We report a variety of rhenium complexes supported by bidentate and tridentate phosphinoamine ligands and their use in the formation of the advanced biofuel isobutanol from methanol and ethanol. Rhenium pincer complexes - are effective catalysts for this process, with giving isobutanol in 35% yields, with 97% selectivity in the liquid fraction, over 16 h with catalyst loadings as low as 0.07 mol %. However, these catalysts show poorer overall selectivity, with the formation of a significant amount of carboxylate salt solid byproduct also being observed. Production of the active catalyst has been followed by P NMR spectroscopy, and the importance of the presence of base and elevated temperatures to catalyst activation has been established. Complexes supported by diphosphine ligands are inactive for Guerbet chemistry; however, complexes supported by bidentate phosphinoamine ligands show greater selectivity for isobutanol formation over carboxylate salts. The novel complex was able to produce isobutanol in 28% yield over 17 h. The importance of the N-H moiety to the catalytic performance has also been established, giving further weight to the hypothesis that these catalysts operate via a cooperative mechanism.
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http://dx.doi.org/10.1021/acs.organomet.1c00313 | DOI Listing |
Adv Sci (Weinh)
August 2024
Division of Arts and Sciences, Texas A&M University at Qatar, Education City, P.O. Box, Doha, 23874, Qatar.
Ethylene dimerization is an efficient industrial chemical process to produce 1-butene, with demanding selectivity and activity requirements on new catalytic systems. Herein, a series of monodentate phosphinoamine-nickel complexes immobilized on UiO-66 are described for ethylene dimerization. These catalysts display extensive molecular tunability of the ligand similar to organometallic catalysis, while maintaining the high stability attributed to the metal-organic framework (MOF) scaffold.
View Article and Find Full Text PDFDalton Trans
October 2022
Department of Inorganic Chemistry, Faculty of Science, Charles University, Hlavova 2030, 128 40 Prague, Czech Republic.
Combining a phosphinoferrocene fragment with extended multidonor moieties affords novel, flexible multidonor pro-ligands. This contribution describes the synthesis of two structurally similar functional phosphines, PhPfcNHC(O)CHPPh (1) and PhPfcNHCHCHPPh (2, fc = ferrocene-1,1'-diyl), and their coordination behaviour towards Pd(II). The former amidophosphine reacts with [PdCl(MeCN)] to produce the chelate complex [PdCl(1-κ,')] as a mixture of and isomers, which convert into bis-chelate [PdCl(PhPfcNC(O)CHPPh-κ,',)] upon reacting with a strong base (KO-Bu).
View Article and Find Full Text PDFOrganometallics
August 2021
Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff CF10 3AT, United Kingdom.
We report a variety of rhenium complexes supported by bidentate and tridentate phosphinoamine ligands and their use in the formation of the advanced biofuel isobutanol from methanol and ethanol. Rhenium pincer complexes - are effective catalysts for this process, with giving isobutanol in 35% yields, with 97% selectivity in the liquid fraction, over 16 h with catalyst loadings as low as 0.07 mol %.
View Article and Find Full Text PDFOrganometallics
November 2020
Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff CF10 3AT, United Kingdom.
We report a variety of manganese-based catalysts containing both chelating diphosphine (bis(diphenylphosphino)methane (dppm: , , and ) or 1,2-bis(diphenylphosphino)ethane (dppe: )), and mixed-donor phosphinoamine (2-(diphenylphosphino)ethylamine (dppea: -)) ligands for the upgrading of ethanol and methanol to the advanced biofuel isobutanol. These catalysts show moderate selectivity up to 74% along with turnover numbers greater than 100 over 90 h, with catalyst supported by dppm demonstrating superior performance. The positive effect of substituting the ligand backbone was also displayed with a catalyst supported by C-phenyl-substituted dppm () having markedly improved performance compared to the parent dppm catalysts.
View Article and Find Full Text PDFMolecules
April 2020
Instrumentation Center, College of Science, National Taiwan University, Taipei City 10617, Taiwan.
In a refluxing chloroform solution the η-pyrimidinyl {pyrimidinyl = CHN} palladium complex [Pd(PPh)(η-CHN)(Br)], exhibited intermolecular displacement of two triphenylphosphine ligands to form the doubly bridged η-pyrimidinyl Dipalladium complex [Pd(PPh)(Br)](μ,η-CHN), . The treatment of with Hdppa {Hdppa = ,-bisdiphenyl phosphinoamine} in refluxing dichloromethane yielded the doubly bridged Hdppa dipalladium complex [Pd(Br)](μ,η-Hdppa), . Complex reacted with the bidentate ligand, NHSCNCH and, NaSCOEt, and the tridentate ligand, KTp {Tp = tris(pyrazoyl-1-yl)borate}, to form the η-dithio η-pyrimidinyl complex [Pd(PPh)(η-CHN)(η-SS)], (: SS = SCNCH; : SS = SCOEt) and η-Tp η-pyrimidinyl complex [Pd(PPh)(η-CHN)(η-Tp)], , respectively.
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