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Extended π-conjugated systems by external ligand-assisted C−H olefination of heterocycles: Facile access to single-molecular white-light-emitting and NIR fluorescence materials
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Ruike Hu, Kangmin Wang, Junxiang Liu, Jingxian Zhang, Guoliang Yang, Liqiu Wan, Bijin Li*
Chinese Chemical Letters | 2025, 36(4) : 110113
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Chinese Chemical Letters | 2025, 36(4): 110113
• Communication •
Extended π-conjugated systems by external ligand-assisted C−H olefination of heterocycles: Facile access to single-molecular white-light-emitting and NIR fluorescence materials
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Ruike Hu, Kangmin Wang, Junxiang Liu, Jingxian Zhang, Guoliang Yang, Liqiu Wan, Bijin Li*
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  • Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, Chongqing 401331, China
Published: 2025-04-15 doi: 10.1016/j.cclet.2024.110113
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The design and synthesis of a novel π-conjugated fluorescent framework by external ligand-assisted C−H olefination of heterocycles with excellent regioselectivity and broad substrate scope are reported herein. These novel fluorescent materials could present full-color-tunable emissions with large Stokes shifts. Furthermore, the protocol provides an opportunity to rapidly screen novel organic single-molecule white-light materials with high fluorescence quantum yields. The robust organic and low-cost white light-emitting diodes could rapidly be fabricated using the white-light-emitting material. Experimental data and theoretical calculations indicate that in the white-light dual emission the relatively short wavelength from high-lying singlet state emission and the relatively long wavelength from low-lying singlet state emission. The anti-Kasha dual-emission systems will provide a foundation for the development and application of organic single-molecule white light materials, effectively promoting the development and innovation of luminescent materials. In addition, this method demonstrated its potential application in the synthesis of new near-infrared (NIR) fluorescence materials with large Stokes shifts based on the olefination of heterocycles.

π-Conjugated fluorescent framework  /  C−H olefination  /  Organic single-molecule white-light materials  /  Heterocycles  /  NIR fluorescence materials
Ruike Hu, Kangmin Wang, Junxiang Liu, Jingxian Zhang, Guoliang Yang, Liqiu Wan, Bijin Li. Extended π-conjugated systems by external ligand-assisted C−H olefination of heterocycles: Facile access to single-molecular white-light-emitting and NIR fluorescence materials[J]. Chinese Chemical Letters, 2025 , 36 (4) : 110113 - . DOI: 10.1016/j.cclet.2024.110113
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Organic fluorescent materials have attracted much attention due to their excellent photophysical properties and high sensitivity to the microenvironment, which were used in memory devices, security systems, sensors, bioprobes, field-effect transistors, organic light-emitting diodes, solid-state lasers, super-resolution microscopy chemosensors, etc. [1–5]. In the past decade, transition-metal-catalyzed C–H functionalization has witnessed exciting and rapid advances in the set-up of various organic fluorescent materials [5–19].
Ligand-assisted C−H olefination is a distinct, facile, and atom-efficient tactic for extended π-conjugated systems, which is usually difficult to prepare using conventional synthetic methods [20–24]. The approaches without the construction and deconstruction of a directing group represent a unique opportunity to access a novel π-conjugated fluorescent framework, which does not require pre-functionalization of starting materials, and does not use stoichiometric organometallic reagents, and can avoid the tiresome multi-step synthesis [20–24]. Recently, the use of an external ligand-assist strategy to achieve palladium-catalyzed C−H olefination has emerged as a promising protocol [20–24]. External ligands can effectively stabilize palladium catalysts, concerted metalation deprotonation, and promote the C–H activation. Yu and co-workers have achieved palladium-catalyzed C–H olefination of arenes using 3,5-bis(trifluoromethyl)pyridin-2-ol as an external ligand (Scheme 1A) [20]. Maiti group recently described using 6-bromo-pyridine-3-ol and amino acid as external ligands to promote palladium-catalyzed C−H/C−F coupling for accessing α-fluoro olefins (Scheme 1B) [21].
