Two Key Descriptors for Designing Second Near-Infrared Dyes and Experimental Validation.

Second near-infrared (NIR-II) optical imaging technology has emerged as a powerful tool for diagnostic and image-guided surgery due to its higher imaging contrast. However, a general strategy for efficiently designing NIR-II organic molecules is still lacking, because NIR-II dyes are usually difficult to synthesize, which has impeded the rapid development of NIR-II bioprobes. Herein, based on the theoretical calculations on 62 multiaryl-pyrrole (MAP) systems with spectra ranging from the visible to the NIR-II region, a continuous red shift of the spectra toward the NIR-II region could be achieved by adjusting the type and site of substituents on the MAPs. Two descriptors (ΔEgs and µgs) were identified as exhibiting strong correlations with the maximum absorption/emission wavelengths, and the descriptors could be used to predict the emission spectrum in the NIR-II region only if ΔEgs ≤ 2.5 eV and µgs ≤ 22.55 D. The experimental absorption and emission spectra of ten MAPs fully confirmed the theoretical predictions, and biological imaging in vivo of newly designed MAP23-BBT showed high spatial resolution in the NIR-II region in deep tissue angiography. More importantly, both descriptors of ΔEgs and µgs have shown general applicability to most of the reported donor-acceptor-donor-type non-MAP NIR-II dyes. These results have broad implications for the efficient design of NIR-II dyes.

Direct Synthesis of Perovskite Quantum Dot Photoresist for Direct Photolithography.

Perovskite quantum dots (PQDs) photoresists are promising building blocks for photolithographically patterned devices. However, their complex synthesis and combination processes limit their optical properties and potential patterning applications. Here, we present an exceptionally simple strategy for the synthesis of PQDs photoresist. Unlike traditional approaches that involve centrifugation, separation, and combination processes, our direct synthesis technique using polymerizable acrylic monomer as solvent to fabricate PQDs photoresists without complex post-synthesis process. We demonstrate that the change in solubility of the precursors is the main reason for the formation of PQDs in the polymerizable monomer. By direct photolithography, colorful PQD patterns with high photoluminescence quantum yields and high thickness are successfully demonstrated. This work opens a new avenue for the direct synthesis of PQDs photoresist, expanding their applications in various integrated applications, such as photonic, energy harvesting, and optoelectronic devices.

Fused-Ring Pyrrole-Based Near-Infrared Emissive Organic RTP Material for Persistent Afterglow Bioimaging.

Organic near-infrared room temperature phosphorescence (RTP) materials offer remarkable advantages in bioimaging due to their characteristic time scales and background noise elimination. However, developing near-infrared RTP materials for deep tissue imaging still faces challenges since the small band gap may increase the non-radiative decay, resulting in weak emission and short phosphorescence lifetime. In this study, fused-ring pyrrole-based structures were employed as the guest molecules for the construction of long wavelength emissive RTP materials. Compared to the decrease of the singlet energy level, the triplet energy level showed a more effectively decrease with the increase of the conjugation of the substituent groups. Moreover, the sufficient conjugation of fused ring structures in the guest molecule suppresses the non-radiative decay of triplet excitons. Therefore, a near-infrared RTP material (764 nm) was achieved for deep penetration bioimaging. Tumor cell membrane is used to coat RTP nanoparticles (NPs) to avoid decreasing the RTP performance compared to traditional coating by amphiphilic surfactants. RTP NPs with tumor-targeting properties show favorable phosphorescent properties, superior stability, and excellent biocompatibility. These NPs are applied for time-resolved luminescence imaging to eliminate background interference with excellent tissue penetration. This study provides a practical solution to prepare long-wavelength and long-lifetime organic RTP materials and their applications in bioimaging.

Helical Self-Assembly and Fe3+ Detection of V-Shaped AIE-Active Chiral Tetraphenylbutadiene-Based Polyamides.

