Browsing by Author "Jora, Elena"

Now showing 1 - 4 of 4

COORDINATION PECULIARITIES OF THE SALICYLALDEHYDE S-METHYLISOTHIOSEMICARBAZONE IN THE PALLADIUM COMPLEXES
(Academia de Ştiinţe a Moldovei, 2006) Revenco, Mihail; Bourosh, Pavlina; Duca, Gheorghe; Simonov, Yurii; Bulmaga, Petru; Jora, Elena; Gdaniec, Maria; Ketrush, Petru
Two coordination modes of salicylaldehyde S-methylthiosemicarbazone (Me-S-HSATSC-NH2) have been observed in the palladium complexes with this ligand. The interaction between Me-S-HSATSC-NH2 and tetrachloropalladate gives rise to the formation of a compound of the composition Pd(Me-S-SATSC-NH2)Cl which one has a planar structure. The organic ligand behaves as a monodeprotonated acid coordinated by O,N,S donor atoms set. This is the only case when the thioalkylated thiosemicarbazone uses the sulfur atom for coordination. The forth position in the coordination polyhedron of the complex is occupied by the chloride ion.figureMolecular structure of [Pd(Me-S-SATSC-NH2)Cl] and [Pd(Me-S-SATSC-N-NO)NO2]When the solution of K2[Pd(NO2)4] was treated with Me-S-HSATSC-NH2, the organic reagent undergoes a more dramatic chemical transformation carrying out to the formation of a new derivative of thiosemicarbazide – nitrozothioamide Me-S-SATSC-N-NO. The newly synthesized organic reagent is a monodeprotonated acid bound via O,N,N donor set, while the alkylated sulfur atom is uncoordinated. The forth site is occupied by NO2-ion coordinated by nitrogen atom (see fig.). The possible causes, driving the system to the formation of nitrosothioamide, and the impact of the anion on the coordination mode of the organic ligand will be discussed.
DERIVAȚI CALCONICI CU GRUPA 4-(DIMETILAMINO)FENIL ÎN APLICAȚII FOTOVOLTAICE
(CEP USM, 2024) Popuşoi, Ana; Potlog, Tamara; Robu, Ştefan; Jora, Elena
In this paper, dye-sensitized solar cells (DSSCs) are fabricated and studied using chalconic derivatives as sensitizing dyes. The chalconic derivatives containing the 4-N,N-dimethyl group present two absorption bands with maxima located at the 241 nm and 416 nm, with maximum intensity in the visible region and absorption coefficient of the order 104 cm-1. The analysis of the current-voltage characteristics of the DSSCs with the respective chalconic derivative indicattes the best solar energy conversion efficiency (η = 0.4%), due to the fact that it has the highest absorption value in the band located in the visible region. The best short-circuits current density with value of 2.45 mA/cm2. are obtained for the DSSCs sensitized with chalconic derivative containing 4-N, N-dimethyl SH group.
STRUCTURE OF PALLADIUM COMPLEXES WITH 8-QUINOLINEALDEHYDE THIOSEMICARBAZONE
(Academia de Ştiinţe a Moldovei, 2006) Bourosh, Pavlina; Bulmaga, Petru; Revenco, Mihail; Jora, Elena; Gdaniec, Maria; Simonov, Yurii A.
The coordination compounds of palladium(II) with 8-quinolinaldehyde thiosemicarbazone (HQATSC) have not been described yet. When a solution of K2[PdCl4] is treated with an equimolar amount of HQATSC in warm ethanol or dimethylformamide a yellow crystalline precipitate of Pd(QATSC)Cl is formed. The solubility of the resulted compound in DMF is increased when thiourea (Thio) is added. During 3 days yellow well defined crystals were formed and selected for X-ray investigation. The composition of the separated crystals can be described with a conventional formula Pd(QATSC)Cl⋅1,5Thio⋅H2O. A detailed X-ray investigation showed that the product is a new type of palladium complexes with HQATSC, formed by the cation [Pd(QATSC)(Thio)]+, Cl- anion, water and thiourea uncoordinated molecules. This result suggests that increasing of the ion solubility in the presence of Thio is due to the substitution of the chloride-ion from the inner sphere by thiourea molecule, resulting in formation of a cation-anion type of the complex. The structure of the complex cation is presented in the figure. The square-planar coordination of Pd(II) is provided by two nitrogen atoms and sulfur atom of the monodeprotonated residue of 8-quinolinealdehyde thiosemicarbazone. The bond distances in the palladium coordination polyhedron are: Pd(1)N(1) 2.116(4), Pd(1)-N(2) 2.013(4), Pd(1)-S(1) 2.44(1), PdS(1A) 2.336(1) Å. The real composition of the complex is [Pd(Q ATSC)(Thio)]Cl.0,5Thio.0.5H2O. The non-coordinated Thio and H2O molecules are randomly disordered over two positions with occupancy factors equal to 0.5. The components are involved into system of hydrogen bonds, and the composition should be formally described by the dimeric formula [Pd(QATSC)(Thio)]2Cl2 .Thio.H2O.
STRUCTURE OF PALLADIUM COMPLEXES WITH TRIDENTATE THIOSEMICARBAZONES
(Academia de Ştiinţe a Moldovei, 2012) Bulmaga, Petru; Bourosh, Pavlina; Jora, Elena; Revenco Mihail; Lipkowski, Janusz; Wicher, B.; Palamarciuc, Oleg