Optical Properties Research Articles

Fluorescent Sensing for the Detection and Quantification of Sulfur-Containing Gases.

Sulfur-containing gases, such as H2S and SO2, play significant roles in a multitude of biological processes affecting human life and health. Precise and efficient detection of these gases is therefore crucial for advancing one's understanding of their biological roles and developing effective diagnostic strategies. Fluorescent sensing offers a highly sensitive and versatile approach for detecting these gases. This Review examines the recent advances in the fluorescent detection of H2S and SO2, highlighting the key mechanisms involved in fluorescence signal transduction, including changes in intensity and wavelength shifts. The diverse array of probe molecules employed for this purpose, including those utilizing mechanisms such as nucleophilic reactions, Förster resonance energy transfer (FRET), and sulfur affinity interactions are explored. In additional to organic sensors, the focus of the Review is particularly directed toward quantum dot (QD) systems, emphasizing their tunable optical properties that hold immense potential for fluorescence sensing. Beyond the traditional III-V QDs, we delve into the emerging fluorescence sensors based on halide perovskite QDs, upconversion nanocrystals, and other novel materials. These advanced QD systems hold promise for the development of highly sensitive and cost-effective gas detectors, paving the way for significant advances in biomedical and environmental monitoring. This Review provides a comprehensive overview of the current state-of-the-art in QD-based fluorescence sensing of sulfur-containing gases and provides a multifaceted discussion comparing organic fluorescent sensors with QD sensors, highlighting the key challenges and opportunities for the integration of fluorescence sensing as it evolves. The Review aims to facilitate further research and development of innovative sensing platforms to enable more accurate and sensitive detection of these important gases.

Cocrystallization‐Induced Red Ultralong Organic Phosphorescence

AbstractOrganic cocrystals formed through multicomponent self‐assembly have attracted significant interest owing to their clear structure and tunable optical properties. However, most cocrystal systems suffer from inefficient long‐wavelength emission and low phosphorescence efficiency due to strong non‐radiative processes governed by the energy gap law. Herein, an efficient long‐lived red afterglow is achieved using a pyrene (Py) cocrystal system incorporating a second component (NPYC4) with thermally activated delayed fluorescence (TADF) and ultralong organic phosphorescence (UOP) properties. The cocrystal (NPYC4‐Py) not only inherits the excellent luminescence of its monomeric counterparts, but also exhibits unique dual‐mode characteristics, including persistent TADF and UOP emission with a high quantum yield of 58 % and a lifetime of 362 ms. The precise cocrystal stacking distinctly reveals that intermolecular interactions lock the cocrystal formation and weaken the intermolecular π‐π interactions between NPYC4 and Py, thereby stabilizing the excited triplet excitons. Furthermore, the favorable energy level of NPYC4 acts as a bridge, reducing the energy gap between the S1 and T1 states for Py, therefore activating its red phosphorescence from Py. This research provides direct insights into achieving efficient red UOP through co‐crystallization.

Uniaxial Strain Engineering of Electronic, Elastic and Optical Properties of Halide Double Perovskites K2NaTIX6 (X = I, Br, and Cl): A DFT Insight

Uniaxial Strain Engineering of Electronic, Elastic and Optical Properties of Halide Double Perovskites K2NaTIX6 (X = I, Br, and Cl): A DFT Insight

Suppressed Nonreciprocal Second-Harmonic Generation of Antiferromagnet MnPSe3 in the MnPSe3/Graphene Heterostructure Due to Interfacial Magnon-Plasmon Coupling.

Interfacial coupling is one of the keys to manipulating magnetic/nonmagnetic two-dimensional (2D) heterostructures for novel functionalities. The MnPSe3/graphene heterostructure is a prospective platform for quantum information and metrology. However, how graphene affects MnPSe3 through interfacial coupling is still poorly understood. Herein, second-harmonic generation (SHG) of antiferromagnet MnPSe3 in the MnPSe3/graphene heterostructure is revealed. Surprisingly, it was found that below TN, nonreciprocal or c-type SHG of MnPSe3 disappeared when interfacing with the graphene, suggesting the existence of interfacial couplings and/or interactions. Most interestingly, different from the short-range interfacial proximity interaction, this interfacial interaction could be contactless and long-range and varied from 2D metallic/semiconducting to insulating underlayers. Interfacial magnon-plasmon coupling probably played an important role in suppressing the c-type SHG signals of MnPSe3 in the MnPSe3/graphene heterostructure. This study will improve our understanding of the manipulation of nonlinear optical properties in 2D heterostructures.