Heterocycles such as phenothiazine, phenoxazine, 5,5-dioxide-phenoxazine, phenoselenazine, dihydrophenazine, and dihydroacridine units are important scaffolds in biologically active natural products, pharmaceuticals, and organic functional materials [25–38]. Especially, phenothiazine possesses electron-rich sulfur and nitrogen heteroatoms, low ionization energy, good hole-transporting ability, and the non-planar "butterfly" structure characteristic, which can enable framework highly twisted conformation and hinder the intermolecular π-π stacking and non-radiative transition to some extent, and thus could be ideal candidates to excavate fluorescent materials. In this study, we would like to report on the design and synthesis of a novel π-conjugated fluorescent framework by external ligand-assisted C−H olefination of heterocycles (Scheme 1C).
We began our investigation by using 10-phenyl-10H-phenothiazine (1a) as a model substrate for alkenylation with ethyl acrylate (2a) (for details, see Table S1 in Supporting information). After the screening of several parameters (e.g., metal source, external ligand, and solvent), the reaction conditions (10 mol% Pd(OAc)2, 1.0 equiv. ligand, 3-nitro-6-(trifluoromethyl)pyridin-2-ol, and 4.0 equiv. Cu(OAc)2 in 1,4-dioxane at 130 ℃ under atmospheric N2) proved to be the most efficient and affording the C3-alkenylated product ethyl (E)−3-(10-phenyl-10H-phenothiazin-3-yl)acrylate (3a) in 60% yield. It was noticed that the external ligand 3-nitro-6-(trifluoromethyl)pyridin-2-ol can significantly increase yield, which plays a crucial role in this catalytic system. The electron-deficient 3-nitro-6-(trifluoromethyl)pyridin-2-ol could coordinate with and stabilize the palladium catalyst and act as an internal base to promote and accelerate the C−H bond cleavage [20,21,39–45]. Furthermore, raw material 1a displays weak fluorescence emission at 449 nm with a meager quantum yield (0.8%) in CH2Cl2 (Fig. S1 in Supporting information). However, C3-alkenylated product 3a displays a strong fluorescence emission at 546 nm with a fluorescence quantum yield (45%) in dichloromethane (Scheme 2 and Fig. S2 in Supporting information), and this result highlights the extended π-conjugated structures by C–H functionalization to discover new organic fluorescent frameworks.
With the optimized alkenylation conditions in hand, a library of C3/C7-alkenylated products was obtained using electronically different 10-aryl-10H-phenothiazines and olefins (Schemes 2 and 3). Both acrylates and acrylamide readily reacted with 1a to produce the C3-alkenylated products in moderate to good yields (3a–3n). Substituted styrenes can also be employed as a coupling partner, giving the desired products in 56%−70% (3o–3r). The reaction exhibited high selectivity at the C3-position, and no C1/C2-alkenylated product was detected (3a–3r). A wide range of heterocycles, such as phenothiazine, phenothiazine 5,5-dioxide-phenoxazine, phenoselenazine, dihydrophenazine, and dihydroacridine smoothly underwent the dehydrogenative coupling reaction to generate the desired C3/C7-alkenylated products in acceptable yields (Scheme 3, 4a–6c). Various functional groups such as methyl (4b, 4c, 4j), naphthyl (4a, 4k), halides (3r), cyano (3r, 4g), nitro (3o), methoxy (4d, 4f), trifluoromethyl (4e, 4q, 4s), acetyl (4h), triphenylamine (4o), and benzothiadiazole (5b, 5c, 6b, 6c) were well tolerated in this reaction. Especially, the aldehyde functional group (3q, 4u-4x, 6a-6c) could be tolerated and thus enabled further synthetic transformations. This work achieves efficient and direct site-selective olefination of heterocycles by an external ligand-assist strategy without the construction and deconstruction of the directing group.
