Metabolic Tumor Imaging with Rapidly Signal-Enhanced 1-13C-Pyruvate-d3

The metabolism of malignant cells differs significantly from that of healthy cells and thus, it is possible to perform metabolic imaging to reveal not only the exact location of a tumor, but also intratumoral areas of high metabolic activity. Herein, we demonstrate the feasibility of metabolic tumor imaging using signal-enhanced 1-¹³C-pyruvate-d₃, which is rapidly enhanced via para-hydrogen, and thus, the signal is amplified by several orders of magnitudes in less than a minute. Using as a model, human melanoma xenografts injected with signal-enhanced 1-¹³C-pyruvate-d3, we show that the conversion of pyruvate into lactate can be monitored along with its kinetics, which could pave the way for rapidly detecting and monitoring changes in tumor metabolism.     

Photoredox-catalyzed [4+2] annulation of cyclobutylanilines with alkenes,alkynes, and diynes in continuous flow

Continuous flow has recently emerged as a powerful enabling technology that greatly improves many reactions’ efficiency. Here, we apply the technology to intermolecular [4+2] annulation of cyclobutylanilines with alkenes, alkynes, and diynes by photoredox catalysis. An across-the-board improvement in the annulation’s efficiency is noticed. Moreover, a gram-scale annulation is successfully demonstrated in continuous flow using a much lower catalyst loading.     

A parallel distributed data CPHF algorithm for analytic Hessians

One of the most commonly used means to characterize potential energy surfaces of reactions and chemical systems is the Hessian calculation, whose analytic evaluation is computationally and memory demanding. A new scalable distributed data analytic Hessian algorithm is presented. Features of the distributed data parallel coupled perturbed Hartree-Fock (CPHF) are (a) columns of density-like and Fock-like matrices are distributed among processors, (b) an efficient static load balancing scheme achieves good work load distribution among the processors, (c) network communication time is minimized, and (d) numerous performance improvements in analytic Hessian steps are made. As a result, the new code has good performance which is demonstrated on large biological systems.     

A first-principles study of the electronic and structural properties of gamma-TaON

The geometric and electronic structure of the recently found new polymorph of tantalum oxynitride, gamma-TaON, and its structural stability were studied quantum-chemically at the density functional level. Results obtained by complementary quantum-chemical techniques with wavefunctions either expanded in atom-centered functions or in plane waves were compared, having employed pure density-functional functionals within the generalized gradient approximation as well as density-functional/Hartree-Fock hybrid methods. In particular, several plausible anion distributions were investigated and, in accordance with Pauling's second rule, it was found that the configuration in which nitrogen occupies crystallographic sites with highest coordination numbers is the most stable one. Theoretically generated local structural parameters were used to improve the accuracy of the experimentally derived information. The bonding situation in the most stable configuration was investigated by an analysis of the density of states.     

Ambient-temperature metal-to-ligand charge-transfer phosphorescence facilitated by triarylboron: Bnpa and its metal complexes

A Cu(I) complex, 1, and a Pt(II) complex, 2a, of a triarylboron ligand, Bnpa, with bright ambient-temperature phosphorescence have been obtained. The phosphorescence of these complexes is highly sensitive toward molecular oxygen and has a distinct response to fluoride ions. For 1, the fluoride ion causes phosphorescent quenching and Bnpa dissociation, and for 2a, it switches phosphorescent color from yellow to green. The Cu(I) complex has an exceptionally high emission quantum yield (0.88) in the solid state.     

High density,high performance optical data storage via volume holography: Viability at last?

The long held promise of using volume holography to deliver high performance optical storage is reviewed. The problems, which limited the development for many years, are accessed. Finally, we describe a series of innovations, which may make the technology viable at last.     

Hecke group algebras as quotients of affine Hecke algebras at level 0

The Hecke group algebra of a finite Coxeter group , as introduced by the first and last authors, is obtained from by gluing appropriately its 0-Hecke algebra and its group algebra. In this paper, we give an equivalent alternative construction in the case when is the finite Weyl group associated to an affine Weyl group W. Namely, we prove that, for q not a root of unity of small order, is the natural quotient of the affine Hecke algebra H(W)(q) through its level 0 representation.The proof relies on the following core combinatorial result: at level 0 the 0-Hecke algebra H(W)(0) acts transitively on . Equivalently, in type A, a word written on a circle can be both sorted and antisorted by elementary bubble sort operators. We further show that the level 0 representation is a calibrated principal series representation M(t) for a suitable choice of character t, so that the quotient factors (non-trivially) through the principal central specialization. This explains in particular the similarities between the representation theory of the 0-Hecke algebra and that of the affine Hecke algebra H(W)(q) at this specialization.     