Potassium and Boron Co-Doping of g-C3N4 Tuned CO2 Reduction Mechanism for Enhanced Photocatalytic Performance: A First-Principles Investigation

Graphitic phase carbon nitride (g-C3N4, abbreviated as CN) can be used as a photocatalyst to reduce the concentration of atmospheric carbon dioxide. However, there is still potential for improvement in the small band gap and carrier migration properties of intrinsic materials. K-B co-doped CN (KBCN) was investigated as a promising photocatalyst for carbon dioxide reduction via the Density Functional Theory (DFT) method. The electronic and optical properties of CN and KBCN indicate that doping K and B can improve the catalytic performance of CN by promoting charge migration and separation. In terms of the Gibbs free energy change, the CO2 reduction reaction catalysed by KBCN results in CH3OH, and its optimal pathway is CO2 → *CO2 → *COOH → CO → *OCH → HCHO → *OCH3 → CH3OH. Compared with CN, the doping elements K and B shift the rate-determining step from CO2 → *CO2 to *CO2 → *COOH. The K and B elements co-doping tuned the charge distribution between the catalyst and the adsorbate and reduced the Gibbs free energy of the rate-determining step from 1.571 to 0.861 eV, suggesting that the CO2 reduction activity of KBCN is superior to that of CN. Our work provides useful insights for the design of metallic–nonmetallic co-doped CN for photocatalytic CO2 reduction (CO2PR) reactions.

Evaluation of the optical and electrical properties of (C8BTBT)(F4TCNQ) charge-transfer complexes according to film formation temperatures during solution-coating

Abstract This study focused on (C8BTBT)(F4TCNQ) charge-transfer complexes, where C8BTBT is 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene and F4TCNQ represents fluorinated derivatives of 7,7,8,8,-tetracyanoquinodimethane. These complexes exhibit excellent thermal and atmospheric stability and near-infrared absorption, serving as transparent thin films for photoelectric conversion. Here, we sought to improve the photoelectric conversion efficiency (and thus the quantum efficiency, QE) of (C8BTBT)(F4TCNQ) thin films by altering the film formation temperatures during solution-coating; we evaluated optical and electrical properties of the films. We found that increased film coverage of a substrate surface (leading to continuous film formation) enhanced optical absorption and improved the photocurrent extraction efficiency when such films were incorporated into devices. C8BTBT and its components, when present alone, negatively affected both the device fabrication yield and photocurrent extraction. It is thus important to maximize (C8BTBT)(F4TCNQ) formation when seeking to improve the QE.

Optical Properties and Antimicrobial Activity of Si/PVP Hybrid Material Combined with Antibiotics

Silica–poly (vinylpyrrolidone) hybrid material was prepared using the sol–gel method. Tetramethyl ortosilane (TMOS) was used as a silica precursor. XRD analysis established that the as-prepared material is amorphous. The morphological structure of the final product was determined by the incorporated PVP. The UV–Vis analysis showed that the obtained hybrid exhibited absorption in the ultraviolet range. The antimicrobial activity of the SiO2/15PVP hybrid material was tested on Staphylococcus epidermidis ATCC 14990, Salmonella typhimurium ATCC BAA-2162, Candida albicans, and Saccharomyces cerevisiae in combination with the following antibiotics: Vancomycin for Gram-positive bacteria, Ciprofloxacin for Gram-negative bacteria, and Nystatin for yeast. The results confirmed a concentration-dependent synergistic effect of the antibiotic in combination with the TM15/PVP hybrid particles, especially at their highest concentration of 100 mg/mL on Gram-positive bacteria and for the Gram-negative Salmonella. On Candida albicans ATCC 18804 and Saccharomyces cerevisiae CCY 21-6-3, the effect was synergistic again, and a fungicidal effect was observed at 6.25 and 1.50 mg/mL for the antibiotic concentration and concentrations of hybrid material at 100 mg/mL. The toxicity on Daphnia magna was also tested. The registered prooxidant activity of SiO2/15PVP shows possible applications at very low concentrations. The obtained results demonstrate the possibility of clinical implementations of the newly synthesized hybrid material.

Does the substrate and a buffer layer have a greater influence on poly(3-Hexylthiophene) films deposited by the chronocoulometry technique?

