Controlling selectivity of polymer‐based monolithic stationary phases

In this work, we aimed to prepare a monolithic capillary column that allowed an isocratic separation of ten dopamine precursors and metabolites in a single run. Segments of five zwitterion sulfobetaine polymer monoliths have been modified by zwitterion phoshorylcholine by using an ultraviolet‐initiated two‐step photografting. Columns with 0, 33, 50, 66, and 100% of modified length were prepared. Effect of length of the modified segment and mobile phase composition has been tested. All columns provided dual‐retention mechanism with reversed‐phase retention in highly aqueous mobile phase and hydrophilic interaction mechanism in highly organic mobile phase. The retention mechanism was controlled by the composition of the mobile phase and has been described by a three‐parameter model. We have used regression parameters to characterize the retention of analyzed compounds and to study individual pathways of dopamine metabolism. Comprehensive optimization of mobile phase composition allowed to find an optimal composition of the mobile phase and stationary phase surface chemistry arrangement to achieve desired separation. Optimized columns provided an isocratic separation of all tested compounds in less than nine min.     

Spirocyclisation of phytoalexin 1-methoxybrassinin in the presence of Grignard reagents

The anti-cancer properties of naturally occurring (2R, 3R)-(?)-1-methoxyspirobrassinol methyl ether (I) and their synthetic amino or piperidyl analogues II inspired us to study the synthesis of new target compounds III with a C—C bond in the 2-position of indole rather than a C—N or C—O bond (I or II respectively). The goal was achieved via electrophilic-nucleophilic 3,2-difunctionalisation of 1-methoxybrassinin (IV) in the presence of bromine and the Grignard reagent leading to the formation of cis- and trans-C—C analogues of I. Finally, the anti-cancer activities of the new compounds were measured and compared with I and II in order to show the importance of a heteroatom in the 2-substituted indole on the anti-cancer activity of spirobrassinols.     

Opportunities in multidimensional trace metal imaging: taking copper-associated disease research to the next level

Copper plays an important role in numerous biological processes across all living systems predominantly because of its versatile redox behavior. Cellular copper homeostasis is tightly regulated and disturbances lead to severe disorders such as Wilson disease and Menkes disease. Age-related changes of copper metabolism have been implicated in other neurodegenerative disorders such as Alzheimer disease. The role of copper in these diseases has been a topic of mostly bioinorganic research efforts for more than a decade, metal–protein interactions have been characterized, and cellular copper pathways have been described. Despite these efforts, crucial aspects of how copper is associated with Alzheimer disease, for example, are still only poorly understood. To take metal-related disease research to the next level, emerging multidimensional imaging techniques are now revealing the copper metallome as the basis to better understand disease mechanisms. This review describes how recent advances in X-ray fluorescence microscopy and fluorescent copper probes have started to contribute to this field, specifically in Wilson disease and Alzheimer disease. It furthermore provides an overview of current developments and future applications in X-ray microscopic methods.

Nonpeptidic Selective Inhibitors of the Chymotrypsin‐Like (β5 i) Subunit of the Immunoproteasome

Elevated expression of the immunoproteasome has been associated with autoimmune diseases, inflammatory diseases, and various types of cancer. Selective inhibitors of the immunoproteasome are not only scarce, but also almost entirely restricted to peptide‐based compounds. Herein, we describe nonpeptidic reversible inhibitors that selectively block the chymotrypsin‐like (β5i) subunit of the human immunoproteasome in the low micromolar range. The most potent of the reversibly acting compounds were then converted into covalent, irreversible, nonpeptidic inhibitors that retained selectivity for the β5i subunit. In addition, these inhibitors discriminate between the immunoproteasome and the constitutive proteasome in cell‐based assays. Along with their lack of cytotoxicity, these data point to these nonpeptidic compounds being suitable for further investigation as β5i‐selective probes for possible application in noncancer diseases related to the immunoproteasome.     

Scope for Accessing the Chain Length Dependence of the Termination Rate Coefficient for Disparate Length Radicals in Acrylate Free Radical Polymerization

A method that utilizes reversible addition fragmentation chain transfer (RAFT) chemistry is evaluated on a theoretical basis to deduce the termination rate coefficient for disparate length radicals k in acrylate free radical polymerization, where s and l represent the arbitrary yet disparate chain lengths from either a “short” or “long” RAFT distribution. The method is based on a previously developed method for elucidation of k for the model monomer system styrene. The method was expanded to account for intramolecular chain transfer (i.e., the formation of mid-chain radicals via backbiting) and the free radical polymerization kinetic parameters of methyl acrylate. Simulations show that the method's predictive capability is sensitive to the polymerization rate's dependence on monomer concentration, i.e., the virtual monomer reaction order, which varies with the termination rate coefficient's value and chain length dependence. However, attaining the virtual monomer reaction order is a facile process and once known the method developed here that accounts for mid-chain radicals and virtual monomer reaction orders other than one seems robust enough to elucidate the chain length dependence of k for the more complex acrylate free radical polymerization.     

