Terpyridine Based Heteroleptic Ruthenium Complexes: Influence of Donor and Acceptor Ligands in Photosensitization

We report heteroleptic ruthenium complexes of terpyridine (tpy) ligands with directly linked carboxylic acid anchors. These complexes feature methyl or methoxy-substituted ^4′−Phtpy as donor ligands. We prepared these heteroleptic complexes from the ruthenium (II) precursor via a milder route to preclude the homoleptic complex formation. The donor−acceptor arrangement of tpy ligands in these ruthenium complexes renders visible light absorption giving metal and ligand-to-ligand charge transfer excitations at c.a. 490 nm. We evaluate the effect of the tpy donor substituents on the light-harvesting ability in Dye-Sensitized Solar Cells (DSSCs) and compare their photosensitizing ability with heteroleptic complexes bearing phenyl spacer at the acceptor end. Further, scrutinizing their photovoltaic performance, we studied their electron transfer kinetics in DSSCs using electrochemical impedance spectroscopy. This paper presents the structure-photosensitization relationship of these heteroleptic ruthenium complexes through a combined experimental and computational approach.     

Bed of polydisperse viscous spherical drops under thermocapillary effects

Viscous flow past an ensemble of polydisperse spherical drops is investigated under thermocapillary effects. We assume that the collection of spherical drops behaves as a porous media and estimates the hydrodynamic interactions analytically via the so- called cell model that is defined around a specific representative particle. In this method, the hydrodynamic interactions are assumed to be accounted by suitable boundary conditions on a fictitious fluid envelope surrounding the representative particle. The force calculated on this representative particle will then be extended to a bed of spherical drops visualized as a Darcy porous bed. Thus, the “effective bed permeability” of such a porous bed will be computed as a function of various parameters and then will be compared with Carman–Kozeny relation. We use cell model approach to a packed bed of spherical drops of uniform size (monodisperse spherical drops) and then extend the work for a packed bed of polydisperse spherical drops, for a specific parameters. Our results show a good agreement with the Carman–Kozeny relation for the case of monodisperse spherical drops. The prediction of overall bed permeability using our present model agrees well with the Carman–Kozeny relation when the packing size distribution is narrow, whereas a small deviation can be noted when the size distribution becomes broader.     

Interplay between hydration and electrostatic attraction in ligand binding: direct observation of hydration barrier at reverse micellar interface

The recognition of a charged biomolecular surface by an oppositely charged ligand is governed by electrostatic attraction and surface hydration. In the present study, the interplay between electrostatic attraction and hydration at the interface of a negatively charged reverse micelle (RM) at different temperatures has been addressed. Temperature-dependent solvation dynamics of a probe H33258 (H258) at the reverse micellar interface explores the nature of hydration at the interface. Up to 45 degrees C, the environmental dynamics reported by the interface-binding probe H258 becomes progressively faster with increasing temperature and follows the Arrhenius model. Above 45 degrees C, the observed dynamics slows down with increasing temperature, thus deviating from the Arrhenius model. The slower dynamics at higher temperatures is interpreted to be due to increasing contributions from the motions of the surfactant head groups, indicating the proximity of the probe to the interface at higher temperatures. This suggests an increased electrostatic attraction between the ligand and interface at higher temperatures and is attributed to the change in hydration. Densimetric and acoustic studies, indeed, show a drastic increase in the apparent specific adiabatic compressibility of the water molecules present in RMs after 45 degrees C, revealing the existence of a softer hydration shell at higher temperatures. Our study indicates that the hydration layer at a charged interface acts both as physical and energetic barrier to electrostatic interactions of small ligands at the interface.     

Discovery of potent and specific fructose-1,6-bisphosphatase inhibitors and a series of orally-bioavailable phosphoramidase-sensitive prodrugs for the treatment of type 2 diabetes

