Glycoluril–tetrathiafulvalene molecular clips: on the influence of electronic and spatial properties for binding neutral accepting guests

Scholarly Works

• Msellem, P.; Dekthiarenko, M.; Hadj Seyd, N.; Vives, G. Switchable molecular tweezers: design and applications. Beilstein journal of organic chemistry 2024, 20, 504–539. doi:10.3762/bjoc.20.45
• Vari, Z.; Ranjbar-Karimi, R.; Mohammadiannejad, K. Synthesis of acyclic triarylmethane-based compounds containing perfluoropyridine subunits using 4,4′-(p-tolylmethylene)bis(2,6-dimethylphenol) as a flexible spacer. Journal of Molecular Structure 2023, 1302, 137360. doi:10.1016/j.molstruc.2023.137360
• Zhou, P.; Nazari Haghighi Pashaki, M.; Frey, H.-M.; Hauser, A.; Decurtins, S.; Cannizzo, A.; Feurer, T.; Häner, R.; Aschauer, U.; Liu, S.-X. Photoinduced asymmetric charge trapping in a symmetric tetraazapyrene-fused bis(tetrathiafulvalene) conjugate. Chemical science 2023, 14, 12715–12722. doi:10.1039/d3sc03184e
• Dekhtiarenko, M.; Mengheres, G.; Levillain, E.; Voitenko, Z.; Nierengarten, I.; Nierengarten, J.-F.; Goeb, S.; Sallé, M. Tetrathiafulvalene and π-extended tetrathiafulvalene pillar[5]arene conjugates: synthesis, electrochemistry and host–guest properties. New Journal of Chemistry 2023, 47, 7757–7764. doi:10.1039/d3nj01025b
• Kotha, S.; Singh, D. Synthesis of New Glycoluril Derivatives via Ring-Closing Metathesis. HETEROCYCLES 2023, 106, 2125. doi:10.3987/com-23-14912
• Alévêque, O.; Achelle, S.; Sanguinet, L. Vinylpyrimidine‐Functionalized Triphenylamines: Bimodal Molecular Switches and Multilevel Systems. ChemPhotoChem 2022, 7. doi:10.1002/cptc.202200201
• Galochkin, A. A.; Baranov, V. V.; Kolotyrkina, N. G.; Kravchenko, A. N. Synthesis of trialkyl semithioglycolurils from alkylthiourea-glyoxal cyclic adducts and dialkylureas. Mendeleev Communications 2022, 32, 771–773. doi:10.1016/j.mencom.2022.11.021
• Topal, S.; Isci, R.; Topal, S.; Karakaya, O.; Amna, B.; Gunturkun, D.; Ozturk, T. Comprehensive Heterocyclic Chemistry IV - 1,3-Dithioles. Comprehensive Heterocyclic Chemistry IV; Elsevier, 2022; pp 834–994. doi:10.1016/b978-0-12-818655-8.00138-4
• Krykun, S.; Croué, V.; Alévêque, O.; Levillain, E.; Allain, M.; Mézière, C.; Carré, V.; Aubriet, F.; Voitenko, Z.; Goeb, S.; Sallé, M. A self-assembled tetrathiafulvalene box. Organic Chemistry Frontiers 2021, 8, 883–890. doi:10.1039/d0qo01543a
• Goeb, S.; Sallé, M. Electron-rich Coordination Receptors Based on Tetrathiafulvalene Derivatives: Controlling the Host-Guest Binding. Accounts of chemical research 2021, 54, 1043–1055. doi:10.1021/acs.accounts.0c00828
• Dekhtiarenko, M.; Krykun, S.; Carré, V.; Aubriet, F.; Canevet, D.; Allain, M.; Voitenko, Z.; Sallé, M.; Goeb, S. Tuning the structure and the properties of dithiafulvene metalla-assembled tweezers. Organic Chemistry Frontiers 2020, 7, 2040–2046. doi:10.1039/d0qo00641f
• Cotelle, Y.; Hardouin-Lerouge, M.; Lemasson, E.; Morille, Y.; Canevet, D.; Legoupy, S.; Hudhomme, P. An original self-assembly using a tetrathiafulvalene-based molecular clip for the recognition of fullerene C60. Chemical communications (Cambridge, England) 2020, 56, 3077–3080. doi:10.1039/c9cc09633g
• Krykun, S.; Dekhtiarenko, M.; Canevet, D.; Carré, V.; Aubriet, F.; Levillain, E.; Allain, M.; Voitenko, Z.; Sallé, M.; Goeb, S. Metalla-Assembled Electron-Rich Tweezers: Redox-Controlled Guest Release Through Supramolecular Dimerization. Angewandte Chemie (International ed. in English) 2019, 59, 716–720. doi:10.1002/anie.201912016
• Krykun, S.; Dekhtiarenko, M.; Canevet, D.; Carré, V.; Aubriet, F.; Levillain, E.; Allain, M.; Voitenko, Z.; Sallé, M.; Goeb, S. Metalla‐Assembled Electron‐Rich Tweezers: Redox‐Controlled Guest Release Through Supramolecular Dimerization. Angewandte Chemie 2019, 132, 726–730. doi:10.1002/ange.201912016
• Alévêque, O.; Gautier, C.; Levillain, E. Real-time absorption spectroelectrochemistry: From solution to monolayer. Current Opinion in Electrochemistry 2019, 15, 34–41. doi:10.1016/j.coelec.2019.03.015
• Aidibi, Y.; Guerrin, C.; Alévêque, O.; Leriche, P.; Delbaere, S.; Sanguinet, L. BT-2-BOX: An Assembly toward Multimodal and Multilevel Molecular System Simple as a Breeze. The Journal of Physical Chemistry C 2019, 123, 11823–11832. doi:10.1021/acs.jpcc.9b00546
• Kikot, L. S.; Kulygina, C. Y.; Lyapunov, A. Y.; Shishkina, S. V.; Zubatyuk, R. I.; Bogashchenko, T. Y.; Kirichenko, T. I. Synthesis and complexation of molecular clips based on diphenylglycoluril and dibenzocrown ethers with alkali metal cations and paraquat. Tetrahedron 2018, 74, 5725–5732. doi:10.1016/j.tet.2018.08.008
• doi:10.1002/9781119126126.ch5
• Zarei, M.; Sepehrmansourie, H.; Zolfigol, M. A.; Karamian, R.; Farida, S. H. M. Novel nano-size and crab-like biological-based glycoluril with sulfonic acid tags as a reusable catalyst: its application to the synthesis of new mono- and bis-spiropyrans and their in vitro biological studies. New Journal of Chemistry 2018, 42, 14308–14317. doi:10.1039/c8nj02470g
• Cova, T. F.; Nunes, S. C.; Valente, A. J.; Pinho e Melo, T. M. V. D.; Pais, A. A. C. C. Properties and patterns in anion-receptors: A closer look at bambusurils. Journal of Molecular Liquids 2017, 242, 640–652. doi:10.1016/j.molliq.2017.07.065

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