A possible mechanism pathway is proposed based on the results and previous reports (Scheme S1 in Supporting information) [20–24,39–45]. Initially, the Pd(Ⅱ) intermediate Ⅰ forms through the Pd(OAc)2 coordinates with two L ligands. Subsequently, the 10-phenyl-10H-phenothiazine (1a) reacts with Ⅰ to give the intermediate Ⅲ through the external ligand-assisted C3-position C–H activation. The intermediate Ⅲ coordinated with an olefin generates the Pd(Ⅱ) intermediate Ⅳ, followed by migratory insertion to yield the intermediate Ⅴ. Finally, the intermediate Ⅴ undergoes β-hydride elimination to offer the desired product 3a and release Pd(0). The Pd(Ⅱ) species is regenerated by the oxidation to finish the catalytic cycle.
Organic single-molecule white-light materials and devices have attracted much attention for their outstanding features such as long-term color balance, stability, and simple device fabrication in practical lighting [46–54]. However, achieving white-light-emission from an organic single molecule is an appealing yet challenging task because white-light-emission requires a broad emission covering the whole visible range (400-700 nm), which is hard to a single chromophore due to the intrinsic limitation of photophysical properties. Hence, organic single-molecule white-light materials are scarce, and only a few have been reported. In theory, anti-Kasha systems held the potential to serve as prime candidates to prepare single-molecular white-light-emitting materials because of their dual-emission behavior involving a high-lying excited state emission with a relatively short wavelength (blue-light component) and a low-lying excited state emission with a relatively long wavelength (orange-light component) [47,50,54].
The photophysical properties of the constructed library of olefination of heterocycles were further measured and the absorption and emission maxima are summarized in Schemes 2 and 3. Their emission spectra are also shown in Fig. S2. All alkenylated products (3a-3r, 4a-4x, 5a-5c, 6a-6c) exhibit bright fluorescent emission and their emission wavelengths are located in the range of purple to orange (408 nm to 608 nm) in dichloromethane. Intriguingly, compounds 4u-4x exhibit apparent dual-emission behavior involving a blue emission and orange emission wavelength, which completely covers the whole visible range (400-700 nm). These four compounds exhibit bright white-light emissions in dichloromethane with CIE1931 coordinates of 4u (0.33, 0.30), 4v (0.29, 0.35), 4w (0.32, 0.33), and 4x (0.33, 0.32), respectively (Fig. 1). It is worth pointing out that based on the compound 4u as the core skeleton of white-light materials, when the electron-donating group (methoxy; 4w) on the phenothiazine moiety, leads to red-shifted emissions, and corresponding CIE coordinates close to pure white light (CIE: 0.33, 0.33). In addition, a slightly blue-shifted emission was observed when the electron-withdrawing group (trifluoromethyl; 4v) was on the phenothiazine unit. White-light molecule 4v exhibits an excellent fluorescence quantum yield of 60% in dichloromethane. Moreover, compound 4w exhibits bright white-light emissions with CIE coordinates of (0.29, 0.33) and a fluorescence quantum yield of 17% in polyvinyl pyrrolidone (PVP) film (0.02 wt%) (Figs. 1a and b). In addition, the room temperature photoluminescence lifetimes of 4u-4x in the dichloromethane solution and 4w in PVP film were investigated and the results are summarized in Table S2 and Figs. S5-S9 (Supporting information). According to observations, the radiative excitons of dual-emission in 4u-4x are several lifetime components with nanosecond order (Table S2 and Figs. S5-S9), and no long-lifetime fluorescence components exist. As demonstrated by the thermogravimetric analyzer, 4u and 4w are thermally stable and show high thermal stability with a 5% weight loss temperature up to 413 ℃ for 4u (Fig. S10 in Supporting information), which is suitable for device fabrication by thermal evaporation. By cyclic voltammetry and the optical bandgap calculation, the HOMO and LUMO levels of 4w are −5.05 eV and −2.57 eV, respectively (Table S3 and Section X in Supporting information).
