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1

Matrix isolation FTIR spectroscopical study of ethene secondary ozonide

100%

Bariseviciute R., Ceponkus J., Sablinskas V.

Open Chemistry

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2007

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vol. 5

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issue 1

71-86

EN

A new method is used for the separation of ethene secondary ozonide (SOZ) from the other products of ethene ozonization reaction. The reaction was performed in the neat films of the reactants at 77 K. Ethene SOZ was separated from other products of the reaction by vacuum distillation at 190–210 K and analyzed by means of the matrix isolation IR absorption spectroscopy. Spectroscopic data from photolysis of the matrix isolated ozonide was used as an argument for assignment of the infrared spectral bands either to ethene SOZ or to other products of the reaction. The spectra of ethene SOZ isolated in the Ar matrix were analyzed by combining experimental results with the theoretical calculations performed at the MP2 6-311+G (3df, 3pd) level. A new assignment of some experimental fundamental bands is proposed taking in to account the Fermi resonance between CH stretch and the five membered ring vibrations. For the first time more than 30 weak infrared absorption bands were observed and assigned to various combination vibrations and overtones. By using new spectral information concerning the overtones and the combination bands it is concluded that the dissociation of unstable ethene SOZ involving breaking of any of the four CO bonds of the five membered ring of ethene SOZ has low probability. Dissociation of the ring starts from breaking of the OO bond. [...]

2

Conformational studies of aliphatic secondary ozonides (propene, 1-butene and 1-heptene) by means of FTIR spectroscopy

100%

Bariseviciute R., Ceponkus J., Gruodis A., Sablinskas V.

Open Chemistry

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2006

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vol. 4

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issue 4

578-591

EN

Ozonization reaction of simple alkenes was studied by means of FT infrared absorption gas spectroscopy. The reaction was performed at 95 K in neat films of the reactants. IR absorption spectra of the gaseous products were recorded. The spectra were analyzed combining experimental results with theoretical calculations performed at B3LYP 6-311++G (3df, 3pd) level. We found that among all theoretically predicted conformers of propene secondary ozonide, only one which has the O-O half-chair configuration for the five membered ring and the radical attached in the equatorial position was present in the sample. Samples of 1-butene and 1-heptene secondary ozonides consist from two conformers of very similar energy (ΔH=0.3 kJ/mol). The most stable conformer for both ozonides is the one with O-O half-chair configuration of the five membered ring and the radical attached in equatorial position and the aliphatic chain in gauche position. The second stable conformer has the aliphatic chain in anti position.

3

Photodynamic therapy (PDT) for disinfection of oral wounds. In vitro study

75%

Matějka Z., Adámková V., Šmucler R., Svobodová J., Hubálková H.

Open Medicine

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2012

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vol. 7

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issue 1

118-123

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2 Bariseviciute R.

2 Ceponkus J.

2 Sablinskas V.

1 Adámková V.

1 Gruodis A.

1 Hubálková H.

1 Matějka Z.

1 Svobodová J.

1 Šmucler R.

Matrix isolation FTIR spectroscopical study of ethene secondary ozonide

Conformational studies of aliphatic secondary ozonides (propene, 1-butene and 1-heptene) by means of FTIR spectroscopy

Photodynamic therapy (PDT) for disinfection of oral wounds. In vitro study