Comparison of large basis set DFT and MP2 calculations in the study of the barrier for internal rotation of 2,3,5,6‐tetrafluoroanisole

The barrier for internal rotation around the ? OCH₃ bond in 2,3,5,6‐tetrafluoroanisole was calculated using the density functional theory (DFT) and second‐order Møller–Plesset (MP2) methods with Pople's basis sets up to 6‐311++G(3df,2p) and Jensen basis sets up to pc‐3. The results are converged only if fairly large basis sets are used (at least 6‐311++G(3df,2pd) or pc‐2). Both the DFT and MP2 potential energy curves show internal structure. Two minima and three maxima are observed on the curves, arising from the interplay between lone‐pair delocalization and changes in the hybridization around the oxygen atom, together with the attraction between the positively polarized hydrogens in the methyl group and the negatively polarized fluorine atom at the ortho position. These critical points are somehow ironed out by the addition of zero‐point and thermal corrections to the energy curves. At this level, the MP2 method can describe reasonably well the previously determined single‐well experimental rotational barrier, 2.7 ± 2.0 kcal/mol at 298 K, while all DFT methods yield a much smaller result. As observed experimentally, the ? OCH₃ group is perpendicular to the aryl ring in the equilibrium structure, although two very close minima with an intermediate hump at 90° are still observable. The theoretical free energy barrier of rotation at the MP2(full)/pc‐2 level is 2.0 ± 1.0 kcal/mol, in reasonable agreement with the experimental determination. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007     

Advanced Computational Strategies for Modelling the Evolution of Full Molecular Weight Distributions Formed During Multiarmed (Star) Polymerisations

Summary: A novel computational strategy is described for the simulation of star polymerisations, allowing for the computation of full molecular weight distributions (MWDs). Whilst the strategy is applicable to a broad range of techniques for the synthesis of star polymers, the focus of the current study is the simulation of MWDs arising from a reversible addition fragmentation chain transfer (RAFT), R‐group approach star polymerisation. In this synthetic methodology, the arms of the star grow from a central, polyfunctional moiety, which is formed initially as the refragmenting R‐group of a polyfunctional RAFT agent. This synthetic methodology produces polymers with complex MWDs and the current simulation strategy is able to account for the features of such complex MWDs. The strategy involves a kinetic model which describes the reactions of a single arm of a star, the kinetics of which are implemented and simulated using the PREDICI® program package. The MWDs resulting from this simulation of single arms are then processed with an algorithm we describe, to generate a full MWD of stars. The algorithm is applicable to stars with an arbitrary number of arms. The kinetic model and subsequent algorithmic processing techniques are described in detail. A simulation has been parameterised using rate coefficients and densities for a 2,2′‐azoisobutyronitrile (AIBN) initiated, bulk polymerisation of styrene at 60 °C. A number of kinetic parameters have been varied over large ranges. Conversion normalised simulations were performed, leading to information regarding star arm length, polydispersity index (PDI) and the fraction of living arms. These screening processes provided a rigorous test for the kinetic model and also insight into the conditions, which lead to optimal star formation. Finally, full MWDs are simulated for several RAFT agent/initiator ratios as well as for stars with a varying number of arms.

Full MWDs from a star with 1, 2, 4, 6 and 8 arms.     

Effect of an Antioxidant Based on Red Beetroot Extract on the Abiotic Stability of Polylactide and Polycaprolactone

This study investigated the effect of natural antioxidants inherent to beetroot (Beta vulgaris var. Vulgaris) on the ageing of environmentally friendly plastics. Certain properties were examined in this context, comprising thermal, mechanical, and morphological properties. A visual evaluation of relevant changes in the given polymers (polylactide and polycaprolactone) was conducted during an ageing test in a UV chamber (45 °C, 70% humidity) for 720 h. The films were prepared by a casting process, in which samples with the extract of beetroot were additionally incorporated in a common filler (bentonite), this serving as a carrier for the extract. The results showed the effect of the incorporated antioxidant, which was added to stabilize the biodegradable films. Its efficiency during the ageing test in the polymers tended to exceed or be comparable to that of the reference sample.     

Conformational and energetic properties of the ammonia dimer—comparison of post-Hartree—Fock and density functional methods

The equilibrium structure of the ammonia dimer has been investigated with density functional and MP2 calculations. We used Slater- and Becke-exchange functionals combined with correlation functionals as recommended by Vosko-Wilk-Nusair, by Perdew, and by Lee-Yang-Parr, respectively. The potential energy surfaces was investigated. The asymmetric cyclic “microwave” structure could be identified as a minimum. Optimization of the intermolecular parameters showed that this structure has nearly the same energy as the centrosymmetric cyclic structure. Full optimization transformed the asymmetric cyclic structure into the linear structure. The interaction energies in the dimer were corrected for the basis set superposition error using the Boys-Bernardi counterpoise method and the a priori chemical Hamiltonian approach, respectively. © 1996 by John Wiley & Sons, Inc.