Chiral aggregation-induced emission (AIE) molecules have drawn attention for their helical self-assembly and special optical properties. The helical self-assembly of AIE-active chiral non-linear main-chain polymers can produce some desired optical features. In this work, a series of V-shaped chiral AIE-active polyamides P1-C3, P1-C6, P1-C12 and linear P2-C3, P2-C6, bearing n-propyl/hexyl/dodecyl side-chains, based on tetraphenylbutadiene (TPB), were prepared. All target main-chain polymers exhibit distinct AIE characteristics. The polymer P1-C6 with moderate length alkyl chains shows better AIE properties. The V-shaped main-chains and the chiral induction of (1R,2R)-(+)-1,2-cyclohexanediamine in each repeating unit promote the polymer chains display helical conformation, and multiple helical polymer chains induce nano-fibers helicity when the polymer chains aggregate and self-assemble in THF/H2 O mixtures. Simultaneously, the helical conformation polymer chains and helical nano-fibers cause P1-C6 produce strong circular dichroism (CD) signals with positive Cotton effect. Moreover, P1-C6 could also occur fluorescence quenching response to Fe3+ selectively with a low detection limit of 3.48 µmol/L.

Microwave-Responsive Flexible Room-Temperature Phosphorescence Materials Based on Poly(vinylidene fluoride) Polymer.

The development of flexible, room-temperature phosphorescence (RTP) materials remains challenging owing to the quenching of their unstable triplet excitons via molecular motion. Therefore, a polymer matrix with Tg higher than room temperature is required to prevent polymer segment movement. In this study, a RTP material was developed by incorporating a 4-biphenylboronic acid (BPBA) phosphor into a poly(vinylidene fluoride) (PVDF) matrix (Tg =-27.1 °C), which exhibits a remarkable UV-light-dependent oxygen consumption phosphorescence with a lifetime of 1275.7 ms. The adjustable RTP performance is influenced by the crystallinity and polymorph (α, ß, and γ phases) fraction of PVDF, therefore, the low Tg of the PVDF matrix enables the polymeric segmental motion upon microwave irradiation. Consequently, a reduction in the crystallinity and an increase in the α phase fraction in PVDF film induces RTP after 2.45 GHz microwave irradiation. These findings open up new avenues for constructing crystalline and phase-dependent RTP materials while demonstrating a promising approach toward microwave detection.

Clusterization-Triggered Color-Tunable Room-Temperature Phosphorescence from 1,4-Dihydropyridine-Based Polymers.

A series of poly(1,4-dihydropyridine)s (PDHPs) were successfully synthesized via one-pot metal-free multicomponent polymerization of diacetylenic esters, benzaldehyde, and aniline derivatives. These PDHPs without traditional luminescent units were endowed with tunable triplet energy levels by through-space conjugation from the formation of different cluster sizes. The large and compact clusters can effectively extend the phosphorescence wavelength. The triplet excitons can be stabilized by using benzophenone as a rigid matrix to achieve room-temperature phosphorescence. The nonconjugated polymeric clusters can show a phosphorescence emission up to 645 nm. A combination of static and dynamic laser light scattering was conducted for insight into the structural information on formed clusters in the host matrix melt. Moreover, both the fluorescence and phosphorescence emission can be easily tuned by the variation of the excitation wavelength, the concentration, and the molecular weight of the guest polymers. This work provides a unique insight for designing polymeric host-guest systems and a new strategy for the development of long wavelength phosphorescence materials.

Constructing Hypoxia-Tolerant and Host Tumor-Enriched Aggregation-Induced Emission Photosensitizer for Suppressing Malignant Tumors Relapse and Metastasis.

Photodynamic immunotherapy is a promising treatment strategy that destroys primary tumors and inhibits the metastasis and relapse of distant tumors. As reactive oxygen species are an intermediary for triggering immune responses, photosensitizers (PSs) that can actively target and efficiently trigger oxidative stress are urgently required. Herein, pyrrolo[3,2-b]pyrrole as an electronic donor is introduced in acceptor-donor-acceptor skeleton PSs (TP-IS1 and TP-IS2) with aggregation-induced emission properties and high absorptivity. Meanwhile, pyrrolo[3,2-b]pyrrole derivatives innovatively prove their ability of type I photoreaction, indicating their promising hypoxia-tolerant advantages. Moreover, M1 macrophages depicting an ultrafast delivery through the cell-to-cell tunneling nanotube pathway emerge to construct TP-IS1@M1 by coating the photosensitizer TP-IS1. Under low concentration of TP-IS1@M1, an effective immune response of TP-IS1@M1 is demonstrated by releasing damage-associated molecular patterns, maturating dendritic cells, and vanishing the distant tumor. These findings reveal insights into developing hypoxia-tolerant PSs and an efficient delivery method with unprecedented performance against tumor metastasis.

