Ionic Liquid Crystals Based on Loop-Shaped Copper(I) Complexes.

This paper describes the synthesis and characterization of liquid crystals based on loop-shaped cationic copper(I) complexes of a multidentate ligand. Their synthesis involves the one-pot reaction of an alkyloxy-decorated pyridine-aldehyde unit with a diamine (2,2'-(ethylenedioxy)bis(ethylamine)) spacer to form in situ a pyridine-imine quadridentate-N-donor ligand, L, which is able to chelate a copper(I) center associated with various noncoordinating anions. All of these compounds were characterized by NMR, IR, and electronic absorption spectroscopy, and more particularly by X-ray diffraction and mass spectroscopy, enabling unambiguous assignment of the [ML] mononuclear nature of the cationic components.

Crossmodal Congruency Between Background Music and the Online Store Environment: The Moderating Role of Shopping Goals.

Despite the robust evidence that congruent background music in the physical store environment positively affects consumer reactions, less is known about its effects in an online context. The present study aims (1) to examine whether congruency via multiple elicited crossmodal correspondences between background music and the online store environment (e.g.

Modified pyridine-triazole and 2,2'-bipyrimidine ligands generating robust titanium complexes constructed around a TiON core.

The synthesis and characterisation of novel chelate nitrogen ligands with phasmidic tails (pyridine-triazole ligand 1b; 2,2'-bipyrimidine ligands 2b and 3b) as well as their titanium(IV) coordination complexes are reported. The analogous ligands 1a, 2a and 3a with methoxy substituents instead of the tails were also synthesized, together with titanium complexes that could be crystallographically characterised. A good agreement is noticed between analytical data of the complexes in solution (NMR) and in the solid state (X-ray diffraction).

Bistable spin-crossover in a new series of [Fe(BPP-R)] (BPP = 2,6-bis(pyrazol-1-yl)pyridine; R = CN) complexes.

Spin-crossover (SCO) active transition metal complexes are a class of switchable molecular materials. Such complexes undergo hysteretic high-spin (HS) to low-spin (LS) transition, and vice versa, rendering them suitable for the development of molecule-based switching and memory elements. Therefore, the search for SCO complexes undergoing abrupt and hysteretic SCO, that is, bistable SCO, is actively carried out by the molecular magnetism community.

A robust Ti(iv)-based mesogen constructed around a TiON core.

Stable complexes [Ti(1a)(2)2] and [Ti(1b)(2)2], where 2 is the 6,6'-diphenyl-2,2'-biphenolato ligand and 1a and 1b ligands are 2,2'-bipyrimidine derivatives, are synthesized. The complex [Ti(1b)(2)2] containing a diimine ligand substituted with long alkyl chains (C16) exhibits a liquid crystal behaviour. This property and self-assembling in the crystalline state are explained by the particular molecular conformation of the complexes.

Ionic liquids at the surface of graphite: Wettability and structure.

The aim of this work is to provide a better understanding of the interface between graphite and different molecular and ionic liquids. Experimental measurements of the liquid surface tension and of the graphite-liquid contact angle for sixteen ionic liquids and three molecular liquids are reported. These experimental values allowed the calculation of the solid/liquid interfacial energy that varies, for the ionic liquids studied, between 14.

Intercalation synthesis of functional hybrid materials based on layered simple hydroxide hosts and ionic liquid guests--a pathway towards multifunctional ionogels without a silica matrix?

Functional hybrid materials on the basis of inorganic hosts and ionic liquids (ILs) as guests hold promise for a virtually unlimited number of applications. In particular, the interaction and the combination of properties of a defined inorganic matrix and a specific IL could lead to synergistic effects in property selection and tuning. Such hybrid materials, generally termed ionogels, are thus an emerging topic in hybrid materials research.

Mesomorphic imidazolium salts: new vectors for efficient siRNA transfection.

The preparation of chloride (1(n)) and bromide (2(n)) derivatives of 1-methyl-3-[3,4-bis(alkoxy)benzyl]-4H-imidazolium with n = 6, 12, 16, 18 is described. The two series of salts possess a rich thermotropic mesomorphism, chain-length dependent. Thus, a lamellar smectic A phase, a bicontinuous cubic Ia3d phase, and a columnar hexagonal liquid crystalline mesophase are induced as a function of increasing chain length.

1-(4-Alkyloxybenzyl)-3-methyl-1H-imidazol-3-ium organic backbone: a versatile smectogenic moiety.

The merger of ionic liquid and liquid crystal fields, obtained by using the imidazolium ring as a common element, has allowed us to tailor a new set of materials which associate specific functionalities. These functionalities are consequences of the original properties of the component, ionic liquids, liquid crystals and their association in a single compound. The study of this interesting association led us to elaborate environment-flexible cationic architectures from which mesomorphic properties emerge.

A convenient method for preparing rigid-core ionic liquid crystals.

An efficient, solvent free method for the N-arylation of imidazole by 1-(dodecyloxy)-4-iodobenzene using Cu(II)-NaY as catalyst and K(2)CO(3) as base is reported. By this synthetic approach, mesomorphic 3-[4-(dodecyloxy)phenyl]-1-methyl-1H-imidazol-3-ium iodide was synthesized in a two-step procedure, and its mesomorphism has been fully investigated by polarised optical microscopy, differential scanning calorimetry and X-ray diffraction. In addition its lamellar crystal structure, electrochemical behaviour and UV (absorption and emission) properties are reported.

Wormlike micelles from a cage amine metallosurfactant.

We have shown that copper and cobalt metallosurfactants derived from Cu(II) and Co(III) complexes of a macrobicyclic hexamine ("cage") can form wormlike micelles in aqueous solution that may coexist with or easily interconvert with vesicle structures. The cylindrical micelle structures are unusual for triple-chain surfactants with a single headgroup and are not easily accounted for using geometrical packing arguments. The solution behavior has been characterized by cryo-TEM and SAXS measurements.

Selective oxidation of a single primary alcohol function in oligopyridine frameworks.

A variety of mono-oxidized pyridine, bipyridine, terpyridine, and pyridine/pyridazine are readily prepared under mild conditions using Pyrolusite MnO2. This phase has been characterized by means of X-ray powder diffraction and scanning electron microscopy. The oxidative activity is in keeping with the nature, morphology, and surface area of the MnO2 reagent.

Mesomorphic phenanthroline derivatives: novel architectures based on hydrogen bonding.

Strong hydrogen bonding has been observed in mesomorphic phenanthroline compounds engineered from diacylaminobenzene platforms: a columnar organization is found in the free ligands (n = 12 or 16) whereas a smectic arrangement is evidenced in a palladium complex (n = 16).

Cation-Induced Macroscopic Ordering of Non-Mesomorphic Modules-A New Application for Metallohelicates.

The subtle balance between organized and chaotic domains in the nondiscoidal ligand in the helicate 1, which displays liquid crystalline properties, represents the key element which enables the local molecular architecture to be integrated into an organized macroscopic ensemble.

π-Stacked ortho-Palladated Bipyridine Complexes Exhibiting Unusual Liquid Crystalline Behavior.

A columnar structure with lamellar morphology in the liquid crystalline state is displayed by the palladium complex salt 1, which is synthesized from nonmesogenic ligands.