Visible-Light-Switchable Tellurium-Based Chalcogen Bonding: Photocontrolled Anion Binding and Anion Abstraction Catalysis.

Exploring new noncovalent bonding motifs with reversibly tunable binding affinity is of fundamental importance in manipulating the properties and functions of supramolecular self-assembly systems and materials. Herein, for the first time, we demonstrate a unique visible-light-switchable telluro-triazole/triazolium-based chalcogen bonding (ChB) system in which the Te moieties are connected by azobenzene cores. The binding strengths between these azo-derived ChB receptors and the halide anions (Cl , Br ) could be reversibly regulated upon irradiation by visible light of different wavelengths.

Photo-Controlled Macroscopic Self-Assembly Based on Photo-Switchable Hetero-Complementary Quadruple Hydrogen Bonds.

A photo-switchable hetero-complementary quadruple H-bonding array, which consists of an azobenzene-derived ureidopyrimidinone (UPy) module (Azo-UPy) and a nonphotoactive diamidonaphthyridine (DAN) derivative (Napy-1), is constructed based on a reversible photo-locking approach. Upon UV (390 nm)/Vis (460 nm) light irradiations, photo-switchable quadruple H-bonded dimerization between Azo-UPy and Napy-1 can be achieved with exhibiting 4.8×10 -fold differences in binding strength (ON/OFF ratios).

Towards photoswitchable quadruple hydrogen bonds a reversible "photolocking" strategy for photocontrolled self-assembly.

Developing new photoswitchable noncovalent interaction motifs with controllable bonding affinity is crucial for the construction of photoresponsive supramolecular systems and materials. Here we describe a unique "photolocking" strategy for realizing photoswitchable control of quadruple hydrogen-bonding interactions on the basis of modifying the ureidopyrimidinone (UPy) module with an -ester substituted azobenzene unit as the "photo-lock". Upon light irradiation, the obtained motif is capable of unlocking/locking the partial H-bonding sites of the UPy unit, leading to photoswitching between homo- and heteroquadruple hydrogen-bonded dimers, which has been further applied for the fabrication of novel tunable hydrogen bonded supramolecular systems.

A Visible-Light-Induced Dynamic Mechanical Bond as a Linkage for Dynamic Materials.

Exploring dynamic bonds and their applications in fabricating dynamic materials has received great attention. A photoinduced [2]rotaxane-based dynamic mechanical bond (DMB) features visible-light-triggered dynamic bonding behavior that is essentially distinguished from conventional dynamic chemical bonds. In this DMB, a photoisomerizable ortho-fluoroazobenzene unit is introduced as a steric-controllable stopper, the visible-light-induced dynamic wagging movement of which enables the photoregulated threading of the macrocycle.

Toward bidirectional photoswitchable colored photochromic molecules with visible light stability.

Photochromic [2]rotaxanes with bidirectional photoswitchability were fabricated, whose colored states exhibit remarkable visible-light and thermal stabilities as revealed by systematically spectroscopic investigations.

Tunable Water-Soluble Supramolecular Polymers by Visible-Light-Regulated Host-Guest Interactions.

The development of artificial self-assembling systems with dynamic photo-regulation features in aqueous solutions has drawn great attention owing to the potential applications in fabricating elaborate biological materials. Here we demonstrate the fabrication of water-soluble cucurbit[8]uril (CB[8])-mediated supramolecular polymers by connecting the fluorinated azobenzene (FAB) containing monomers through host-enhanced heteroternary π-π stacking interactions. Benefiting from the unique visible-light-induced E→Z photoisomerization of the FAB photochromophores, the encapsulation behaviors between the CB[8] macrocycle and the monomers could be regulated upon visible light irradiation, resulting in the depolymerization of such CB[8]-mediated supramolecular polymers.

Ultrahigh volatile iodine uptake by hollow microspheres formed from a heteropore covalent organic framework.

We herein report the construction of a new heteropore COF which consists of two different kinds of micropores with unprecedented shapes. It exists as hollow microspheres and exhibits an extremely high volatile iodine uptake (up to 481 wt%) by encapsulating iodine in the inner cavities and porous shells of the microspheres.

A Case Study on the Influence of Substitutes on Interlayer Stacking of 2D Covalent Organic Frameworks.

Interlayer stacking of 2D covalent organic frameworks (COFs) plays a crucial role in determining not only the geometry of channels inside COFs but also the mobility of carrier transport between COF layers. However, though topological structures of 2D COFs monolayers can be precisely predicted through the structures of building blocks, factors affecting their interlayer stacking remain poorly understood. In this work, a truxene-based building block on which six methyl groups are introduced was designed.