Halogen Bonding: A New Platform for Achieving Multi-Stimuli-Responsive Persistent Phosphorescence.

Monotonous luminescence has always been a major factor limiting the application of organic room-temperature phosphorescence (RTP) materials. Enhancing and regulating the intermolecular interactions between the host and guest is an effective strategy to achieve excellent phosphorescence performance. In this study, intermolecular halogen bonding (CN⋅⋅⋅Br) was introduced into the host-guest RTP system. The interaction promoted intersystem crossing and stabilized the triplet excitons, thus helping to achieve strong phosphorescence emission. In addition, the weak intermolecular interaction of halogen bonding is sensitive to external stimuli such as heat, mechanical force, and X-rays. Therefore, the triplet excitons were easily quenched and colorimetric multi-stimuli responsive behaviors were realized, which greatly enriched the luminescence functionality of the RTP materials. This method provides a new platform for the future design of responsive RTP materials based on weak intermolecular interactions between the host and guest molecules.

On-Chip Multicolor Photoacoustic Imaging Flow Cytometry.

On-chip imaging flow cytometry has been widely used in cancer biology, immunology, microbiology, and drug discovery. Pure optical imaging combined with flow cytometry to derive chemical, structural, and morphological features of cells provides systematic insights into biological processes. However, due to the high concentration and strong optical attenuation of red blood cells, preprocessing is necessary for optical flow cytometry while dealing with whole blood. In this study, we develop an on-chip photoacoustic imaging flow cytometry (PAIFC), which combines multicolor high-speed photoacoustic microscopy and microfluidics for cell imaging. The device employs a micro-optical scanner to achieve a miniaturized outer size of 30 × 17 × 24 mm3 and ultrafast cross-sectional imaging at a frame rate of 1758 Hz and provides lateral and axial resolutions of 2.2 and 33 µm, respectively. Using a multicolor strategy, PAIFC is able to differentiate cells labeled by external contrast agents, detect melanoma cells with an endogenous contrast in whole blood, and image melanoma cells in blood samples from tumor-bearing mice. The results suggest that PAIFC has sufficient sensitivity and specificity for future cell-on-chip applications.

Functional Isocyanide-Based Polymers.

Research interest in the isocyanide-based reaction can be traced back to 1921 when the Passerini reaction was first reported. However, most of these research efforts did not lead to important progress in the synthesis of isocyanide-based polymers (IBPs). The major challenge resides in the lack of highly efficient polymerization methods, which limits large-scale preparation and applications. Modern organic chemistry provides efficient access to develop functional IBPs on the basis of isocyanide chemistry. However, it is still challenging to prepare the IBPs with small molecular isocyanide reaction. Our investigations into catalyst exploration and polymerization methodology have prompted the synthesis of a series of IBPs. Two classes of isocyanide monomers can be used for the construction of IBPs. The first class includes monomers with a single isocyanide. Novel catalysts for the synthetic chemistry of isocyanide allow the introduction of functional pendants into the linear polymer chains. This molecular functionalization endows the polymers with an array of new functional properties. For example, the incorporation of a chromophore on the polymeric side chain provides novel functional properties, such as aggregation-induced emission and optical activity. Diisocyanide monomers can be also utilized for the construction of heterocyclic, spiro-heterocyclic, and bispiro-heterocyclic polymers in the polymeric backbones. A new concept of "multi-component spiropolymerization" has been developed for the preparation of spiropolymers using the catalysis-free one-pot reaction. Proper structural design allows for the preparation of a heterocyclic polymeric chain with natural bioactivity and biological compatibility, generating new IBPs with biofunctionalities.In this Account, we discuss progress mainly made in our lab and related fields for the design of isocyanide monomers, exploration of new catalysts, and optimization of reaction conditions. The subsequent section discusses the characteristic properties and applications of selected examples of these functional polymers, mainly focusing on their optical applications. We have investigated the UV-sensitive IBPs that could potentially be used for lithography applications. One-pot highly efficient polymerization of diisocyanides and CO2 under mild conditions can provide a new method for realizing the reuse of CO2 and reducing the greenhouse effect. Through a combination of structural modifications, IBPs bearing dimethylbenzene moieties exhibit characteristics of black materials that can be potentially utilized as pyroelectric sensors, thermal detectors, and optical instruments. Most recently, our group synthesized a spiro-heterocyclic IBP with clusterization-triggered emission properties that can be used to discriminate cancer cells from normal cells and provides a new method for the treatment of cancer. The studies reviewed in this Account suggest that polymerization with isocyanide chemistry can be implemented in diverse functional macromolecules and materials.

