Thermodynamic studies of some binary mixtures containing a self-associated component. II. Excess volumes of some mixtures of tetrahydrofuran with alcohols

Excess volumes of mixing, V^E, for binary mixtures of tetrahydrofuran (THF) with methanol, ethanol, n-butanol, tert-butanol, 2-bromoethanol and ethylene glycol have been determined from the experimental density measurements at 298.15 K over the entire composition range. The V^E data follow the order: ethylene glycol < 2-bromoethanol < methanol < ethanol < n-butanol < tert-butanol. The results have been explained in terms of self-association and the hydrogen bond-donating abilities of alcohols.     

Freezing temperatures of aqueous solutions of methyl formate and ethyl acetate with a variety of nonelectrolytes. Gibbs energy of interaction of the ester group with other functional groups

Freezing temperatures of dilute aqueous solutions of ethyl acetate and mixtures with myo-inositol, D-mannitol, formamide, 1,3,5-trioxane, 1,4-dioxane, acetamide, hexamethylenetetramine, and methyl formate have been measured. In addition, freezing temperatures of dilute aqueous solutions of methyl formate and mixtures with the above solutes have been measured. From these data, the pairwise molecular Gibbs energies of interaction between the molecules were calculated. Using the additivity principle, the pairwise functional group Gibbs energies of interaction were calculated for ester group interactions with a variety of other functional groups.     

Point‐of‐Care Amperometric Testing of Diabetic Marker (HbA1c) Using Specific Electroactive Antibodies

Specific immune detection of glycated hemoglobin is still a great challenge owing to the small epitopic difference between Hemoglobin (Hb) and HbA1c. We report a new electrochemical immunoassay format for point of care testing of HbA1c. A conducting self‐assembled monolayer of mercaptophenyl boronic acid (MPBA) was used as a capture layer for binding of glycated proteins and ferrocene tagged anti‐HbA1c antibody (FcAb) as a tracer molecule on a gold screen printed electrode. Validation of the new HbA1c assay was carried out using 6 clinical samples with known HPLC values and a correlation coefficient of 98 % was observed.     

Systematic trends in optogalvanic signals of some transitions in a uranium hollow cathode discharge

A study of optogalvanic (OG) signals in a uranium hollow cathode discharge using a tunable pulsed dye laser with intensities above saturation revealed certain systematic trends. The peaks of OG signals, for a given hollow cathode current, due to all transitions involving the ground state are within a certain range of values. The same is true of the OG signals due to transitions involving the 620 cm^-1 and 3800 cm^-1 lower metastable levels. For all transitions involving the same lower state, the peaks of OG signal vary linearly with the discharge current. The slopes of such straight lines are different for transitions involving different lower levels of uranium. Effects of radiation trapping are seen in the OG signals due to transitions involving the ground state of uranium at currents above 60 mA. Details of our observations are presented and discussed.     

A Constant Bound for Geometric Permutations of Disjoint Unit Balls

   Abstract. We prove that a set of n disjoint unit balls in R ^d admits at most four distinct geometric permutations, or line transversals, thus settling a long-standing conjecture in combinatorial geometry. The constant bound significantly improves upon the Θ (n ^d-1 ) bound for disjoint balls of unrestricted radii.     

Morphing Simple Polygons

In this paper we investigate the problem of morphing (i.e., continuously deforming) one simple polygon into another. We assume that our two initial polygons have the same number of sides n , and that corresponding sides are parallel. We show that a morph is always possible through an interpolating simple polygon whose n sides vary but stay parallel to those of the two original ones. If we consider a uniform scaling or translation of part of the polygon as an atomic morphing step, then we show that O(n log n) such steps are sufficient for the morph. Furthermore, the sequence of steps can be computed in O(n log n) time. Received May 25, 1999, and in revised form November 15, 1999.     

Dihydroxyacetone variants in the organocatalytic construction of carbohydrates: mimicking tagatose and fuculose aldolases

Dihydroxyacetone variants have been explored as donors in organocatalytic aldol reactions with various aldehyde and ketone acceptors. The protected form of dihydroxyacetone that was chosen for in-depth study was 2,2-dimethyl-1,3-dioxan-5-one, 1. Among the catalysts surveyed here, proline proved to be superior in terms of yield and stereoselectivities in the construction of various carbohydrate scaffolds. In a fashion analogous to aldolase enzymes, the de novo preparation of L-ribulose, L-lyxose, D-ribose, D-tagatose, 1-amino-1-deoxy-D-lyxitol, and other carbohydrates was accomplished via the use of 1 and proline. In reactions using 2,2-dimethyl-1,3-dioxan-5-one 1 as a donor, (S)-proline can be used as a functional mimic of tagatose aldolase, whereas (R)-proline can be regarded as an organocatalytic mimic of fuculose aldolase.     

Synthesis of orthogonal end functionalized oligoethylene glycols of defined lengths

The synthesis of oligoethylene glycols of defined lengths possessing different end functionalities is described. The utility of these molecules towards the development of a generic membrane anchor is demonstrated.