Dingyong Zhong

Linear Alkane Polymerization on a Gold Surface

The confining channel geometry of a gold surface induces selective end-to-end linking of hydrocarbon chains. In contrast to the many methods of selectively coupling olefins, few protocols catenate saturated hydrocarbons in a predictable manner. We report here the highly selective carbon-hydrogen (C–H) activation and subsequent dehydrogenative C–C coupling reaction of long-chain (>C20) linear alkanes on an anisotropic gold(110) surface, which undergoes an appropriate reconstruction by adsorption of the molecules and subsequent mild annealing, resulting in nanometer-sized channels (1.22 nanometers in width). Owing to the orientational constraint of the reactant molecules in these one-dimensional channels, the reaction takes place exclusively at specific sites (terminal CH3 or penultimate CH2 groups) in the chains at intermediate temperatures (420 to 470 kelvin) and selects for aliphatic over aromatic C–H activation.

On-Surface Synthesis of Rylene-Type Graphene Nanoribbons

The narrowest armchair graphene nanoribbon (AGNR) with five carbons across the width of the GNR (5-AGNR) was synthesized on Au(111) surfaces via sequential dehalogenation processes in a mild condition by using 1,4,5,8-tetrabromonaphthalene as the molecular precursor. Gold-organic hybrids were observed by using high-resolution scanning tunneling microscopy and considered as intermediate states upon AGNR formation. Scanning tunneling spectroscopy reveals an unexpectedly large band gap of Δ = 2.8 ± 0.1 eV on Au(111) surface which can be interpreted by the hybridization of the surface states and the molecular states of the 5-AGNR.

Surface Supported Gold–Organic Hybrids: On‐Surface Synthesis and Surface Directed Orientation

The surface-assisted synthesis of gold-organic hybrids on Au (111) and Au (100) surfaces is repotred by thermally initiated dehalogenation of chloro-substituted perylene-3,4,9,10-tetracarboxylic acid bisimides (PBIs). Structures and surface-directed alignment of the Au-PBI chains are investigated by scanning tunnelling microscopy in ultra high vacuum conditions. Using dichloro-PBI as a model system, the mechanism for the formation of Au-PBI dimer is revealed with scanning tunnelling microscopy studies and density functional theory calculations. A PBI radical generated from the homolytic C-Cl bond dissociation can covalently bind a surface gold atom and partially pull it out of the surface to form stable PBI-Au hybrid species, which also gives rise to the surface-directed alignment of the Au-PBI chains on reconstructed Au (100) surfaces.

Atomic Structures of CH3NH3PbI3 (001) Surfaces

We report on the atomic structures of methylammonium (MA) lead iodide (CH3NH3PbI3) perovskite surfaces, based on a combined scanning tunneling microscopy and density functional theory calculation study. A reconstructed surface phase with iodine dimers, coexisting with the pristine zigzag phase, was found at the MA-iodine-terminated (001) surfaces of the orthorhombic perovskite films grown on Au(111) surfaces. The reorientation of surface MA dipoles, which strengthens the interactions with surface iodine anions, resulting in a slight energy reduction of 34 meV per unit cell, is responsible for the surface iodine dimerization. According to our calculation, the surface MA dipoles weaken the surface polarity and are therefore considered to be stabilizing the surface structures.

Surface-mounted molecular rotors with variable functional groups and rotation radii.

A strategy for designing and activating surface-mounted molecular rotors with variable rotation radii and functional groups is proposed and demonstrated. The key point of the strategy is to separate the anchor and the rotating functional group from each other by using a connector of adjustable length. The three independent parts of the molecule are responsible for different functions to support the rotating movement of the molecule as a whole. In this way, one can easily change each part to obtain molecular rotors with different sizes, anchors, and functional rotating groups.

Graphene-like nanoribbons periodically embedded with four- and eight-membered rings

Embedding non-hexagonal rings into sp2-hybridized carbon networks is considered a promising strategy to enrich the family of low-dimensional graphenic structures. However, non-hexagonal rings are energetically unstable compared to the hexagonal counterparts, making it challenging to embed non-hexagonal rings into carbon-based nanostructures in a controllable manner. Here, we report an on-surface synthesis of graphene-like nanoribbons with periodically embedded four- and eight-membered rings. The scanning tunnelling microscopy and atomic force microscopy study revealed that four- and eight-membered rings are formed between adjacent perylene backbones with a planar configuration. The non-hexagonal rings as a topological modification markedly change the electronic properties of the nanoribbons. The highest occupied and lowest unoccupied ribbon states are mainly distributed around the eight- and four-membered rings, respectively. The realization of graphene-like nanoribbons comprising non-hexagonal rings demonstrates a controllable route to fabricate non-hexagonal rings in nanoribbons and makes it possible to unveil their unique properties induced by non-hexagonal rings.

Multilevel Supramolecular Architectures Self-Assembled on Metal Surfaces

We report the controllability of the complexity of surface-supported supramolecular assembly on metal surfaces. By introducing mismatch between the molecular packing and the surface atomic periodicity in the systems with comparable strength of intermolecular and molecule-substrate interactions, a homomolecular assembly exhibiting two-dimensional multilevel structures up to quaternary level was observed. In such a multiperiodicity modulated system, neither the intermolecular nor molecule-substrate interactions solely dominate the assembly, resulting in complicated multilevel structures. We further demonstrated that the multilevel assemblies can serve as templates for site-selective adsorption of guest molecules.

Synthesis and Characterization of Hexapole [7]Helicene, A Circularly Twisted Chiral Nanographene

We report the synthesis and characterization of two hexapole [7]helicenes (H7Hs). Single crystal X-ray diffraction unambiguously confirms the molecular structure. H7H absorbs light, with distinct Cotton effect, from ultraviolet to the near-infrared (λmax = 618 nm). Cyclic voltammetry reveals nine reversible redox states, consecutively from -2 to +6. These chiroptical and electronic properties of H7H are inaccessible from helicenes small homologues.

Gold DNA-conjugates: ion specific self-assembly of gold nanoparticles via the dG-quartet.

The Oxytricha telomere DNA hairpin 5′-d(G4T4G4) immobilized on 13 nm gold nanoparticles forms a supramolecular assembly via dG-quartets, as determined by the color change and by SEM. The aggregation is ion-dependent and selective for sodium ions. K+ is less efficient while Li+ and Cs+ do not drive the aggregation. This work is the first effort exploring the use of secondary structures of DNA (quadruplexes) for producing self-assemblies of gold nanoparticles.

Linear Alkane CC Bond Chemistry Mediated by Metal Surfaces

Linear alkanes undergo different C-C bond chemistry (coupling or dissociation) thermally activated on anisotropic metal surfaces depending on the choice of the substrate material. Owing to the one-dimensional geometrical constraint, selective dehydrogenation and C-C coupling (polymerization) of linear alkanes take place on Au(110) surfaces with missing-row reconstruction. However, the case is dramatically different on Pt(110) surfaces, which exhibit similar reconstruction as Au(110). Instead of dehydrogenative polymerization, alkanes tend to dehydrogenative pyrolysis, resulting in hydrocarbon fragments. Density functional theory calculations reveal that dehydrogenation of alkanes on Au(110) surfaces is an endothermic process, but further C-C coupling between alkyl intermediates is exothermic. On the contrary, due to the much stronger C-Pt bonds, dehydrogenation on Pt(110) surfaces is energetically favorable, resulting in multiple hydrogen loss followed by C-C bond dissociation.