Reviews & Analysis

A new concept termed 'robust dynamics' is presented as the intellectual centerpiece to the union between metal–organic frameworks (MOFs) and mechanically interlocking molecules. Robust dynamics allows highly flexible entities, which are bound covalently to MOF backbones, to carry out repeated movements without affecting the integrity of the overall structure.

Molecular 'boxes' can hold other molecules and often serve as the moving parts in molecular switches. The latest addition to this class of compounds is a simple-to-prepare positively charged macrocycle that can encircle molecular guests of appropriate size and charge — and offers new opportunities for assembling stimuli-responsive structures.

To improve organic electronic devices, the principles underlying organic-film/metal-electrode interfaces must be understood. A comprehensive study of the organic electron acceptor TCNQ on a copper surface reveals a structural rearrangement of both the organic molecule and the metal surface atoms after charge transfer across the interface.

The iron active sites of enzymes routinely cleave strong C–H bonds, but synthetic complexes have so far been much slower and less efficient. Now, the reactivity of a biomimetic diiron complex has been dramatically enhanced by converting its oxo bridge into a terminal ligand, and its iron centre from low spin to high spin.

Single-molecule magnets are coordination clusters with magnetic properties that are typically reliant on the coupling between pairs of metal centres. Now, a cluster in which magnetism arises from delocalized electrons — built using an imidazolate bridge, a common linker in metal–organic architectures — shows promise for molecular memory devices.

Spin transitions are the most common mechanism for switching molecules between two distinct energy states, for uses as diverse as memory devices and displays. How the transition is triggered is crucial, and a pentanuclear cluster has now been reported in which the spin transition is promoted by redox transfer between different metal ions.

The synthesis or separation of chiral compounds is crucial for many areas of chemistry, with chiral solids having important roles as catalysts or separating agents. This Review covers recent progress and future avenues for developing methods of preparing chiral solids from achiral starting materials.

The convergent total synthesis of the pore-forming polytheonamide B — a linear peptide natural product — pokes holes through perceived limitations in de novo peptide synthesis, and provides access to novel synthetic membrane channels.

Macrocyclic compounds can serve as hosts for smaller organic molecules, but precise control over the uptake and release of the guests remains challenging. Now, a host–guest system has been built that responds to the addition of metal ions, showing promise for drug-delivery applications.

A strong acid catalyst and a small change to one reactant have transformed a 37-year-old 'curiosity' into a useful chemical reaction that has great potential in organic synthesis.

Electrochemistry has so far been mostly centred around measuring factors and coefficients. Through the reversible reduction and oxidation of an electrode coating formed from three-dimensional hybrid aniline–gold nanoparticles, it has now moved on to controlling the pH of a solution, thus triggering specific reactions.

Rare-earth metal dialkyl complexes can be readily transformed into the corresponding cationic monoalkyl species — which have been shown to catalyse a range of (co)polymerization processes — as well as into polyhydride complexes that have unique structures and a rich reaction chemistry.

The interactions of electrons and water molecules are not just of great fundamental interest but are also studied to understand the role electrons have in damaging biomolecules. Now using ultrafast photoelectron spectroscopy, key details about the energy and lifetime of the hydrated electron in bulk and at an interface have been determined.

Monomers that contain masked ketene groups provide new opportunities for facile crosslinking and post-synthetic modification of polymers in a wide variety of materials applications.

The long-awaited first total synthesis of the structurally intriguing natural product palau'amine has now been achieved. The synthesis features cascade reactions and an 'across ring' stitching of a 'macropalau'amine', and sets the bar for future efforts towards an enantioselective variant.

Public acceptance of the expansion of nuclear power may hinge on the safe disposal of nuclear waste. Ion exchangers that remove radioactive metals — such as caesium ions — from the waste could provide part of the answer, so a flexible-framework material that selectively grab them from solution is a step in the right direction.