Synthesis and characterization of bis(2-aminophenyl)disulphide diimine derivatives and their ruthenium complexes

Condensation of bis(2-aminophenyl)disulphide with aromatic aldehydes yielded the corresponding dithiophenyldiimines. Dinuclear ruthenium complexes were obtained by reacting the diimines (3) [bis(3-nitrobenzaldehyde)-phenyldisulphide diimine], (5) [bis(2-chlorobenzaldehyde)-phenyldisulphide diimine], (8) [bis(2-methoxybenzaldehyde)-phenyldisulphide diimine] and (9) [bis(2-hydroxybenzaldehyde)-phenyldisulphide diimine], with RuCl₃ in the presence of L (L=2,2-bipyridine, 1,10-phenanthroline, 3,4-diaminotoluene, pyridine and PPh₃) in EtOH. The two metal centres, connected through bridging chlorides, are in octahedral environments with one metal centre coordinated to sulphur and water while the other is coordinated to L.     

Benzoboroxoles as efficient glycopyranoside-binding agents in physiological conditions: structure and selectivity of complex formation

In contrast to normal boronic acids, o-hydroxymethyl phenylboronic acid (benzoboroxole) has the capability of complexing glycopyranosides efficiently in neutral water. The measurement of association constants with a panel of model hexopyranosides indicates that the preferred mode of binding is through a cis-3,4-diol, such as that found in galactopyranosides, and mass spectrometric studies support a 1:1 binding stoichiometry. The complexation of glucopyranosides is weaker, and they are bound through their 4,6-diol unit. Although several factors may explain the exceptional carbohydrate-binding behavior of this class of hemiboronic acids, the relatively high Lewis acidity of benzoboroxoles is a likely contributing factor along with subtle factors such as intramolecular hydrogen bonds with other hydroxyl groups in the resulting anionic complex. These results with hexopyranosides suggest that biologically relevant cell-surface oligosaccharides could be targeted in water using oligomeric benzoboroxole receptors.     

An Efficient Low‐Temperature Stille–Migita Cross‐Coupling Reaction for Heteroaromatic Compounds by Pd–PEPPSI–IPent

The reactivity of Pd–PEPPSI (Pyridine, Enhanced, Precatalyst, Preparation, Stabilization, and Initiation) precatalysts in the Stille–Migita cross‐coupling reaction between heteroaryl stannanes and aryl or heteroaryl halides was evaluated. In general, Pd–PEPPSI–IPent (IPent=diisopentylphenylimidazolium derivative) demonstrated high efficiency over a variety of challenging aryl or heteroaryl halides with thiophene‐, furan‐, pyrrole‐, and thiazole‐based organostannanes when compared with Pd–PEPPSI–IPr (IPr=diisopropylphenylimidazolium derivative). The transformations proceeded at appreciably lower temperatures (30–80 °C) than triarylphosphine‐based Pd catalysts, improving the scope of this useful carbon–carbon bond‐forming process.     

Palladium(II) complexes of (t-butyl salicylidene) diphenyl disulfide diamine: synthesis,structure, spectral characterization and catalytic properties

The hexadentate N₂S₂O₂ donor ligand N,N’-bis(3,5-tert-butylsalicylidene) diphenyl disulfide-2,2’-diamine was synthesised by the condensation of 2-aminophenyl disulfide and 3,5-di-tert-butyl-2-hydroxybenzaldehyde and its molecular structure was confirmed by X-ray studies. One of the tert-butyl groups in the Schiff base has rotational disorder around the C–C bond with ratio 0.56:0.44. The palladium complexes were prepared by the direct reaction of PdCl₂(CH₃CN)₂ and Schiff base ligands N,N’-bis (5-tert-butylsalicylidene) diphenyl disulfide-2,2’-diamine and N,N’-bis(3,5-tert-butylsalicylidene) diphenyl disulfide-2,2’-diamine, respectively. The structure of the metal complexes was characterized by physico-chemical and spectroscopic methods. Palladium is in square-planar geometry bonded to imine nitrogen and phenolic O in both the complexes. The catalytic efficiency of the palladium complexes was evaluated in the cross-coupling reactions; Heck-Mizoroki reaction of iodobenzene and methyl acrylate and the Suzuki-Miyaura reaction of phenylboronic acid and iodobenzene, which gave low to moderate yields. Higher conversions were obtained for 2a as catalyst due to the increase in the number of bulky tertiary butyl groups in the structure.

     

An improved class of sugar-binding boronic acids, soluble and capable of complexing glycosides in neutral water

This study describes a new class of carbohydrate-binding boronic acids. ortho-Hydroxymethyl phenylboronic acid (boronophthalide) was shown to be superior to the well-established dialkylamino ("Wulff-type") analogues, and it is more soluble in aqueous solvents. The most significant finding in this work is the surprising ability of ortho-hydroxyalkyl arylboronic acids to complex model glycopyranosides under physiologically relevant conditions. These boronic acid units appear to complex hexopyranosides mainly using their 4,6-diol. This behavior is significant because a majority of cell-surface glycoconjugates present free 4,6-diols. Thus, conjugatable forms of these boronic acids could be used in the design of oligomeric receptors and sensors to exploit multivalency effects. Such receptors could dramatically expand the potential of boronic acids toward the selective recognition of cell-surface glycoconjugates.     

Investigation of nonspecific effects of different dyes in the screening of labeled carbohydrates against immobilized proteins

[structure: see text] Carbohydrates play an important role in life processes, and combinatorial chemistry can provide useful sources of thousands of synthetic carbohydrates as potential ligands for biological receptors. To accelerate the detection of positive hits arising from specific interactions between a carbohydrate and a protein, the use of fluorescent dyes can serve as a reliable detecting tool. A study of labeled carbohydrates to lectins conjugated to a solid-support shows that succinimidyl 6-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino)hexanoate (NBD-X) dye provides by far the lowest level of nonspecific interaction with immobilized protein. This observation is in stark contrast with the commonly used labeling reagents constituted of charged and aromatic groups, for instance, FITC and TAMRA dyes.     

Heat Release Imaging in Turbulent Premixed Ethylene-Air Flames Near Blow-off

The focus of this work is to visualise the regions of CH₂O and heat release (HR) of an unconfined turbulent premixed bluff body stabilised ethylene-air flame at conditions approaching lean blow-off using simultaneous imaging of OH- and CH₂O-PLIF. The HR regions are estimated from the product of the OH and CH₂O profiles. At conditions near blow-off, wide regions of CH₂O are observed inside the recirculation zone (RZ). The presence of CH₂O and HR inside the RZ is observed to follow fragmentation of the downstream flame parts near the top of the RZ. The presence of wide regions void of both OH and CH₂O inside the RZ at conditions very close to blow-off indicates the possible entrainment of un-reacted gases into the RZ. The behaviour of the lean ethylene-air flame with Lewis number (Le) greater than 1 is compared to that of a lean methane-air flame with Le of approximately 1. For both fuels, qualitatively similar observations of flame fragmentation downstream followed by build-up of CH₂O and HR inside the RZ are observed at conditions near lean blow-off. Also, a similar trend of flame front curvature conditioned on HR was observed for both the ethylene-air and methane-air flames, where the magnitude of HR was observed to increase with the absolute value of curvature.