White light-emitting diodes (LEDs) have attracted enormous interest because of their various applications in solid-state lighting and display applications [53,55–59]. Most current commercial white light-emitting diodes are manufactured by coating the LED chip with green and/or inorganic phosphor [53,55–59]. To further demonstrate the potential application of these newly developed white-light materials, 4w film (0.02 wt% in PVP) was coated onto the surface of a commercially available UV LED chip, and bright white light could be formed when turning the LED on (Figs. 1c and d). This result unlocks an opportunity to rapidly fabricate low-cost white LEDs based on organic single-molecule white-light materials.
The anti-Kasha character of 4u was further studied by experiments and theoretical calculations (Fig. 2). The decay experiments of the excited states show only several lifetime components with nanosecond order in the dual-emission (Fig. S5). Hence, the relatively short wavelength from high-lying singlet state emission (S4 → S0) and the relatively long wavelength from low-lying singlet state emission (S1 → S0) (Fig. 2b). Notably, the large energy gap ΔE(S4 → S3) value is 0.61 eV, which can effectively suppress the partial internal conversion (IC) from the S4 to the S3 state [47,50,54]. Furthermore, the relative intensities of the dual-emission are very dependent on the excitation wavelength, with lower energy excitation resulting in weakened emissions at shorter wavelengths (Fig. 2a). These results strongly indicate that 4u possesses an anti-Kasha dual-emission character [47,50,54].
To increase the degree of conjugation of the heterocycles further, a series of dialkenylated products (7a-7h) were synthesized with moderate to good yields and high regioselectivity by modifying the reaction conditions slightly (Scheme 4a). Furthermore, the structure of 7e was confirmed through single-crystal X-ray analysis.
In recent years, near-infrared (NIR) fluorescence materials (emission wavelengths 650–900 nm) have attracted considerable attention in vivo bioanalysis and bioimaging because of their low light scattering, small photodamage, and deep tissue penetration [60–67]. Hence, the development of novel NIR fluorophores is an appealing and significantly challenging task. Derivatives of dicyanoisophorone (DCI) with ultra-fast intramolecular charge transfer are ideal candidates for designing NIR fluorescence probes with large Stokes shifts because the DCI group is well-known as a quality acceptor [66,67]. The phenothiazine or triphenylamine (TPA) group possesses good electron-donating properties and could be used as an excellent donor. Therefore, we designed DCI-bearing alkenylated-phenothiazine derivatives (8a-8c) as novel NIR fluorescence probes.
Given that the external ligand-assisted C−H olefination protocol developed here can tolerate the reactive aldehyde group, 6a-6c were used as starting materials to avoid tedious multiple-step synthesis and thus greatly streamline synthetic routes. The NIR fluorescence molecules 8a-8c with large Stokes shifts were obtained by reaction of the 6a-6c with 2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile, respectively (Scheme 4b).
Furthermore, NIR fluorescence molecules 8b and 8c were fabricated as water-dispersed nanoparticles (NPs) with Poloxamer 188 as a matrix (Section XI in Supporting information). The hydrodynamic diameter of 8b and 8c NPs are 169.5 nm and 158.2 nm, respectively by dynamic light scattering (DLS) measurement (Fig. S12 in Supporting information). Scanning electron microscopy (SEM) images indicated that the 8b and 8c NPs have a spherical shape and are almost in size to those of DLS measurement (Figs. S13 and S14 in Supporting information). In addition, the cytotoxicity experiments reveal 8b and 8c NPs with almost no toxicity in HeLa cells (Fig. S17 and Section XII in Supporting information), which means they can be used for biomedical applications. Subsequently, staining experiments of 8b and 8c NPs in HeLa cells were conducted and the 4′, 6-diamidino-2-phenylindole (DAPI) was used as a reference dye for fluorescence staining. The corresponding NIR fluorescence signal can be detected in HeLa cells by confocal laser scanning microscopy (Figs. 3a-f). Furthermore, the co-staining experiments of Hela cells with 8b NPs and the commercially available Mito-Tracker Green (mitochondria-specific tracker) indicated that it could specifically targeted the mitochondria of living cells with Pearson's coefficient in 0.87 (Figs. S18 and 19, and Section XII in Supporting information). Moreover, the obvious NIR fluorescence signal fluorescence signals were clearly observed in HeLa cells by two-photon irradiation, indicating that 8b and 8c NPs possess good two-photon excitation fluorescence imaging character (Fig. S20 in Supporting information). These results reveal that the 8b and 8c NPs can be efficiently endocytosed into the HeLa cells and potentially applied for NIR fluorescence imaging probes.
