Regioselective 1,4-hydroboration of pyridines catalyzed by an acid-initiated boronium cation

The reaction of the commercially available ammonium salt NH4BPh4 with a pyridine-activated pinacolborane species generates a boronium cation that facilitates the 1,4-selective hydroboration of pyridines in polar solvents. This catalytic reaction is amenable to a host of reactive functional groups and provides access to sterically bulky hydroboration products, previously inaccessible by metal-free routes. Further, the regioselectivity of this reaction can be altered by reducing the polarity of the reaction solvent, resulting in greater proportions of the 1,2-hydroboration product.E. N. K. thanks NSERC of Canada for a PGSD as well as the Cambridge Commonwealth, European, and International Trust and Gonville and Caius College for funding

Exploring Cation-Anion Redox Processes in One-Dimensional Linear Chain Vanadium Tetrasulfide Rechargeable Magnesium Ion Cathodes.

For magnesium ion batteries (MIBs) to be used commercially, new cathodes must be developed that show stable reversible Mg intercalation. VS4 is one such promising material, with vanadium and disulfide anions [S2]2- forming one-dimensional linear chains, with a large interchain spacing (5.83 Å) enabling reversible Mg insertion. However, little is known about the details of the redox processes and structural transformations that occur upon Mg intercalation and deintercalation. Here, employing a suite of local structure characterization methods including X-ray photoelectron spectroscopy (XPS), V and S X-ray absorption near-edge spectroscopy (XANES), and 51V Hahn echo and magic-angle turning with phase-adjusted sideband separation (MATPASS) NMR, we show that the reaction proceeds via internal electron transfer from V4+ to [S2]2-, resulting in the simultaneous and coupled oxidation of V4+ to V5+ and reduction of [S2]2- to S2-. We report the formation of a previously unknown intermediate in the Mg-V-S compositional space, Mg3V2S8, comprising [VS4]3- tetrahedral units, identified by using density functional theory coupled with an evolutionary structure-predicting algorithm. The structure is verified experimentally via X-ray pair distribution function analysis. The voltage associated with the competing conversion reaction to form MgS plus V metal directly is similar to that of intermediate formation, resulting in two competing reaction pathways. Partial reversibility is seen to re-form the V5+ and S2- containing intermediate on charging instead of VS4. This work showcases the possibility of developing a family of transition metal polychalcogenides functioning via coupled cationic-anionic redox processes as a potential way of achieving higher capacities for MIBs.S. D. acknowledges DST Overseas Visiting Fellowship in Nano Science and Technology, Government of India (July 2018− June 2019) and EPSRC Programme Grant (EP/M009521/1) for fellowships and funding. This work used the ARCHER UK National Super-computing Service (http://www.archer.ac.uk). This research used resources of the Center for Functional Nanomaterials, which is a U.S. DOE Office of Science Facility, and the Scientific Data and Computing Center, a component of the Computational Science Initiative, at Brookhaven National Laboratory under Contract No. DE-SC0012704. The XPS data collection was performed at the EPSRC National Facility for XPS ("HarwellXPS"), operated by Cardiff University and UCL, under Contract No. PR16195. via our membership of the UK's HEC Materials Chemistry Consortium, which is funded by EPSRC (EP/L000202)

Strengthening the Magnetic Interactions in Pseudobinary First-Row Transition Metal Thiocyanates, M(NCS)2.

Understanding the effect of chemical composition on the strength of magnetic interactions is key to the design of magnets with high operating temperatures. The magnetic divalent first-row transition metal (TM) thiocyanates are a class of chemically simple layered molecular frameworks. Here, we report two new members of the family, manganese(II) thiocyanate, Mn(NCS)2, and iron(II) thiocyanate, Fe(NCS)2. Using magnetic susceptibility measurements on these materials and on cobalt(II) thiocyanate and nickel(II) thiocyanate, Co(NCS)2 and Ni(NCS)2, respectively, we identify significantly stronger net antiferromagnetic interactions between the earlier TM ions-a decrease in the Weiss constant, θ, from 29 K for Ni(NCS)2 to -115 K for Mn(NCS)2-a consequence of more diffuse 3d orbitals, increased orbital overlap, and increasing numbers of unpaired t2g electrons. We elucidate the magnetic structures of these materials: Mn(NCS)2, Fe(NCS)2, and Co(NCS)2 order into the same antiferromagnetic commensurate ground state, while Ni(NCS)2 adopts a ground state structure consisting of ferromagnetically ordered layers stacked antiferromagnetically. We show that significantly stronger exchange interactions can be realized in these thiocyanate frameworks by using earlier TMs.EPSRC NPIF 2018 fund Laboratory Directed Research and Development Program of Oak Ridge National Laboratory NSERC of Canada PGSD fund Trinity College, Cambridge School of Chemistry, University of Nottingham Hobday Fellowship EPSRC Strategic Equipment Grant EP/M000524/

