ISBN-13: 9783639266207 / Angielski / Miękka / 2010 / 144 str.
The synthesis physical nature and spectroscopic characterization of several phthaloylamino acids (ligands) have been carried out. Initially, series of two different types of complexes are produced i.e. A-type: Monomeric dibutyltin diphthaloyl-N-carboxylates with 2:1 molar ratio of general formula C6H4(CO)2NRCOO]2SnBu2, B-type: Dimcric tetraorgano dibutyl distannoxane diphthaloyl-N-carboxylates with 1:1 molar ratio of general formula {C6H4(CO)2NRCOO-SnBu2}2O]2 Where R = -CH2, -C2H4, -C4H7, -C5H9, -C2H3C6 H5, -C2H3 C6H5OH. They are characterized by CHN analyzer, FTIR, 1H-, 13C-, l19Sn-multinuclear FTNMR and Mossbauer Spectrometer. The monomeric dibutyltin diphthaloyl-N-Carboxylates complexes behave as hexa- coordinate and possess trans octahedral geometry. The dimeric tetraorgano dibutyl distannoxane diphthaloyl carboxylate complexes have penta coordinate environment with a pair of exo- and endo-cyclic structure having fluxional behavior of organic moieties. It is found that most of the mono and dimeric compounds are biocidally active as well as the triorgano- tins show high biocidal activity against various bacteria and fungi."
The synthesis physical nature and spectroscopic characterization of several phthaloylamino acids (ligands) have been carried out. Initially, series of two different types of complexes are produced i.e. A-type: Monomeric dibutyltin diphthaloyl-N-carboxylates with 2:1 molar ratio of general formula [C6H4(CO)2NRCOO]2SnBu2, B-type: Dimcric tetraorgano dibutyl distannoxane diphthaloyl-N-carboxylates with 1:1 molar ratio of general formula [{C6H4(CO)2NRCOO-SnBu2}2O]2 Where R = -CH2,-C2H4, -C4H7, -C5H9, -C2H3C6 H5, -C2H3 C6H5OH. They are characterized by CHN analyzer, FTIR, 1H-, 13C-, l19Sn-multinuclear FTNMR and Mössbauer Spectrometer. The monomeric dibutyltin diphthaloyl-N-Carboxylates complexes behave as hexa- coordinate and possess trans octahedral geometry. The dimeric tetraorgano dibutyl distannoxane diphthaloyl carboxylate complexes have penta coordinate environment with a pair of exo- and endo-cyclic structure having fluxional behavior of organic moieties. It is found that most of the mono and dimeric compounds are biocidally active as well as the triorgano- tins show high biocidal activity against various bacteria and fungi.