Abstract In this study, we investigate the interface morphology and optical properties of electrochemical poly(3-hexylthiophene) (P3HT) films deposited by electrochemical synthesis using the chronocoulometry technique on tin-doped indium oxide (ITO) and fluorine-doped tin oxide (FTO) and how the substrate used influences in the deposition of the films and their optical and morphological properties, as well as the buffer layer and the interface effect, with and without spin-coating films of poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS). P3HT polymeric films were synthesized and deposited via the oxidation of the 3-hexylthiophene (3-HT) monomer and characterized via Raman spectroscopy. The morphology and thickness of the P3HT layer present in the samples ITO/P3HT, FTO/P3HT, ITO/PEDOT:PSS/P3HT, and FTO/PEDOT:PSS/P3HT were carried out using atomic force microscopy (AFM). The optical and electronic gap energy of P3HT were calculated from UV‒Vis spectra and cyclic voltammetry curves, respectively. The photoluminescence (PL) spectra showed broad and asymmetrical line shapes fitted by multi-Gaussian functions identifying different emission species. Emission ellipsometry spectroscopy was performed to study the energy transference between adjacent polymer chains. Our results show a higher linear polarized light emitted by ITO/PEDOT:PSS/P3HT film, ∼37%, thus demonstrating a significant decrease in the energy transfer. Based on these results, the efficiency of organic solar cells can be improved via the interaction of the polymer/polymer interface.

Low temperature, concentration dependent synthesis of MoS2/PEDOT:PSS nanocomposites: effect on morphological and optical properties

Low temperature, concentration dependent synthesis of MoS2/PEDOT:PSS nanocomposites: effect on morphological and optical properties

Facile Access to Phosphorus Ylide-fused Heteroarenes Possessing Tunable Optoelectronic Properties and High Nonlinear Optical Performances.

We report here a novel family of ylidic P-heteroarenes (P1-P6), structurally featuring unique phosphonium cyclopentadienylide (P-Cp)-fused π-skeletons and synthetically prepared via an unexpected one-pot [2+3]/[3+3] phospha-annulation reaction. While the facile and modular synthesis allows the fine-tuning of their optical absorptions and redox properties, single-crystallographic and theoretical analysis of these P-heteroarenes further reveal that the fusion of P-Cp moiety leads to substantial intramolecular charge-separated features with high ylidic character values of up to 84 %. Benefitted from such dipolar structures, these P-heteroarenes not only allows stepwise electrophilic substitution reaction for further structural π-expansions, but also exhibit excellent nonlinear optical (NLO) responses and optical limiting (OL) performances comparable to or exceed those of C60. As a model compound, the persistent radical-anion salt of P5a was also prepared through chemical reduction, thus offering valuable insights into the electronic structures of reduced P-ylidic species. Our work not only established a highly efficient synthetic method toward new P-heteroarenes, but also provide fundamental understanding of those fused-ring ylidic P-heterocycles with promising NLO/OL applications.

Nanotechnology-enhanced Phytonutraceuticals: Innovations in Characterization, Formulation, and Therapeutic Applications

Nanotechnology refers to the branch of science and engineering devoted to designing, producing, and using structures, devices, and systems by manipulating atoms and molecules at nano-scale, having one or more dimensions of the order of 100 nanometres (100 millionth of a millimetre) or less. Nanotechnology is the exploitation of the unique properties of materials at the nanoscale. Nanotechnology has gained popularity in several industries, as it offers better built and smarter products. The ability to manipulate structures at the atomic scale allows for the creation of nanomaterials. Nanomaterials have unique optical, electrical and/or magnetic properties at the nanoscale, and these can be used in the fields of electronics and medicine, amongst other scenarios. Nanomaterials are unique as they provide a large surface area to volume ratio. Unlike other large-scaled engineered objects and systems, nanomaterials are governed by the laws of quantum mechanics instead of the classical laws of physics and chemistry. Nanotechnology is the engineering of useful objects and functional systems at the molecular or atomic scale. Nano-formulations are widely used for phyto-nutraceuticals and drug delivery systems. These substances are generally having low solubility, leading to their poor absorption and bioavailability in the human body. In this regard, one of the most important applications of nanotechnology in food sector has been the formulation of novel neutraceutical compounds with improved properties viz., enhanced solubility, stability, bioavailability and efficacy. This is achieved by encapsulation of neutraceutical by nanoparticles, which modifies their pharmacokinetics (PK) and biodistribution (BD). Nano-formulations widely used for the purpose are nanoliposomes, nanoemulsions, nanoparticles, nanofibres. The particles are characterized by scanning probe microscope (SPM), Ultraviolet-visible spectroscopy (UV-Vis spectrophotometer, SEM, TEM, Dynamic light scattering (DLS).

