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1.  Synthesis, Characterization and In Vitro Antibacterial Studies of Organotin(IV) Complexes with 2-Hydroxyacetophenone-2-methylphenylthiosemicarbazone (H2dampt) 
Five new organotin(IV) complexes of 2-hydroxyacetophenone-2-methylphenylthiosemicarbazone [H2dampt, (1)] with formula [RSnCln-1(dampt)] (where R = Me, n = 2 (2); R = Bu, n = 2 (3); R = Ph, n = 2 (4); R = Me2, n = 1 (5); R = Ph2, n = 1 (6)) have been synthesized by direct reaction of H2dampt (1) with organotin(IV) chloride(s) in absolute methanol. The ligand (1) and its organotin(IV) complexes (2–6) were characterized by CHN analyses, molar conductivity, UV-Vis, FT-IR, 1H, 13C, and 119Sn NMR spectral studies. H2dampt (1) is newly synthesized and has been structurally characterized by X-ray crystallography. Spectroscopic data suggested that H2dampt (1) is coordinated to the tin(IV) atom through the thiolate-S, azomethine-N, and phenoxide-O atoms; the coordination number of tin is five. The in vitro antibacterial activity has been evaluated against Staphylococcus aureus, Enterobacter aerogenes, Escherichia coli, and Salmonella typhi. The screening results have shown that the organotin(IV) complexes (2–6) have better antibacterial activities and have potential as drugs. Furthermore, it has been shown that diphenyltin(IV) derivative (6) exhibits significantly better activity than the other organotin(IV) derivatives (2–5).
doi:10.1155/2012/698491
PMCID: PMC3352140  PMID: 22611347
2.  {4-Hy­droxy-N′-[(2E,3Z)-4-oxido-4-phenyl­but-3-en-2-yl­idene]benzo­hydrazidato}dimethyl­tin(IV) 
The SnIV atom in the title compound, [Sn(CH3)2(C17H14N2O3)], is five-coordinated within a C2N2O donor set provided by the N,N,O-tridentate ligand and two methyl groups. The resultant coordination geometry is inter­mediate between trigonal-bipyramidal and square-pyramidal. In the crystal, supra­molecular zigzag chains propagating along the c- axis direction are mediated by O—H⋯O hydrogen bonds, and weak C—H⋯π inter­actions consolidate the packing.
doi:10.1107/S1600536811023506
PMCID: PMC3151873  PMID: 21836942
3.  {4-Hy­droxy-N′-[(2E,3Z)-4-oxido-4-phenyl­but-3-en-2-yl­idene]benzo­hydra­zidato}diphenyl­tin(IV) methanol monosolvate 
Two independent diphenyl­tin mol­ecules and two independent methanol mol­ecules comprise the asymmetric unit of the title compound, [Sn(C6H5)2(C17H14N2O3)]·CH3OH. The Sn atom in each is five-coordinated by a tridentate ligand and the ipso-C atoms of the Sn-bound benzene substituents. The resulting C2N2O donor set defines a coordination geometry that is inter­mediate between trigonal-bipyramidal (TP) and square-pyramidal (SP), with one mol­ecule slightly tending towards TP and the other slightly towards SP. The mol­ecules differ in terms of the relative orientations of the terminal benzene rings [dihedral angles = 45.71 (18) and 53.98 (17)°] and of the Sn-bound benzene substituents [dihedral angles = 59.5 (2) and 45.77 (18)°, respectively]. The most prominent feature of the crystal packing is the formation of four-mol­ecule aggregates via O—H⋯O and O—H⋯N hydrogen bonds, in which the hy­droxy group is connected to a methanol mol­ecule which, in turn, is linked to a non-coordinating N atom. Weak C—H⋯π inter­actions also occur.
doi:10.1107/S1600536811023415
PMCID: PMC3151954  PMID: 21836941
4.  (2E)-2-[2-(Cyclo­hexyl­carbamothio­yl)hydrazinylidene]­propanoic acid 
In the title thio­urea derivative, C10H17N3O2S, the carboxyl group and the least-squares plane through the cyclo­hexyl ring are twisted out of the plane through the central CN3S residue; the respective dihedral angles are 7.18 (8) and 62.29 (4)°. The conformation about the azomethine bond [1.275 (2) Å] is E. The NH groups are anti, with one forming an intra­molecular N—H⋯N hydrogen bond. The main feature of the crystal structure is the formation of linear supra­molecular chains along [110] mediated by alternating pairs of O—H⋯O and pairs of N—H⋯S hydrogen bonds.
doi:10.1107/S1600536811014449
PMCID: PMC3089072  PMID: 21754495
5.  1-Cyclo­hexyl-3-{(E)-[1-(pyridin-2-yl)ethyl­idene]amino}­thio­urea 
In the title thio­urea derivative, C14H20N4S, the non-ring non-H atoms are approximately planar, with an r.m.s. deviation of 0.0720 Å. The pyridine ring is twisted out of this plane and makes a dihedral angle of 16.85 (13)° with it. The mean plane passing through the cyclo­hexyl ring is almost normal to the central plane [dihedral angle = 69.23 (8)°]. An intra­molecular N—H⋯N(imine) hydrogen bond occurs. Centrosymmetric dimers are formed in the crystal structure via pairs of N—H⋯S hydrogen bonds, and these are connected into a supra­molecular chain along the a axis via C—H⋯π(pyrid­yl) inter­actions.