Excessive glucose production by the liver coupled with decreased glucose uptake and metabolism by muscle, fat, and liver results in chronically elevated blood glucose levels in patients with type 2 diabetes. Efforts to treat diabetes by reducing glucose production have largely focused on the gluconeogenesis pathway and rate-limiting enzymes within this pathway such as fructose-1,6-bisphosphatase (FBPase). The first potent FBPase inhibitors were identified using a structure-guided drug design strategy (Erion, M. D.; et al. J. Am. Chem. Soc. 2007, 129, 15480-15490) but proved difficult to deliver orally. Herein, we report the synthesis and characterization of a series of orally bioavailable FBPase inhibitors identified following the combined discoveries of a low molecular weight inhibitor series with increased potency and a phosphonate prodrug class suitable for their oral delivery. The lead inhibitor, 10A, was designed with the aid of X-ray crystallography and molecular modeling to bind to the allosteric AMP binding site of FBPase. High potency (IC50 = 16 nM) and FBPase specificity were achieved by linking a 2-aminothiazole with a phosphonic acid. Free-energy perturbation calculations provided insight into the factors that contributed to the high binding affinity. 10A and standard phosphonate prodrugs of 10A exhibited poor oral bioavailability (0.2-11%). Improved oral bioavailability (22-47%) was achieved using phosphonate diamides that convert to the corresponding phosphonic acid by sequential action of an esterase and a phosphoramidase. Oral administration of the lead prodrug, MB06322 (30, CS-917), to Zucker Diabetic Fatty rats led to dose-dependent inhibition of gluconeogenesis and endogenous glucose production and consequently to significant blood glucose reduction.     

Dual-labeled oligonucleotide probe for sensing adenosine via FRET: a novel alternative to SNPs genotyping

A novel FRET based strategy for DNA sequence analysis utilising base-discriminating fluorescence (BDF) nucleoside, (Py)U/(2-Ant)U, as donor in the dual-labelled oligonucleotide probe is reported; a selective/specific emission from acceptor, was observed upon excitation at the donor, only when the opposite base of the "smart" fluorescently labeled BDF nucleoside, (Py)U/(2-Ant)U, is adenine on the complementary target sequence.     

Design of a novel G-quenched molecular beacon: a simple and efficient strategy for DNA sequence analysis

G-quenched MBs are devised from readily available starting materials and used for sequence specific DNA detection with high efficiency.     

A high-performance selective oxidation system for the facile production of fine chemicals

Mn(III)AlPO-5 and Cr(VI)AlPO-5 redox (microporous) catalysts are effective, in the presence of dissolved acetylperoxyborate (APB) under mild conditions (333-373 K), and much superior to the titanosilicate, TS-1 (also a single-site heterogeneous catalyst), in the selective oxidation of primary, secondary, benzylic and other unsaturated alcohols, p-cymene, methyl cyclohexene and other speciality organics which are of value in the fine-chemical and pharmaceutical industries.     

Hydration in protein folding: thermal unfolding/refolding of human serum albumin

Human serum albumin (HSA) is known to undergo both reversible and irreversible thermal unfolding and refolding, depending upon the experimental conditions (end temperature) at neutral pH. In this report we have used high precision densimetric and ultrasonic measurements to determine the apparent specific volume (phi v) and compressibility (phi k) of HSA at different unfolded and refolded states at two different end temperatures, 55 degrees C and 70 degrees C. The unfolded and refolded states were characterized using dynamic light scattering (DLS), circular dichroism (CD), picosecond-resolved fluorescence decay, and anisotropy of the single-tryptophan residue in HSA (Trp214). Both the unfolded states were allowed to refold by cooling wherein the former and latter processes were found to be reversible and irreversible, respectively, in nature. The results obtained from the densimetric and ultrasonic measurements reveal that the apparent specific volume and compressibility of the protein in the reversible protein unfolding process is preserved upon restoration of HSA to ambient temperature. However, a significant change in phi v and phi k occurs in the process of irreversible protein refolding (from 70 to 20 degrees C). The experimental observation is rationalized in terms of the exposure of domain IIA to an aqueous environment, resulting in the swelling of the protein to a higher hydrodynamic diameter. Our studies attempt to explore the extent of hydration associated with the structural integrity of the popular protein HSA.     

On a Class of Hungarian Semigroups and the Factorization Theorem of Khinchin

Let G be a connected reductive Lie group and K be a maximal compact subgroup of G. We prove that the semigroup of all K-biinvariant probability measures on G is a strongly stable Hungarian semigroup. Combining with the result [see Rusza and Szekely⁽⁹⁾], we get that the factorization theorem of Khinchin holds for the aforementioned semigroup. We also prove that certain subsemigroups of K-biinvariant measures on G are Hungarian semigroups when G is a connected Lie group such that Ad G is almost algebraic and K is a maximal compact subgroup of G. We also prove a p-adic analogue of these results.