Structural Modifications of CdS/Graphene Oxide with Ionic Dopants of Fe/Ag for Degradation of Methylene Blue

AbstractGlobal demand for pollution removal agents requires advanced materials to provide a good protocol to keep clean water resources. The composition of CdS was modified with ionic dopants including iron (Fe) and silver (Ag) and is incorporated into graphene oxide (GO) nanoparticles. The obtained compositions are CdS, Fe-CdS, Ag-CdS, CdS@GO, Fe-CdS@GO, and Ag-CdS@GO that have been fabricated by the co-precipitation method and examined by several techniques to estimate the morphological, optical, and structural properties using TEM, SEM, UV–Vis analysis, and XRD. The crystallite size of the CdS@Go was measured using the Williamson-Hall (W–H) method and was found to be around 28.6 nm. Furthermore, the a-axis was found to be 5.78 Å and 5.80 Å for cubic crystals and the a-axis achieved 14.28 to 14.24 Å for an orthorhombic crystal of CdS, respectively. The average roughness varied from 32.30 ± 3.3 to 66.65 ± 10.9 nm for CdS and Ag-CdS@GO. The degradation of methylene blue (MB) is increased from 75.56, 73.87, 76.01, 81.53, 89.34, and 91.68% for CdS, Fe-CdS, Ag-CdS, CdS@GO, Fe-CdS@GO, and Ag-CdS@GO after 60 min of exposure under visible light irradiation. The pseudo-first-order constant (Kapp) is increased from 4.4 × 10−3 to 39.4 × 10−3 min−1 for CdS and Ag-CdS@GO.

Trigonal Planar Heteroleptic Lanthanide(III) Bis(silyl)amide Complexes Containing Aminoxyl Radicals and Anions.

Modulation of the crystal field (CF) in lanthanide (Ln) complexes can enhance optical and magnetic properties, and large CF splitting can be achieved with low coordination numbers in specific geometries. We previously reported that the homoleptic near-linear Sm2+ complex [SmII{N(SiiPr3)2}2] (1-Sm) is oxidized by the 2,2,6,6-tetramethylpiperidinyl-1-oxy (TEMPO•) radical to give the heteroleptic, approximately trigonal planar Sm3+ complex, [SmIII{N(SiiPr3)2}2(TEMPO-)] (2-Sm). Here, we report the synthesis of homologous [LnIII{N(SiiPr3)2}2(TEMPO-)] (2-Ln; Ln = Tm, Yb) complexes by the oxidation of the parent [Ln{N(SiiPr3)2}2] (1-Ln; Ln = Tm, Yb) with TEMPO•; complexes 2-Ln all contain TEMPO- anions. The homoleptic bent Ln3+ complexes [LnIII{N(SiiPr3)2}2][B(C6F5)4] (3-Ln; Ln = Sm, Tm, Yb) were also treated with TEMPO• to yield the heteroleptic, approximately trigonal planar Ln3+ complexes [LnIII{N(SiiPr3)2}2(TEMPO•)][B(C6F5)4] (4-Ln; Ln = Sm, Tm, Yb); the cations of 4-Ln all contain TEMPO• radicals. We have compared the electronic structures of the two geometrically similar families of Ln3+ complexes with the TEMPO- anion (2-Ln) or TEMPO• radical (4-Ln) using a combination of UV-vis-NIR and EPR spectroscopy, magnetic measurements, and ab initio calculations. These studies revealed no single-molecule magnet behavior for 2-Yb despite evidence for sizable CF splitting and a high degree of purity of the ground stabilized mJ = |±7/2⟩ state, while the radical TEMPO• in 4-Yb did not significantly improve performance.

