Synthesis, Spectroscopic Properties and Crystal Structures of Dibenzyltin（IV） Dithiobenzoate and Chlorodibenzyltin（IV） Thiobenzoate

Two dibenzyltin(IV) complexes with thiobenzoate ligand, (PhCH2)2Sn(SOCPh)2 (1) and (PhCH2)2Sn(C1)SOCPh (2), have been synthesized by the reaction of dibenzyltin(IV) dichloride with thiobenzoic acid in the presence of organic base Et3N and characterized by IR, ^1H NMR spectroscopy and elemental analysis. Their crystal structures were determined by X-ray single crystal diffraction analysis. In the crystals of 1, the tin atom is six-coordinated in a distorted octahedron configuration. In the crystals of 2, the molecular packing in unit cell reveals that the two adjacent molecules are symmetrically linked to each other to form a dimer with intermolecular Sn…C1 distances of 0.3591 (2) nm and the tin atom is five-coordinated in a distorted trigonal bipyramid configuration.     

丙酮酸异烟酰腙四核有机锡配合物的合成、表征及{[nBu2Sn(C9H8N3O3)O]SnBu3n}2的晶体结构

The tetranuclear alkyltin(Ⅳ) compounds {[R2Sn(C9H8N3O3)O]SnR3}2 [R=n-Bu (1), 4-CNC6H4CH2 (2),C6H5CH2 (3), 4-ClC6H4CH2 (4)] were prepared by the reaction of Schiff base ligand pyruvic acid isonicotinyl hydrazone with (R3Sn)2O in the corresponding molar ratio of 1:1. All compounds have been characterized by elemental analysis, IR and ^1H NMR spectra. The crystal structure of compound 1 was determined by X-ray single crystal diffractional analysis. This compound exhibits a dimeric structure containing distannoxane units with two types of the tin atoms. For the first tin atom, it appears to be seven-coordinated with a distorted pentagonal bipyramid geometry, and the other is five-coordinated with a distorted trigonal bipyramidal geometry. The molecules are packed in the unit cell in two-dimensional network structure through an interaction between the N atoms of the pyridine and the tin atoms of an adjacent molecule.     

Studies on the Synthesis,Crystal Structure and Quantum Chemistry of Di（o-cyanobenzyl）tin Bis（quinoline-2-carboxylate）

Di（o-cyanobenzyl）tin bis（quinoline-2-carboxylate） was synthesized by the reaction of tri（o-cyanobenzyl）tin chloride with quinoline-2-carboxylic acid. The molecular structure of the compound was characterized by elemental analysis, IR, 1H NMR and X-ray diffraction. Crystal data for the compound： tficlinic, space group P1, a = 0.80734（7）, b = 1.00681（9）, c = 1.04811（9） nm, a = 81.7570（10）, β = 7.7240（10）,γ = 81.2850（10）°, V = 0.77581（12） nm3, Z = 1, Dc = 1.488 g/cm3, μ（MoKa） = 0.870 mm^-1 and F（000） = 350. The final R= 0.0204 and wR= 0.0530 for 2677 observed reflections with I 〉2σ（I）, and R = 0.0208 and wR = 0.0532 for all reflections. The molecular structure adopts a distorted octahedral geometry around the Sn atom. The title compound molecules are connected via hydrogen bonding interactions to form a 3D network structure. Quantum chemistry calculation study on the title compound has been performed by means of G98W package at the Lanl2dz basis set. The stability of the compound, orbital energies and some frontier molecular orbital composition characteristics have also been investigated.     

Synthesis,Characterization and Crystal Structure of (PhCH2)2Sn(S2CENt2) and (PhCH2)2Sn(S2CNC4H8)2

Two new dibenzyltin bisditiocarbamates(PhCH2)2 Sn(S2CNEt2)2(1) and (PhCH2)2 Sn(S2CNC4H8)2(2) were synthesized by the reaction of dibenzyltin dichloride with dithiocarbamates and characterized by elemental analysis ,IR,^1H NMR and MS spectra.The crystal structures were determined by X-ray single crystal diffraction analysis.In both complexes,the tin atom is six-coordinated in a distorted octahedral configuration.In the crystals of 1,the molecular packing in unit cell reveals that the two adjacent molecules are symmetrically linked to each other in dimers by two Sn S interactions of 0.3816nm.In the crystals of 2,the molecules are packed in the unit cell in one-dimensional chain structure linked by weaker intermolecular S S conmtacts.     

