2026-06-28T15:23:34Zhttps://docta.ucm.es/rest/oai/request
oai:docta.ucm.es:20.500.14352/1058462025-03-18T13:09:33Zcom_20.500.14352_14col_20.500.14352_15
Docta Complutense author Dorca, Yeray author Sánchez-Naya, Roberto author Cerdá, Jesús author Calbo, Joaquín author Aragó, Juan author Gómez Aspe, Rafael author Ortí, Enrique author Sánchez Martín, Luis 2024-07-09T11:20:57Z 2024-07-09T11:20:57Z 2020 10.1002/CHEM.202002879 https://hdl.handle.net/20.500.14352/105846 A comparative investigation of the chiral amplification features of a series of three families of C3-symmetric tricarboxamides, 1,3,5-triphenylbenzenetricarboxamides (TPBAs), benzenetricarboxamides (BTAs) and oligo(phenylene ethynylene) tricarboxamides (OPE-TAs), is here reported. As previously observed for BTAs and OPE-TAs, a similar dichroic response is obtained for TPBAs decorated with one, two or three chiral side chains bearing stereogenic centers, thus confirming the efficient transfer of point chirality to the supramolecular helical aggregates. Unlike BTAs and OPE-TAs, the chiral amplification ability of TPBAs in majority rules experiments shows a negligible dependence on the number of chiral centers per monomeric unit, and stands the largest among the series of tricarboxamides. Detailed experimental and theoretical studies demonstrate that the rotation angle between the TPBA units in the helical stack is intermediate to that observed for BTAs and OPE-TAs. This feature strongly conditions the steric interactions between vicinal molecules in the stack and the final chiral amplification outcome. Furthermore, theoretical calculations show that achiral side chains favor the interdigitation of the helical aggregates and thereby the formation of bundle superstructures. eng Impact of molecular size and shape on the supramolecular co-assembly of chiral ticarboxamides: a comparative study journal article 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