In this study, we would like to report on the design and synthesis of a novel π-conjugated fluorescent framework by external ligand-assisted C−H olefination of heterocycles strategy. The developed reaction showed a broad substrate scope of olefins and heterocycles, and various olefination of heterocycles compounds were synthesized in moderate to good yields. It is worth noting that these novel fluorescent materials could present full-color-tunable emissions (λem: 408–665 nm in DCM) with large Stokes shifts (up to 195 nm) (Figs. 3g and h).
In addition, novel organic single-molecule white-light materials based on olefination of heterocycles were developed herein and exhibits bright white-light emissions with high fluorescence quantum yields. The obtained single-molecule white-light material 4w is thermally stable and shows a CIE coordinate of (0.32, 0.33), which is very close to pure white light (CIE: 0.33, 0.33). Experimental data and theoretical calculations indicate that white light emission from a relatively short wavelength anti-Kasha emission and a relatively long wavelength Kasha emission. More importantly, novel olefination of heterocycles can be applied to fabricate robust organic and low-cost white LEDs. Furthermore, the novel NIR fluorescence materials based on the olefination of heterocycles were designed, synthesized, and fabricated as water-dispersed NPs, which can be efficiently endocytosed into the HeLa cells and potentially applied for NIR fluorescence imaging probes. The easy access to external ligand-assisted C−H olefination of heterocycles developed herein has well exemplified the great appeal of C−H activation and unlocks an opportunity for rapid screening of single-molecular white-light-emitting and NIR fluorescence materials.
Declaration of competing interest
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The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
CRediT authorship contribution statement
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Ruike Hu: Project administration, Methodology, Investigation, Formal analysis, Data curation. Kangmin Wang: Methodology, Data curation. Junxiang Liu: Methodology, Investigation. Jingxian Zhang: Methodology, Data curation. Guoliang Yang: Methodology, Data curation. Liqiu Wan: Methodology, Investigation. Bijin Li: Writing – review & editing, Writing – original draft, Project administration, Methodology, Funding acquisition, Formal analysis, Data curation.
Acknowledgments
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We thank the Fundamental Research Funds for the Central Universities (Nos. 2024CDJXY002; 2023CDJYGRH-YB17; 2022CDJXY-025), the Venture & Innovation Support Program for Chongqing Overseas Returnees (No. cx2022061), the Natural Science Foundation of Chongqing (No. CSTB2022NSCQ-MSX1123), the Chongqing Talents: Exceptional Young Talents Project (No. cstc2021ycjh-bgzxm0067), the Hongshen Young Scholars Program from Chongqing University (No. 0247001104426) for financial support.
Supplementary materials
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Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.cclet.2024.110113.
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Year 2025 volume 36 Issue 4
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doi: 10.1016/j.cclet.2024.110113
  • Receive Date：2024-04-15
  • Online Date：2025-11-19
  • Published：2025-04-15
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  • Received：2024-04-15
  • Revised：2024-05-27
  • Accepted：2024-06-11
Affiliations
    Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, Chongqing 401331, China
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表12种不同金属材料的力学参数
科
Family		 属数
Number of
genus		 种数
Number of
species		 占总种数比例
Percentage of
total species (%)		 属
Genus		 种数
Number of
species		 占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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