Investigating Hydrogen Bonding in Quinoxaline-Based Thermally Activated Delayed Fluorescent Materials.

In recent years, hydrogen bonding (H bonding) as an intramolecular locking strategy has been proposed to enhance photoluminescence, color purity, and photostability in thermally activated delayed fluorescence (TADF) materials. Rigidification as a design strategy is particularly relevant when using electron-deficient N-heterocycles as electron acceptors, because these materials often suffer from poor performance as orange to near-infrared emitters as a result of the energy gap law. To critically evaluate the presence of H bonding in such materials, two TADF-active donor-acceptor dyads, ACR-DQ and ACR-PQ, were synthesized. Despite their potential sites for intramolecular H bonding and emissions spanning yellow to deep red, computational analyses (including frequency, natural bond orbital, non-covalent interaction, and potential energy surface assessments) and crystal structure examinations collectively suggest the absence of H bonding in these materials. Our results indicate that invoking intramolecular H bonding should be done with caution in the design of rigidified TADF materials.

Dopants Induce Persistent Room Temperature Phosphorescence in Triarylamine Boronate Esters.

Purely organic materials exhibiting room temperature phosphorescence (RTP) are promising candidates for oxygen sensors and information encryption owing to their cost-effective and environmentally friendly nature. Herein, we report a bimolecular RTP system where DTBU acts as the guest and TBBU serves as the host. In contrast to previously reported results, we find that both pure DTBU and TBBU do not exhibit RTP in the solid state even under N2 atmosphere. A DTBU/TBBU system with a low doping ratio (0.1 mol %) exhibits persistent yellowish-green afterglow with a lifetime of 340 ms and is highly sensitive to oxygen. A DTBU/TBBU system with a higher doping ratio (10 mol %) maintains a phosphorescence lifetime of 179 ms under air. Applications of DTBU/TBBU at varied doping ratios in both oxygen sensing and information encryption are demonstrated. We propose that the T1 state of TBBU acts as an energy transfer intermediate between Tn and T1 of DTBU, ultimately leading to the generation of persistent RTP. Overall, this work demonstrates the critical importance of material purity in the design of RTP systems, and how an understanding of host-guest doping enables their photophysical properties to be precisely tuned.

Excited-state dynamics of C3-symmetric heptazine-based thermally activated delayed-fluorescence emitters.

Heptazine-based materials have recently emerged as a promising motif for thermally activated delayed fluorescence, as their near-zero or negative singlet-triplet energy gaps enable extremely fast reverse intersystem crossing (rISC) rates. Another method for achieving a high rate of rISC is through the use of highly symmetric emitters, which benefit from energy-level degeneracies and a high density of states. Here, we investigate the effect of combining these two design strategies on the excited-state dynamics of C3-symmetric emitters containing heptazine cores. We find that in two of the four emitters studied, the S1 state has a high degree of locally excited (LE) character with density on the heptazine moiety, preventing excited-state localization and a loss of symmetry in the energy-minimized S1 geometry. Surprisingly, these symmetric molecules still suffer from a loss of density of triplet states below the S1 state. Overall, we find that maintaining C3 symmetry will not necessarily maintain density of states, but that heptazine-based materials with LE S1 states still benefit from maximized rISC rates via increased spin-orbit coupling with low-lying charge-transfer triplet states and exhibit advantageous photophysical properties, such as near-unity photoluminescence quantum yields and high colour purity.

Red-Shifted Emission in Multiple Resonance Thermally Activated Delayed Fluorescent Materials through Malononitrile Incorporation.

Multiple resonance thermally activated delayed fluorescent (MR-TADF) materials offer higher color purity than conventional TADF materials but suffer from aggregation-caused quenching (ACQ) and rarely exhibit red emission. Herein, two malononitrile-substituted emitters are synthesized from a quinolino[3,2,1-de]acridine-5,9-dione (QAO) MR-TADF precursor. Both materials maintain MR-TADF, while they display red-shifted fluorescence. They also overcome ACQ, displaying enhanced emission upon aggregation in solution and forming red-emissive J-aggregates in the solid state with photoluminescent quantum yields of 9 and 11%.

Imidazophenothiazine-Based Thermally Activated Delayed Fluorescence Materials with Ultra-Long-Lived Excited States for Energy Transfer Photocatalysis.