Phosphorescent Cu(I) complexes of 2-(2'-pyridylbenzimidazolyl)benzene: impact of phosphine ancillary ligands on electronic and photophysical properties of the Cu(I) complexes

Four mononuclear Cu(I) complexes of 2-(2'-pyridyl)benzimidazolylbenzene (pbb) with four different ancillary phosphine ligands PPh(3), bis[2-(diphenylphosphino)phenyl]ether (DPEphos), bis(diphenylphosphino)ethane (dppe), and bis(diphenylphosphinomethyl)diphenylborate (DPPMB) have been synthesized. The crystal structures of [Cu(pbb)(PPh(3))(2)][BF(4)] (1), [Cu(pbb)(dppe)][BF(4)] (2), [Cu(pbb)(DPEphos)][BF(4)] (3), and the neutral complex [Cu(pbb)(DPPMB)] (4) were determined by single-crystal X-ray diffraction analyses. The impact of the phosphine ligands on the structures of the copper(I) complexes was examined, revealing that the most significant impact of the phosphine ligands is on the P-Cu-P bond angle. The electronic and photophysical properties of the new complexes were examined by using UV-vis, fluorescence, and phosphorescence spectroscopies and electrochemical analysis. All four complexes display a weak MLCT absorption band that varies considerably with the phosphine ligand. At ambient temperature, no emission was observed for any of the complexes in solution. However, when doped into PMMA polymer (20 wt %), at ambient temperature, all four complexes emit light with a color ranging from green to red-orange, depending on the phosphine ligand. The emission of the new copper complexes has an exceptionally long decay lifetime (>200 micros). Ab initio MO calculations established that the lowest electronic transition in the copper(I) complexes is MLCT in nature. The electronic and photophysical properties of the new mononuclear Cu(I) complexes were compared with those of the corresponding polynuclear Cu(I) complexes based on the 2-(2'-dipyridyl)benzimidazolyl derivative ligands and the previously extensively studied phenanthroline-based Cu(I) complexes.     

Development of a gradient elution preparative high performance liquid chromatography method for the recovery of the antibiotic ertapenem from crystallization process streams

A gradient elution preparative chromatography method was developed for the recovery of the antibiotic ertapenem from crystallization mother-liquor streams. The preparative HPLC method that was developed on the lab-scale employs an analytical size column of conventional dimensions (25 cm x 0.46 cm) packed with Kromasil C8 stationary phase. Gradient elution was used with aqueous acetic acid and acetonitrile as mobile phases. A target of processing approximately 30 mg of ertapenem per half an hour at a flow rate of 1.5 mL/min with high yield and adequate rejection of all major impurities was achieved. This corresponds to a productivity of approximately 0.6 kg ertapenem as free acid per kilogram of stationary phase per day (kkd). The scalability of the method was demonstrated by using a 5 cm i.d. column configuration to generate 10 g of purified ertapenem. This work complements a previous study improving on the productivity and throughput of the method by employing gradient elution and the use of crystallization to remove some key impurities that are chromatographically difficult to resolve [A. Vailaya, P. Sajonz, O. Sudah, V. Capodanno, R. Helmy, F.D. Antia, J. Chromatogr. A 1079 (2005) 80].     

The synthesis of N,O-ferrocenyl pyrrolidine-containing ligands and their application in the diethyl- and diphenylzinc addition to aromatic aldehydes

A facile route to a series of planar chiral N,O-ferrocenyl pyrrolidine-containing ligands with varying substituents at the nitrogen and oxygen donor atoms is described. The oxygen donor atom was introduced via a diastereoselective ortho-metalation of N-methylpyrrolidinyl and N-allylpyrrolidinyl ferrocene intermediates and was quenched with various ketones. The nitrogen substituent was varied through deallylation and subsequent derivatization of a secondary pyrrolidine. The efficacy of these novel ligands was investigated in the enantioselective addition of diethylzinc and diphenylzinc to aromatic aldehydes. The ligands proved highly effective in the diethylzinc addition to benzaldehyde that resulted in high yields of up to 99% and enantioselectivities (ee's) of up to 95%. The role of planar chirality was explored and the results indicated that the planar chirality, and not the central chirality, of the ferrocenyl ligands was the dominant stereo-controlling element. Employment of a mixed ethyl-phenylzinc reagent in the phenylation of aromatic aldehydes led to a mixture of the two additional products, and the phenylated product was obtained in up to 37% ee.