Abstract 4139162: Optical coherence tomography measures mechanical contractile properties of the beating murine heart

Introduction: Optical imaging techniques can characterize properties of tissue at high temporal and spatial resolution, offering unique insights into electrically excitable tissues such as nerve and muscle. We hypothesized that the gated high-speed optical coherence tomography (OCT) could profile the contractile properties of mouse myocardial tissue and facilitate investigations of microscale mechanical function in the beating heart. Methods: C57BL/6 male mice (n=6) underwent a sternotomy while anesthetized and ventilated and were imaged at baseline with OCT. Another cohort of C57BL/6 male mice (n=6) were sacrificed and the hearts were ex vivo perfused with crystalloid using a Langendorff system. These hearts were imaged at baseline and after inhibition of contractile function with blebbistatin. OCT was performed using a custom tissue stabilizer and a Thorlabs TEL 321 OCT system, which was synchronized to physiologic signals using custom hardware and software and cardiac pacing protocols (Fig. 1A and 1B). OCT cross-sectional B-scan images (Fig. 1C) were obtained throughout multiple cardiac cycles in both in vivo and ex vivo preparations. Data were processed in MATLAB and ImageJ using the workflow in Fig. 1D. Results: Highly reproducible cross-sectional mean intensity changes were observed over the contractile cycle in vivo and ex vivo (Fig. 1E, left and middle). With mechanical contraction inhibited by blebbistatin, this cyclical intensity extinguished, linking the optical scattering change measured by OCT to myocardial contraction (Fig. 1E, right). B-scan curves averaged over multiple mice and temporally aligned with the ECG waveform (Fig. 1F) demonstrate a signal intensity waveform that reproducibly varies with the contractile cycle for both in vivo and ex vivo preparations. In vivo and ex vivo baseline waveforms both had peak intensity during systole and minimum in end-diastole (Fig. 1F). Reproducibility in ex vivo beating heart preparations without blood perfusion provides evidence that myocardial mechanical properties, not red blood cell flow, generate the intensity changes. Conclusion: Gated high-speed OCT imaging can quantify the mechanical contraction wave in the myocardium. Combined with gated OCT angiography, OCT techniques will provide high resolution imaging of both blood flow and mechanical contractility of the beating heart in small animal models of heart disease.

Tuning Electronic and Functional Properties in Defected MoS2 Films by Surface Patterning of Sulphur Atomic Vacancies.

Defects are inherent in transition metal dichalcogenides and significantly affect their chemical and physical properties. In this study, surface defect electrochemical nanopatterning is proposed as a promising method to tune in a controlled manner the electronic and functional properties of defective MoS₂ thin films. Using parallel electrochemical nanolithography, MoS₂ thin films are patterned, creating sulphur vacancy-rich active zones alternated with defect-free regions over a centimetre scale area, with sub-micrometre spatial resolution. The patterned films display tailored optical and electronic properties due to the formation of sulphur vacancy-rich areas. Moreover, the effectiveness of defect nanopatterning in tuning functional properties is demonstrated by studying the electrocatalytic activity for the hydrogen evolution reaction.

Preparation and properties of Cu2MgSnS4 thin films and fabrication of heterojunction devices

Abstract Copper based chalcogenides have garnered growing importance in the area of thin film photovoltaics. Cu2MgSnS4 (CMTS) is one of the newest materials in this family of materials. It is a p-type material which find multiple applications in the field of photovoltaics. Cu2MgSnS4 thin films were deposited onto soda lime glass substrates using automated vacuum spray pyrolysis technique at a substrate temperature of 300 °C and annealed at different temperatures from 300 °C to 375 °C in steps of 25°C. The structural, elemental, morphological, optical, and electrical properties of the material were studied. X-Ray Diffraction studies showed that annealing eliminates impurity phases and improves crystallinity. Field Emission Scanning Electron Microscopy studies showed improved grain size and uniform deposition of the films. The energy bandgap of the as-prepared film is 2.02 eV and that of annealed films are around 2.5 eV. Hall measurements show that the material exhibit p-type conductivity with high value of conductivity, mobility and bulk concentration. Heterojunction devices were fabricated with chemical bath deposited CdS as a buffer layer and spray deposited Aluminium doped Zinc Oxide (Al:ZnO) as n-layer. Silver contacts were placed as electrodes over the top layer. The fabricated device architecture is <FTO/AZO/CdS/CMTS/Ag>. The junction parameters including rectification ratio, knee voltage, series resistance and Ideality factor of all the devices are calculated. The device annealed at 375 °C showed an ideality factor of 2.23, which is the best among all the fabricated devices.

Unlocking the Potential of Push-Pull Pyridinic Photobases: Aggregation-Induced Excited-State Proton Transfer.

