A spectrophotometric assay for solid phase primary amino groups

A rapid, sensitive, and convenient spectrophotometric assay was developed for the measurement of amino groups on solid supports. This method is based on the reaction of amino groups of solids with an excess ofo-phthaldialdehyde (OPA) and subsequent quantitative determination of unreacted OPA by reaction with glycine. Four solids possessing variable quantities of amino groups were examined. Results indicate that about 70% of the total surface amino concentration (determined by the microKjeldahl method) are available for ligand attachment. Unlike the spectrophotometric 2,4,6-trinitrobenzenesulfonic acid method, the OPA spectrophotometric assay is more rapid, sensitive, and convenient, and unlike the spectrofluorimetric OPA, it does not require sophisticated instrumentation.     

Another look at complete positivity in generalized quantum dynamics: Reply to Raggio and Primas

In this rejoinder to a critique by Raggio and Primas of our paper, On Completely Positive Maps in Generalized Quantum Dynamics, we acknowledge that, contrary to our original assertion, the Bloch equations are indeed completely positive. We then explain briefly why this modification of our analysis does not alter its main conclusions.     

Effects of structure on properties of some new aromatic-aliphatic polybenzimidazoles

Polybenzimidazoles were prepared in poly(phosphoric acid) from isophthalic, m- and p-phenylene diacetic, succinic, adipic, suberic, and sebacic acids and 3,3′-diaminobenzidine, 3,3′,4,4′-tetraaminodiphenyl ether and 3,3′,4,4′-tetraaminodiphenylmethane. The thermal, mechanical, and bonding properties were studied. A 3:1 copolymer of isophthalic and m-phenylenediacetic acid with 3,3′-diaminobenzidine showed the best results as far as isothermal oxidation resistance and thermal and processing characteristics.     

A comparative study on methods of optimal sample preparation for the analysis of oligonucleotides by matrix-assisted laser desorption/ionization mass spectrometry

Metal adducts (e.g., Na+ and K+) significantly hinder the analysis of oligonucleotides by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). Although a number of sample purification methods exist, to date no comparative study exists to determine the most efficient method for purifying oligonucleotides. The objective of this work was to perform such a study. Several different oligonucleotide samples were synthesized. Aliquots of these samples were then purposely contaminated with sodium acetate to generate representative contaminated (salted) oligonucleotide samples. A number of popular oligonucleotide purification techniques were then tested as to their effectiveness at removing Na+ from the salted samples. The effectiveness of Na+ removal was qualitatively assessed by comparing the MALDI mass spectra of the original sample, the salted sample, and the salted sample after purification. Micropipet tips packed with C18 reversed-phase packing material (e.g., Zip Tips) appear to be the most effective means of purifying the oligonucleotides investigated. Minidialysis was found to be an effective alternative for purifying higher molecular weight oligonucleotides (> 10,000 u).     

The hall effect in some liquid alloys

The Hall coefficient has been measured for (a) liquid CuTe, AgTe and AuTe₂ and (b) liquid Cu-Sn alloy. The results are discussed in terms of the possible semiconducting nature of liquids comprising group (a) and in terms of bound state formation around the Sn atoms for those in group (b).     

Orbital nature in the electronic states of cyclopropene

Self-consistent field results for the excited electronic states of cyclopropene, with regard to the spatial extent of the π* orbital in the lowest energy ¹(π, π*) state, are found to be identical with that for ethylene. Due to the forced planarity of the ring structure, dihedrally twisted conformers of the upper electronic state cannot contribute significantly to the oscillator strength which must therefore receive a substantial contribution from the vertical transition; this conclusion is contrary to the self-consistent field results. For a proper theoretical treatment of the problem the importance of a multi-configuration approach in an extended basis with ¹(σ, σ*)-type states is emphasized.     

Phase Transfer Catalysis Preparation of Acyl Isothiocyanates

The use of phase transfer catalysis, PTC, for nucleophillic substitution reactions is well documented.^1,2 Included among these reactions is the preparation of both alkyl³ and aryl⁴ thiocyanates. However, PTC reactions at an acyl carbon are much less common. Brándstróm⁵ has reported the preparation of acyl azides and Weber⁶ has used PTC to prepare benzoyl cyanide. Recently Illi⁷ has used PTC to acylate sterically crowded phenols.     

Double Bruhat Cells in Kac–Moody Groups and Integrable Systems

We construct a family of integrable Hamiltonian systems generalizing the relativistic periodic Toda lattice, which is recovered as a special case. The phase spaces of these systems are double Bruhat cells corresponding to pairs of Coxeter elements in the affine Weyl group. In the process we extend various results on double Bruhat cells in simple algebraic groups to the setting of Kac–Moody groups. We also generalize some fundamental results in Poisson–Lie theory to the setting of ind-algebraic groups, which is of interest beyond our immediate applications to integrable systems.