Solid-state red-emissive (cyano)vinylene heteroaromatics via Pd-catalysed C-H homocoupling.

Thiophene-based π-conjugated systems are important materials for organic electronics; thus, their synthesis is of topical interest. We report fluorescent thiophene/furan-based vinylene and cyanovinylene systems via Pd-catalysed homocoupling [Pd(OAc)2, pivalic acid, KOAc, DMAc, 140 °C]. The methodology is versatile and allows the development of a variety of π-conjugated systems without the need for pre-functionalized building units. The reaction tolerates electron-rich, electron-deficient and large π-conjugated substrates. The developed compounds absorb in the visible region (400-515 nm) and emit green to orange fluorescence in the solution state (510-600 nm). Most importantly, the compounds exhibit strong aggregation-induced emission (AIE) in the NIR region (λem = 650 nm), with quantum yields reaching up to 10%. Steric hindrance imparted by vinylene/cyanovinylene units is responsible for the strong solid-state luminescence. DFT-optimized structures reveal an apparent twist of 20-40° in the molecular backbone of the compounds, supporting the AIE behaviour of the compounds.

Synthesis of mesoscale ordered two-dimensional π-conjugated polymers with semiconducting properties.

Two-dimensional materials with high charge carrier mobility and tunable band gaps have attracted intense research effort for their potential use in nanoelectronics. Two-dimensional π-conjugated polymers constitute a promising subclass because the band structure can be manipulated by varying the molecular building blocks while preserving key features such as Dirac cones and high charge mobility. The major barriers to the application of two-dimensional π-conjugated polymers have been the small domain size and high defect density attained in the syntheses explored so far. Here, we demonstrate the fabrication of mesoscale ordered two-dimensional π-conjugated polymer kagome lattices with semiconducting properties, Dirac cone structures and flat bands on Au(111). This material has been obtained by combining a rigid azatriangulene precursor and a hot dosing approach, which favours molecular diffusion and eliminates voids in the network. These results open opportunities for the synthesis of two-dimensional π-conjugated polymer Dirac cone materials and their integration into devices.

Functional π-Conjugated Two-Dimensional Covalent Organic Frameworks.

Fingerprints of π-conjugated compounds are ubiquitous in nature and play a crucial part in human existence. For instance, cis-retinal, an endogenous π-conjugated molecule present in the eye, performs a vital role in the function of visual perception. π-Conjugated molecules have also received a great deal of attention owing to their intriguing optical properties and created a surge in optoelectronics. Varieties of π-conjugated molecules/oligomers have been developed and explored for a number of applications such as organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), organic photovoltaics (OPVs), and sensors, among others. While the extended π-delocalization in one-dimensional (1D) polymers versus oligomers produce superior optical and electronic properties, further extension of π-delocalization to the second dimension (2D) is expected to give rise even more intriguing properties as revealed by theoretical studies. As a matter of fact, graphene is the best example of 2D-conjugated polymers, but its zero-band-gap behavior is a major impediment for semiconducting applications. In contrast, it was challenging to prepare 2D crystalline polymers until the discovery of boroxine/boronate ester linked covalent organic frameworks (COFs) by Yaghi and co-workers. COFs are a new class of porous crystalline polymers in which organic building blocks are held together by covalent bonds. These polymers exhibit potential applications in gas storage, energy storage, photocatalyst, heterogeneous catalysis, sensors, etc. However, the first π-conjugated COF was realized in 2009 via the introduction of imine linker (-C═N-) between the building blocks. Since then, wide varieties of COFs with various π-delocalization promoting spacers have been developed and explored their electronic and optical properties and pertinent applications. In this review, we will highlight the importance of 2D π-conjugated COFs and their achievements in developing novel functionalities.

Construction of Novel Cyclic Tetrads by Axial Coordination of Thiaporphyrins to Tin(IV) Porphyrin.

We report the formation of new cyclic porphyrin tetrads 1 and 2, which were obtained from the reaction between dihydroxytin(IV) porphyrin and cis-dihydroxy-21-thiaporphyrin/21,23-dithiaporphyrin. The unique oxophilicity of tin(IV) porphyrin was the driving force for the formation of these tetrads. Moreover, these novel tetrads represent the first examples of cyclic porphyrins containing tin(IV) that are constructed exclusively on the basis of the "Sn-O" interaction without any other complementary, noncompetitive mode of interactions. The molecular structures of the cyclic tetrads have been investigated by matrix-assisted laser desorption ionization time-of-flight mass spectrometry, NMR spectroscopy, quantum-mechanical calculations, and, in one case, single-crystal X-ray crystallography. The X-ray structure revealed that the two cis-dihydroxy-N2S2 porphyrins were coordinated at the axial positions of two tin(IV) porphyrins, leading to the symmetric cyclic tetrad structure. The optical properties of tetrads were studied, and these compounds were stable under redox conditions. Preliminary photophysical studies carried out on the tetrads indicated efficient energy transfer from tin(IV) porphyrin to the thiaporphyrin unit, which highlights their potential applications in energy and electron transfer in the future.

Hybrid Macrocycles of Subporphyrins and Triphyrins.

The dibenzofuran/dibenzothiophene-based nonaromatic hybrid macrocycles, exhibiting the features of both contracted macrocycles, subporphyrins and triphyrins, have been synthesized under simple reaction conditions using readily available precursors. The monoanionic new macrocyclic ligands with three donor atoms, such as two pyrrole nitrogens and one dibenzofuran oxygen or dibenzothiophene sulfur, readily form Re(I) complexes.