The pH effect on the photophysics of three push-pull compounds bearing dimethoxytriphenylamine (TPA-OMe) as electron donor and pyridine as electron acceptor, with different ortho-functionalization (-H, -Br, -TPA-OMe), is assessed through steady-state and time-resolved spectroscopic techniques in DMSO/water mixed solutions and in water dispersions over a wide pH range. The enhanced intramolecular charge transfer upon protonation of the pyridineleads to the acidochromic (from colorless to yellow) and acido(fluoro)chromic (from cyan to pink) behaviours of the investigated compounds. In dilute DMSO/buffer mixtures these molecules exhibited low pKa values (≤ 3.5) and short singlet lifetimes. Nevertheless, it is by exploiting the aggregation phenomenon in aqueous environment that the practical use of these compounds largely expands: i) the basicity increases (pKa ≈ 4.5) approaching the optimum values for pH-sensing in cancer cell recognition; ii) the fluorescence efficiencies are boosted due to Aggregation-Induced Emission (AIE), making these compounds appealing as fluorescent probes; iii) longer singlet lifetimes enable Excited-State Proton Transfer, paving the way for the application of these molecules as photobases (pKa* = 9.1). The synergy of charge and proton transfers combined to the AIE behaviour in these pyridines allows tunable multi-responsive optical properties providing valuable information for the design of new light-emitting photobases.

Synthesis, Functionalization, and Biomedical Applications of Iron Oxide Nanoparticles (IONPs)

Iron oxide nanoparticles (IONPs) have garnered significant attention in biomedical applications due to their unique magnetic properties, biocompatibility, and versatility. This review comprehensively examines the synthesis methods, surface functionalization techniques, and diverse biomedical applications of IONPs. Various chemical and physical synthesis techniques, including coprecipitation, sol–gel processes, thermal decomposition, hydrothermal synthesis, and sonochemical routes, are discussed in detail, highlighting their advantages and limitations. Surface functionalization strategies, such as ligand exchange, encapsulation, and silanization, are explored to enhance the biocompatibility and functionality of IONPs. Special emphasis is placed on the role of IONPs in biosensing technologies, where their magnetic and optical properties enable significant advancements, including in surface-enhanced Raman scattering (SERS)-based biosensors, fluorescence biosensors, and field-effect transistor (FET) biosensors. The review explores how IONPs enhance sensitivity and selectivity in detecting biomolecules, demonstrating their potential for point-of-care diagnostics. Additionally, biomedical applications such as magnetic resonance imaging (MRI), targeted drug delivery, tissue engineering, and stem cell tracking are discussed. The challenges and future perspectives in the clinical translation of IONPs are also addressed, emphasizing the need for further research to optimize their properties and ensure safety and efficacy in medical applications. This review aims to provide a comprehensive understanding of the current state and future potential of IONPs in both biosensing and broader biomedical fields.

Exact Equations for the Back and Effective Focal Lengths of a Plano-Concave Thick Lens

In this work, we present the exact equations for the back and effective focal lengths of a plano-concave thick lens. These equations are derived through a detailed ray-tracing approach, calculating the meridional ray’s path parallel to the optical axis while taking into account lens thickness, refractive index, and surface curvature. Our analysis bridges the gap between paraxial approximations and exact ray behavior, highlighting how traditional models (e.g., thin-lens equations) can be extended to thick lenses. Additionally, we review recent advancements in negative refraction and surface phase manipulation techniques to demonstrate how our equations compare to modern numerical methods and metacoating-enhanced designs. This work provides a comprehensive and exact framework for understanding the optical properties of plano-concave thick lenses, offering new insights into their application in precision optics.

Construction of Luminescent Terpyridine-Based Metallo-Bowties with Alkyl Chain-Bridged Dimerized Building Blocks.

Numerous metallo-supramolecules with well-defined sizes and shapes have been successfully constructed via the strong coordination interaction between terpyridine (TPY) moieties and ruthenium cations. However, the pseudo-octahedral geometry of <TPY-Ru-TPY> unit hampers the luminescent properties of such metallo-architectures, thus limiting their applications as optical materials. To address this issue, we herein use a flexible alkyl chain to bridge TPY building blocks, replacing conventional <TPY-Ru-TPY> linkage. The introduction of alkyl chain guides the self-assembly into desired architecture while simultaneously eliminating the quenching effects typically associated with the <TPY-Ru-TPY> linkage. More importantly, this design strategy enables the precise construction of bowtie-shaped metallo-supramolecules with significantly enhanced emission. The incorporation of alkyl chain linkage not only maintains structural integrity but also enhances optical performance, making these metallo-supramolecular assemblies highly promising for applications in advanced photonic and luminescent materials. This study offers a versatile approach to construct complex metallo-supramolecular architectures with desired optical properties.