Strongly coloured thiocyanate frameworks with perovskite-analogue structures

We report the first examples of thiocyanate-based analogues of the cyanide Prussian Blue compounds, MIII[Bi(SCN)6], M= Fe, Cr, Sc. These compounds adopt the primitive cubic pcu topology and show strict cation order. Optical absorption measurements show these compounds have band gaps within the visible and near IR region, suggesting that they may be useful for applications where light harvesting is key, such as photocatalysis. We also show that Cr[Bi(SCN)6] can reversibly uptake water into its framework structure pointing towards the possibility of using these frameworks for host/guest chemistry

Post-Assembly Reactivity of N-Aryl Iminoboronates: Reversible Radical Coupling and Unusual B-N Dynamic Covalent Chemistry.

Post-assembly reaction of a dynamic covalent iminoboronate system following addition of Cp2 Co resulted in the formation of a series of new reductively coupled dianionic dimers via C-C bond formation. The dimers formed as a mixture of BN-containing isomeric products: diastereomers rac5 and meso5, with coupled five-membered rings, and enantiomeric rac6, with a fused six-membered ring bicyclic system from C-C bond formation and rearrangement of the B-N bonds. Each isomer was identified using 1 H NMR spectroscopy in combination with single crystal X-ray structure determination. Interestingly, interconversion between the coupled five-membered rings (rac5 ) and fused bicyclic systems (rac6 ) was found to occur through an unprecedented breaking and reforming of the B-N covalent bond. Further, the coupled products could be converted quantitatively back to their iminoboronate precursors with addition of the electron abstractor Ph3 C+ .European Research Council (695009) EPSRC (EP/M01083X/1

The structures of ordered defects in thiocyanate analogues of Prussian Blue.

We report the structures of six new divalent transition metal hexathiocyanatobismuthate frameworks with the generic formula , M = Mn, Co, Ni and Zn. These frameworks are defective analogues of the perovskite-derived trivalent transition metal hexathiocyanatobismuthates MIII[Bi(SCN)6]. The defects in these new thiocyanate frameworks order and produce complex superstructures due to the low symmetry of the parent structure, in contrast to the related and more well-studied cyanide Prussian Blue analogues. Despite the close similarities in the chemistries of these four transition metal cations, we find that each framework contains a different mechanism for accommodating the lowered transition metal charge, making use of some combination of Bi(SCN)6 3- vacancies, MBi antisite defects, water substitution for thiocyanate, adventitious extra-framework cations and reduced metal coordination number. These materials provide an unusually clear view of defects in molecular framework materials and their variety suggests that similar richness may be waiting to be uncovered in other hybrid perovskite frameworks

Exploring the Peierls-Distorted Vanadium Sulphide as A Rechargeable Mg-Ion Cathod .pdf

For magnesium ion batteries (MIB) to be used commercially, new cathodes must be developed that show stable reversible Mg intercalation. VS4 is one such promising material, with vanadium and disulphide anions [S2]2- forming one dimensional linear chains, with a large interlayer spacing (5.83 Å) enabling Mg insertion. However, little is known about the details of the redox processes and structural transformations that occur upon Mg intercalation and deintercalation of VS4. Here we use a suite of local structure characterization methods including XPS, V and S X-ray Absorption Near Edge Spectroscopy and 51V Hahn-Echo and Magic Angle Turning with Phase Adjusted Sideband Separation NMR to elucidate the complex electrochemical reaction pathways. We show that the reaction proceeds via internal electron transfer from V4+ to [S2]2, resulting in the simultaneous and coupled oxidation of V4+ to V5+ and reduction of [S2]2- to S2-. We report the formation of a previously unknown intermediate in the Mg-V-S compositional space, Mg3V2S8, which is made of [VS4]3- tetrahedral units and identified using an evolutionary structure predicting algorithm and verified experimentally via X-ray Pair Distribution Function analysis. Subsequent magnesiation gives rise to the reduction of V5+ towards V4+. Further magnesiation sees conversion to MgS plus V metal; this reaction potential is close to the conversion potential of VS4 to Mg3V2S8, leading to competing reaction pathways. Demagnesiation results in the reformation of the V5+, S2- containing intermediate instead of VS4. This work showcases the possibility of developing a family of transition metal polychalcogenides functioning via anionic as well as combined cationic-anionic redox processes, as a potential way of achieving higher capacities for MIBs.</p