Extending the star order to Rickart rings

Star partial order was initially introduced for semigroups and rings with (proper) involution. In particular, this order has recently been studied on Rickart *-rings. It is known that the star order in such rings can be characterized by conditions not involving involution explicitly. Owing to these characterizations, the order can be extended to certain special Rickart rings named strong in the paper; this extension is the objective of the paper. The corresponding order structure of strong Rickart rings is studied more thoroughly. In particular, the most significant lattice properties of star-ordered Rickart *-rings are successfully transferred to strong Rickart rings; also several new results are obtained.     

Temporal Control of Gelation and Polymerization Fronts Driven by an Autocatalytic Enzyme Reaction

Chemical systems that remain kinetically dormant until activated have numerous applications in materials science. Herein we present a method for the control of gelation that exploits an inbuilt switch: the increase in pH after an induction period in the urease‐catalyzed hydrolysis of urea was used to trigger the base‐catalyzed Michael addition of a water‐soluble trithiol to a polyethylene glycol diacrylate. The time to gelation (minutes to hours) was either preset through the initial concentrations or the reaction was initiated locally by a base, thus resulting in polymerization fronts that converted the mixture from a liquid into a gel (ca. 0.1 mm min^?1). The rate of hydrolytic degradation of the hydrogel depended on the initial concentrations, thus resulting in a gel lifetime of hours to months. In this way, temporal programming of gelation was possible under mild conditions by using the output of an autocatalytic enzyme reaction to drive both the polymerization and subsequent degradation of a hydrogel.     

Julia-Kocienski Olefination: A Tutorial Review

Over the past two decades, Julia-Kocienski olefination has become one of the most powerful and reliable C=C double-bond construction methods typically furnishing E-configured alkenes. This review summarizes the scientific literature of the past decade focusing on the key aspects for successful execution of the olefination step. The main stereoselectivity and yield-determining aspects have been outlined in separate chapters providing all the necessary information for the synthesis of Julia-Kocienski reagents as well as the most commonly used reaction optimization techniques.     

Synthesis of 2-substituted oxazoloquinazolinones

Chemistry of Heterocyclic Compounds - The reaction of methyl 2-isothiocyanatobenzoate and 1-azido-3-(4-substituted phenyl)propan-2-ones in the presence of triphenyl phosphine in dioxane by heating...     

Estimation of laminate stiffness reduction due to cracking of a transverse ply by employing crack initiation-and propagation-based master curves

The applicability range of toughness-and strength-based criteria for progressive cracking of a transverse layer in a cross-ply composite laminate subjected to tensile loading is considered. Using a deterministic cracking model, approximate relations for the crack density as a function of stress are derived for initiation-and propagation-controlled types of cracking. The master-curve approach is applied to progressive cracking in glass/epoxy laminates. The accuracy of estimation of laminate stiffness reduction by using crack density master curves is evaluated. Russian translation published in Mekhanika Kompozitnykh Materialov, Vol. 44, No. 5, pp. 633–646, September–October, 2008.     

Structure of polymer and particle aggregates in hydrogel composites

Knowledge of the structure of a biomaterial is usually vital to control its function. This article provides a structural characterization of a hyaluronan scaffold that has demonstrated good biocompatibility and is used to induce bone regeneration. Hyaluronan hydrogels are appealing materials that can function as a matrix to incorporate both organic and inorganic substances to enhance tissue growth. Because of the intrinsic properties of this swollen matrix, one needs a very sensitive technique that can be applied in situ to determine the organization of the polymers in a gel. Small-angle neutron scattering is used to determine the characteristics of the inhomogeneous structure of the hydrogel both with and without added particles. The results are interpreted using models of structure with two length scales that are beyond the traditional picture of homogeneous gels. The observed structure and the dimensions can explain the previously reported rheological properties of gels containing different amount of polymers. Hydroxyapatite nanoparticles added to the gel are frozen in the gel matrix. We are able to determine the distribution and shape of these particles as they aggregate around the polymer chains. We have also concluded, in this case, that the particle structure is concentration independent. Information about the nanostructure for an applicable biomaterial guides the formulation, preparation, and use that should lead to further understanding of its exploitation. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2013     

Interplay between H‐Bonding and Alkyl‐Chain Ordering in Self‐Assembly of Monodendritic L‐Alanine Derivatives

This paper reports on the synthesis and self‐organizing properties of monodendrons consisting of L ‐alanine at the focal point and alkyl chains with different length at the periphery. The structures of thin films and monolayers are studied by temperature‐resolved grazing‐incidence X‐ray diffraction and scanning force microscopy. The interplay between H‐bonding and ordering of the alkyl chains results in a rich temperature‐dependent phase behavior. The monodendrons form H‐bonded stabilized clusters with the number of molecules depending on the length of the aliphatic chains and temperature. The clusters play the role of constitutive units in the subsequent self‐assembly. Short alkyl chains allow the material to form thermodynamically stable crystalline phases. The molecules with longer side groups exhibit additional transitions from the crystalline phase to thermotropic columnar hexagonal or columnar rectangular liquid‐crystalline phases. In monolayers deposited on highly ordered pyrolytic graphite, the materials show ordering similar to thin films. However, for the compound bearing hexadecyl chains the affinity of the alkyl groups to graphite dominates the self‐assembly and thereby allows epitaxial growth of a 2D lattice with flat‐on oriented molecules.