Synthesis, Spectroscopic Properties and Structural Characterization of Tri（o-chlorobenzyl）tin Ester of 4-Pyridinecarboxylic Acid

The tri(2-chlorobenzyl)tin(IV) complex with 4-pyridinylcarboxylate ligand tri(o-chlorobenzyl)tin ester of 4-pyridinecarboxylic acid has been synthesized by the reaction of tri(2-chlorobenzyl)tin(Ⅳ) chloride with 4-pyridinyl carboxylic acid and characterized by elemental analysis, IR and ^1HNMR, and its crystal structure was determined by X-ray single-crystal diffraction.     

RESEARCH ON TRINUCLEAR MOLYBDENUM CLUSTER COMPOUNDS——CRYSTAL AND MOLECULAR STRUCTURES OF (Et_4N)_2[Mo_3(μ_3-O)(μ_2-Cl)_3(Oac)_2Cl_5]

The title compound forms black crystals shaped like pseudo-octahedrons, which belong to the orthorhombic system The space group is Pna 2_1 with unit cell parametrs of a=17.815(1), b=16.629(2), c=12.003(1), and with Z=4, D_(obs)=1.80g·cm~(-3), and D_(calc)=1.804g·cm~(-3). The crystal structure was solved by the heavy atom method and refiened by fullmatrix least-squares to a final conventional R factor of 0.048 for 2584 unique reflections with I≥σ(Ⅰ). The investigation confirms that the crystal structure consists of tetraethylammonium cations and trinuclear Mo cluster anions. The anion is a μ_3-O monocapped trinuclear cluster with an average Mo-Mo bond length of 2.60 (2). On the side of the Mo_3 triangular plane opposite to the μ_3-O atom, each two Mo atoms are bridged by a Cl atom with the result that these seven atoms (3 Me, 1 O and 3 Cl atoms)form an apex-deficient quasicubane configuration. In addition, each Mo atom is coordinated to three additional atoms resulting in a pseudo-octahedral geome     

Synthesis, Crystal Structure and Quantum Chemistry of Tris[（2-methyl- 2-phenyl）propyl] （2,4-dinitro-phenolato）tin

The tris[(2-methyl-2-phenyl)propyl](2,4-dinitro-phenolato)tin was synthesized by the reaction of bis[tri(2-methyl-2-phenyl)propyltin] oxide with 2,4-dinitrophenol. The compound was characterized by IR, 1H NMR spectra and elemental analysis. The crystal structure has been determined by X-ray diffraction. The crystal belongs to the monoclinic system, space group P21/n with a = 0.9649(0), b = 1.0087(8), c = 3.4867(4) nm, β = 90.965(7) , Z = 4, V = 3.3933(7) nm3, Dc = 1.369 Mg·m-3, (MoKa) = 0.796 mm-1, F(000) = 1440, R = 0.0345 and wR = 0.0821. The tin atom has a distorted tetrahedral geometry. The 2D network structure of the complex is formed by hydrogen bonds and π-π effects. The stabilities, orbital energies and composition characteristics of some frontier molecular orbitals of the complexes have been investigated with the aid of G98W software.     

Synthesis and Structural Characterization of Mono- and Di-nuclear Zinc(Ⅱ) Coordination Compounds of Triphenylphosphoniopropionate

Two novel coordination compounds of Zn(Ⅱ) with Ph3P (CH2)2CO-2(L), namely, [ZnL4(H2O)2]·(ClO4)2·2H2O(compound 1) and [Zn2Cl4(μ-L-O,O′)2](compound 2), have been prepared. The single crystal X-ray structure analysis of these compounds indicates that in compound 1 the Zn(Ⅱ) atom is coordinated by four monodentate carboxylato groups on the equatorial plane and two aqua ligands occupy the axial coordination positions. The pendant oxygen atoms form strong hydrogen bonds with the aqua molecules which results in the stability of this structure. In compound 2, two Zn(Ⅱ) atoms are bridged by a pair of carboxylato groups, showing a skew-bridge mode, and thus enabling a long Zn(Ⅱ)…Zn(Ⅱ) separation. As we know, it is a dinuclear coordination compound with the longest Zn…Zn separation.     

