Chiral pincer ruthenium complexes of formula [RuCl(CNN)(Josiphos)] (2-7; Josiphos = 1-[1-(dicyclohexylphosphano)ethyl]-2-(diarylphosphano)ferrocene) have been prepared by treating [RuCl(2)(PPh(3))(3)] with (S,R)-Josiphos diphosphanes and 1-substituted-1-(6-arylpyridin-2-yl)methanamines (HCNN; substituent = H (1 a), Me (1 b), and tBu (1 c)) with NEt(3). By using 1 b and 1 c as a racemic mixture, complexes 4-7 were obtained through a diastereoselective synthesis promoted by acetic acid. These pincer complexes, which display correctly matched chiral PP and CNN ligands, are remarkably active catalysts for the asymmetric reduction of alkyl aryl ketones in basic alcohol media by both transfer hydrogenation (TH) and hydrogenation (HY), achieving enantioselectivities of up to 99 %. In 2-propanol, the enantioselective TH of ketones was accomplished by using a catalyst loading as low as 0.002 mol % and afforded a turnover frequency (TOF) of 10(5)-10(6) h(-1) (60 and 82 degrees C). In methanol/ethanol mixtures, the CNN pincer complexes catalyzed the asymmetric HY of ketones with H(2) (5 atm) at 0.01 mol % relative to the complex with a TOF of approximately 10(4) h(-1) at 40 degrees C.
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http://dx.doi.org/10.1002/chem.200802112 | DOI Listing |
J Am Chem Soc
December 2022
Institut für Anorganische Chemie, University of Göttingen, Tammannstraße 4, 37077 Göttingen, Germany.
Transition metal complexes with a doubly deprotonated diazomethane (CNN) ligand have been proposed as fleeting intermediates in nitrogen transfer reactions. However, in contrast to isoelectronic azide (N), well-defined examples are unknown. We here report the synthesis and characterization of isolable complexes with terminal and bridging CNN ligands, stabilized by platinum(II) pincer fragments.
View Article and Find Full Text PDFTalanta
February 2023
Hubei Key Lab on Organic and Polymeric Optoelectronic Materials, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, Hubei, China; Engineering Research Center of Organosilicon Compounds & Materials, Ministry of Education, College of Chemistry and Molecular Science, Wuhan University, Wuhan, 430072, Hubei, China. Electronic address:
According to the assumption that the formation of C-Pd bond becomes a cyclopalladated complex (CPC), we designed and synthesized two C-N-N pincer ligands of BODIPY appended 2,2'-bipyridine derivatives (BP and BPB). It has been confirmed that the C-Pd bond does exist and plays a crucial role in "on-off" fluorescence behavior. Based on it, a coordination-induced fluorescence quenching sensor for Pd was constructed.
View Article and Find Full Text PDFPhotochem Photobiol
March 2023
Institut für Anorganische und Analytische Chemie, Westfälische Wilhelms-Universität Münster, Münster, Germany.
In this work, we explored coordination compounds featuring caffeine-based carbene co-ligands and tridentate dianionic pincer luminophores derived from 2,6-bis(1H-1,2,4-triazol-5-yl)pyridine (N), as well as from 2-phenyl-6-(1H-1,2,4-triazol-5-yl)pyridine (C), bearing either Ad (adamantyl) or tBu (tertiary butyl) substituents. The new 2-phenyl-6-(1H-1,2,4-triazol-5-yl)pyridine-based ligand precursors along with four Pt(II) complexes, namely Pt(C-tBu), Pt(C-Ad), Pt(N-tBu) and Pt(N-Ad) were characterized. Further on, the influence of the different substituents at the chelating luminophores and of the caffeine-based NHC-co-ligand on the photophysical properties (including photoluminescence quantum yields (Φ ), excited-state lifetimes (τ), radiative (k ), and non-radiative (k ) deactivation rate constants) was assessed in fluid solutions at room temperature (RT) and in frozen glassy matrices at 77 K.
View Article and Find Full Text PDFJ Phys Chem A
April 2022
Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, 14040-901 Ribeirão Preto, São Paulo, Brazil.
Computational modeling at the DLPNO-CCSD(T)/CBS//M06-L/def2-TZVP level of theory was used to propose four different iron catalysts whose structures were inspired on the [Fe]-hydrogenase active site: [Fe(PNHP)(acmp)] (, PNHP = 2,6-bis(dimethylphosphine), acmp = acylmethylpyridine), [Fe(CNHC)(acmp)] (, CNHC = 2,6-bis(methylimidazol-2-ylidene)), [Fe(PNP)(acmp)] (, PNP = 2,6-bis((dimethylphosphine)pyridine)), and [Fe(CNC)(acmp)] (, CNC = 2,6-bis((methylimidazol-2-ylidene) pyridine)). Through these electronic structure calculations, the catalytic mechanism of the reaction was explored. The intermediates and transition states present along the reaction coordinate were identified and described as to their equilibrium geometries, vibrational frequencies, and energies.
View Article and Find Full Text PDFInorg Chem
December 2021
Instituto de Investigaciones Químicas (IIQ), Departamento de Química Inorgánica and Centro de Innovación en Química Avanzada (ORFEO-CINQA). CSIC and Universidad de Sevilla. Avda. Américo Vespucio 49, 41092 Sevilla, Spain.
Metal complexes incorporating proton-responsive ligands have been proved to be superior catalysts in reactions involving the H molecule. In this contribution, a series of Ir complexes based on lutidine-derived CNN pincers containing N-heterocyclic carbene and secondary amino NHR [R = Ph (), Bu (), benzyl ()] donors as flanking groups have been synthesized and tested in the dehydrogenation of ammonia-borane (NHBH, AB) in the presence of substoichiometric amounts (2.5 equiv) of BuOK.
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