Synthesis, characterization, kinetic investigation and biological evaluation of Re( i ) di- and tricarbonyl complexes with tertiary phosphine ligands

Autor: Bruno Goud, Mazzarine Dotou, Marta Jakubaszek, Gilles Gasser, Hendrik G. Visser, Verity Lindy Gantsho, Marietjie Schutte-Smith
Rok vydání: 2020
Předmět:
Zdroj: Dalton Transactions
ISSN: 1477-9226
DOI: 10.1039/c9dt04025k
Popis: Rhenium(I) di- and tri-carbonyl complexes of the form fac-[Re(CO)3(L,L′-Bid)X] and [Re(CO)2(L,L′-Bid)X2], where X = aqua (H2O), methanol (CH3OH), triphenylphosphine (PPh3), 1,3,5-triaza-7-phosphaadamantane (PTA), tricyclohexylphosphine (PCy3) and L,L′-Bid = O,O′ bidentate ligands (tropolone = TropH and 3-hydroxyflavone = FlavH) and N,O bidentate ligands (8-hydroxyquinoline = QuinH, 5,7-chloro-8-hydroxyquinoline = diCl-QuinH and quinoline-2,4-dicarboxylic acid = QuinH2), were synthesized and unambiguously characterized by 1H-, 13C-and 31P-NMR, IR, UV/Vis and micro-analysis. The crystal structures of four complexes, namely fac-[Re(CO)3(QuinH)(H2O)]·H2O (5), fac-[Re(CO)3(Quin)(PPh3)] (11), fac-[Re(CO)3(diCl-Quin)(PPh3)] (12) and [Re(CO)2(Trop)(PPh3)2]·2C6H5CH3 (20) were obtained. Re–P bonding distances for 11 and 12 are 2.4948(8) and 2.4908(8) A, respectively, indicating the effect of the electron-withdrawing substituents of the diCl-Quin− ligand. The second-order rate constants for the substitutions of methanol at 25.1 °C in fac-[Re(CO)3(L,L′-Bid)(CH3OH)] (L,L′-Bid = Trop, Flav and QuinH) type complexes by different entering phosphine ligands (PPh3, PCy3, and PTA) varied between 7.23(7) × 10−5 and 1.32(3) × 10−3 M−1 s−1 and were found to depend on the coordinated bidentate ligand (in general k1 (QuinH) 25 μM in RPE-1 cells).
Databáze: OpenAIRE