doi:10.1107/S1600536811009317
PMCID: PMC3099887  PMID: 21754220
6.  Dichlorido{4-cyclo­hexyl-1-[1-(2-pyridyl-κN)ethyl­idene]thio­semicarbazidato-κ2 N 1,S}phenyl­tin(IV) 
The SnIV atom in the title compound, [Sn(C6H5)(C14H19N4S)Cl2], exists within a distorted octa­hedral geometry defined by the N,N′,S-tridentate monodeprotonated Schiff base ligand, two mutually trans Cl atoms, and the ipso-C atom of the Sn-bound phenyl group; the latter is trans to the azo-N atom. The greatest distortion from the ideal geometry is found in the nominally trans angle formed by the S and pyridyl-N atoms at Sn [151.03 (4)°]. With the exception of the cyclo­hexyl group (chair form), the Schiff base ligand is almost planar (r.m.s. deviation of non-H and Sn atoms = 0.053 Å). The nearly orthogonal orientation of the Sn-bound phenyl group [N—Sn—C—C torsion angle = 70.8 (5)°] to the planar portion of the Schiff base allows for the formation of significant intra­molecular C—H⋯Cl inter­actions which preclude the Cl atoms from participating in N—H⋯Cl hydrogen bonds. Instead, C—H⋯π contacts, involving methyl­ene H and the Sn-bound phenyl group, lead to the formation of supra­molecular chains that pack in the bc plane. Connections between these layers are of the type C—H⋯Cl.
doi:10.1107/S1600536810044247
PMCID: PMC3011751  PMID: 21589211
7.  n-Butyl­dichlorido(2-{(1E)-1-[2-(pyridin-2-yl)hydrazin-1-yl­idene]eth­yl}phenolato)tin(IV) 
Two independent mol­ecules comprise the asymmetric unit of the title compound, [Sn(C4H9)(C13H12N3O)Cl2]. The Sn atom in each is coordinated by the tridentate ligand via the phenoxide O, hydrazine N and pyridyl N atoms, forming five- and six-membered chelate rings. The approximately octa­hedral coordination geometry is completed by the α-C atom of the n-butyl group (which is trans to the hydrazine N atom) and two mutually trans Cl atoms. Differences between the mol­ecules are evident in the relative planarity of the chelate rings and in the conformations of the n-butyl groups [C—C—C—C = 177.2 (5) and −64.4 (11)°]. Significant differences in the Sn—Cl bond lengths are related to the formation of N—H⋯Cl hydrogen bonds, which link the mol­ecules comprising the asymmetric unit into dimeric aggregates. These are consolidated in the crystal packing by C—H⋯Cl contacts. The structure was refined as an inversion twin; the minor twin component is 37 (3)%.
doi:10.1107/S1600536810040572
PMCID: PMC3009310  PMID: 21588842
8.  {4-Hy­droxy-N′-[(2-oxido-1-naphthyl-κO)methyl­idene]benzohydrazidato-κ2 N′,O}dimethyl­tin(IV) 
Two independent but very similar mol­ecules comprise the asymmetric unit of the title compound, [Sn(CH3)2(C18H12N2O3)]. Each Sn atom is coordinated by two methyl groups and two O atoms and an N atom from the dinegative tridentate ligand. The resultant C2NO2 donor set defines a coordination geometry inter­mediate between square-pyramidal and trigonal-pyramidal, with a small tendency towards the former. Zigzag chains running along the a axis mediated by O—H⋯N hydrogen bonding characterize the crystal packing. These are connected into layers in the ab plane by a combination of C—H⋯N and π–π [centroid–centroid distances = 3.658 (2) and 3.6740 (18) Å] inter­actions. The layers are connected along the c axis via C—H⋯O inter­actions.
doi:10.1107/S1600536810027078
PMCID: PMC3007549  PMID: 21588158
9.  1,5-Bis[(E)-1-(2-hydroxyphenyl)ethyl­idene]thiocarbonohydrazide mono­hydrate 
In the title compound, C17H18N4O2S·H2O, the thio­urea derivative is almost planar, with an r.m.s. deviation for the non-H atoms of 0.057 Å. The hydroxyl groups lie to the same side of the mol­ecule as the thione S atom, a conformation that allows the formation of intra­molecular O—H⋯S and O—H⋯N hydrogen bonds. In the crystal structure, the thio­urea and water mol­ecules self-assemble into a two-dimensional array by a combination of Owater—H⋯Ohydrox­yl, N—H⋯Owater and Owater—H⋯S hydrogen bonds and C—H⋯π inter­actions.
doi:10.1107/S1600536810004241
PMCID: PMC2983601  PMID: 21580324

Results 1-9 (9)