A tridentate Ni pincer for aqueous electrocatalytic hydrogen production
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The first complete structurally and spectroscopically characterized series of isostructural Group 6 N 2 complexes is reported in this paper. Protonolysis experiments on cis-[M(N 2 ) 2 (P Et N R P Et ) 2 ] (M = Cr, Mo, W; R = 2,6-difluorobenzyl) reveal that only Cr affords N 2 H 5 + and NH 4 + from the reduction of the N 2 ligands.
Excitation of the first overtone of bending mode results in a significant enhancement in the HD + OH channel due to the 1 : 2 Fermi resonance between the fundamental OD stretch and the first overtone of the bend.
Clostridium thermocellum is among the most efficient bacteria to convert cellulosic biomass into H 2 during dark fermentation.
A series of viologen related redox mediators of varying reduction potential has been characterized and their utility as electron shuttles between CdSe quantum dots and hydrogenase enzyme has been demonstrated.
The facet-dependent strain effects on the hydrogen evolution reaction catalyzed by CoP were studied using density functional theory methods. We show that both atomic and electronic effects need to be taken into consideration to understand the strain effects. For the (111) surface, tensile strain promotes hydrogen evolution at all the levels of hydrogen coverage. For the (101) surface, a moderate tensile strain of ~3% endows this facet with optimum performance.
A process that upgrades biomass-derived sugars to 5-hydroxymethylfurfural (HMF), a value-added platform molecule, is presented. The proposed process is ideally suited for integration with the current HFCS process and has the potential for long-term process improvement.
Poly(methylhydrosiloxane) (PMHS) has been examined for its ability to reduce and subsequently cyclize carbohydrate substrates using catalytic tris(pentafluorophenyl)borane (BCF).
Lubricant ranged alkanes of controlled branching and molecular size with excellent yields were synthesized by catalytic conjugate addition-hydroxylalkylation/alkylation (CA-HAA) of biomass derived 2-alkylfurans with enals followed by hydrodeoxygenation.
Flow-through solvolysis offers an opportunity to limit lignin condensation reactions that prevent isolation of native lignin in biomass processing, thus allowing for the study of intrinsic lignin properties and steady-state lignin depolymerization.
We report the continuous, gas-phase synthesis of α-methylene-δ-valerolactone (MVL) from δ-valerolactone (DVL) and formaldehyde (FA) over alkaline earth oxide catalysts.
Ethanol can be converted into diesel fuel ethers using a three-step catalytic approach that involves ethanol oligomerization to larger alcohols, hydrogenolysis of the esters followed by dehydration of the C4 to C8 alcohols into ethers. In this paper we report results for the dehydration of a mixture of C4 – C8 alcohols using a zeolite Y catalyst in a continuous flow reactor. Mono-molecular dehydration of the alcohols produces olefins while bi-molecular dehydration of the alcohol produces ethers. Increasing the pressure increases the ether selectivity while decreasing the pressure produces more olefins. Linear alcohol feeds produce more C8+ ethers, while branched and secondary alcohols lead to more olefins. Olefin and coke selectivities increase with increasing carbon chain length of alcohols. Secondary alcohols lead to higher coke selectivities. Furthermore, ethanol/Butanol oligomerization experiments showed that the incoming dehydration feedstock can be grown to larger C6+ alcohol fractions, leading to higher yields of C10+ diesel-range ethers.
Na-doped BiFeO 3 demonstrates an enhanced p-type behavior compared to p-type BiFeO 3 prepared without extrinsic dopants, and Na-doped BiFeO 3 can serve as a photocathode for solar O 2 reduction to H 2 O 2 when coupled with Ag nanoparticle catalysts.
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