It is shown that exceptional automorphisms exist for semi-local group rings of groups involving extensions of certain generalized dihedral, semi-dihedral, or quaternion groups 相似文献
In this article, the implementation of electrochemical plasmonic nanostructures functionalized with DNA‐based structure‐switching sensors is presented. eNanoSPR devices with open and microfluidic measurement cells are developed on the base of nanohole arrays in 100 nm gold film and applied for combined microscopic and electrochemical surface plasmon (eSPR) visualization. eSPR voltammograms and spectroscopy are performed using planar three electrode schematic with plasmonic nanostructure operated as working electrode. Limit of detection of eNanoSPR devices for oligonucleotide hybridization is estimated in the low nanomolar and applications for structure‐switching electro‐plasmonic sensing in complex liquids are discussed. 相似文献
The photochemical and electrochemical investigations of commercially available, safe, and cheap fluorescent brighteners, namely, triazinylstilbene (commercial name: fluorescent brightener 28) and 2,5‐bis(5‐tert‐butyl‐benzoxazol‐2‐yl)thiophene, as well as their original use as photoinitiators of polymerization upon light emitting diode (LED) irradiation are reported. Remarkably, their excellent near‐UV–visible absorption properties combined with outstanding fluorescent properties allow them to act as high‐performance photoinitiators when used in combination with diaryliodonium salt. These two‐component photoinitiating systems can be employed for free radical polymerizations of acrylate. In addition, this brightener‐initiated photopolymerization is able to overcome oxygen inhibition even upon irradiation with low LED light intensity. The underlying photochemical mechanisms are investigated by electron‐spin resonance‐spin trapping, fluorescence, cyclic voltammetry, and steady‐state photolysis techniques.
A simple and sensitive electrochemical method for the determination of antioxidant capacity has been studied. 4‐hydroxybenzoic acid (4‐HBA) was used as a trapping agent for photogenerated .OH radicals, leading to 3,4‐dihydroxybenzoic acid (3,4‐DHBA). Square‐wave voltammetry was used to quantify the amount of 3,4‐DHBA formed from the reaction between 4‐HBA and .OH. Addition of antioxidants induced the competition between 4‐HBA and antioxidants toward .OH elimination, resulting in a decrease of the measured current. The IC50 for different standard antioxidants was calculated and expressed in Trolox equivalent antioxidant capacity (TEAC). The proposed method was successfully compared to a fluorimetric one. 相似文献
A composite dilation wavelet is a collection of functions generating an orthonormal basis for L2(ℝn) under the actions of translations from a full rank lattice and dilations by products of elements of non-commuting groups A and B. A minimally supported frequency composite dilation wavelet has generating functions whose Fourier transforms are characteristic
functions of a lattice tiling set. In this paper, we study the case where A is the group of integer powers of some expanding matrix while B is a finite subgroup of the invertible n×n matrices. This paper establishes that with any finite group B together with almost any full rank lattice, one can generate a minimally supported frequency composite dilation wavelet system.
The paper proceeds by demonstrating the ability to find such minimally supported frequency composite dilation wavelets with
a single generator. 相似文献
A series of oligothienylenevinylenes, pi-conjugated oligomers rigidified by ethylene bridges attached at different sites of the conjugated backbone, have been constructed by multistep synthetic methodologies. Electronic absorption spectra show that the rigidification of the conjugated system produces a bathochromic shift of the absorption maximum and a narrowing of the HOMO-LUMO energy gap, as compared to the spectra of an open-chain reference compound. The cyclic voltammograms of all oligomers show that these compounds can be reversibly oxidized into their cation radicals and dications and that rigidification produces a large negative shift of the first oxidation potential, which is indicative of a considerable increase of the HOMO level. Electrochemical data confirm that covalent bridging strongly affects the HOMO and LUMO levels and these data demonstrate that the sites of fixation of the bridges on the pi-conjugated backbone exert a determining effect on the relative stability of the cation radical and dication. Examination of these various results in the light of theoretical calculations shows that in addition to a local control of bond length alternation, and hence of the HOMO-LUMO gap, the fixation of covalent bridges at selected positions of the pi-conjugated system limits the deformation of the pi-conjugated structure upon oxidation to the charged states. 相似文献
AT2433, an indolocarbazole antitumor antibiotic, is structurally distinguished by its aminodideoxypentose-containing disaccharide and asymmetrically halogenated N-methylated aglycon. Cloning and sequence analysis of AT2433 gene cluster and comparison of this locus with that encoding for rebeccamycin and the gene cluster encoding calicheamicin present an opportunity to study the aminodideoxypentose biosynthesis via comparative genomics. The locus was confirmed via in vitro biochemical characterization of two methyltransferases--one common to AT2433 and rebeccamycin, the other unique to AT2433--as well as via heterologous expression and in vivo bioconversion experiments using the AT2433 N-glycosyltransferase. Preliminary studies of substrate tolerance for these three enzymes reveal the potential to expand upon the enzymatic diversification of indolocarbazoles. Moreover, this work sets the stage for future studies regarding the origins of the indolocarbazole maleimide nitrogen and indolocarbazole asymmetry. 相似文献