Block copolymer nanoparticles of controlled sizes via ring‐opening metathesis polymerization

This article describes the formation and characterization of self‐assembled nanoparticles of controlled sizes based on amphiphilic block copolymers synthesized by ring‐opening metathesis polymerization. We synthesized a novel hydrophobic derivative of norbornene; this monomer could be polymerized using Grubbs' catalyst [Cl₂Ru(CHPh)(PCy₃)₂] forming polymers of controlled molecular weight. We synthesized amphiphilic block copolymers of controlled composition and showed that they assemble into nanoparticles of controlled size. The nanoparticles were characterized using dynamic light scattering and transmission electron microscopy. Tuning the composition of the block copolymer enables the tuning of the diameters of the nanoparticles in the 30‐ to 80‐nm range. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3352–3359, 2004     

Controlled/living polymerization of 2‐(diethylamino)ethyl methacrylate and its block copolymer with tert‐butyl methacrylate by atom transfer radical polymerization

Polymerization of 2‐(diethylamino)ethyl methacrylate (DEAEMA) via homogeneous atom transfer radical polymerization under various reaction conditions is described. The effects of the initiators and solvents were examined. With 1,1,4,7,10,10‐hexamethyl triethylenetetramine/copper(I) chloride/p‐toluenesulfonyl chloride as the ligand/catalyst/initiator system in methanol, poly(DEAEMA) with a polydispersity index as low as 1.07 was synthesized. Kinetic studies demonstrated the polymerization was very well controlled and exhibited the living characteristic of the process. Well‐defined block copolymers of DEAEMA and tert‐butyl methacrylate (tBMA) were successfully synthesized. The copolymers could be synthesized with equally good results by starting with either p(DEAEMA) or p(tBMA) as the macroinitiators. However, only the macroinitiators terminated with chlorine should be used. The corresponding macroinitiators with bromine as a transferable group did not yield well‐defined copolymers. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2688–2695, 2003     

Partitioning multi-edge graphs

We introduce a new kind of graph called multi-edge graph which arises in many applications such as finite state Markov chains and broadcasting communication networks. A cluster in such a graph is a set of nodes such that for any ordered pair of nodes, there is a path of multi-edges from one to the other such that these edges remain within the same set. We give two algorithms to partition a multi-edge graph into maximal clusters. Both these algorithms are based on the depth-first search algorithm to find strongly connected components of the directed graph. We also discuss some applications of clustering in multi-edge graphs.     

Local magnetism of Rh in Ni-Rh alloys near the critical composition for ferromagnetism

Local magnetic behaviour of Rh implanted into Ni-Rh alloys near the critical Rh compositionx=0.37 has been studied using the TDPAC method. The observed Curie-Weiss type local susceptibility reflects the presence of large d spin polarization around Rh yielding a total moment of 4.7 _B. Our results show that the magnetism of Rh in the alloys depends strongly on the number of Ni near neighbour atoms.     

Photoluminescence and atomic force microscopy studies on pre- and post-irradiated ruby with Fe3+ ion

Photoluminescence spectra measured for pristine ruby and its two irradiated samples with Fe³⁺ ion show R₁, R₂, N lines and a broad band. Decrease in intensities of these features is observed with irradiation of Fe³⁺ ion in ruby. Progressive structural changes and modifications on surface of irradiated rubies with Fe³⁺ ion have been observed by atomic force microscopy. Decrease in intensities is discussed in terms of pair formation.     

Controlled hydrothermal growth of ZnO nanostructures by sequestering the Zn metal ions with the chelating agent EDTA

In the present work, a controlled growth of ZnO nanostructures by manipulating Zn metal ion concentration by the chelating action of ethylene diaminetetra acetic acid in hydrothermal method is studied. EDTA produces metal–chelate complex by the formation of bidentate ligand with Zn²⁺ in the solution and diminishes the reactivity of Zn metal cations. Concentration of EDTA in the mother solution was varied in different ranges like 3, 5 and 10 mM while retaining the zinc metal salt and the NaOH concentration the same. Three different morphologies of wurtzite structured ZnO nanostructures such as nanorods-bunch, separate/discrete uniformly sized hexagonal nanorods and tapered flower petals like shapes are achieved by 3, 5 and 10 mM strengths of EDTA, respectively. The medium concentration 5 mM of EDTA is found to have moderate control over producing ZnO nanostructures of uniform diameter and a high aspect (length to diameter) ratio. An array of vertically aligned free standing ZnO nanorods with uniform spacing is successfully achieved by the addition of 5 mM of EDTA in the mother solution and the same is studied for its fluorescence property at an excitation of 325 nm and it has exhibited a characteristic UV emission of ZnO around 383 nm.