N-heterocyclic carbenes with three and six fluorous ponytails and their highly fluorophilic Rh and Ir complexes

0569339 - ÚCHP 2024 RIV CH eng J - Článek v odborném periodiku
Dušková, T. - Prajapati, D.S. - Kaule, P. - Červenková Šťastná, Lucie - Strašák, Tomáš - Čermák, Jan
N-heterocyclic carbenes with three and six fluorous ponytails and their highly fluorophilic Rh and Ir complexes.
Journal of Organometallic Chemistry. Roč. 986, FEB 15 (2023), č. článku 122605. ISSN 0022-328X. E-ISSN 1872-8561
Institucionální podpora: RVO:67985858
Klíčová slova: N-heterocyclic carbene * fluorous chemistry * rhodium complexes * iridium complexes
Obor OECD: Organic chemistry
Impakt faktor: 2.3, rok: 2022
Způsob publikování: Open access s časovým embargem

Reactions of 1-methylimidazole and 1-(1-methylethyl)imidazole with (3-iodopropyl)tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silane gave the corresponding 1-alkyl-3-(3-(tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl) silyl) propyl) imidazolium iodides 1 and 2. Reaction of imidazole in excess with (3-iodopropyl)tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silane afforded 1-(3-(tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl) silyl) propyl) imidazole 3 which was further reacted with (3-iodopropyl)tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silane to produce the doubly tagged 1,3-bis[3-(tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl) silyl) propyl] imidazolium iodide 4 and by anion exchange a tetrafluoroborate salt 5. The prepared imidazolium iodides 1,2, and 4 were then used as pre-cursors in synthesis of chlorido(cycloocta-1,5-diene)rhodium or-iridium complexes bearing Nheterocyclic carbenes with one 3-[tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silyl]propyl-substituent and methyl-, 1-methylethyl-and another 3-[ tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl )silyl]propyl-substituent on nitrogens, 6 11. The metal complexes were equimolar mixtures of conformational enantiomers as was best documented by the 1H NMR signals of diastereotopic CH2 protons next to nitrogen. Fluorophilicity fi as the natural logarithm of partition coefficient Pi between fluorous and organic phase of the complexes was determined in the standard solvent system (perfluoro)methylcyclohexane/toluene. All the complexes are fluorophilic with variation of fi between 0.96 and 4.06, the complexes with high values may be classified as highly fluorophilic (heavy fluorous).(c) 2022 Elsevier B.V. All rights reserved.
Trvalý link: https://hdl.handle.net/11104/0340756