scholarly journals Synthesis, Structure Determination and Catalytic Activity of a Novel Ruthenium(II) [RuCl(dppb)(44bipy)(4-pic)]PF6 Complex

2021 ◽  
Author(s):  
Rafael da Silveira ◽  
Angel Higuera-Padilla ◽  
Beatriz da Cunha ◽  
João de Araujo Neto ◽  
Anderson Catão ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Molecular Orbital ◽  
Density Functional ◽  
Hydrogenation Reaction ◽  
Transfer Hydrogenation ◽  
Dft Methods ◽  
X Ray ◽  
Td Dft ◽  
Dft Simulations ◽  
Transfer Hydrogenation Reaction

This work reports the synthesis, structure and catalytic activity of a novel ruthenium(II) complex, [RuCl(dppb)(44bipy)(4-pic)]PF6 (where dppb = 1,4-bis(diphenylphosphine)butane; 44bipy = 4,4’-dimethyl-2,2’-dipyridyl; 4-pic = 4-picoline). The molecular structure and catalytic activity were studied by Fourier transform infrared (FTIR), UV-Vis and nuclear magnetic resonance (NMR) spectroscopies, cyclic voltammetry, and X-ray crystallography, while the electronic structure was investigated by density-functional theory (DFT) and time dependent DFT (TD-DFT) methods. Electrochemical studies showed the substitution of the chlorido ligand from the precursor by the 4-pic ligand, exhibiting the RuII/RuIII process at 1.21 V. The structure of the compound was optimized using DFT simulations and showed data similar to the X-ray structure. The UV-Vis absorption spectrum showed a good agreement with TD-DFT simulations. The highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) energies were determined at the Becke, 3-parameter, Lee-Yang-Parr (B3LYP) level. The study of the catalytic activity in the transfer hydrogenation of ketones by the 1H NMR showed efficient transfer hydrogenation reaction at 60 ºC, employing acetophenone as substrate and resulting in a high conversion. The formation of two ruthenium-hydride species was observed.

scholarly journals Synthesis of lignin-derived nitrogen-doped carbon as a novel catalyst for 4-NP reduction evaluation

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Yun Liu ◽  
Huanghui Xu ◽  
Hongfei Yu ◽  
Haihua Yang ◽  
Tao Chen
Keyword(s):  
Density Functional ◽  
Catalytic Reduction ◽  
Hydrogenation Reaction ◽  
Transfer Hydrogenation ◽  
Functional Theory ◽  
Nitrogen Doped ◽  
Ft Ir ◽  
Transfer Hydrogenation Reaction ◽  
Novel Catalyst ◽  
Nitrogen Doped Carbon

AbstractIn this study, nitrogen-doped carbon (NC) was fabricated using lignin as carbon source and g-C3N4 as sacrificial template and nitrogen source. The structural properties of as-prepared NC were characterized by TEM, XRD, FT-IR, Raman, XPS and BET techniques. Attractively, NC has proved efficient for reducing 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) using NaBH4 as hydrogen donor with high apparent rate constant (kapp = 4.77 min−1) and specific mass activity (s = 361 mol kgcat−1 h−1), which values are superior to the previously reported catalysts in the literature. Density functional theory (DFT) calculations demonstrate that four kinds of N dopants can change the electronic structure of the adjacent carbon atoms and contribute to their catalytic properties dependant on N species, however, graphitic N species has much greater contribution to 4-NP adsorption and catalytic reduction. Furthermore, The preliminary mechanism of this transfer hydrogenation reaction over as-prepared NC is proposed on the basis of XPS and DFT data. Astoundingly, NC has excellent stability and reusability of six consecutive runs without loss of catalytic activity. These findings open up a vista to engineer lignin-derived NC as metal-free catalyst for hydrogenation reaction.

scholarly journals One-Pot Microwave-Assisted Synthesis of Water-Soluble Pyran-2,4,5-triol Glucose Amine Schiff Base Derivative: XRD/HSA Interactions, Crystal Structure, Spectral, Thermal and a DFT/TD-DFT

