Selective nickel-catalyzed fluoroalkylations of olefins.

Mild and selective nickel-catalyzed trifluoromethylation and perfluoroalkylation reactions of alkenes were developed to provide fluorinated olefins, including natural products, pharmaceuticals, and variety of synthetic building blocks in good to excellent yields (38 examples). Control experiments, kinetic measurements and in situ EPR studies reveal the importance of radical species and the formation of 1,2-adducts as intermediates.

Lewis Acid Catalyzed Synthesis of Cyanidophosphates.

Salts containing new cyanido(fluorido)phosphate anions of the general formula [PF6-n(CN)n](-) (n=1-4) were synthesized by a very mild Lewis-acid-catalyzed synthetic protocol and fully characterized. All [PF6-n(CN)n](-) (n=1-4) salts could be isolated on a preparative scale. It was also possible to detect the [PF(CN)5](-) but not the [P(CN)6](-) anion. The best results with respect to purity, yield, and low cost were obtained when the F(-)/CN(-) substitution reactions were carried out in ionic liquids.

Palladium-Catalyzed Trifluoromethylation of (Hetero)Arenes with CF3 Br.

The CF3 group is an omnipresent motif found in many pharmaceuticals, agrochemicals, catalysts, materials, and industrial chemicals. Despite well-established trifluoromethylation methodologies, the straightforward and selective introduction of such groups into (hetero)arenes using available and less expensive sources is still a major challenge. In this regard, the selective synthesis of various trifluoromethyl-substituted (hetero)arenes by palladium-catalyzed C-H functionalization is herein reported. This novel methodology proceeds under comparably mild reaction conditions with good regio- and chemoselectivity. As examples, trifluoromethylations of biologically important molecules, such as melatonin, theophylline, caffeine, and pentoxifylline, are showcased.

Tetracyanido(difluorido)phosphates M(+) [PF2 (CN)4 ](.).

The systematic study of the reaction of M[PF6 ] salts and Me3 SiCN led to a synthetic method for the synthesis and isolation of a series of salts containing the unprecedented [PF2 (CN)4 ](-) ion in good yields. The reaction temperature, pressure, and stoichiometry were optimized. The crystal structures of M[PF2 (CN)4 ] (M=[nBu4 N](+) , Ag(+) , K(+) , Li(+) , H5 O2 (+) ) were determined. X-ray crystallography showed the exclusive formation of the cis isomer in accord with (31) P and (19) F solution NMR spectroscopy data. Starting with the K[PF2 (CN)4 ] the room temperature ionic liquid EMIm[PF2 (CN)4 ] was prepared exhibiting a rather low viscosity.

Omeprazole inhibits proliferation and modulates autophagy in pancreatic cancer cells.

BACKGROUND: Omeprazole has recently been described as a modulator of tumour chemoresistance, although its underlying molecular mechanisms remain controversial. Since pancreatic tumours are highly chemoresistant, a logical step would be to investigate the pharmacodynamic, morphological and biochemical effects of omeprazole on pancreatic cancer cell lines. METHODOLOGY/PRINCIPAL FINDINGS: Dose-effect curves of omeprazole, pantoprazole, gemcitabine, 5-fluorouracil and the combinations of omeprazole and 5-fluorouracil or gemcitabine were generated for the pancreatic cancer cell lines MiaPaCa-2, ASPC-1, Colo357, PancTu-1, Panc1 and Panc89. They revealed that omeprazole inhibited proliferation at probably non-toxic concentrations and reversed the hormesis phenomena of 5-fluorouracil. Electron microscopy showed that omeprazole led to accumulation of phagophores and early autophagosomes in ASPC-1 and MiaPaCa-2 cells. Signal changes indicating inhibited proliferation and programmed cell death were found by proton NMR spectroscopy of both cell lines when treated with omeprazole which was identified intracellularly. Omeprazole modulates the lysosomal transport pathway as shown by Western blot analysis of the expression of LAMP-1, Cathepsin-D and ß-COP in lysosome- and Golgi complex containing cell fractions. Acridine orange staining revealed that the pump function of the vATPase was not specifically inhibited by omeprazole. Gene expression of the autophagy-related LC3 gene as well as of Bad, Mdr-1, Atg12 and the vATPase was analysed after treatment of cells with 5-fluorouracil and omeprazole and confirmed the above mentioned results. CONCLUSIONS: We hypothesise that omeprazole interacts with the regulatory functions of the vATPase without inhibiting its pump function. A modulation of the lysosomal transport pathway and autophagy is caused in pancreatic cancer cells leading to programmed cell death. This may circumvent common resistance mechanisms of pancreatic cancer. Since omeprazole use has already been established in clinical practice these results could lead to new clinical applications.

