Towards green, scalable peptide synthesis: leveraging DEG-crosslinked polystyrene resins to overcome hydrophobicity challenges.

Diethylene glycol dimethacrylate (DEG)-crosslinked polystyrene (PS) resin offers a promising alternative to traditional divinyl benzene (DVB)-PS resin for solid-phase peptide synthesis (SPPS), particularly for challenging sequences with hydrophobic or bulky amino acids. DEG-PS resin's reduced hydrophobicity and enhanced flexibility improve synthesis efficiency, yielding peptides up to 28 residues with higher purities and yields compared to DVB-PS. In various syntheses, DEG-PS outperformed DVB-PS resin, with higher purities and yields for challenging peptides such as ABC analogue (73.

Re-assessing viologens for modern bio-electrocatalysis.

Viologens, 1,1'-disubstituted-4,4'-bipyridinium salts, are organic redox species that can be used in place of NADPH as mediators for redox enzymes. In this study, using the reduction of oxidized glutathione by glutathione reductase as a model system, a rationally designed library of viologens covering a range of polarities and functional groups were explored as electron transfer mediators for bio-electrocatalysis. Through a series of electrochemical investigations, the reduction potential was found to be the primary determining factor for electron transfer between the viologen and enzyme.

Enzymatic Fluoromethylation as a Tool for ATP-Independent Ligation.

-adenosylmethionine-dependent methyltransferases are involved in countless biological processes, including signal transduction, epigenetics, natural product biosynthesis, and detoxification. Only a handful of carboxylate methyltransferases have evolved to participate in amide bond formation. In this report we show that enzyme-catalyzed F-methylation of carboxylate substrates produces F-methyl esters that readily react with - or -nucleophiles under physiological conditions.

Semisynthesis reveals apoptin as a tumour-selective protein prodrug that causes cytoskeletal collapse.

Apoptin is a small viral protein capable of inducing cell death selectively in cancer cells. Despite its potential as an anticancer agent, relatively little is known about its mechanism of toxicity and cancer-selectivity. Previous experiments suggest that cancer-selective phosphorylation modulates apoptin toxicity, although a lack of chemical tools has hampered the dissection of underlying mechanisms.

Direct measurement of the genuine efficiency of thermogalvanic heat-to-electricity conversion in thermocells.

Harvesting wasted thermal energy could make important contributions to global energy sustainability. Thermogalvanic devices are simple, chemistry-based devices which can convert heat to electricity, through facile redox chemistry. The efficiency of this process is the ratio of electrical energy generated by the cell (in Watts) to the quantity of thermal energy that passes through the cell (also in Watts).

Size Effects of the Anions in the Ionothermal Synthesis of Carbon Nitride Materials.

Semiconducting carbon nitride polymers are used in metal-free photocatalysts and in opto-electronic devices. Conventionally, they are obtained using thermal and ionothermal syntheses in inscrutable, closed systems and therefore, their condensation behavior is poorly understood. Here, the synthetic protocols and properties are compared for two types of carbon nitride materials - 2D layered poly(triazine imide) (PTI) and hydrogen-bonded melem hydrate - obtained from three low-melting salt eutectics taken from the systematic series of the alkali metal halides: LiCl/KCl, LiBr/KBr, and LiI/KI.

Development of Strong Visible-Light-Absorbing Cyclometalated Iridium(III) Complexes for Robust and Efficient Light-Driven Hydrogen Production.

Weak light absorption of common Ir(III) complexes (e. g., using phenylpyridine as the ligand) has hindered their applications in photocatalytic hydrogen generation from water as an efficient photosensitizer.

Synthesis of ternary sulfide nanomaterials using dithiocarbamate complexes as single source precursors.

We report the use of cheap, readily accessible and easy to handle di-isobutyl-dithiocarbamate complexes, [M(SCNBu) ], as single source precursors (SSPs) to ternary sulfides of iron-nickel, iron-copper and nickel-cobalt. Varying decomposition temperature and precursor concentrations has a significant effect on both the phase and size of the nanomaterials, and in some instances meta-stable phases are accessible. Decomposition of [Fe(SCNBu)]/[Ni(SCNBu)] at 210-230 °C affords metastable FeNiS (violarite) nanoparticles, while at higher temperatures the thermodynamic product (Fe,Ni)S (pentlandite) results.

An atom efficient, single-source precursor route to plasmonic CuS nanocrystals.

The synthesis of colloidal semiconductor nanocrystals (NCs) from single-source precursors offers simplified manufacturing processes at the cost of reduced atom efficiency. Self-capping routes have the potential to maximise this efficiency although investigation has so far been limited to organic solvents. Here we present the synthesis of copper sulfide NCs the decomposition of a copper dithiocarbamate complex in water.