Triclinic modification of di-n-butyl­bis(2-hydroxy­benzoato-κ 2 O 1,O 1′)tin(IV)

The Sn atom in the title compound, [Sn(C4H9)2(C7H5O3)2], is chelated by the carboxyl­ate groups of 2-hydroxy­benzoate liagnds, and exists in a six-coordinate skew-trapezoidal bipyramidal coordination geometry [C—Sn—C = 140.1 (3)°]

(μ-Piperazine-1,4-dicarbodithioato-κ4 S,S′:S′′,S′′′)bis­[triphenyl­tin(IV)] dichloro­methane solvate

The dinuclear centrosymmetric title compound, [Sn2(C6H5)6(C6H8N2S4)]·CH2Cl2, features a distorted cis-trigonal–bipyramidal coordination geometry for Sn based on a C3S2 donor set. The dinuclear mol­ecule lies across a centre of inversion. The solvent dichloro­methane mol­ecule is disordered about a centre of inversion

(Ethanol-κO)[2-(4-hydroxy­phen­yl)quinoline-4-carboxyl­ato-κO]triphenyl­tin(IV)

The Sn atom in the title mol­ecule, [Sn(C6H5)3(C16H10NO3)(C2H6O)], shows a trans-C3SnO2 trigonal bipyramidal coord­in­ation. Adjacent mol­ecules are linked by O—H⋯O and O—H⋯N hydrogen bonds into a two-dimensional array parallel to (100). The ethanol ligand is disordered, with two sites of equal occupancy being resolved for the ethyl group

μ-1,2-Di-4-pyridylethane-κ2 N:N′-bis­[bis­(N,N-diisopropyl­dithio­carbamato-κ2 S,S′)zinc(II)]

In the dinuclear title compound, [Zn{S2CN(n-Pr)2}2{(NC5H4)CH2CH2(C5H4N)}] or [Zn2(C7H14NS2)4(C12H12N2)], each Zn atom adopts a distorted trigonal–bipyramidal ZnNS4 geometry. The crystal structure involves intermolecular C—H⋯S hydrogen bonds

Perplexing Coordination Behaviour of Potentially Bridging Bipyridyl-Type Ligands in the Coordination Chemistry of Zinc and Cadmium 1,1-Dithiolate Compounds

The X-ray structural chemistry of zinc and cadmium 1,1-dithiolates (for example, xanthate, dithiophosphate and dithiocarbamate) with potentially bridging bipyridyl-type ligands (for example, 4,40-bipyridine) is reviewed. For zinc, the xanthates and dithiophosphates uniformly form one-dimensional coordination polymers, whereas the zinc dithiocarbamates are always zero-dimensional, reflecting the exceptional chelating ability of dithiocarbamate ligands compared with xanthates and dithiophosphates. For cadmium, one-dimensional coordination polymers are usually found, reflecting the larger size of cadmium compared with zinc, but zero-dimensional aggregates are sometimes found. Steric effects associated with the 1,1-dithiolate-bound R groups are shown to influence supramolecular aggregation and, when formed, polymer topology in order to reduce steric hindrance; the nature of the bipyridyl-type ligand can also be influential. For the dithiocarbamates of both zinc and cadmium, in instances where the dithiocarbamate ligand is functionalised with hydrogen bonding potential, extended supramolecular architectures are often formed via hydrogen bonding interactions. Of particular interest is the observation that the bipyridyl-type ligands do not always bridge zinc or cadmium 1,1-dithiolates, being monodentate instead, often in the presence of hydrogen bonding. Thus, hydroxyl-O–H . . . N(pyridyl) hydrogen bonds are sometimes formed in preference toM N(pyridyl) coordinate-bonds, suggesting a competition between the two modes of association

Adventures in crystal engineering

Crystals are all around us and are aesthetically pleasing as they arise from the ordered, three-dimensional assembly of chemical species which can be minerals (e.g. salt), macromolecules (e.g. proteins) or smaller chemical species (e.g. drugs, natural products, coordination complexes, etc.). Scientists need to know the precise structure of all these materials in order to rationalise the way they work. To put it in another way, “structure determines function”. Single-crystal X-ray crystallography is the crucial technique behind the determination of crystal structure. Despite the prevalence and obvious importance of crystals, what remains an enormous challenge in contemporary science is to answer the fundamental question of “How do crystals form?”. The goal of crystal engineering is to control the way molecules self-assemble in the condensed phase and the present discussion relates to this topic, an on-going research programme undertaken at Sunway University

Exploring the topological landscape exhibited by Binary Zinc-triad 1,1-dithiolates

The crystal chemistry of the zinc-triad binary 1,1-dithiolates, that is, compounds of xanthate [−S2COR], dithiophosphate [−S2P(OR)2], and dithiocarbamate [−S2CNR2] ligands, is reviewed. Owing to a wide range of coordination modes that can be adopted by 1,1-dithiolate anions, such as monodentate, chelating, μ2-bridging, μ3-bridging, etc., there exists a rich diversity in supramolecular assemblies for these compounds, including examples of zero-, one-, and two-dimensional architectures. While there are similarities in structural motifs across the series of 1,1-dithiolate ligands, specific architectures are sometimes found, depending on the metal centre and/or on the 1,1-dithiolate ligand. Further, an influence of steric bulk upon supramolecular aggregation is apparent. Thus, bulky R groups generally preclude the close approach of molecules in order to reduce steric hindrance and therefore, lead to lower dimensional aggregation patterns. The ligating ability of the 1,1-dithiolate ligands also proves crucial in determining the extent of supramolecular aggregation, in particular for dithiocarbamate species where the relatively greater chelating ability of this ligand reduces the Lewis acidity of the zinc-triad element, which thereby reduces its ability to significantly expand its coordination number. Often, the functionalisation of the organic substituents in the 1,1-dithiolate ligands, for example, by incorporating pyridyl groups, can lead to different supramolecular association patterns. Herein, the diverse assemblies of supramolecular architectures are classified and compared. In all, 27 structurally distinct motifs have been identified

Phosphinegold(I) Thiolates – Pharmacological Use and Potential

A brief overview of the use of gold compounds in medicine, namely in the treatment of rheumatoid arthritis is presented, including that of the orally-administered triethylphosphinegold(I) tetraacetylatedthioglucose species, auranofin. A summary of an evaluation for anti-arthritic activity of novel phosphinegold(I) thiolate analogues containing biologically active thiols is given. This shows that compounds with greater efficacy and reduced toxic side-effects, at least in the in vivo model studied, can be developed. More recent investigations on this class of compound have focussed on their putative anti-tumour activity. Significant cytotoxicity and apparent cellular specificity have been discovered for certain phosphinegold(I) thiolates carrying water-solubilising groups. All indications are there that the continued exploration of the medicinal properties of phosphinegold(I) thiolates offers very real opportunities in metallotherapeutics

catena-Poly[[tetra­aqua­copper(II)]-μ-tri­thionato-κ2 O:O′]

The title supra­molecular polymer, [Cu(S3O6)(H2O)4]n, features a tetra­gonally distorted octa­hedral CuII centre within an O6 donor set with the longer Cu—O bonds linking the dication and the trithio­nate dianion. Extensive O—H⋯O hydrogen-bonding inter­actions connect the supra­molecular chains into a three-dimensional network