Electron-transfer-induced decomposition of 1,2-dioxetanes in negative-mode matrix- assisted laser desorption/ionization time-of-flight mass spectrometry

1,2-Dioxetanes bearing an aromatic electron donor undergo intramolecular charge-transfer-induced chemiluminescence (CTICL). Although there has been some controversy regarding the mechanisms involved, there is little experimental evidence to strongly support any of the proposed mechanisms. In the course of our investigations, to clarify these mechanisms, we tried to effectively ionize dioxetanes bearing a phenolic group and found that poly(3-octylthiophene-2,5-diyl) was a promising matrix for negative-mode matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-ToF-MS). Electron-transfer ionization was found to take place for dioxetanes bearing a hydroxyphenyl moiety that had been further substituted with an aromatic group, which acted as an antenna to catch an electron from the matrix. Furthermore, the characteristic fragmentation of dioxetanes 3c-3d was thought to occur by the elimination of 2-methyl-1-propene (56 u) and pivalaldehyde (86 u) from deprotonated ion [M - H](-) of dioxetanes, based on the results of muliple mass spectrometry measurements of dioxetanes using MALDI quadrupole ion trap ToF-MS. Based on a comparison of fragmentation in dioxetanes and the corresponding keto esters, dioxetanes were presumed to initially generate excited keto esters from which fragmentation took place.     

Qualitative and quantitative analysis of Swertia herbs by high performance liquid chromatography-diode array detector-mass spectrometry (HPLC-DAD-MS)

We evaluated the composition of Swertia herbs using high performance liquid chromatography-diode array detector-mass spectrometry (HPLC-DAD-MS). Eleven peaks of 6 species were unequivocally identified by comparing their retention times, UV spectra, on-line electrospray ionization mass (ESI-MS) spectra, and collision-induced dissociation mass spectrometry/mass spectrometry (CID-MS/MS) data with those of authentic compounds. We adopted wavelengths of 254 nm, 340 nm and 230 nm to simultaneously determine these 11 compounds. By comparing the overall DAD and total ion current (TIC) profiles of various samples, the 6 species were differentiated in terms of the occurrence and/or relative concentrations of the eleven compounds. Our novel validated HPLC-DAD-MS method not only facilitates quality control and identification of Swertia herbs, but is also applicable to systematic investigations of the distribution of secoiridoids, flavonoids, and xanthones in the genus Swertia.     

Computational Results for Regular Difference Systems of Sets Attaining or Being Close to the Levenshtein Bound

Difference systems of sets (DSSs) are combinatorial structures arising in connection with code synchronization that were introduced by Levenshtein in 1971, and are a generalization of cyclic difference sets. In this paper, we consider a collection of m‐subsets in a finite field of prime order to be a regular DSS for an integer m, and give a lower bound on the parameter ρ of the DSS using cyclotomic numbers. We show that when we choose ‐subsets from the multiplicative group of order e, the lower bound on ρ is independent of the choice of subsets. In addition, we present some computational results for DSSs with block sizes and , whose parameter ρ attains or comes close to the Levenshtein bound for .     

A structural isomer of nonaromatic porphyrin: preparation of 20pi-conjugated porphycene based on electronic perturbation

A porphycene having four CF3 groups at the beta-pyrrolic positions affords a stable 20pi-conjugated form in the presence of a 2H+-2e- donor due to the high redox potential of the tetrapyrrole ring framework. No visible band in the UV-vis spectrum and the highly ruffled structure determined by X-ray crystallography support its nonaromatic character. The ethylene bridge moiety in the 20pi-conjugated framework displayed the olefinic reactivities.     

