9 research outputs found
Knots in Charged Polymers
The interplay of topological constraints and Coulomb interactions in static
and dynamic properties of charged polymers is investigated by numerical
simulations and scaling arguments. In the absence of screening, the long-range
interaction localizes irreducible topological constraints into tight molecular
knots, while composite constraints are factored and separated. Even when the
forces are screened, tight knots may survive as local (or even global)
equilibria, as long as the overall rigidity of the polymer is dominated by the
Coulomb interactions. As entanglements involving tight knots are not easy to
eliminate, their presence greatly influences the relaxation times of the
system. In particular, we find that tight knots in open polymers are removed by
diffusion along the chain, rather than by opening up. The knot diffusion
coefficient actually decreases with its charge density, and for highly charged
polymers the knot's position appears frozen.Comment: Revtex4, 9 pages, 9 eps figure
Quantization of energy and writhe in self-repelling knots
Probably the most natural energy functional to be considered for knotted strings is that given by electrostatic repulsion. In the absence of counter-charges, a charged, knotted string evolving along the energy gradient of electrostatic repulsion would progressively tighten its knotted domain into a point on a perfectly circular string. However, in the presence of charge screening self-repelling knotted strings can be stabilized. It is known that energy functionals in which repulsive forces between repelling charges grow inversely proportionally to the third or higher power of their relative distance stabilize self-repelling knots. Especially interesting is the case of the third power since the repulsive energy becomes scale invariant and does not change upon Mobius transformations (reflections in spheres) of knotted trajectories. We observe here that knots minimizing their repulsive Mobius energy show quantization of the energy and writhe (measure of chirality) within several tested families of knots
Halide‐Substituted Phosphacyclohexadienyl Iron Complexes: Covalent Structures vs. Ion Pairs
Invited for the cover of this issue is the group of Robert Wolf from the University of Regensburg, Germany. The cover image shows the structure of the first transition metal complexes bearing pi-coordinated lambda(3)-halophosphacyclohexadienyl ligands, featuring polarized P-halogen bonds
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Synthesis of a Cyclic Co2Sn2 Cluster Using a Co- Synthon.
[Ar'SnCo]2 (1, Ar' = C6H3-2,6{C6H3-2,6- iPr2}2), a rare metal-metal bonded cobalt-tin cluster with low-coordinate tin atoms, was prepared by the reaction of [K(thf)0.2][Co(1,5-cod)2] (cod = 1,5-cyclooctadiene) with [Ar'Sn(μ-Cl)]2. This reaction illustrates a promising synthetic strategy to access uncommon metal clusters. The structure of 1 features a rhomboidal Co2Sn2 core with strong metal-metal bonds between tin and cobalt and a weaker tin-tin interaction. Reaction of 1 with white phosphorus afforded [Ar'2Sn2Co2P4] (2), the first molecular cluster compound containing phosphorus, cobalt and tin