Synthesis of carboxylate arsenobetaines based on (carboxyalkyl)triphenylarsonium halides

© 2015 Pleiades Publishing, Ltd. It has been found that the reaction of triphenylarsine with unsaturated carboxylic acids (acrylic, maleic, and itaconic ones) supposed to yield the arsenobetaines does not occur, in contrast to similar reactions of carboxylic acids with tertiary phosphines. However, the interaction of tertiary arsines with the halogenated carboxylic acids has resulted in the corresponding tertiary arsonium salts, dehydrohalogenation of the latter affording the target carboxylate betaines in the quantitative yield; the products structure has been elucidated using a set of chemical, physical, and physico-chemical methods. Antibacterial activity of the prepared compounds has been studied

New di- and tricarboxylate phosphabetaines

© 2016, Springer Science+Business Media New York.New stable tricarboxylate phosphabetaines were synthesized based on 3-(diphenylphosphino)propionic acid and unsaturated dicarboxylic acids (maleic and itaconic). A new dicarboxylate phosphabetaine was synthesized based on 1,3-bis(diphenylphosphino)propane, which did not contain any proton-donor reagents in its crystal lattice

Crystal structure of new carboxylate phosphabetaines and phosphonium salts conjugated with them

© 2016, Springer Science+Business Media New York.Earlier unknown crystalline forms of three carboxylate phosphabetaines and conjugated with them phosphonium salts differing by β substituent with respect to the carboxylate group were studied. The structure of studied compounds in crystal is determined by intermolecular electrostatic interactions. This leads to the trans arrangement of the carboxylate and the phosphonium groups

Synthesis and biological evaluation of novel carboxylate phosphabetaines derivatives with long alkyl chains

© 2016 Taylor & Francis Group, LLC.The purpose of the present study was to investigate the antibacterial activity of novel alkyl esters of carboxylate phosphabetaine: β-(carboxyalkyl)ethyltributylphosphonium bromides 4–8. The in vitro microbiological activity of the synthesized phosphonium bromides against gram-positive, gram-negative bacteria and the yeast Candida albicans was determined in comparison to standard agents. Microbiological results indicate the synthesized phosphonium salts possess a broad spectrum of activity against the testedmicroorganisms. Every newly synthesized compound was characterized by elemental analyses, IR, 1H NMR, 31P NMR spectral studies

Triphenylphosphine in reactions with ω-haloalkylcarboxylic acids

© 2016 Taylor & Francis Group, LLC.Stable phosphonium salts were synthesized by the phosphorylation of a series of ω-haloalkylcarboxylic acids with triphenylphosphine. In a second step the resulting phosphonium salts have been treated with 1 M aqueous solution of sodium hydroxide to form the corresponding carboxylate phosphabetaines. The structure of the isolated compounds was determined by IR and NMR spectroscopy, elemental analysis, and X-ray crystallographic studies. Their thermal stability was studied by simultaneous thermogravimetry and differential scanning calorimetry

Synthesis of carboxylate arsenobetaines based on (carboxyalkyl)triphenylarsonium halides

© 2015 Pleiades Publishing, Ltd. It has been found that the reaction of triphenylarsine with unsaturated carboxylic acids (acrylic, maleic, and itaconic ones) supposed to yield the arsenobetaines does not occur, in contrast to similar reactions of carboxylic acids with tertiary phosphines. However, the interaction of tertiary arsines with the halogenated carboxylic acids has resulted in the corresponding tertiary arsonium salts, dehydrohalogenation of the latter affording the target carboxylate betaines in the quantitative yield; the products structure has been elucidated using a set of chemical, physical, and physico-chemical methods. Antibacterial activity of the prepared compounds has been studied

Synthesis of carboxylate arsenobetaines based on (carboxyalkyl)triphenylarsonium halides

© 2015 Pleiades Publishing, Ltd. It has been found that the reaction of triphenylarsine with unsaturated carboxylic acids (acrylic, maleic, and itaconic ones) supposed to yield the arsenobetaines does not occur, in contrast to similar reactions of carboxylic acids with tertiary phosphines. However, the interaction of tertiary arsines with the halogenated carboxylic acids has resulted in the corresponding tertiary arsonium salts, dehydrohalogenation of the latter affording the target carboxylate betaines in the quantitative yield; the products structure has been elucidated using a set of chemical, physical, and physico-chemical methods. Antibacterial activity of the prepared compounds has been studied

Synthesis of carboxylate arsenobetaines based on (carboxyalkyl)triphenylarsonium halides

© 2015 Pleiades Publishing, Ltd. It has been found that the reaction of triphenylarsine with unsaturated carboxylic acids (acrylic, maleic, and itaconic ones) supposed to yield the arsenobetaines does not occur, in contrast to similar reactions of carboxylic acids with tertiary phosphines. However, the interaction of tertiary arsines with the halogenated carboxylic acids has resulted in the corresponding tertiary arsonium salts, dehydrohalogenation of the latter affording the target carboxylate betaines in the quantitative yield; the products structure has been elucidated using a set of chemical, physical, and physico-chemical methods. Antibacterial activity of the prepared compounds has been studied

New di- and tricarboxylate phosphabetaines

© 2016, Springer Science+Business Media New York.New stable tricarboxylate phosphabetaines were synthesized based on 3-(diphenylphosphino)propionic acid and unsaturated dicarboxylic acids (maleic and itaconic). A new dicarboxylate phosphabetaine was synthesized based on 1,3-bis(diphenylphosphino)propane, which did not contain any proton-donor reagents in its crystal lattice

New di- and tricarboxylate phosphabetaines

© 2016, Springer Science+Business Media New York.New stable tricarboxylate phosphabetaines were synthesized based on 3-(diphenylphosphino)propionic acid and unsaturated dicarboxylic acids (maleic and itaconic). A new dicarboxylate phosphabetaine was synthesized based on 1,3-bis(diphenylphosphino)propane, which did not contain any proton-donor reagents in its crystal lattice