Percolation clusters above criticality form Kardar-Parisi-Zhang surfaces

This study is concerned with the characteristics of regular (isotropic) percolation clusters above the critical threshold p{c}. Analytic arguments for the general dimension case, and numerical results for the two-dimensional case, lead to the conclusion that the characteristics of the shortest paths (defined as the chemical distance l) between given two sites on a percolation cluster are similar to the characteristics of optimal paths in the directed polymer model. A corollary which should be valid for the general dimension case, and verified by numerical results for the two-dimensional case, is that a cluster whose sites are at chemical distance l from a given site forms a Kardar-Parisi-Zhang surface.     

Insulating phases and superfluid-insulator transition of disordered boson chains

Using a strong disorder real-space renormalization group, we study the phase diagram of a fully disordered chain of interacting bosons. Since this approach does not suffer from runaway flows, it allows a direct study of the insulating phases, not accessible in a weak disorder perturbative treatment. We find that the universal properties of the insulating phase are determined by the details and symmetries of the on-site chemical-potential disorder. Three insulating phases are possible: (i) an incompressible Mott glass with a finite superfluid susceptibility, (ii) a random-singlet glass with diverging compressibility and superfluid susceptibility, (iii) a Bose glass with a finite compressibility but diverging superfluid susceptibility. In addition to characterizing the insulating phases, we show that the superfluid-insulator transition is always described by Kosterlitz-Thouless-like flows.     

Reactions in dry media: reactions of cholesterol and cholestanes on silica bound ferric chloride : Cholestane—diacholestene rearrangement

Reaction of cholesterol with silica bound FeCl₃ resulted in a mixture of 3β-cholesteryl chloride and dicholesteryl ether.5-Cholestene and hydroxy- and halogeno-substituted cholestane derivatives gave on heating at 100° with this reagent a 1:1 mixture of 20-epimeric diacholestenes. The 20(R)-isomer gave with meta-chloroperbenzoic acid 20(R)-α-epoxide, while the 20(S)-gave a mixture of 20(S)-α- and 20(S)-β-epoxides.5α,6β-Dihydrocholestane reacted with the FeCl₃/SiO₂ under milder conditions (50°) to give 6β-hydroxy-20(R)-diacholestene, which was converted to the 20(R)-diacholestene.     

INACTIVATION OF Trypanosoma cruzi TRYPOMASTIGOTE FORMS IN BLOOD COMPONENTS BY PHOTODYNAMIC TREATMENT WITH PHTHALOCYANINES

Abstract— -Three phthalocyanine dyes HOSiPcOSi(CH₃)₂(CH₂)₃N(CH₃)₂ (Pc 4), HOSiPc-OSi(CH₃)₂(CH₂)₃N+(CH₃)3I- (Pc 5) and aluminum tetrasulfophthalocyanine hydroxide (AlOHPcS₄) were evaluated for their ability to inactivate the trypomastigote form of Trypanosoma cruzi in fresh frozen plasma (FFP) and red blood cell concentrates (RBCC). The compound Pc 4 was found to be highly effective in killing T. cruzi, Pc 5 less effective and AlOHPcS₄ ineffective. With FFP as the medium, a complete loss of parasite infectivity in vitro (≥5 log₁₀) was found to occur with 2 μ M Pc 4 after irradiation with red light (>600 nm) at a fiuence of 7.5 J/cm², while with RBCC as the medium, a complete loss was found to occur at a fiuence of 15 J/cm². Even without illumination, Pc 4 at 2 μ M also killed about 3.7-4.1 log₁₀ of T. cruzi in FFP during 30 min. Observed differences in T. cruzi killing by the various phthalocyanines may relate to differences in binding; Pc 4 binds to the parasites about twice as much as Pc 5. Ultrastructural analysis of treated parasites suggests that mitochondria are a primary target of this photodynamic treatment. The data indicate that Pc 4 combined with exposure to red light could be used to eliminate bloodborne T. cruzi parasites from blood components intended for transfusion. The inactivation of T. cruzi by Pc 4 in the dark suggests a possible therapeutic application.     

Exploring Helical Peptides and Foldamers for the Design of Metal Helix Frameworks: Current Trends and Future Perspectives

Flexible and biocompatible metal peptide frameworks ( MPFs) derived from short and ultra-short peptides have been explored for the storage of greenhouse gases, molecular recognition, and chiral transformations. In addition to short flexible peptides, peptides with specifically folded conformations have recently been utilized to fabricate a variety of metal helix frameworks ( MHFs ). The secondary structures of the peptides govern the structure-assembly relationship and thereby control the formation of three-dimensional (3D)- MHFs . Particularly, the hierarchical structural organization of peptide-based MHFs has not yet been discussed in detail. Here, we describe the recent progress of metal-driven folded peptide assembly to construct 3D porous structures for use in future energy storage, chiral recognition, and biomedical applications, which could be envisioned as an alternative to the conventional metal-organic frameworks (MOFs).     

Properties of stable organic bond-stretched non-Lewis molecules

The conditions required for the existence of a stable bond-stretched singlet isomer of hetero derivatives of bicyclo[2.1.0]pentane (which is a cyclopentane-1,3-diyl derivative) are discussed. Such species are non-Lewis systems with a ruptured C-C bond (formally diradicals), in which two electrons occupy the nonbonding orbital. A high-level calculation shows that in contrast with the carbon substituted compounds, in which the open form is a transition state between two classical-bonded closed bicyclic forms, in the heterosubstituted molecules, the open form is calculated to be a stable minimum. The ionization potentials of the open forms are considerably lower than those of their bicyclic isomers and also of regular organic radicals/diradicals. Nitrogen atoms are found to be more effective than oxygen or sulfur in stabilizing the open isomer. In this case, the open isomer is calculated to be a little more stable than the bicyclic compound, and a barrier of approximately 40 kcal/mol is computed for the ring closing reaction. Thus, the open isomer is both thermodynamically and kinetically stable. This result rationalizes some experimental observations that indicated the existence of non-Lewis singlet species.