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Integrated amperometric biosensors for the determination of l-malic and l-lactic acids were developed by coimmobilization of the enzymes l-malate dehydrogenase (MDH) and diaphorase (DP), or l-lactate oxidase (LOX) and horseradish peroxidase (HRP), respectively, together with the redox mediator tetrathiafulvalene (TTF), on a 3-mercaptopropionic acid (MPA) self-assembled monolayer (SAM)-modified gold electrode by using a dialysis membrane. The electrochemical oxidation of TTF at +100 mV (vs. Ag/AgCl), and the reduction of TTF+ at -50 mV were used for the monitoring of the enzyme reactions involved in l-malic and l-lactic acid determinations, respectively. Experimental variables concerning the biosensors composition and the detection conditions were optimized for each biosensor. Good relative standard deviation values were obtained in both cases for the measurements carried out with the same biosensor, with no need of cleaning or pretreatment of the bioelectrodes surface, and with different biosensors constructed in the same manner. After 7 days of continuous use, the MDH/DP biosensor still exhibited 90% of the original sensitivity, while the LOX/HRP biosensor yielded a 91% of the original response after 5 days. Calibration graphs for l-malic and l-lactic were obtained with linear ranges of 5.2 × 10-7 to 2.0 × 10-5 and 4.2 × 10-7 to 2.0 × 10-5 M, respectively. The calculated detection limits were 5.2 × 10-7 and 4.2 × 10-7 M, respectively. The biosensors exhibited a high selectivity with no significant interferences. They were applied to monitor malolactic fermentation (MLF) induced by inoculation of Lactobacillus plantarum CECT 748T into a synthetic wine. Samples collected during MLF were assayed for l-malic and l-lactic acids, and the results obtained with the biosensors exhibited a very good correlation when plotted against those obtained by using commercial enzymatic kits.

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Reference:
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

Discovery of 1,1′-Dibromoferrocene

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We have measured the optical absorption of gaseous ferrocene, 1,1 prime -dimethylferrocene, 1,1 prime -dibromoferrocene, and 1,1 prime -dichloroferrocene using synchrotron radiation. From these data we have estimated the ligand field parameters and noted increasing e//2//g(d) to Cp( pi ) overlap with increasing charge transfer from the Cp ring to the substitution. The optical absorption spectra for ferrocene, dibromoferrocene, and dichloroferrocene are remarkably similar. The halogen substitutions result in greater Cp( pi ) to e//2//g-(d(x2-y2)) hybridization. The e//2//g orbitals become more bonding while the a//1//g and e//1//g orbitals become more non-bonding or antibonding. This change is reflected in a change of the ligand field parameters.

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Reference:
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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This work proposes the use of an electronic tongue based on flow injection coulometry for the rapid determination of the antioxidant capacity of fresh lettuce. The e-tongue consisted of a series of 16 porous carbon electrodes, each poised at a fixed potential from +100 to +850 mV. Each injection leaded to a characteristic hydrodynamic voltammogram, whose profile reflects the composition of antioxidants. The correlation between the peak area recorded by each sensor and the 1,1-Diphenyl-2-picryl-hydrazyl (DPPH) assay was maximum in the range of potentials between +400 and 750 mV (R2>0.97). Accordingly, the charge measured provided a direct and simple index of the antioxidant capacity. The practical utility of such index was initially demonstrated by determining the best extraction conditions. This consisted in freeze-drying of lettuce followed by methanolic extraction. Later, the e-tongue was used to evaluate the effect of storage (one week at 5 C) on lettuce. The e-tongue revealed that lettuce lost up to 25 % of their initial antioxidant activity during storage. However, when lettuce samples were pre-treated with fast cooling or vacuum cooling, the decrease of the antioxidant index was limited to 14 and 15 %. Overall, the e-tongue is a rapid, simple and sensitive method for the determination of the antioxidant capacity of fresh lettuce samples. Indirectly, these findings suggest also that lettuce may serve as potential dietary sources of natural phenolic antioxidants.

