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A molecular loaded dice: When the π conjugation breaks the statistical addressability of an octastate multimodal molecular switch

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Abstract

The elaboration of multichromophoric system which can undergo a reversible transformation over more than two different states can be easily performed by the covalent assembly of several identical switching subunits around a central node. However, the selective addressability of each of them still represents a challenging task. This study reports on the elaboration of multichromophoric systems incorporating three identical indolino-oxazolidine (BOX) moieties as multimodal addressable units. Depending of the open/closed oxazolidine ring status of each of them, these systems can be interconverted between four different states in stepwise manner by using indifferently acid addition or electrochemical stimulation. More important, we have demonstrated by using a dissymmetric triarylamine node that the classical statistical BOX opening is broken then reaching a regioselective addressability. The switching of the three identical BOX units differentiated by their π conjugated junction to the central core follows a preferential order leading to the preponderant and successive formation of only four forms over the eight theoretically and equally expected. To provide limitations and outlooks for such strategy, their switching capacities have been rationalized by DFT calculations.

Original languageEnglish
Article number110270
JournalDyes and pigments
Volume202
DOIs
Publication statusPublished - Jun 2022

Funding

Y.A. thanks the University of Angers for granting. All authors thank the CARMA and ASTRAL platforms of the Structure Fédérative de Recherche MATRIX. This work, carried out within the MORIARTY project, has benefited from financial support from Wallonie-Bruxelles International (WBI), from the Fund for Scientific Research (F.R.S.-FNRS), from the French Ministry of Foreign and European Affairs, and from the Ministry of Higher Education and Research in the frame of the Hubert Curien partnerships. The calculations were performed on the computers of the Consortium des Équipements de Calcul Intensif, including those of the Technological Platform of High-Performance Computing, for which we gratefully acknowledge the financial support of the FNRS-FRFC, of the Walloon Region, and of the University of Namur (Conventions 2.5020.11, GEQ U.G006.15, 1610468, and RW/GEQ2016). Y.A. thanks the University of Angers for granting. All authors thank the CARMA and ASTRAL platforms of the Structure Fédérative de Recherche MATRIX. This work, carried out within the MORIARTY project, has benefited from financial support from Wallonie-Bruxelles International (WBI), from the Fund for Scientific Research (F.R.S.- FNRS ), from the French Ministry of Foreign and European Affairs , and from the Ministry of Higher Education and Research in the frame of the Hubert Curien partnerships. The calculations were performed on the computers of the Consortium des Équipements de Calcul Intensif, including those of the Technological Platform of High-Performance Computing, for which we gratefully acknowledge the financial support of the FNRS-FRFC, of the Walloon Region, and of the University of Namur (Conventions 2.5020.11, GEQ U.G006.15 , 1610468 , and RW/GEQ2016 ).

Keywords

  • Electrochromism
  • Halochromism
  • Indolino-oxazolidine
  • Molecular switch

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