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 117
Author(s):  
Yousef Hijji ◽  
Rajeesha Rajan ◽  
Hamdi Ben Yahia ◽  
Said Mansour ◽  
Abdelkader Zarrouk ◽  
...  
Keyword(s):  
Schiff Base ◽  
Molecular Orbital ◽  
Density Functional ◽  
Condensation Reaction ◽  
3D Structure ◽  
Water Soluble ◽  
Microwave Assisted Synthesis ◽  
One Pot ◽  
Microwave Assisted ◽  
Td Dft

The(3R,4R,6R)-3-(((E)-2-hydroxybenzylidene)amino)-6-(hydroxymethyl)tetrahydro-2H-pyran-2,4,5-triol water-soluble Glucose amine Schiff base (GASB-1) product was made available by condensation of 2-hydroxybenzaldehyde with (3R,6R)-3-amino-6-(hydroxymethyl)-tetra-hydro-2H-pyran-2,4,5-triol under mono-mode microwave heating. A one-pot 5-minute microwave-assisted reaction was required to complete the condensation reaction with 90% yield and without having byproducts. The 3D structure of GASB-1 was solved from single crystal X-ray diffraction data and computed by DFT/6-311G(d,p). The Hirshfeld surface analysis (HSA), molecular electronic potential (MEP), Mulliken atomic charge (MAC), and natural population analysis (NPA) were performed. The IR and UV-Vis spectra were matched to their density functional theory (DFT) relatives and the thermal behavior was resolved in an open-room condition via thermogravimetry/Derivative thermogravimetry (TG/DTG) and differential scanning calorimetry (DSC). The highest occupied molecular orbital/lowest unoccupied molecular orbital (HOMO/LUMO), density of state (DOS), and time-dependence TD-DFT computations were correlated to the experimental electron transfer in water and acrylonitrile solvents.

scholarly journals TD-DFT simulations of K-edge resonant inelastic X-ray scattering within the restricted subspace approximation

2021 ◽  
Author(s):  
Vinícius Vaz da Cruz ◽  
Sebastian Eckert ◽  
Alexander Föhlisch
Keyword(s):  
Accurate Description ◽  
X Ray ◽  
X Ray Scattering ◽  
Td Dft ◽  
Dft Simulations ◽  
Subspace Approximation ◽  
Ray Scattering

Truncation of orbital subspaces in TD-DFT yields an accurate description of RIXS spectra for soft X-ray K-edges.

scholarly journals Bis-NHC–Ag/Pd(OAc)2 Catalytic System Catalyzed Transfer Hydrogenation Reaction

Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 8
Author(s):  
Hui-Ju Chen ◽  
Chien-Cheng Chiu ◽  
Tsui Wang ◽  
Dong-Sheng Lee ◽  
Ta-Jung Lu
Keyword(s):  
Functional Groups ◽  
Catalytic System ◽  
High Efficiency ◽  
Aqueous Media ◽  
Hydrogenation Reaction ◽  
Transfer Hydrogenation ◽  
Terminal Alkynes ◽  
Wide Range ◽  
Transfer Hydrogenation Reaction

The bis-NHC–Ag/Pd(OAc)2 catalytic system (NHC = N-heterocyclic carbene), a combination of bis-NHC–Ag complex and Pd(OAc)2, was found to be a smart catalyst in the Pd-catalyzed transfer hydrogenation of various functionalized arenes and internal/terminal alkynes. The catalytic system demonstrated high efficiency for the reduction of a wide range of various functional groups such as carbonyls, alkynes, olefins, and nitro groups in good to excellent yields and high chemoselectivity for the reduction of functional groups. In addition, the protocol was successfully exploited to stereoselectivity for the transformation of alkynes to alkenes in aqueous media under air. This methodology successfully provided an alternative useful protocol for reducing various functional groups and a simple operational protocol for transfer hydrogenation.

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