Tailoring structure-property relationships in dithienosilole-benzothiadiazole donor-acceptor copolymers.

Four new DTS-BTD copolymers (P1-P4) differing by the concentration of electron-donating and -withdrawing substituents along the backbone have been synthesized and characterized by 2D-WAXS and in bottom-contact FETs. While all copolymers can self-assemble into lamellar superstructures, only P2 and P4 show a propensity to pi-stack. P4 exhibits a hole mobility as high as 0.02 cm(2) V(-1) s(-1) in excellent agreement with the close pi-stacking and lamellar distances found by structural analysis (0.36 and 1.84 nm, respectively) and absorbs homogenously across the entire visible spectrum as solar cell applications require.

A spray-processable, low bandgap, and ambipolar donor-acceptor conjugated polymer.

Combining a strong donor, tris(dodecyloxy)phenyl)-dithieno[3,2-b:2',3'-d]pyrrole, with a strong acceptor, 4,8-dithien-2-yl-2lambda(4)delta(2)-benzo[1,2-c;4,5-c']bis[1,2,5]thiadiazole, has yielded the lowest bandgap, soluble, spray-processable polymer to date. The polymer has access to four different redox states and shows ambipolar behavior in OFETs. Multiple techniques, including transmission/absorption spectroscopy on SWCNTs and reflectance spectroscopy on gold were used to accurately estimate the optical bandgap at 0.5-0.6 eV, which correlates well to theoretical calculations.

Efficient green solar cells via a chemically polymerizable donor-acceptor heterocyclic pentamer.

In this contribution, we report on bulk-heterojunction solar cells using a solution-processable neutral green conjugated copolymer based on 3,4-dioxythiophene and 2,1,3-benzothiadiazole as the donor and [6,6]phenyl-C61 butyric acid methyl ester (PCBM) as the acceptor. We have found that the short-circuit current is very sensitive to the composition of the donor-acceptor blend and it increases with increasing acceptor concentration. The device with a donor-acceptor ratio of 1:8 gives the best performance with a short-circuit current of 5.56 mA/cm(2), an open-circuit voltage of 0.77 V, and a power conversion efficiency of 1.9% under AM 1.5 solar illumination. The incident photon-to-current efficiency (IPCE) of the green solar cells shows two bands, one with a maximum of 57% in the UV region corresponding to absorption of PCBM and a second one with a maximum of 42% at longer wavelengths corresponding to the absorption of the green polymer.

Spray Processable Green to Highly Transmissive Electrochromics via Chemically Polymerizable Donor-Acceptor Heterocyclic Pentamers.

Electrochromic polymers (ECPs) of tunable green: Two symmetrical donor-acceptor based oligomers were designed, synthesized and chemically polymerized affording solution-processable conjugated polymers of distinct green hues in their neutral state. The polyheterocyclic hybrids exhibited highly transmissive oxidized states, excellent optical contrasts both in the visible and in the near infrared, fast switching times and long-term redox switching stability as expected for practical ECP devices.

High-resolution gas chromatography retention data as a basis for estimation of the octanol-water distribution coefficients (Kow) of PCB: the effect of experimental conditions.

The semi-experimental approach to approximating physicochemical data relevant to environmental distribution (vapor pressure and gas-octanol distribution) by correlation with gas chromatography (GC) retention data has been extended to the determination of Kow values. We estimated Kow values >10(4) for polychlorinated biphenyls (PCB), which are often derived by liquid chromatography, by correlation with gas chromatographic retention data. Selecting a set of reference compounds with known Kow values for relative retention time (RRT) correlation enables easy and accurate semi-empirical calculation of further Kow values for a given group of congeners. The RRT/log Kow correlation is validated in this paper with regard to the following gas chromatographic conditions: (1) isothermal versus temperature-programmed elution, (2) the possible effect of the polarity of the stationary phase, and (3) the effect of the format of the standardized GC retention data. The advantages of our Kow(GC) method can be summarized as follows: complex mixtures can be analyzed, only amounts in the nanogram-range or less are required, Kow values of isomers can be determined and the exact structure of compounds need not be known. Normalized GC retention data of persistent organic pollutants are readily available. The quality of the Kow values obtained by the GC method compares well with that for other Kow estimation methods. It depends mainly on the accuracy of the Kow data of the structurally correlated compounds used as standards for the correlation cohort. The Kow(GC) data for all 209 PCB congeners are given.