A Smoothing Newton Method with Fischer-Burmeister Function for Second-Order Cone Complementarity Problems

The second-order cone complementarity problem (SOCCP) is an important class of problems containing a lot of optimization problems. The SOCCP can be transformed into a system of nonsmooth equations. To solve this nonsmooth system, smoothing techniques are often used. Fukushima, Luo and Tseng (SIAM J. Optim. 12:436–460, 2001) studied concrete theories and properties of smoothing functions for the SOCCP. Recently, a practical computational method using the smoothed natural residual function to solve the SOCCP was given by Chen, Sun and Sun (Comput. Optim. Appl. 25:39–56, 2003). In the present paper, we propose an algorithm to solve the SOCCP by using the smoothed Fischer-Burmeister function. Some preliminary numerical results are given.     

Crucial dependence of chemiluminescence efficiency on the syn/anti conformation for intramolecular charge-transfer-induced decomposition of bicyclic dioxetanes bearing an oxidoaryl group

Thermally stable rotamers of bicyclic dioxetanes bearing 6-hydroxynaphthalen-1-yl (anti-5a and syn-5a), 3-hydroxynaphthalen-1-yl (anti-5b and syn-5b), and 5-hydroxy-2-methylphenyl groups (anti-5c and syn-5c) were synthesized. These dioxetanes underwent TBAF (tetrabutylammonium fluoride)-induced decomposition accompanied by the emission of light in DMSO and in acetonitrile at 25 °C. For all three pairs of rotamers, the chemiluminescence efficiency Φ(CL) for anti-5 was 8-19 times higher than that for syn-5, and the rate of CTID (charge-transfer-induced decomposition) for anti-5 was faster than that for syn-5. The chemiluminescence spectra of the rotamers for 5a and 5c, respectively, were different. This discrepancy in the chemiluminescence spectra between rotamers can presumably be attributed to the difference in the structures of de novo keto imide anti-14 and syn-14 in an excited state, which inherit the structures of the corresponding intermediary anionic dioxetanes anti-13 and syn-13. The important difference in chemiluminescence efficiency between anti-5 and syn-5 is discussed from the viewpoint of a chemiexcitation mechanism for CTID of oxidophenyl-substituted dioxetane.     

Preparation of Hemispherical Polymer Particles by Cleavage of a Janus Poly(methyl Methacrylate) /Polystyrene Composite Particle

Micrometer-sized, hemispherical particles were successfully prepared as a result of the cleavage of Janus PMMA/PS composite particles by dispersion into acetone/water (9/1-10/0 v/v) media or a THF/water (8/2 v/v) medium. The spherical composite particles having a Janus structure were prepared by the slow evaporation of toluene from homogeneous PMMA/PS/toluene droplets dispersed in an aqueous medium in advance. It was clarified that the difference in affinity between PMMA and PS phases with respect to the media caused the cleavage of the composite particles. This method is expected to be a novel approach to the preparation of nonspherical polymer particles.     

TLC‐SERS study of Syrian rue (Peganum harmala) and its main alkaloid constituents

Surface‐enhanced Raman spectroscopy (SERS) has found increasing acceptance in art conservation and forensic science for its great potential in detecting trace amounts of material. However, SERS is not a separation technique, and, therefore, it is not always suitable for distinguishing different components in a mixture. Coupling of thin layer chromatography (TLC) and SERS has been investigated in this article as a tool for the separation and identification of four alkaloids, namely harmalol, harmaline, harmane and harmine, from the seed extract of Syrian rue (Peganum harmala). The alkaloids contained in this plant were historically used as a dye and for medicinal purposes and have recently drawn attention due to their antitumor activity. The use of TLC over high‐performance liquid chromatography (HPLC) is a convenient way to reduce the amount of material, equipment and time needed for the analysis, and coupling of TLC with SERS provides vibrational information on each compound in the mixture. HPLC analyses with diode array detection were also carried out as a test of our technique, to ascertain the composition of Syrian rue extract and validate the results obtained from TLC‐SERS investigations. In addition, Syrian rue extract and its commercial alkaloid components were characterized by SERS and normal Raman spectroscopy here for the first time, in order to provide valuable reference data to be used for identification purposes. Copyright © 2012 John Wiley & Sons, Ltd.