Colorimetric Interconversion of Helical Polymers Accompanied by a Tunable Self‐Assembly Processjournal article10.1002/smll.2018054131613-6829open access