On-Surface Polymerization: From Polyarylenes to Graphene Nanoribbons and Two-Dimensional Networks

On-surface polymerization is a novel technique for the fabrication of one- and two-dimensional molecular networks confined on a surface and is a rapidly developing field in surface science. The molecular building blocks exhibit pre-defined connection sites at which, after thermal activation and diffusion on the surface, the molecules are linked in a clean environment. Depending on the position and number of these connection sites, activated molecules polymerize to yield chains or two-dimensional networks. The chemical composition of the resulting polymer is precisely defined by the precursor molecules. We review current developments in the field of on-surface polymerization and present different examples, including the fabrication of graphene nanoribbons. We introduce reductive Ullmann-type coupling as well as Scholl-type cyclodehydrogenation for fabrication of graphene nanoribbons of increasing width. The surface plays a crucial role during the activation and polymerization processes because it serves as a catalyst, promotes molecular diffusion, and has a huge influence on the final molecular architecture. One-dimensional polymers can act as molecular wires and their conductance has been studied at the level of individual chains. In addition, we discuss two-dimensional networks and describe recent progress in attempts to improve their quality using sequential activation or defect-healing

Wafer-sized multifunctional polyimine-based two-dimensional conjugated polymers with high mechanical stiffness

One of the key challenges in two-dimensional (2D) materials is to go beyond graphene, a prototype 2D polymer (2DP), and to synthesize its organic analogues with structural control at the atomic- or molecular-level. Here we show the successful preparation of porphyrin-containing monolayer and multilayer 2DPs through Schiff-base polycondensation reaction at an air–water and liquid–liquid interface, respectively. Both the monolayer and multilayer 2DPs have crystalline structures as indicated by selected area electron diffraction. The monolayer 2DP has a thickness of∼0.7 nm with a lateral size of 4-inch wafer, and it has a Young's modulus of 267±30 GPa. Notably, the monolayer 2DP functions as an active semiconducting layer in a thin film transistor, while the multilayer 2DP from cobalt-porphyrin monomer efficiently catalyses hydrogen generation from water. This work presents an advance in the synthesis of novel 2D materials for electronics and energy-related applications

Translation of rod-like template sequences into homochiral assemblies of stacked helical oligomers

International audienceTranslating a molecular sequence into a chemically different sequence has been powerfully exploited by nature, for example to produce proteins from mRNA templates. Yet, artificial systems inspired from this process are rare and far from optimized. Here we show that rod-like oligocarbamates may template the formation of well-defined sequences of stacked aromatic amide helices wound around them. Features of the rods, including the number and distance between carbamate functions and the presence of stereogenic centres, template the high fidelity formation of complementary stacks of helices each having a defined handedness, length and single or double helicity, through a self-assembly process allowing error correction. The outcome is unprecedentedly large abiotic folded architectures that may serve as scaffolds to organize appended functional features at positions in space defined with atomic precision across nanometric distances

Polymeric pseudo-crown ether for cation recognition via cation template-assisted cyclopolymerization

Cyclopolymerization is a chain polymerization of bifunctional monomers via alternating processes of intramolecular cyclization and intermolecular addition, to give soluble linear polymers consisting of in-chain cyclic structures. Though cyclopolymers comprising in-chain multiple large rings potentially show unique functionality, they generally require the elaborate design of bifunctional monomers. Here we report cation template-assisted cyclopolymerization of poly(ethylene glycol) dimethacrylates as an efficient strategy directly yielding polymeric pseudo-crown ethers with large in-chain cavities (up to 30-membered rings) for selective molecular recognition. The key is to select a size-fit metal cation for the spacer unit of the divinyl monomers to form a pseudo-cyclic conformation, where the two vinyl groups are suitably positioned for intramolecular cyclization. The marriage of supramolecular chemistry and polymer chemistry affords efficient, one-pot chemical transformation from common chemical reagents with simple templates to functional cyclopolymers

Anion-induced reconstitution of a self-assembling system to express a chloride-binding Co(10)L(15) pentagonal prism

Biochemical systems are adaptable, capable of reconstitution at all levels to achieve the functions associated with life. Synthetic chemical systems are more limited in their ability to reorganize to achieve new functions; they can reconfigure to bind an added substrate (template effect) or one binding event may modulate a receptor's affinity for a second substrate (allosteric effect). Here we describe a synthetic chemical system that is capable of structural reconstitution on receipt of one anionic signal (perchlorate) to create a tight binding pocket for another anion (chloride). The complex, barrel-like structure of the chloride receptor is templated by five perchlorate anions. This second-order templation phenomenon allows chemical networks to be envisaged that express more complex responses to chemical signals than is currently feasible