Multicomponent Spiropolymerization of Diisocyanides, Diethyl Acetylenedicarboxylate, and Halogenated Quinones.

Multicomponent spiropolymerization (MCSP) provides an efficient synthetic tool for the construction of spiropolymers based on nonspiro monomers. In this study, a method of MCSP using diisocyanides 1, diethyl acetylenedicarboxylate 2, and halogenated quinones 3 is developed for the in situ construction of bis-spiropolymers with high molecular weights (Mw up to 29 200) and good yields (up to 87.7%) under mild reaction conditions. The structure of the obtained bis-spiropolymers is confirmed by gel permeation chromatography, Fourier transform infrared spectroscopy, and nuclear magnetic resonance analysis. Halogenated bis-spiropolymers show good thermal stability, good solubility, and film-forming ability. The photosensitizer rhodamine B is used as a doping agent to induce the photodegradation of the polymer P1a3c into small-molecule segments, which results in the slow release of halogenated spiro-groups under irradiation with simulated sunlight. This finding reveals that P1a3c has the potential to be applied in pesticides. Therefore, this MCSP is a novel method for preparing halogen-containing bis-spiropolymers, which accelerates the development of multifunctional polymer materials.

Catalyst-Free Multicomponent Cyclopolymerizations of Diisocyanides, Activated Alkynes, and 1,4-Dibromo-2,3-Butanedione: a Facile Strategy toward Functional Polyiminofurans Containing Bromomethyl Groups.

Polymers containing iminofuran (PIFs) are rarely reported due to the lack of simple and effective synthesis methods. In this work, a novel multicomponent cyclopolymerization (MCCP) of diisocyanides, activated alkynes, and 1,4-dibromo-2,3-butanedione using catalyst-free one-pot reactions under mild conditions to prepare PIFs containing bromomethyl groups is reported. PIFs with good solubility and thermal stability are obtained with high Mw s (up to 19 600) and good yields (up to 89.5%) under optimized polymerization conditions. The structure of the PIFs is characterized by nuclear magnetic resonance, Fourier transform infrared spectroscopy, and gel permeation chromatography. The photophysical properties indicate that polymers P1a2b3 and P1c2b3 have cluster-triggered emission characteristics. Thin films made from PIFs quickly degrade under UV irradiation. Moreover, the obtained polymers are decorated with bromomethyl and carboxylate groups in the side chain, which can be postfunctionalized to prepare multifunctional materials, such as star branched polymers and biomedical carrier materials. Thus, this work not only enriches the field of polymerization based on isocyanates and activated alkynes but also provides a facile strategy toward functional iminofuran polymers.

The Aggregation Regularity Effect of Multiarylpyrroles on Their Near-Infrared Aggregation-Enhanced Emission Property.

Increasing the quantum yield of near-infrared (NIR) emissive dyes is critical for biological applications because these fluorescent dyes generally show decreased emission efficiency under aqueous conditions. In this work, we designed and synthesized several multiarylpyrrole (MAP) derivatives, in which a furanylidene (FE) group at the 3-position of the pyrrole forms donor-π-acceptor molecules, MAP-FE, with a NIR emissive wavelength and aggregation-enhanced emission (AEE) features. Different alkyl chains of MAP-FEs linked to phenyl groups at the 2,5-position of the pyrrole ring resulted in different emissive wavelengths and quantum yields in aggregated states, such as powders or single crystals. Powder XRD data and single crystal analysis elucidated that the different lengths of alkyl chains had a significant impact on the regularity of MAP-FEs when they were forced to aggregate or precipitate, which affected the intermolecular interaction and the restriction degree of the rotating parts, which are essential components. Therefore, an increasing number of NIR dyes could be developed by this design strategy to produce efficient NIR dyes with AEE. Moreover, this method can provide general guidance for other related fields, such as organic solar cells and organic light-emitting materials, because they are all applied in the aggregated state.