Crystal Structure of 5—（l—Menthyloxy）—3—chloro—4— Pyrrolidinyl—2（5H0—f

The molecular structure of the title compound 5-(l-menthyloxy)-3-chloro-4-pyrrolidinyl-2(5H)-furanone, C18H28ClNO3(Ⅰ), has been determined by X-ray diffraction at 296(1)K. The crystal is monoclinic with space group P21, a=9.457(3), b=10.413(3), c=9.525(2), β=95.19(2)°, V=934(1) 3, Z=2, Mr=341.88, Dx=1.22 g/cm3, μ=2.15 cm-1, F(000)=368. The final R factor is 0.059, and Rw is 0.065 for 1020 observed reflections with I≥3σ(I). The absolute configuration at C(14) of the acetal carbon was proved to be S, taking into account the known configuration of 1R, 2S, 5R-menthyl moiety. There are three rings in the molecule of this compound: the furanone ring, the pyrrolidine ring and the mentholoxy group ring. The franone ring is connected with the pyrrolidine ring and the mentholoxy ring by N atom and μ2-O bridge atom respectively.     

Studies on the Synthesis,Crystal Structure and Quantum Chemistry of Di(o-cyanobenzyl)tin Bis(quinoline-2-carboxylate)

Di(o-cyanobenzyl)tin bis(quinoline-2-carboxylate)was synthesized by the reaction of tri(o-cyanobenzyl)tin chloride with quinoline-2-carboxylic acid.The molecular structure of the compound Was characterized by elemental analysis,IR,1H NMR and X-ray diffraction.Crystal data for the compound:triclinic,space group P1,a=0.80734(7),b=1.00681(9),c=1.04811(9)nm,α=81.7570(10),β=7.7240(10),γ=81.2850(10)°,V=0.77581(12)nm3,Z=1,Dc=1.488 g/cm3,μ(MoKa)=0.870 mm-1 and F(000)=350.1 The final R=0.0204 and wR=0.0530 for 2677 observed reflections with I＞2σ(I),and R=0.0208 and wR=0.0532 for all reflections.The molecular structure adopts a distorted octahedral geometry around the Sn atom.The title compound molecules are connected via hydrogen bonding interactions to form a 3D network structure.Quantum chemistry calculation study on the title compound has been performed by means of G98W package at the Lanl2dz basis set.The stability of the compound,orbital energies and some frontier molecular orbital composition characteristics have also been investigated.     

One-dimensional Infinite Chain Organotin Compounds: Synthesis and Structural Characterization of Triphenyltin Thiazole-2-carboxylate and Triphenyltin 3-Pyridinylcarboxylate

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A three‐dimensional polymeric potassium complex of 5‐sulfonobenzene‐1,2,4‐tricarboxylic acid: poly[μ‐aqua‐aqua‐μ9‐(2,4‐dicarboxy‐5‐sulfonatobenzoato)‐dipotassium(I)]

The asymmetric unit in the structure of the title compound, [K₂(C₉H₄O₉S)(H₂O)₂]_n, consists of two eight‐coordinated K^I cations, one 2,4‐dicarboxy‐5‐sulfonatobenzoate dianion (H₂SBTC²⁻), one bridging water molecule and one terminal coordinated water molecule. One K^I cation is coordinated by three carboxylate O atoms and three sulfonate O atoms from four H₂SBTC²⁻ ligands and by two bridging water molecules. The second K^I cation is coordinated by four sulfonate O atoms and three carboxylate O atoms from five H₂SBTC²⁻ ligands and by one terminal coordinated water molecule. The K^I cations are linked by sulfonate groups to give a one‐dimensional inorganic chain with cage‐like K₄(SO₃)₂ repeat units. These one‐dimensional chains are bridged by one of the carboxylic acid groups of the H₂SBTC²⁻ ligand to form a two‐dimensional layer, and these layers are further linked by the remaining carboxylate groups and the benzene rings of the H₂SBTC²⁻ ligands to generate a three‐dimensional framework. The compound displays a photoluminescent emission at 460 nm upon excitation at 358 nm. In addition, the thermal stability of the title compound has been studied.     

