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Starting out from Flory`s most probable Distribution concept, correct and incorrect evaluations of SEC measurements are discussed. Using the correct mode, polyesters prepared by irreversible and reversible polycondensation methods were studied. Polyesters of α,ω−alkanediols and isophthalic acid or polyesters of diphenols and sebacic acid were prepared by three different irreversible polyconcensation methods. Formation of cyclic oligo and polyesters was monitored by MALDI-TOF mass spectrometry and dispersities were measured by SEC. The results are compared with the theories of Flory and Odian.
Eqilibrated polyesters were prepared by reversible polycondensation of ethyl 6-hydroxycaproate or by alcohol-initiated ring-opening polymerization of ε-caprolactone. Various catalysts were compared. The influence of dilution and of di- or multifunctional initiators was evaluated. Furthermore, equilibrated polylactides were prepared from L- or meso-lactide at 120, 160 and 180°C. A fast even-odd equilibration was discovered in addition to reversible cyclization and intermolecular transesterification. The influence of these different equilibration mechanisms on the dispersity was investigated. The preparative and theoretical consequences are discussed.
Anemophilous plants produce pollen grains, which have to be monitored to provide an information network for persons suffering from an allergy. The current conventional characterization and identification of pollen is performed by time-consuming microscopic examinations on the basis of the genus-specific pollen shape and size. These examinations are in need of proficient researchers, are not statistically validated, and additionally rely on relatively inaccurate observations of the pollination process. A variety of new analytical approaches have been proposed in order to develop a fast and reliable pollen identification using specific molecular information. Recently, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) was initially applied for the rapid investigation of such complex biological samples. The combination of the obtained patterns of pollen mass spectra and multivariate statistics provide a powerful tool for identifying taxonomic relationships. Here promising results obtained by the reduction and optimization of sample preparation prior to MALDI-TOF MS mapping are presented. Based on a novel application of conductive carbon tape as target, the signal information of the species-specific mass peak patterns of pollen was enhanced. This leads to a clear separation in a subsequent pattern analysis, which is important when analyzing pollen grains in natural species mixtures. As a proof-of-concept, artificial pollen mixtures were investigated by MALDI imaging and evaluated by innovative multivariate data analysis strategies, to assign individual pollen species in the mixtures. Our results can be used to improve the taxonomic differentiation and identification of pollen species and might be useful for the development of a routine method to identify pollen based on mass spectrometry.
About one in seven German citizens is suffering from respiratory allergies, which are mainly caused by anemophilous plant pollen. These pollen grains are monitored to provide a national information network. Their conventional identification is performed by time-consuming microscopic examinations based on the genus-specific pollen morphology. A variety of spectroscopic and spectrometric approaches have been proposed to develop a fast and reliable pollen identification using specific molecular information. Amongst them, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) showed a high potential for the successful investigation of such complex biological samples. The evaluation of the obtained peak patterns from pollen mass spectra with multivariate statistics enables a consistent and rapid identification of the taxonomic relationships.
We will report on a new kind of ring-expansion polymerization (REP) of cyclic esters based of three classes of catalysts.
In contrast to REP described previously these new polymerizations are characterized by a self-extrusion of the catalysts resulting in cyclic homopolyesters as the only reaction product. These REP of L-lactide were performed in bulk at temperatures between 100 and 180°C without racemization. A simplified scheme of a REP catalyzed by BuCa or SnBi is presented below. With meso-lactide temperatures down to 60°C were realized. Depending on catalyst, time and temperature with equal quantities of even and odd-numbered cycles a strong predominance of either even or odd-numbered cycles was found.
Eine neue Art einer Ring-Expansion Polymerization (REP) von zyklischen Polylaktiden mittels neuer Katalysatoren wird präsentiert.
MALDI-TOF Massenspektrometrie und andere analytische Techniken wurden zur Aufklärung des Mechanismus eingesetzt. Dabei zeigte sich, dass im Gegensatz zu anderen REP, ausschließlich zyklische Polymere gebildet wurden. Diese stellen neue Kandidatenmaterialien für zukünftige neue CRM dar.
Various catalysts and polycondensation mechanisms (ROPPOC/REP/ROP)were presented and discussed with regard to the Formation of cyclic and linear polylactides. It could be shown that depending on the structure of the catalyst even- and od numbered cyclics were selectively formed. These data were supported by various analytical techniques like MALDI-TOF mass spectrometry and Size Exclusion Chromatography.
Since its introduction mass spectrometric techniques like Matrix-assisted Laser Desorption/ionization (MALDI) and Electrospray Ionization (ESI) have become indispensable for synthetic polymer analyses. Ideally, various polymer properties (monomer structure, masses, mass distribution, end groups) can be determined simultaneously. However, in real life these experiments are always affected by important structural parameters and instrumental limitations.
A short introduction focussing on latest findings with respect to ionisation principles and mechanisms will be given. Recent results from our group will be presented and efforts to avoid common drawbacks of polymer mass spectrometry will be discussed. In this regard, MALDI - Imaging mass spectrometry and the 2D hyphenation of MS with different chromatographic separation techniques were especially useful, since they can provide additional information and reduce the complexity of polymer analyses.