MDM2-Associated Clusterization-Triggered Emission and Apoptosis Induction Effectuated by a Theranostic Spiropolymer.

Heteroatom-containing spiropolymers were constructed in a facile manner by a catalyst-free multicomponent spiropolymerization route. P1a2b as the most potent of these spiropolymers, demonstrates cluster-triggered emission resulting from strong interactions with the MDM2 protein. By preventing the anti-apoptotic p53/MDM2 interaction, P1a2b triggers apoptosis in cancerous cells, while demonstrating a good biocompatibility and non-toxicity in non-cancerous cells. The combined results from solution and cell-based cluster-triggered emission studies, docking, protein expression experiments and cytotoxicity data strongly support the MDM2-binding hypothesis and indicate a potential application as a fluorescent cancer marker as well as therapeutic for this spiropolymer.

Wide-Range Color-Tunable Organic Phosphorescence Materials for Printable and Writable Security Inks.

Organic materials with long-lived, color-tunable phosphorescence are potentially useful for optical recording, anti-counterfeiting, and bioimaging. Herein, we develop a series of novel host-guest organic phosphors allowing dynamic color tuning from the cyan (502 nm) to orange red (608 nm). Guest materials are employed to tune the phosphorescent color, while the host materials interact with the guest to activate the phosphorescence emission. These organic phosphors have an ultra-long lifetime of 0.7 s and a maximum phosphorescence efficiency of 18.2 %. Although color-tunable inks have already been developed using visible dyes, solution-processed security inks that are temperature dependent and display time-resolved printed images are unprecedented. This strategy can provide a crucial step towards the next-generation of security technologies for information handling.

1,2,5-Triphenylpyrrole Derivatives with Dual Intense Photoluminescence in Both Solution and the Solid State: Solvatochromism and Polymorphic Luminescence Properties.

Five organic luminophores, 1,2,5-triphenylpyrrole (TPP) derivatives 3 a-e bearing electron-withdrawing or electron-donating groups, have been synthesized by Pd-catalyzed Suzuki coupling of 1-phenyl-2,5-di(4'-bromophenyl)pyrrole and para-substituted phenylboronic acid derivatives. They possess good thermal stabilities with high decomposition temperatures above 310 °C. Investigation of the photophysical properties of the luminogens 3 a-e indicated that they exhibited dual intense photoluminescence in both solution and the solid state due to their twisted conformations, and their fluorescence quantum yields (ΦF ) were determined as 68.7-94.9 % in THF solution and 19.1-52.0 % in solid powder form. Compounds 3 a-c bearing electron-accepting groups exhibited remarkable solvatochromism with large Stokes shifts, attributable to their D-π-A structure and intramolecular charge-transfer effect. In particular, 3 a, bearing aldehyde groups, displayed an obvious red-shift of the emission band from 445 to 564 nm with increasing solvent polarity. However, no obvious solvatochromic behavior was observed for compounds 3 d,e bearing electron-donating groups. The luminophore 3 a exhibited polymorphic luminescence properties and crystallization-induced emission enhancement.

Aggregation-Induced Emission of Multiphenyl-Substituted 1,3-Butadiene Derivatives: Synthesis, Properties and Application.