Synthesis,structural characterization and cytotoxic activity of triorganotin 5‐(salicylideneamino)salicylates

Six new triorganotin complexes ( 1a – 1c and 2a – 2c ) of 5‐(salicylideneamino)salicylic acid, [5‐(3‐X‐2‐HOC₆H₃CH═N)‐2‐HOC₆H₃COO]SnR₃ (X = H, 1 ; CH₃O, 2 ; R = Ph, a ; Cy, b ; CH₂C(CH₃)₂Ph, c ), have been synthesized by one‐pot reaction of 5‐aminosalicylic acid, salicylaldehyde and triorganotin hydroxide and characterized using elemental analysis and infrared and NMR (¹H, ¹³C and ¹¹⁹Sn) spectra. The crystal structures of 1a , 1b , 2a ·CH₃OH, 2b ·CH₃OH and 2c ·CHCl₃ have been determined using single‐crystal X‐ray diffraction. In non‐coordinated solvent CDCl₃, the tin atoms in the complexes are all four‐coordinated. In the crystalline state, these compounds adopt a four‐ or five‐coordination mode. Complex 1a exhibits a 44‐membered macrocyclic tetrameric structure with trigonal bipyramidal geometry around the tin atoms in which the axial positions are occupied by the oxygen atom of carboxylate group of the ligand and the phenolic oxygen atom from the adjacent ligand. The coordination geometry of tin atom in 1b and 2c ·CHCl₃ is a distorted tetrahedron shaped by three carbon atoms of alkyl groups and a carboxylate oxygen atom of the ligand. In 2a ·CH₃OH and 2b ·CH₃OH, the tin atom has a distorted trans‐C₃SnO₂ trigonal bipyramidal geometry formed by three alkyl groups, a monodentate carboxylate group and a coordinated methanol molecule. The molecules of 2a ·CH₃OH and 2b ·CH₃OH are linked via O─H···O hydrogen bonds into a one‐dimensional supramolecular chain and a centrosymmetric R₄⁴(22) macrocycle, respectively. Bioassay results against two human tumor cell types (A549 and HeLa) show the complexes are efficient cytostatic agents and may be explored as potential antitumor drugs.     

Coordination polymers based on building blocks of dimethyltin(IV) Chloride iso‐thiocyanate and dimethyltin(IV) di‐iso‐thiocyanate with pyrazine‐2‐carboxylate and 4, 4′‐bipyridine

The reaction of 4,4′‐bipy with dimethyltin(IV) chloride iso‐thiocyanate affords the one‐dimensional (1D) coordination polymer, [Me₂Sn(NCS)Cl·(4,4′‐bipy)]_n ( 1 ), whereas reaction of dimethyltin(IV) dichloride with sodium pyrazine‐2‐carboxylate in the presence of potassium iso‐thiocyanate affords the two‐dimensional (2D) coordination polymer, {[Me₂Sn(C₄H₃N₂COO)₂]₂ [Me₂Sn(NCS)₂]}_n ( 2 ). Both coordination polymers were characterized by elemental analysis and infrared spectroscopy in addition to ¹H and ¹³C NMR spectroscopy of the soluble coordination polymer ( 1 ). A single‐crystal structure determination showed that the asymmetric unit in 1 contains Me₂Sn(NCS)Cl and 4,4′‐bipy moieties and a 1D infinite rigid chain structure forms through bridging of the 4,4′‐bipy ligand between tin atoms and the geometry around the tin atom is a distorted octahedral. Coordination polymer 2 contains two distinct tin atom geometrics in which one tin atom is seven coordinate, and the other is six coordinate. The two tin atom environments are best described as a pentagonal bipyramidal in the former and distorted octahedral in the latter where the carboxylate groups bridge the two tin atoms and construct a 2D‐coordination polymer. The ¹¹⁹Sn NMR spectroscopy indicates the octahedral geometry of 1 retains in solution. © 2011 Wiley Periodicals, Inc. Heteroatom Chem 22:699–706, 2011; View this article online at wileyonlinelibrary.com . DOI 10.1002/.20736     

catena‐Poly[[[triaquazinc(II)]‐μ‐2‐nitroterephthalato‐κO1:κ2O4,O4′] monohydrate]

The title complex, {[Zn(C₈H₃NO₆)(H₂O)₃]·H₂O}_n, has a one‐dimensional chain structure. The two carboxylate groups of the dianionic 2‐nitroterephthalate ligand adopt mono‐ and bidentate chelating modes. The Zn atom shows distorted octahedral coordination, bonded to three O atoms from two carboxylate groups and three O atoms of three non‐equivalent coordinated water molecules. The one‐dimensional chains are aggregated into two‐dimensional layers through inter‐chain hydrogen bonding. The whole three‐dimensional structure is further stabilized by inter‐layer hydrogen bonds.     

