Acetate | EPFL Graph Search

An acetate is a salt formed by the combination of acetic acid with a base (e.g. alkaline, earthy, metallic, nonmetallic or radical base). "Acetate" also describes the conjugate base or ion (specifically, the negatively charged ion called an anion) typically found in aqueous solution and written with the chemical formula C2H3O2-. The neutral molecules formed by the combination of the acetate ion and a positive ion (called a cation) are also commonly called "acetates" (hence, acetate of lead, acetate of aluminium, etc.). The simplest of these is hydrogen acetate (called acetic acid) with corresponding salts, esters, and the polyatomic anion CH3CO2-, or CH3COO-. Most of the approximately 5 million tonnes of acetic acid produced annually in industry are used in the production of acetates, which usually take the form of polymers. In nature, acetate is the most common building block for biosynthesis. Nomenclature and common formula When part of a salt, the formula of the acetate

New Synthetic Applications of Water Acetate Pd/TPPTS Catalyst Generated in situ. Evidence for true Pd(0) Valent Species Intermediate

Christian Amatore

Studies on the sp-sp intermolecular coupling reactions with the palladium water-soluble catalyst prepared in situ from palladium(II) acetate and sulfonated triphenylphosphine P(C6H4-m-SO3Na)(3) (TPPTS) in a homogeneous acetonitrile-water system, without Cu(I) promotor, afford diynes with moderate yields (45-65%). Under the same conditions, the sp(2)-sp coupling of 2-iodophenols or 2-iodoanilines and terminal alkynes followed by intramolecular cyclization gives indolic and furanic products in good yields (60-99%). Under these aqueous conditions, an efficient and short synthesis of eutypine illustrated the synthetic potentiality of the coupling. Furthermore, through a series of kinetic and P-31 NMR experiments, we have demonstrated that a mixture of Pd(OAc)(2) and TPPTS affords spontaneously a palladium(0) complex, through formation of bivalent complex Pd(OAc)(2)-(TPPTS)(2). A detailed mechanism of the reaction has been investigated thoroughly and the pertinent rate constants measured. The resulting palladium(0) complex reacts with phenyl iodide via an oxidative addition. This complex is considerably less reactive than the corresponding complex generated from PPh(3), probably due to steric effects.

1995

Wastewater and green waste biorefinery Degradation of simple sugars using mixed cultures of purple non-sulfur bacteria: an insight into microbial interactions

Guillaume Crosset-Perrotin

Purple non-sulfur bacteria (PNSB) are phototrophic organisms that have raised interest for both industrial and domestic wastewater treatment and valorization because of their very high assimilation (~1 g CODX g-1 COD substrate) and valuable compounds production (i.e hydrogen, polyhydroxyalkanoates, pigments). PNSB have been studied mostly in pure- or co-cultures with fermentative bacteria. Mixed cultures have been little described. This work aims to enrich a stable association of fermenters and PNSB on a carbohydrate-rich wastewater in a single-step process with a mixed culture. Batches with glucose and acetate at different concentrations were inoculated with an in-house mixed-culture. A chemostat was continuously supplied with glucose (5 g COD L-1) and run at a dilution rate of 0.05 h-1 after start-up under batch mode and baseline stabilization of the PNSB enrichment with acetate. The reactor was constantly illuminated with a light filtered at wavelengths superior to 700 nm. Biomass, pigments expression and substrate depletion were tracked along the experiment. A model was developed to anticipate the biomass growth and the substrates consumption. In the batches fed with acetate, PNSB were dominant in purple biomass (>80% vs. total sequencing read count). The main PNSB population were Rhodopseudomonas and Rhodobacter. With glucose, the biomass turned white. The fermenter Enterobacter dominated the microbiomes (>95% abundance). In the stirred-tank reactor, batch operation with acetate led to the production of a substantial biomass enriched in PNSB (4.0 g VSS L-1) that assimilated the nutrients in a molar C-N-P ratio of 100:9.5:0.1 (- n/n/n). Under chemostat regime with glucose, PNSB were efficiently associated with fermenters in a biomass of 1.0-1.5 g VSS L-1. Phase-contrast microscopy displayed the typical morphotypes of Rhodopseudomonas and the fermenter Clostridium. The glucose was completely depleted. The main fermentation products were acetate (between 3 and 10 mmol L-1), ethanol (between 6 and 9 mmol L-1) and butyrate (between 2 and 4 mmol L-1). The hydrogen yield was low (0.033±0.012 mol H2 mol-1 glucose). A fermenters-PNSB mixed culture was successfully built by microbial community engineering by harnessing the chemostat regime to establish the ecological niches and interactions of these organisms. It provides an excellent opportunity to clean carbohydrate-rich wastewater in a compact single-stage process. In the case of direct application of PNSB, a concentrated biomass can be produced. The biomass can even find interesting applications for resource recovery in the form of, e.g., a protein-rich fertilizing biomass (on food and agricultural aqueous wastes), biogas, bulk chemicals and biopolymers.

