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Chiral molecular switches are attracting attention as they could pave the way to chiral molecular machines. Herein, we report on the design and synthesis of a single molecule chiral switch based on a cyclotriveratrylene scaffold, in which the chirality inversion is controlled by the solvent. Hemicryptophanes are built around a C 3 cyclotriveratrylene chiral unit, with either M or P handedness, connected to another tripod and usually displaying an "out" configuration. Here, we demonstrate that solvents are able to control the "in" and "out" configurations of the CTV unit, creating a chiral molecular switch from (M/P)"in" to (P/M)"out" handedness. The full characterization of the "in" and "out" configurations and of the chirality switch were made possible by combining NMR, HPLC, ECD, DFT and molecular dynamics. Interestingly, bulky aromatic solvents such as 2-t-butylphenol favor the "in" configuration while polar aprotic solvents such as acetone favor the "out" configuration. This chiral switch was found to be fully reversible allowing the system to oscillate between two different M and P configurations several times upon the action of solvents stimuli., (© 2023 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.)

Constructing a sensitive and efficient sensor for determination of metronidazole (MNZ) is crucial in food field. Herein, a new cyclotriveratrylene-based metal-organic framework (MOF), namely, [Cd 6 L 2 (cyclen) 2 (H 2 O) 2 ] (1), was constructed by self-assembly of functionalized 5,6,12,13,19,20-hexacarboxy-propoxy-cyclotriveratrylene (H 6 L), 1,4,7,10-tetraazacyclododecane (cyclen) and Cd(II) cation under solvothermal condition. In 1, adjacent Cd(II) cations are linked by L 6- to produce a 2D polymeric structure with carboxylate and phenolic oxygen atoms. To enhance conductivity of 1, it was combined with conducting carbon materials, including mesoporous carbon (MC), reduced graphene oxide (RGO) and multi-walled carbon nanotubes (MWCNT), respectively, producing a series of composite materials. Remarkably, electrochemical tests showed that 1@MWCNT(1:1) featured a much better electrochemical detection performance for metronidazole (MNZ) than 1@MC and 1@RGO. The linear range for the detection of MNZ is up to 0.4-500 μM and the limit of detection (LOD) for MNZ reached 0.25 μM. Importantly, the fabricated sensor 1@MWCNT(1:1) was employed for the detection of MNZ in honey and egg with satisfactory result. High-performance liquid chromatography (HPLC) validated the high accuracy of the electrochemical method for the determination of honey and egg., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

A new and innovative fluorescent structure was constructed on Cyclotriveratrylene affiliated to Dansyl chloride (DNSC) and was used to detect Cr (III) and Fe (III) among the various cations by using spectrofluorimetric method. The characterization of the new compound was carried out using the 1 H-NMR, 13 C-NMR, and ESI-MS techniques. The interaction and role of DNSC-CTV with cations was reviewed. A change in the spectra of absorption directed to the conclusion that there is substantial interaction of Cr (III) and Fe (III) with DNSC-CTV. Furthermore the interaction of the ligand DNSC-CTV with the metal ions Chromium (III) and Iron (III) showed quenching in the emission spectra. Quantum yield of the complexes were calculated and the stern volmer analysis was done to deduce the quenching mechanism of fluorescence to being either static or dynamic. The molecule DNSC-CTV was further studied with the help of computational methods such as molecular docking to study the binding interactions and properties of the molecule., (© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

The five-steps synthesis of a hemicryptophane cage combining a benzene-1,3,5-tricarboxamide unit and a cyclotriveratrylene (CTV) moiety is described. Chiral high-performance liquid chromatography (HPLC) was used to resolve the racemic mixture. The absolute configuration of the isolated enantiomers was assigned by comparison of the experimental electronic circular dichroism (ECD) spectra with the calculated ones. X-ray molecular structures reveal that the capped benzene-1,3,5-tricarboxamide unit adopts a structurally chiral conformation in solid state: the chirality of CTV moiety controls the Λ or Δ orientation of the three amides., (© 2019 Wiley Periodicals, Inc.)

Mononuclear and trinuclear bis-cyclometallated Ir III complexes of the host ligands tris(4-[4'-methyl-2,2'-bipyridyl]methyl)cyclotriguaiacylene (L1) and tris(4-(4'-methyl-2,2'- bipyridyl)carboxy)cyclotriguaiacylene (L2) have been prepared. Complexes [{Ir(ppy) 2 } 3 (L1)](PF 6 ) 3 (1.1), [{Ir(ppy) 2 }(L1)](PF 6 ) 3 (1.2), [{Ir(ppy) 2 } 3 (L2)](PF 6 ) 3 (2.1) and [{Ir(ppy) 2 }(L2)](PF 6 ) 3 (2.2) (where ppy=phenylpyridinato) showed distinct photophysical properties depending on the L ligand. Complexes featuring the L1 ligand were comparatively blue-shifted in solution, with longer lifetimes and higher quantum yields. The mixed bis-cyclometallated Ir III complexes [{Ir(ppy) 2 }{Ir(dFppy) 2 } 2 (L1)](PF 6 ) 3 (1.3), [{Ir(ppy) 2 }{Ir(dFppy) 2 } 2 (L2)](PF 6 ) 3 (2.3), [{Ir(ppy) 2 } 2 {Ir(dFppy) 2 }(L1)](PF 6 ) 3 (1.4) and [{Ir(ppy) 2 } 2 {Ir(dFppy) 2 }(L2)](PF 6 ) 3 (2.4) (where dFppy=2,4-difluorophenylpyrinato) were also synthesised. Steady-state and time-resolved spectroscopy, along with electrochemical investigations, show that the Ir(III) chromophores within these mixed Ir-environment species behave as isolated centres, with no energy transfer or electronic communication between them., (© 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.)