Poly[[aqua(4,4′‐diazenediyldibenzoato‐κ4O,O′:O′′,O′′′)cadmium(II)]: a twofold interpenetrated three‐dimensional coordination polymer of PtS topology

In the title coordination compound, [Cd(C₁₄H₈N₂O₄)(H₂O)]_n, the Cd^II cation and the coordinated water molecule lie on a twofold axis, whereas the ligand lies on an inversion center. The Cd^II center is five‐coordinated in a distorted square‐pyramidal geometry by four carboxylate O atoms from four different 4,4′‐diazenediyldibenzoate (ddb) anions and one water O atom. The three‐dimensional frameworks thus formed by the bridging ddb anions interpenetrate to generate a three‐dimensional PtS‐type network. Additionally, the coordination water molecule and the carboxylate O atom form a hydrogen‐bonding interaction, stabilizing the three‐dimensional framework structure.     

Poly[[triaquazinc(II)]‐μ3‐4‐nitrophthalato‐κ3O1:O2:O2′]

In the title complex, [Zn(C₈H₃NO₆)(H₂O)₃]_n, the two carboxylate groups of the 4‐nitrophthalate dianion ligands have monodentate and 1,3‐bridging modes, and Zn atoms are interconnected by three O atoms from the two carboxylate groups into a zigzag one‐dimensional chain along the b‐axis direction. The Zn atom shows distorted octahedral coordination as it is bonded to three O atoms from carboxylate groups of three 4‐nitrophthalate ligands and to three O atoms of three non‐equivalent coordinated water molecules. The one‐dimensional chains are aggregated into two‐dimensional layers through inter‐chain hydrogen bonding. The whole three‐dimensional structure is further maintained and stabilized by inter‐layer hydrogen bonds.     

Poly[bis(μ‐5‐iodoisophthalato)(methanol)dilead(II)] exhibiting a novel centrosymmetric rhombus‐shaped I4 unit

The asymmetric unit of the title compound, [Pb₂(C₈H₃IO₄)₂(CH₄O)]_n, contains two Pb^II atoms, two 5‐iodoisophthalate (5‐IIP²⁻) ligands and one coordinated methanol molecule. One Pb atom is eight‐coordinated, surrounded by seven carboxylate O atoms from five 5‐IIP²⁻ ligands and one O atom from the terminal methanol ligand. The other Pb atom is seven‐coordinated in a hemidirected geometry, surrounded by seven carboxylate O atoms from five 5‐IIP²⁻ ligands. Both Pb atoms are connected by carboxylate groups to form a one‐dimensional infinite rod along the a axis; neighbouring rods are further linked by the aromatic rings of 5‐IIP²⁻ to generate the final three‐dimensional structure with channels in the a direction. An O—H...O hydrogen bond between the methanol ligand and one of the carboxylate groups of a 5‐IIP²⁻ ligand stablizes the three‐dimensional framework. Interestingly, a centrosymmetric rhombus‐shaped I₄ unit is formed by four 5‐IIP²⁻ ligands, with I...I distances of 3.8841 (8) and 3.9204 (8) Å.     

A novel helical copper complex: catena‐poly[[[aquacopper(II)]‐μ‐N‐(3‐carboxy‐2‐oxidobenzylidene‐κO2)glycinato‐κ3N,O′:O′] monohydrate]

In the polymeric title compound, {[Cu(C₁₀H₇NO₅)(H₂O)]·H₂O}_n, the Cu atom adopts a square‐based pyramidal coordination involving a N,O,O′‐tridentate glycine dianionic ligand, a water O atom and an apical bridging carboxylate O atom from an adjacent ligand. The title compound also adopts a carboxylate‐bridged chain structure. The molecular chain propagates in a helical fashion along the b axis of the monoclinic unit cell. Neighbouring chains are linked together to form a three‐dimensional network via hydrogen‐bonding interactions between coordinated and uncoordinated water molecules and O atoms of the bridging carboxylate groups.     

[Bis(3,5‐dimethylpyrazol‐1‐yl‐κN2)dithioacetato‐κS](triphenylphosphine‐κP)copper(I)

In the title compound, [Cu(C₁₂H₁₅N₄S₂)(C₁₈H₁₅P)], the copper(I) center is tetrahedrally coordinated by one S atom and two N atoms from one bis(3,5‐dimethylpyrazol‐1‐yl)dithioacetate ligand and one P atom from a triphenylphosphine ligand. In the crystal structure, adjacent pyrazole rings are involved in weak π–π interactions, thereby forming a one‐dimensional zigzag chain running along the b axis.