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Reference:
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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We report an innovative supramolecular architecture for bienzymatic glucose biosensing based on the non-covalently functionalization of multi-walled carbon nanotubes (MWCNTs) with two proteins, glucose oxidase (GOx) (to recognize glucose) and avidin (to allow the specific anchoring of biotinylated horseradish peroxidase (b-HRP)). The optimum functionalization was obtained by sonicating for 10 min 0.50 mg mL?1 MWCNTs in a solution of 2.00 mg mL?1 GOx+1.00 mg mL?1avidin prepared in 50 : 50 v/v ethanol/water. The sensitivity to glucose for glassy carbon electrodes (GCE) modified with MWCNTs-GOx-avidin dispersion and b-HRP (GCE/MWCNTs-GOx-avidin/b-HRP), obtained from amperometric experiments performed at ?0.100 V in the presence of 5.0×10?4 M hydroquinone, was (4.8±0.3) muA mM?1 (r2=0.9986) and the detection limit was 1.2 muM. The reproducibility for 5 electrodes using the same MWCNTs/GOx-avidin dispersion was 4.0 %, while the reproducibility for 3 different dispersions and 9 electrodes was 6.0 %. The GCE/MWCNT-GOx-avidin/b-HRP was successfully used for the quantification of glucose in a pharmaceutical product and milk.

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Reference:
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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The present review aims to highlight the potential of an emerging 2D single element material: phosphorene. Attention is focused on the more recent studies on phosphorene, in terms of synthetic approaches, modification aimed at its stabilization, and potential applications in the biomedical field. Critical aspects for a practical use of phosphorene are discussed, in order to show a realistic scenario and challenges facing researchers.

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Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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Chemical engineers work across a number of sectors, processes differ within each of these areas, but chemistry and chemical engineering roles are found throughout, creation and manufacturing process of chemical products and materials. Reference of 1273-94-5. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. Introducing a new discovery about 1273-94-5, Name is 1,1′-Diacetylferrocene

An efficient method for the synthesis of 2-ferrocenyl-substituted quinoline-4-carboxylic acids via the reaction of acetyl- and 1,1?-diacetylferrocene with isatin under the conditions of the Pfitzinger reaction was developed. Starting from the obtained acids methyl esters, amides, N-methyl-N-methoxyamides, and oximes (at one of the free acetyl groups) of some of these compounds were synthesized.

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Reference:
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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Cation transport through a cellulose acetate-poly(N,N-dimethylaminoethyl methacrylate) membrane (CA:PDMAEMA) was studied with scanning electrochemical microscope (SECM) and the thickness increase of the membrane was monitored with ellipsometry. Upon addition of the polyelectrolyte PDMAEMA, the permeability of the probe cation (ferrocenium methanol, FcMeOH) was increased as much as 40-fold. Soaking membranes in an electrolyte solution doubled the permeability in plain CA membranes, whereas for PDMAEMA containing membranes the opposite was observed and the permeability was reduced by 20?40%. This time-dependent behavior is shown to be a result of the presence of PDMAEMA within the membrane matrix, thus providing an interesting platform for controllable membrane permeability.

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Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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Accurate and detailed measurements of average magnetic susceptibility (4-100 K) and magnetization (2-20 K and 10-50 kOe)) are reported on a number of high spin iron (III) porphyrins, namely protoporphyrin-, octaethylporphyrin-, and deuteroporphyrin iron (III) chlorides.Adequate percautions were taken to ensure that the crystallities did not orient during the magnetization measurements, in high magnetic fields at low temperatures.The experimental magnetization data show complete saturation below 4 K at magnetic fields above 40 kOe and the saturation moment lies between 3.0-3.4 in these compounds. indicating large deviation from the expected value of 5.0, due to sizeable zero-field splitting.The magnetization results at low temperatures show varying degrees of exchange interaction, which was considered within molecular field framework to quantitatively account for the data.A fit to the data gave reasonable values for the zero-filed splitting and exchange-interaction parameters.

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Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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Treatment of [(PCy3)2Cl2Ru=CH-Ph] (I) with vinylferrocene 1 and 1-ferrocenyl-1,3-butadiene 2 yielded solid products. These new complexes were characterized by 1H NMR, 31P NMR and 13C NMR spectroscopy. X-ray crystal structures of both the complexes have been solved. The crystal structure of II confirmed the assigned structure and revealed existence of two sets of intermolecular C-H-Cl(M) type interactions, viz. (Ru)Cl-H-C(ferrocene) and (Ru)Cl-H-CHCl2. The air-stable, dark solid II is an efficient catalyst for ring-opening metathesis polymerization (ROMP) of cyclopentene, norbornene and cycloocta-1,5-diene. Electrochemical behavior of the complexes clearly reflects electronic communication between two metal centers.

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Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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The present invention is safe photodynamic agents and their use in treating microbial contamination.

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Reference:
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion