The synthesis of the first unsupported dicationic arene complexes of calcium and strontium [(η6-HMB)AE(oDFB)4]2+ is reported (HMB = hexamethylbenzene; AE = alkaline earth metal; oDFB = ortho-difluorobenzene). They were prepared by direct oxidation of the elemental metals employing the ligand-forming radical cation salt [HMB][WCA] as an oxidant (WCA = [Al(ORF)4] or [μF-Al(ORF)32]; RF = C(CF3)3). In addition, monocationic η6-HMB complexes of calcium, strontium and barium supported by coordination of the monodentate anion [F-Al(ORF)3]- are reported. In all examples, almost undistorted η6-HMB coordination is observed with rather short M-arenecentroid distances approaching those observed with the isoelectronic but negatively charged pentamethylcyclopentadienyl ligand. The structure and bonding, thermodynamic stability and Lewis acidity (fluoride/hydride ion affinities, FIA/HIA) of the generated complexes were assessed by DFT methods. It followed that the gaseous dications [(η6-HMB)AE(oDFB)4]2+ are extremely hard Lewis acids that retain FIAs close to superacidity in solution. This journal is © The Royal Society of Chemistry 2020.Non-canonical DNA i-motifs and G-quadruplexes are postulated as genetic switches for the transcriptional regulation of proto-oncogenes. However, in comparison to G-quadruplexes, the therapeutic potential of i-motifs is less explored. The development of i-motif selective ligands by conventional approaches is challenging due to the structural complexity of i-motifs. The target guided synthetic (TGS) approach involving in situ cycloaddition could provide specific ligands for these dynamic DNA structures. Herein, we have used i-motif forming C-rich DNA and their complementary G-quadruplex forming DNA sequences of c-MYC and BCL2 promoter regions as well as a control self-complementary duplex DNA sequence as the templates to generate selective ligands from a pool of reactive azide-alkyne building blocks. In our approach, thiolated DNA targets are immobilized on the surface of gold-coated iron nanoparticles to enable efficient isolation of the newly generated ligands from the solution mixture by simple magnetic decantation. The combinatorial in situ cycloaddition generated cell-membrane permeable triazole leads for respective DNA targets (c-MYC and BCL2 i-motifs and G-quadruplexes) that selectively promote their formation. In vitro cellular studies reveal that the c-MYC i-motif and G-quadruplex leads downregulate c-MYC gene expression whereas the BCL2 i-motif lead upregulates and the BCL2 G-quadruplex lead represses BCL2 gene expression. The TGS strategy using i-motif DNA nanotemplates represents a promising platform for the direct in situ formation of i-motif specific ligands for therapeutic intervention. This journal is © The Royal Society of Chemistry 2020.The preparation of a range of tetraaryl-substituted bicyclo[4.2.0]octa-1,5,7-trienes using a one-pot procedure starting from terminal aryl alkynes and catalysed by a rhodium(i) complex is reported. This synthesis proceeds by a reaction sequence involving head-to-tail homocoupling of the terminal alkyne and zipper annulation of the resulting gem-enyne. The rhodium catalyst employed is notable for the incorporation of a flexible NHC-based pincer ligand, which is suggested to interconvert between mer- and fac-coordination modes to fulfil the orthogonal mechanistic demands of the two transformations. https://www.selleckchem.com/products/gsk3368715.html Evidence for this interesting auto-tandem action of the catalyst is provided by reactions of the precatalyst with model substrates, corroborating proposed intermediates in both component cycles, and norbornadiene, which reversibly captures the change in pincer ligand coordination mode, along with a DFT-based computational analysis. This journal is © The Royal Society of Chemistry 2020.Many contrast agents for magnetic resonance imaging are based on gadolinium, however side effects limit their use in some patients. Organic radical contrast agents (ORCAs) are potential alternatives, but are reduced rapidly in physiological conditions and have low relaxivities as single molecule contrast agents. Herein, we use a supramolecular strategy where cucurbit[8]uril binds with nanomolar affinities to ORCAs and protects them against biological reductants to create a stable radical in vivo. We further overcame the weak contrast by conjugating this complex on the surface of a self-assembled biomacromolecule derived from the tobacco mosaic virus. This journal is © The Royal Society of Chemistry 2020.Despite the prevalence of lithium ion batteries in modern technology, the search for alternative electrochemical systems to complement the global battery portfolio is an ongoing effort. The search has resulted in numerous candidates, among which mildly acidic aqueous zinc ion batteries have recently garnered significant academic interest, mostly due to their inherent safety. As the anode is often fixed as zinc metal in these systems, most studies address the absence of a suitable cathode for reaction with zinc ions. This has led to aggressive research into viable intercalation cathodes, some of which have shown impressive results. However, many investigations often overlook the implications of the zinc metal anode, when in fact the anode is key to determining the energy density of the entire cell. In this regard, we aim to shed light on the importance of the zinc metal anode. This perspective offers a brief discussion of zinc electrochemistry in mildly acidic aqueous environments, along with an overview of recent efforts to improve the performance of zinc metal to extract key lessons for future research initiatives. Furthermore, we discuss the energy density ramifications of the zinc anode with respect to its weight and reversibility through simple calculations for numerous influential reports in the field. Finally, we offer some perspectives on the importance of optimizing zinc anodes as well as a future direction for developing high-performance aqueous zinc ion batteries. This journal is © The Royal Society of Chemistry 2020.The electrochemical oxidation of biomass platforms such as 5-hydroxymethylfurfural (HMF) to value-added chemicals is an emerging clean energy technology. However, mechanistic knowledge of this reaction in an electrochemical context is still lacking and operando studies are even more rare. In this work, we utilize core-shell gold-metal oxide nanostructures which enable operando surface-enhanced Raman spectroelectrochemical studies to simultaneously visualize catalyst material transformation and surface reaction intermediates under an applied voltage. As a case study, we show how the transformation of NiOOH from ∼1-2 nm amorphous Ni layers facilitates the onset of HMF oxidation to 2,5-furandicarboxylic acid (FDCA), which is attained with 99% faradaic efficiency in 1 M KOH. In contrast to the case in 1 M KOH, NiOOH formation is suppressed, and consequently HMF oxidation is sluggish in 10 mM KOH, even at highly oxidizing potentials. Operando Raman experiments elucidate how surface adsorption and interaction dictates product selectivity and how the surface intermediates evolve with applied potential.