2019

Proton diffusion spectroscopy and modeling of brain metabolism at 14.1T

Masoumeh Dehghani Moghadam

As a field at the CIBM, Nuclear magnetic resonance (NMR)spectroscopy can be applied non-invasively to explore the metabolic fate of energy fuel substrates, as well as the rate at which they are consumed, using 13C and 1H nuclei. The work of this thesis encompasses both nuclei, and focuses on (1) improving the quantification and modeling of glucose-derived metabolites; and (2) characterizing diffusion-related parameters of the purportedly glial-specific energy substrate, acetate. Both aim to quantitatively explore cerebral energy metabolism, at ultra-high magnetic field, in vivo, in the healthy rat. 13C NMR spectroscopy, as a tool, enables measuring the progressive incorporation of 13C-glucose into brain glucose and then NMR detectable amino acids (glutamate and glutamine); this relies on the infusion of the 13C-labeled energy substrate. The experimentally obtained 13C labelling curves are analyzed using suitable mathematical models to provide an estimation of cerebral metabolic rates. Here, a dynamic model of time-courses of 13C multiplets arising from isotopomers was considered. So beyond the two-compartment neuronal-glial model, we took into account additional data on the dynamics of 13C isotopomers, available from the fine structure multiplets in 13C spectra of glutamate and glutamine, measured under prolonged [1-6,13C] glucose infusion. We concluded that the dynamic analyses of 13C multiplet time courses of glutamate and glutamine resulted in a higher precision for estimating the absolute values of most cerebral metabolic rates. Acetate metabolism is challenging because dynamic metabolic modeling requires prior knowledge of the transport and uptake kinetics of infused acetate. We sought this information by determining the apparent concentration and distribution volume (V_d) of cerebral acetate between the intracellular and the extracellular compartments. Experimentally, the diffusion characteristics of cerebral acetate were measured, relative to that of N-Acetylaspartate (NAA, known to be mainly intracellular) using diffusion-weighted 1H NMR spectroscopy at 14.1T, under prolonged acetate infusion. The detection of an acetate and NAA signal at large diffusion weighting provided direct experimental evidence of intracellular cerebral acetate and NAA, although a substantial fraction of acetate was extracellular. To estimate the apparent concentration of in vivo brain acetate, T1 and T2 relaxation times of acetate were measured. The longer T1 relaxation and shorter T2 relaxation times of acetate compared with NAA provided evidence of its small molecular size, and possibly different chemical environment. Our experimentally determined value of V_dled to cerebral metabolic rates of acetate (CMR acetate) of the same order reported for the glial Krebâs cycle rate, an indication that estimates of CMR acetate are highly dependent on V_d. Finally, in order to pursue metabolic mapping of cerebral acetate uptake in the rat, in vivo, at 14.1 T, the design and construction of a combined transmit-birdcage coil and receive-quadrature pair surface coil was considered. Its performance was compared to a single birdcage coil in the transmit/receive mode. So far, the preliminary results of the 2-coil configuration are promising: homogenous excitation and a gain in sensitivity up to a distance of 5 mm are achievable. Improvements are ongoing for NMR spectroscopic and imaging applications at 14.1 T.

EPFL2016