In search of a new way to fabricate graphene-like materials, isostatic graphite targets were ablated using high peak power with a nanosecond-pulsed infrared laser. We conducted dry ablations in an argon atmosphere and liquid-phase ablations in the presence of a liquid medium (water or toluene). After the dry ablation, the SEM images of the target showed carbon in the form of a volcano-like grain structure, which seemed to be the result of liquid carbon ejected from the ablation center.
View Article and Find Full Text PDFWe use two pore-forming proteins, alpha-hemolysin and aerolysin, to compare the polymer size-dependence of ionic current block by two types of ethyleneglycol polymers: 1) linear and 2) 3-arm star poly(ethylene glycol), both applied as a polydisperse mixture of average mass 1kDa under high salt conditions. The results demonstrate that monomer size sensitivity, as known for linear PEGs, is conserved for the star polymers with only subtle differences in the dependence of the residual conductance on monomer number. To explain this absence of a dominant effect of polymer architecture, we propose that PEG adsorbs to the inner pore wall in a collapsed, salted-out state, likely due to the effect of hydrophobic residues in the pore wall on the availability of water for hydration.
View Article and Find Full Text PDFA highly active nickel catalyst with a hybrid P,N ligand is successfully used for the first time for the polymerization of a thiophene monomer with sterically very demanding side groups. The performance of this catalyst is by far not achievable with commercially available standard catalysts. Polythiophenes with special side chain patterns can thus be made with predetermined molecular weight, low dispersity, and high regioregularity, which enable the preparation of various large crystalline superstructures for the investigation of anisotropic optoelectronic properties in the absence of π-π interactions.
View Article and Find Full Text PDFMacromol Rapid Commun
August 2009
Hyperbranched polythiophenes were prepared via a simple one-pot synthesis approach based on oxidative coupling of branched conjugated monomers. Only small variations in the building unit and architecture lead to large differences of absorption and photoluminescence properties. Interestingly, soluble hyperbranched polythiophenes with relatively small molecular weights show enhanced absorption at low and high wavelengths compared to linear analogues, such as poly(3-hexyl thiophenes) with high molecular weights.
View Article and Find Full Text PDFPoly(ethylene glycol)s (PEGs) are potential drug carriers for improving the therapeutic index of anticancer agents. In this work, the anticancer drug methotrexate (MTX) was activated with N,N'-dicyclohexylcarbodiimide (DCC) and coupled to amino group bearing PEGs of MW 750, 2000, 5000, 10 000, 20,000, and 40,000. First, the activation process of MTX with DCC in the presence and absence of N-hydroxysuccinimide was analyzed through HPLC.
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