Organic functional materials, including conjugated molecules and fluorescent dyes, have been intensely developed in recent years because they can be applied in many fields, such as solar cells, biosensing and bioimaging, and medical adjuvant therapy. Organic functional materials with aggregation-induced emission or aggregation-enhanced emission (AIE/AEE) characteristics have increasingly attracted attention due to their high quantum efficiency in the aggregated or solid state. A large variety of AIE/AEE materials have been designed and applied during the exponential growth of research interest in the abovementioned fields. Multiphenyl-substituted 1,3-butadiene (MPB), as a core structure that includes tetraphenyl-1,3-butadiene, hexaphenyl-1,3-butadiene and their derivatives, show a typical AIE/AEE feature and can be potentially used in all the above-mentioned fields. This review summarizes the design principles, the corresponding syntheses, and the structure-property relationships of MPBs, as well as their excellent innovative functionalities and applications. This review will be useful for scientists conducting chemistry, materials, and biomedical research in AIE/AEE-related fields.

The Dual-State Luminescent Mechanism of 2,3,4,5-Tetraphenyl-1H-pyrrole.

2,3,4,5-Tetraphenyl-1H-pyrrole (TePP) was synthesized by a simple one-step reaction. The compound showed a balanced emission in both the solution and solid state with the absolute quantum yield of ΦF/THF =65.6 % and ΦF/solid =74.3 %, respectively. Temperature and viscosity variation measurements demonstrated that the phenyl group at the 1-position (N-position) of the pyrrole core can act as a rotor in pyrrole-based molecules, which can consume the excited energy and reduce the molecular emission in solution. TePP without the phenyl group at the 1-position can effectively enhance the emission in solution. Single-crystal analysis showed that the phenyl groups at the 2,5-positions of pyrrole extend the molecular conjugation and lock the conformation. The phenyl groups at the 3,4-positions with a twisted conformation prevent their molecules from close packing and are helpful for aggregated emission. A delicate balance between the twisting conformation and rigid conjugation takes advantage of both ACQ and AIE luminogens. The strategy can tune the AIE, ACQ, or solution and solid dual-state emission properties of pyrrole-based molecules by simply altering the position of phenyl groups, which provides a great opportunity to explore the luminescent mechanism in greater detail and to facilitate practical applications.

The Synergistic Effect between Triphenylpyrrole Isomers as Donors, Linking Groups, and Acceptors on the Fluorescence Properties of D-π-A Compounds in the Solid State.

Eight donor-π-acceptor (D-π-A) compounds employing triphenylpyrrole isomers (TPP-1,2,5 and TPP-1,3,4) as donors, malononitrile (CN) and 1H-indene-1,3(2H)-dione (CO) as acceptors, pyridone (P) and benzopyran (B) as π-linking groups were synthesized. The compounds exhibited aggregation-induced emission and piezochromic properties. Compared with previously reported donors, triphenylpyrroles induced all the compounds to have more remarkable photophysical properties. The compounds containing TPP-1,2,5 and P moieties displayed stronger fluorescence intensities, shorter emission wavelengths, and more distinct piezochromic properties. However, the same phenomenon was observed in the TPP-1,3,4-containing system if B was as π-linker. Moreover, the CN acceptor endowed the compound to have a relatively strong fluorescent intensity, in which CO induced a relatively long emission wavelength. That is, the photophysical properties of D-π-A compounds can be controlled by adjusting the structure of donor, linker and acceptor.

Tetraphenylethylene derivative capped CH3NH3PbBr3 nanocrystals: AIE-activated assembly into superstructures.

The surfaces of semiconductor nanocrystals have been known to be a very important factor in determining their optical properties. The introduction of functionalized ligands can further enhance the interactions between nanocrystals, which is beneficial for the assembly of nanocrystals. In a previous report, we developed a ligand-assisted reprecipitation method to fabricate organometal halide perovskite nanocrystals capped with octylamine and oleic acid. Here, a TPE derivative 3-(4-(1,2,2-triphenylvinyl)phenoxy)propan-1-amine, which shows a typical aggregation induced emission feature, is applied to replace octylamine to fabricate CH3NH3PbBr3 nanocrystals. The obtained CH3NH3PbBr3 nanocrystals were nanocubes (average diameter ∼ 11.1 nm) and are likely to assemble into ordered superstructures. By adjusting the chain length of the TPE derivative, we found that the assembly of the CH3NH3PbBr3 nanocrystals was correlated with the interactions between the TPE groups. This provides a new platform to investigate the ligand effects in nanocrystal solids and may potentially achieve enhanced optical and electrical properties.