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Magdalena Frańska

Publications and source records attributed to Magdalena Frańska.

7 recordsLinked to original sources

Cationization versus surface activity--the effect on electrospray ionization.

Ethoxylated fatty alcohols, C(12)E(1), C(12)E(2), C(18)E(1) and C(18)E(2), were studied by electrospray ionization mass spectrometry (E is the ethoxylene unit OCH(2)CH(2)). For compounds containing two ethoxylene units, which form quite stable adducts with sodium cation, the abundances of [M + Na](+) ions were not affected by alkyl chain, so the hydrophobic effect was not observed. For the compounds containing one ethoxylene unit, forming rather unstable adducts with sodium, the hydrophobic effect was clearly seen since the [C(18)E(1) + Na](+) ion was more abundant than the [C(12)E(1) + Na](+) ion. Two ethoxylene units are not able to form stable adducts with potassium cations, therefore the hydrophobic effect was observed for the [C(12)E(2) + K](+) and [C(18)E(2) + Na](+) ions, the latter being more abundant than the former. For lithium cation adducts with C(12)E(1) and C(18)E(1), the hydrophobic effect was observed, but was less manifested than for sodium cations since lithium adducts are more stable than sodium ones. C(18)E(1) and C(18)E(2) gave more intense signals at higher cone voltage values than C(12)E(1) and C(12)E(2), respectively. However, this is not related to the hydrophobic effect but to the collisions being less effective for the former.

Journal Article↗

Isotachophoretic determination of carboxylic acids in biodegradation samples.

In the current study a method of isotachophoretic separation of selected carboxylic acids was developed. The method was used for the determination of carboxylated oligo(ethylene glycol)s and their degradation products in biodegradation tests of PEG 250 DA [a mixture of dicarboxylated oligo(ethylene glycol)s]. Two tests were performed in the studies: the Organization for Economic Cooperation and Development (OECD) screening test and the river water die-away test. Both the biodegradation tests proved relatively fast biodegradation of the studied compounds. In the OECD screening test the biodegradation was faster than in the river water die-away test which can be ascribed to a higher concentration of bacteria in the biodegradation liquor. The minimal sample pretreatment and relatively low cost of analysis by the isotachophoretic method used here make it a good alternative to existing methods of carboxylic acids analysis.

Biodegradation, Environmental↗

Electrospray ionization mass spectrometric study of purine base-cisplatin complexes.

By mixing cisplatin (cis-diamminedichloroplatinum(II)) with purine base the following ions have been obtained under electrospray ionization conditions: [A+Pt(NH3)2 Cl]+, [A+PtNH3Cl]+, [G+Pt(NH3)2 Cl]+ and [G+PtNH3)Cl]+. Their collision-induced dissociation led to the loss of NH3 and HCl and formation of the protonated base. The last process is strongly favoured for adenine over guanine. It confirms that, analogously as for DNA, formation of the guanine-cisplatin complex is favoured over that of the adenine complex and, as a consequence, it suggests that the mass spectrometric study of nucleic base complexes with platinum may provide some information on the interactions of DNA with other platinum drugs. The loss of NH3 accompanied by that of CO from the guanine ring has experimentally confirmed the presence of a strong hydrogen bond between the NH3 molecule and the O=C6 moiety of guanine found by theoretical calculations.

Adenine↗

Electrospray ionization mass spectrometry of pyrimidine base-rubidium complexes.

Nucleobases and alkali metal cations, under electrospray ionisation conditions, tend to form the so-called magic number clusters (unusually stable clusters in comparison with the neighbouring ones). The effect of the ion source parameters, namely cone voltage and desolvation temperature and relative concentrations of thymine and RbCl on the [T5+Rb]+ ion abundance has been studied.

Hydrogen Bonding↗

Mass spectrometric behaviour of carboxylated polyethylene glycols and carboxylated octylphenol ethoxylates.

Mass spectrometric behaviour of mono- and di-carboxylated polyethylene glycols (PEGCs and CPEGCs) and carboxylated octylphenol ethoxylates (OPECs) are discussed. The tendency for ionisation (deprotonation, protonation and cationisation by alkali metal cations) of carboxylated PEGs was compared with that of non-carboxylated correspondents by using both secondary ion mass spectrometry (SIMS) and electrospray ionisation (ESI). The fragmentation of the PEGCs and CPEGCs is discussed and also compared with their neutral correspondents, PEGs. The B/E mass spectra were recorded, using secondary ion mass spectrometry as a method for generation, for deprotonated and protonated molecules and molecules cationised by alkali metal cations. The fragmentation behaviour of PEGs is found to be different from that of CPEGCs, The presence of carboxylic groups may be confirmed not only by the determination of molecular weights of the ethoxylates studied, but also on the basis of the fragment ions formed. The metastable decomposition of the [OPEC-H](-) ions proceed through the cleavage of the bond between the octylphenol moiety and the ethoxylene chain leading to the octylphenoxy anions. It permits determination of the mass of the hydrophobic moiety of the studied carboxylated alkylphenol ethoxylate. ESI mass spectra recorded in the negative ion mode were found to be more suitable for the determination of the average molecular weight of carboxylated ethoxylates than SI mass spectra.

Journal Article↗

Investigation of ion-pair precipitates of selected alkoxylates and complex salts of specific metal cations by liquid secondary ion mass spectrometry.

Liquid secondary ion (LSI) mass spectra of ion-pair precipitates obtained for Triton X-100 with strontium, lead, cadmium and mercury tetraphenylborates and for selected butoxylene-ethoxylene monoalkyl ethers with barium tetraiodobismuthate(III) are discussed. On the basis of LSI mass spectra, recorded in both positive and negative modes, the formulae of the ion-pair precipitates were determined. On the basis of B/E mass spectra, the fragmentation routes of [M - H + Ba](+) ions for butoxylene-ethoxylene monoalkyl ether complexes of barium and [M - H + Cd](+) ions for the Triton X-100 complex of cadmium are proposed.

Barium↗