192 research outputs found
Bis[(4-methylphenyl)ethynyl] telluride
The tellurium atom in the title bis-ethynyl telluride, Te(C9H7)2 or C18H14Te, is located on a crystallographic twofold axis, the C—Te—C angle being 92.23 (15)°. The dihedral angle between the rings is 87.27 (7)°. In the crystal structure, molecules are connected in chains parallel to the b axis and mediated by C—H⋯π interactions
2-(4-Methoxyphenylsulfinyl)cyclohexan-1-one
The cyclohexanone ring in the title compound, C13H16O3S, is in a distorted chair conformation. The intramolecular S⋯Ocarbonyl distance is 2.814 (2) Å. Molecules are connected into a two-dimensional array via C—H⋯O contacts involving the carbonyl and sulfinyl O atoms
1-(4-Bromophenyl)-2-ethylsulfinyl-2-(phenylselanyl)ethanone monohydrate
In the title hydrate, C16H15BrO2SSe·H2O, the sulfinyl O atom lies on the opposite side of the molecule to the Se and carbonyl O atoms. The benzene rings form a dihedral angle of 51.66 (17)° and are splayed with respect to each other. The observed conformation allows the water molecules to bridge sulfinyl O atoms via O—H⋯O hydrogen bonds, generating a linear supramolecular chain along the b axis; the chain is further stabilized by C—H⋯O contacts. The chains are held in place in the crystal structure by C⋯H⋯π and C—Br⋯π interactions
A new non-covalent bonding mode in supramolecular chemistry: main group element lone-pair- [small pi] (arene) interactions
Main group metal lone-pair⋯π(arene) interactions: a new bonding mode for supramolecular associations
Crystal structures of the heavier main group elements in low oxidation states have been evaluated for the
presence of supramolecular elementIJlp)⋯π(arene) interactions that are structure-directing. It is revealed
that when present, these interactions lead to zero-dimensional, binuclear aggregates but higher-nuclearity
species are sometimes observed, with one-dimensional supramolecular chains of varying topology being
prominent. By contrast, two-dimensional aggregation based on elementIJlp)⋯π(arene) interactions are rare.
In summary, interactions of main group metal lone-pairs with aromatic rings are revealed as synthons capable
of assembling molecules into supramolecular aggregates
An inorganic helix in the supramolecular structure of trimethyltin diphenylarsinate, [me3sn(o2asph2)]n: a structural comparison of triorganotin arsinates and phosphinates
The crystallographic structure analysis of [Me3Sn(O2AsPh2)]n reveals
supramolecular association owing to symmetric bridges between Me3Sn
centres afforded by O2AsPh2 groups. The resulting polymer has a helical
topology. A systematic analysis of triorganotin arsinato and phosphinato
analogues indicates a role for the remote substituents on aggregations patterns
1-Methyl-3-phenylsulfonyl-2-piperidone
The piperidone ring in the title compound, C12H15NO3S, has a slightly distorted half-chair conformation with the methyl, carbonyl and phenylsulfonyl ring substituents occupying equatorial, equatorial and axial positions, respectively. Molecules are connected into centrosymmetric dimers via C—H⋯O interactions and these associate into layers via C—H⋯O—S contacts. Further C—H⋯O interactions involving both the carbonyl and sulfonyl O atoms consolidate the crystal packing by providing connections between the layers
Methyl 3-[(1-benzyl-4-phenyl-1H-1,2,3-triazol-5-yl)formamido]propanoate: crystal structure, Hirshfeld surface analysis and computational chemistry
Synthesis of 1,3-diynes via detelluration of bis(ethynyl)tellurides
The synthesis of symmetric conjugated diyne systems with electron-withdrawing or electron-donating substituents via a palladium-catalyzed detelluration of bis(arylethynyl)tellurides and bis(alkylethynyl)tellurides is described. This procedure is effected under atmospheric conditions in DMF using Pd(OAc)2 as a catalyst and AgOAc as an additive in the presence of triethylamine. This route offers efficient access to conjugated diyne systems in short reaction time. X-ray crystallographic structure and solid-state conformation of bis(p-tolylethynyl)telluride show a supramolecular chain aligned along the b axis, sustained by C-H...π interactions.Neste artigo é descrita a síntese de sistemas diínicos conjugados contendo substituintes elétronatratores e elétron-doadores via a deteluração catalizada por paládio de bis-(ariletinil)teluretos e bis-(alquiletinil)teluretos. Este procedimento foi realizado sob condições atmosféricas em DMF usando Pd(Oac)2 como catalisador e AgOAc como um aditivo na presença de trietilamina. Esta rota oferece acesso eficiente a sistemas diínicos conjugados em um curto período de tempo. A estrutura cristalográfica por difração de raios X do telureto de bis(p-toluiletinila) e a conformação no estado sólido mostram uma cadeia supramolecular alinhada ao longo do eixo b, sustentada por interações CH...π.FAPESPCNP
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