Triplet-triplet energy transfer (EnT) is a powerful activation pathway in photocatalysis that unlocks new organic transformations and improves the sustainability of organic synthesis. Many current examples, however, still rely on platinum-group metal complexes as photosensitizers, with associated high costs and environmental impacts. Photosensitizers that exhibit thermally activated delayed fluorescence (TADF) are attractive fully organic alternatives in EnT photocatalysis. However, TADF photocatalysts incorporating heavy atoms remain rare, despite their utility in inducing efficient spin-orbit-coupling, intersystem-crossing, and consequently a high triplet population. Here, we describe the synthesis of imidazo-phenothiazine (IPTZ), a sulfur-containing heterocycle with a locked planar structure and a shallow LUMO level. This acceptor is used to prepare seven TADF-active photocatalysts with triplet energies up to 63.9 kcal mol-1. We show that sulfur incorporation improves spin-orbit coupling and increases triplet lifetimes up to 3.64 ms, while also allowing for tuning of photophysical properties via oxidation at the sulfur atom. These IPTZ materials are applied as photocatalysts in five seminal EnT reactions: [2 + 2] cycloaddition, the disulfide-ene reaction, and Ni-mediated C-O and C-N cross-coupling to afford etherification, esterification, and amination products, outcompeting the industry-standard TADF photocatalyst 2CzPN in four of the five studied scenarios. Detailed photophysical and theoretical studies are used to understand structure-activity relationships and to demonstrate the key role of the heavy atom effect in the design of TADF materials with superior photocatalytic performance.

Uncovering the Mechanism of Thermally Activated Delayed Fluorescence in Coplanar Emitters Using Potential Energy Surface Analysis.

Planarized emitters exhibiting thermally activated delayed fluorescence (TADF) have attracted attention due to their narrow emission spectra, improved photostability, and high quantum yields, but with large singlet-triplet energy gaps (ΔEST) and no heavy atoms, the origin of their TADF remains a subject of debate. Here we prepare two isomeric, coplanar donor-acceptor compounds, with HMAT-2PYM performing dual TADF and room-temperature phosphorescence but with HMAT-4PYM exhibiting only prompt fluorescence. Although conventional TADF design principles suggest that neither isomer should exhibit TADF, we reveal differences in the excited state potential energy surfaces that enable spin-flip processes in only one isomer. We also find that hydrogen bonding is absent between the planar units of these emitters, despite earlier claims of intramolecular hydrogen bonding in similar compounds. Overall, this work demonstrates that potential energy surface analysis is a practical strategy for designing coplanar TADF materials that might otherwise be overlooked by conventional TADF design metrics.

The Tunable Photophysical Properties of Enamine Intermediates Involved in Light-Driven Aminocatalysis.

In this study, the photosensitive nature of reactive enamine and polyenamine intermediates is investigated to improve our understanding of light-mediated aminocatalytic reactions. Experimental optical absorption data and TD-DFT calculations reveal that these intermediates are excited directly from the HOMO on the enamine moiety to low-lying unoccupied orbitals localized on the catalyst scaffold. This indicates that the photophysical properties of enamine intermediates can be tuned for visible light-mediated reactions by modifications to the aminocatalyst.

Rotational Spectroscopic and Ab Initio Investigation of the Rotamer Geometries of 2-Fluoroanisole and 3-Fluoroanisole.

The rotational spectra of 2-fluoroanisole and 3-fluoroanisole were investigated using Fourier transform microwave spectroscopy in the 4-26 GHz range. Assigned transitions correspond to the lowest energy rotamer for 2-fluoroanisole which has the O-CH3 group directed away (anti) from the fluorine substituent whereas for 3-fluoroanisole, the spectrum is consistent with the presence of two rotamers arising from syn and anti orientations of the methoxy moiety relative to fluorine. Ab initio calculations at the MP2/cc-pVTZ level were used to estimate the equilibrium (re) geometries of the three observed rotamers. Their assignments were confirmed through the observation of the rotational transitions of eight minor isotopologues (13C and 18O) in natural abundance for each species. The mass dependence (rm(1)) structures derived using the experimentally determined rotational constants compare favorably with the ab initio estimates. The resulting sets of geometric parameters suggest that the aromatic ring backbone is distorted by the introduction of the angular methoxy substituent, with a tendency to induce bond length alternation around the ring, and by the electron withdrawing effects of fluorine.