Search results for "Nod"

On The Incompatibility of Dextran and Pullulan in Aqueous Solutions and Its Modeling

2012

Joint aqueous solutions of branched dextran and linear pullulan are investigated with respect to their phase separation. The experiments demonstrate that the polymers are – depending on the molar mass of dextran – incompatible in aqueous solutions despite their chemical similarity. This finding can be modeled on the basis of an approach accounting for chain connectivity and conformational relaxation of the components. According to these calculations, the polymers exhibit a miscibility gap in joint solutions despite the favorable interactions between them. Using information on the subsystems H2O/dextran and H2O/pullulan, the assumption of complete miscibility of the polysaccharides is requir…

Cell wall-degrading enzymes produced in vitro by isolates of Phaeosphaeria nodorum differing in aggressiveness

2000

The relationships between in vitro production of cell wall-degrading enzymes and aggressiveness of three Phaeosphaeria nodorum isolates were investigated. When grown in liquid medium containing 1% cell wall from wheat leaves as the carbon source, the isolates secreted xylanase, α-arabinosidase, β-xylosidase, polygalacturonase, β-galactosidase, cellulase, β-1,3-glucanase, β-glucosidase, acetyl esterase and butyrate esterase. Time-course experiments showed different levels of enzyme production and different kinetics between isolates. A highly aggressive isolate produced more xylanase, cellulase, polygalacturonase and butyrate esterase than did the two weakly aggressive isolates. Xylanase was …

Saponins as immunoadjuvants and immunostimulants

1999

Saponins are either triterpene or steroid glycosides widely distributed in the plant and animal kingdom and include a large number of biologically active compounds. Most of them have surface-active and cholesterol-binding properties.

Glycoside derivatives of scopoletin and β-sitosterol from Hymenodictyon floribundum

2003

MCM-41 silica monoliths with independent control of meso- and macroporosity

2007

Centimetre sized macroporous silica monoliths consisting of MCM-41 have been prepared by a two-step procedure allowing an independent control of the meso- and macro-porosity. In the first step a monolith with a macroporosity tailored between 2 and 20 μm is prepared under acidic medium by a phase separation, named spinodal decomposition, leading to a bicontinuous structure of a silica/polymer phase and a water phase. The monolith is then reacted in an alkaline solution of cetyltrimethyl ammonium to transform the silica skeleton into MCM-41 under conditions which preserve the original morphology and macroporosity of the material. The combination of spinodal decomposition and pseudomorphic tra…

Michael additions to double bonds of esters of N-protected (s)-phenylalanyldehydroalanine (X-(s)-Phe-ΔAla-OMe) and its phosphonic acid counterpart (X…

2017

Electrophilic addition of amines, thiols and bromide to the double bonds of model dehydrodipeptides and dehydrophosphonodipeptide was studied. The double bond in these two classes of peptides reacted similarly and gave the same products. These results indicate that dehydropeptides are very good candidates as substrates for modifications of peptide side-chains.

ChemInform Abstract: Electrical Breakdown and Pitting in Anodic Films on Tungsten in Halogen Ion-Containing Solutions.

1988

Abstract The systematic investigation of the anodic behaviour of W in halogen ion-containing solutions reveals noticeable differences in the presence of different anions. Strong generalized dissolution is observed in fluoride solutions, the oxide growth being hindered at low anodizing current densities. Sparking phenomena occur in the presence of Br− and I− anions as in nitrate and sulphate solutions. Only in Cl− containing solutions is the growth of the anodic films limited by the occurrence of pitting phenomena at a critical thickness of the oxide. The laws of dependence of the phenomenon on the experimental parameters and the influence of ferrous ions on the voltage at which pitting occu…

Electrochemical Oxidative C – C Bond Formation

2021

Optimization Strategies for the Anodic Phenol‐Arene Cross‐Coupling Reaction

2021

Electroactivation of Transition Metal Redox Couples for the Carbonylation of Alcohols to Dialkylcarbonates

1998

Electrochemical systems which promote the carbonylation of methanol to dimethylcarbonate, based on the anodic activation of transition metal redox couples, or the Br−/Br2 couple, are poorly active for the carbonylation of ethanol to diethylcarbonate at room temperature and atmospheric pressure. Positive results have been obtained by combined addiction of PdBr2 and Bu4NBr to the system. In this way yields up to 50% in diethylcarbonate were obtained, with very good conductivities in long range electrolyses.