Construction of 2D covalent organic frameworks by taking advantage of the variable orientation of imine bonds.

A model system has been established to construct two-dimensional (2D) covalent organic frameworks (COFs) by taking advantage of the variable orientation of imine bonds. During the assembly process, the imine bonds adopt an unprecedented heterodromous orientation to facilitate the formation of the COFs.

Dual absorption spectral changes by light-triggered shuttling in bistable [2]rotaxanes with non-destructive readout.

Light-triggered photoisomerization of the azobenzene (AB) unit in bistable [2]rotaxanes can cause the shuttling of the macrocycle on the dumbbell, resulting in distinctive dual spectral variation characteristics: (1) the spectral change of the photochromic unit and (2) the variation of the charge-transfer band. By employing the CT bond region as an output signal, non-destructive readout of optical information could be achieved.

Precision Construction of 2D Heteropore Covalent Organic Frameworks by a Multiple-Linking-Site Strategy.

Integrating different kinds of pores into one covalent organic framework (COF) endows it with hierarchical porosity and thus generates a member of a new class of COFs, namely, heteropore COFs. Whereas the construction of COFs with homoporosity has already been well developed, the fabrication of heteropore COFs still faces great challenges. Although two strategies have recently been developed to successfully construct heteropore COFs from noncyclic building blocks, they suffer from the generation of COF isomers, which decreases the predictability and controllability of construction of this type of reticular materials.

Fluorescence enhancement through the formation of a single-layer two-dimensional supramolecular organic framework and its application in highly selective recognition of picric acid.

A two-dimensional (2D) supramolecular organic framework (SOF) has been constructed through the co-assembly of a triphenylamine-based building block and cucurbit[8]uril (CB[8]). Fluorescence turn-on of the non-emissive building block was observed upon the formation of the 2D SOF, which displayed highly selective and sensitive recognition of picric acid over a variety of nitroaromatics.

Construction of Covalent Organic Frameworks Bearing Three Different Kinds of Pores through the Heterostructural Mixed Linker Strategy.

It is very important to create novel topologies and improve structural complexity for covalent organic frameworks (COFs) that might lead to unprecedented properties and applications. Despite the progress achieved over the past decade, the structural diversity and complexity of COFs are quite limited. In this Communication, we report the construction of COFs bearing three different kinds of pores through the heterostructural mixed linker strategy involving the condensation of a D2h-symmetric tetraamine and two C2-symmetric dialdehydes of different lengths.

Synthesis, Photophysical and Electrochemical Properties, and Self-assembly Behavior of Two Hexaazatriphenylene Derivatives: A Single Bond Makes a Big Difference.

A hexaazatriphenylene (HAT) derivative (compound 1) that bears four n-octyl chains and two thienyl groups was designed and synthesized. Further light-induced oxidation coupling reaction led to thienyl-fused compound 2. Their photophysical and electrochemical properties and self-assembly behavior have been investigated by UV/Vis, fluorescence, and (1)H NMR spectroscopies, cyclic voltammetry (CV), scanning electron microscopy (SEM), and powder X-ray diffraction (PXRD).

The construction of rigid supramolecular polymers in water through the self-assembly of rod-like monomers and cucurbit[8]uril.

Two new types of supramolecular polymers have been constructed via the self-assembly of rigid rod-like monomers and cucurbit[8]uril (CB[8]) in water. These supramolecular polymers possessed rigid backbones and further aggregated into stick-like bunched fibres.

Self-assembly of chiral propeller-like supermolecules with unusual "sergeants-and-soldiers" and "majority-rules" effects.

Chiral amplification is an interesting phenomenon in supramolecular chemistry mainly observed in complicated systems in which cooperative effect dominate. Herein, chiral, supramolecular, propeller-like architectures have been constructed through coassembly of an achiral disk-shaped molecule and chiral amino acid derivatives driven by intermolecular hydrogen bonding. Both the "sergeants-and-soldiers" principle and "majority-rules" effect are applicable in these discrete four-component supermolecules, which are the simplest supramolecular system ever reported that exhibit chiral amplification.

Oligo(quinoxalineethynylene)s: synthesis, properties, and Ag+-mediated complanation.

A series of oligo(quinoxalineethylene)s which exhibit n-type semi-conducting features were synthesized, and adding Ag(+) to their solutions induced the backbones to adopt coplanar conformations due to Ag(+)-N coordination.