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In the design of dynamic supramolecular systems used in molecular machines, it is important to understand the binding preferences between the macrocycle and stations along the thread. Here, we apply 1H NMR spectroscopy to investigate the relative stabilities of a series of linear alkylammonium templated pseudorotaxanes with the general formula [H2NRR'][Cr7CoF8(O2CCH2tBu)16] by exchanging the cation in solution. Our results show that the pseudorotaxanes are able to exchange threads via a dissociative mechanism. The position of equilibrium is dependent upon the ammonium cation and solvent used. Short chain primary ammonium cations are shown to be far less favourable macrocycle stations than secondary ammonium cations. Collision‐induced dissociation mass spectrometry (CID‐MS) has been used to look at disassembly of the pseudorotaxanes in a solvent‐free environment and stability trends compared to those in acetone‐d6. The energy needed to induce 50 % of the precursor ion loss (E50) is used and shows a similar trend to the equilibria measured by NMR. The relative stabilities of these hybrid inorganic‐organic pseudo‐rotaxanes are different to those of host‐guest compounds involving crown ethers and this may be valuable for the design of molecular machines. [ABSTRACT FROM AUTHOR]

A synthetic strategy is demonstrated to prepare two distinct trimers of antiferromagnetically coupled {Cr7Ni} rings, substantially varying the magnetic interactions between the spin centres. The interactions were studied using multi‐frequency cw EPR: in a trimer linked via non‐covalent H‐bonding interactions no measurable interaction between rings was seen, while in a trimer linked via iso‐nicotinate groups isotropic and anisotropic exchange interactions of +0.42 and −0.8 GHz, respectively, were observed. The latter are the same as those for a simpler hetero‐dimer system, showing how the spin‐spin interactions can be built in a predictable and modular manner in these systems. [ABSTRACT FROM AUTHOR]

Despite being known for decades the chemical reactivity of homoatomic seven‐atom phosphorus clusters towards small molecules remains largely unexplored. Here, we report that neutral tris(silyl) functionalised heptaphosphane (P7(SiR3)3) cages are capable of heteroallene capture between the P−Si bonds of the cluster. A range of isocyanates and an isothiocyanate were investigated. In the case of isocyanates, silyl bonding at oxygen or nitrogen is regioselectively directed by the functional group on the isocyanate and substituents on the silyl moiety. Above all, we find that captured isothiocyanate molecules can be exchanged for isocyanate molecules, indicative of small molecule catch and release. Small molecule catch and release at these Zintl‐derived clusters reveals their potential application as chemical storage materials or as reusable probes. [ABSTRACT FROM AUTHOR]

A series of new IrIII complexes with carbene ligands that contain a range of benzyl wingtip groups have been prepared and fully characterised by NMR spectroscopy, HRMS, elemental analysis and X-ray diffraction. All the complexes were active in the acceptorless dehydrogenation of alcohol substrates in 2,2,2-trifluoroethanol to give the corresponding carbonyl compounds. The most active complex bore an electron-rich carbene ligand; this complex was used to catalyse the highly efficient and chemoselective dehydrogenation of a wide range of secondary alcohols to their respective ketones, with turnover numbers up to 1660. Mechanistic studies suggested that the turnover of the dehydrogenation reaction is limited by the H2-formation step. [ABSTRACT FROM AUTHOR]