Adsorption of fluorinated ethers and alcohols on fresh and oxidized carbon overcoats for magnetic data storage

Temperature programmed desorption has been used to study the desorption kinetics and desorption energies of perfluorodiethylether, (CF3CF2)2O, and 2,2,2-trifluoroethanol, CF3CH2OH, adsorbed on fresh and oxidized hydrogenated amorphous carbon (a-CHx) films. (CF3CF2)2O and CF3CH2OH serve as models for the ether backbone and hydroxyl end-groups of Fomblin Zdol, the lubricant most commonly used to lubricate the surfaces of amorphous carbon overcoats on magnetic data storage hard disks. Our measurements clearly reveal, for the first time, the effects of surface oxidation on the adsorption of fluorocarbon lubricants such as Fomblin Zdol on a-CHx films. Oxidation of the a-CHx surface increases the desorption energy of CF3CH2OH but has no observable impact on the desorption energy of (CF3CF2)2O. These results support the suggestion that the alcohols interact with the surface via hydrogen bonding. From a practical perspective, these results imply that the oxidation of the fresh a-CHx film may serve as a means to control or tailor the a-CHx surface to optimize the properties of the lubricant-overcoat interface in hard disks.     

Crystallographic characterization of helical secondary structures in alpha/beta-peptides with 1:1 residue alternation

Oligomers that contain both alpha- and beta-amino acid residues in a 1:1 alternating pattern have recently been shown by several groups to adopt helical secondary structures in solution. The beta-residue substitution pattern has a profound effect on the type of helix formed and the stability of the helical conformation. On the basis of two-dimensional NMR data, we have previously proposed that beta-residues with a five-membered ring constraint promote two different types of alpha/beta-peptide helix. The "11-helix" contains i, i+3 CO...H-N hydrogen bonds between backbone amide groups; these hydrogen bonds occur in 11-atom rings. The alpha/beta-peptide "14/15-helix" contains i, i+4 CO...H-N hydrogen bonds, which occur in alternating 14- and 15-atom rings. Here we provide crystallographic data for 14 alpha/beta-peptides that form the 11-helix and/or the 14/15-helix. These results were obtained for a series of oligomers containing beta-residues derived from ( S,S)- trans-2-aminocyclopentanecarboxylic acid (ACPC) and alpha-residues derived from alpha-aminoisobutyric acid (Aib) or l-alanine (Ala). The crystallized alpha/beta-peptides range in length from 4 to 10 residues. Nine of the alpha/beta-peptides display the 11-helix in the solid state, three display the 14/15-helix, and two display conformations that contain both i, i+3 and i, i+4 CO...H-N hydrogen bonds, but not bifurcated hydrogen bonds. Only 3 of the 14 crystal structures presented here have been previously described. These results suggest that longer alpha/beta-peptides prefer the 14/15-helix over the 11-helix, a conclusion that is consistent with previously reported NMR data obtained in solution.     

Reaction of Dimethyl Acetylene-Dicarobxylate With Triazinone

Abstract

The addition of dimethyl acetylenedicarboxylate (DMAD) to 6-menthy-1, 2,4-triazlne-3(2H)thione-5(4H)-one afforded 2-methoxylcarboxy-7-methyl-1,3-thiazino[3,2-b][1,2,4]triazine-4,8-dione.     

Microwave-assisted parallel synthesis of a 14-helical beta-peptide library

To facilitate the preparation of beta-peptide libraries in parallel, we have adapted reaction conditions for the solid-phase synthesis of 14-helical beta-peptides for use in a multimode microwave reactor. The low temperature/pressure requirements of microwave-assisted beta-peptide synthesis were found to be compatible with multiwell filter plates composed of polypropylene. Microwave heating of the 96-well plate was sufficiently homogeneous to allow the rapid preparation of a beta-peptide library in acceptable purity.     

A Relation Between Closure Operators on a Small Category and Its Category of Presheaves

In this paper we show that each factorization structure on a small category , satisfying certain conditions, yields a presheaf on and a morphism of presheaves . We then give connections, and set up one to one correspondences, between subclasses of the following classes: (a) closure operators on (b) subobjects of (c) morphisms from to (d) weak Lawvere–Tierney topologies (e) weak Grothendieck topologies (f) closure operators on .     

Influence of anionic substitutions on hyperfine interactions and ionic ordering in ferrites

Hyperfine Interactions -     

Synthesis and 12-helical secondary structure of beta-peptides containing (2R,3R)-aminoproline

[structure: see text] (2R,3R)-Aminoproline, a pyrrolidine-based beta-amino acid, was synthesized and incorporated into hexa-beta-peptide 4. This residue confers water solubility when the ring nitrogen is protonated and allows for 12-helix formation in aqueous solution. Circular dichroism spectra display the 12-helical signature, and 12-helical structure was confirmed by 2D NMR analysis.     

Efficient synthesis of enantiomerically pure beta2-amino acids via chiral isoxazolidinones

We report a practical and scalable synthetic route for the preparation of alpha-substituted beta-amino acids (beta(2)-amino acids). Michael addition of a chiral hydroxylamine, derived from alpha-methylbenzylamine, to an alpha-alkylacrylate followed by cyclization gives a diastereomeric mixture of alpha-substituted isoxazolidinones. These diastereomers are separable by column chromatography. Subsequent hydrogenation of the purified isoxazolidinones followed by Fmoc protection affords enantiomerically pure Fmoc-beta(2)-amino acids, which are useful for beta-peptide synthesis. This route provides access to both enantiomers of a protected beta(2)-amino acid.     

Tolerance of acyclic residues in the beta-peptide 12-helix: access to diverse side-chain arrays for biological applications

Oligomeric backbones with well-defined conformational propensities can serve as scaffolds for displaying sets of functional groups in specific three-dimensional arrangements. beta-Peptides are particularly interesting in this regard because several distinct secondary structures can be induced by appropriate choice of beta-amino acid substitution pattern.3 The beta-peptide 12-helix (defined by 12-membered ring C=O(i)- -H-N(i + 3) hydrogen bonds) is of particular interest because this helix resembles the alpha-helix. To date 12-helices have been observed in beta-peptides comprised exclusively of residues containing a five-membered ring constraint. Here we show that 12-helical propensity is maintained when some cyclic beta-amino acid residues are replaced with more flexible acyclic residues. This result is important because use of acyclic residues greatly facilitates introduction of diverse side chains at specific sites along the 12-helix. We demonstrate the utility of this advance in the context of antibiotic design.