Alleviating NIR-II emission quenching in ring-fused fluorophore via manipulating dimer populations for superior fluorescence imaging
Open accessAbstract
Emission quenching resulting from fluorophore aggregation has long been a significant challenge in optimizing emission-based technologies, such as fluorescence imaging and optoelectronic devices. Alleviating this quenching in aggregates is crucial, yet progress is impeded by the limited understanding of the nature and impact of aggregates on emission. Here, we elucidate the critical role of dimeric aggregate (dimer) in alleviating second near-infrared (NIR-II, 900-1700 nm) emission quenching from ring-fused fluorophore 4F for superior fluorescence imaging. Spectral decomposition and molecular dynamics simulations demonstrate the predominance of dimer populations in 4F aggregates. Notably, dimers exhibit significantly weaker emission but intense intermolecular nonradiative ( inter NR) decay compared to monomers, as demonstrated by ultrafast spectra and quantum calculation. Therefore, the predominant population of dimers with weak emission and pronounced inter NR feature underlies the emission quenching in 4F aggregates. This discovery guides the preparation of ultrabright NIR-II 4F nanofluorophore (4F NP3s) by decreasing dimer populations, which show 5-fold greater NIR-II brightness than indocyanine green, enabling superior resolution in visualizing blood vessels. This work offers valuable insights into aggregation-caused quenching, with broad implications extending far beyond NIR-II fluorescence imaging.
AI snapshot
Written from the paper’s full text.
TL;DR
This study shows that dimeric aggregates dominate in nanoparticles of the ring-fused NIR-II fluorophore 4F and drive emission quenching through weak dimer emission and intense intermolecular nonradiative decay. Reducing the dimer population yields ultrabright 4F NP3s with 7.1 × 10³ M⁻¹ cm⁻¹ NIR-II brightness, enabling high-resolution vascular and tumor imaging in mice.
Key findings
- In 4F NP1s, spectral decomposition assigns monomer emission at ~940 nm and dimer emission at ~1050 nm, with dimers predominating (64.3% vs. 35.7% monomers); ΦPL drops from 17.1% for 4F in THF to 2.6% in 4F NP1s, and brightness falls from 1.09 × 10⁴ to 1.79 × 10³ M⁻¹ cm⁻¹.
- Femtosecond transient absorption shows 4F NP1s have a 0.43 ps component assigned to dimer intermolecular nonradiative decay, a 7.73 ps dimer emission component, and a 179 ps monomer fluorescence component, versus 4.6 and 134 ps components for 4F in THF; dimer radiative decay is ~30 times faster than monomer decay (7.7 vs. 179 ps).
- Reducing dimer population produces 4F NP3s with ΦPL increased from 2.6% to 7.5%, ε at 808 nm increased from 6.8 × 10⁴ to 9.5 × 10⁴ M⁻¹ cm⁻¹, and brightness of 7.1 × 10³ M⁻¹ cm⁻¹, about 4 times that of 4F NP1s and ~5 times that of ICG (1560 M⁻¹ cm⁻¹).
- In vivo, 4F NP3s under 1500 nm LP gave FWHM of 0.25 mm and SBR of 4.04, compared with 0.30 mm/2.75 at 1300 nm LP and 0.49 mm/1.71 at 980 nm LP; tumor signal peaked at 24 h and remained detectable at 36 h, with accumulation mainly in liver and spleen and no significant H&E organ damage.
Methods
- 4F was synthesized as a ring-fused donor–acceptor fluorophore and encapsulated in Pluronic F-127 to form water-soluble nanoparticles at 1, 0.1, and 0.01 mg mL⁻¹, yielding 4F NP1s, NP2s, and NP3s; nanoparticles were characterized by DLS, TEM, zeta potential, and stability tests.
- Optical and mechanistic analyses included absorption/PL spectroscopy, ΦPL determination relative to IR-26 (0.5%), Gaussian spectral decomposition, molecular dynamics simulations, quantum chemical calculations, femtosecond transient absorption, and femtosecond transient fluorescence spectroscopy.
- In vivo studies used Balb/c mice for whole-body vascular imaging after tail-vein injection of 4F NP3s (200 μL, 1 mg mL⁻¹) with 980, 1300, and 1500 nm LP filters, and BALB/c nude mice bearing 143B osteosarcoma for tumor imaging from 0 to 48 h, plus biodistribution and H&E staining.
Limitations
- The paper states that femtosecond transient fluorescence spectroscopy could not measure fluorescence lifetimes for 4F NP2s, 4F NP1s, and 4F because of its detection limit (~300 ps).
- The paper notes that the clinical and translational path is “undeniably complex,” despite arguing that 4F NP3s satisfy brightness, photostability, and biosafety requirements.
- Evident from the text: in vivo validation is limited to mouse models, and the reported dimer-population percentages are not fully internally consistent (4F NP1s are stated as 64.3% dimers, while 4F NP3s are later described as reduced from 73.5% to 64.3%), so the quantitative dimer fractions should be interpreted cautiously.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 17 cited sources checked · 0 supported · 0 flagged
- Findingcitation
Femtosecond transient absorption spectra provide experimental evidence of weak emission and intense intermolecular nonradiative decay from dimers in 4F NP1s.
“Femtosecond transient absorption (fs-TA) spectra provided experimental evidence of the weak emission and intense interNR decay from dimers in 4F NP1s37,38.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [37] Maiuri, M., Garavelli, M. & Cerullo, G. Ultrafast spectroscopy: state of the art and open challenges. J. Am. Chem. Soc. 142, 3–15 (2020). source
Not checked in the free run.
- cites [38] Hu, W. B., Prasad, P. N. & Huang, W. Manipulating the dynamics of dark excited states in organic materials for phototheranostics. Acc. Chem. Res. 54, 697–706 (2021). source
Not checked in the free run.
- Findingown data
4F in tetrahydrofuran exhibits intense NIR-II emission with photoluminescence quantum yield up to 17.1%.
“and intense NIR-II emission with ultrahigh ΦPL of up to 17.1% (reference: IR-26, ΦPL = 0.5%, Fig. 2b, Fig. S10).”
Quote in the paperSubstantial claim - Findingown data
Spectral decomposition reveals a reduced dimer population from 73.5% to 64.3% in 4F NP3s.
“Spectral decomposition revealed a reduced dimer population from 73.5% to 64.3% in 4F NP3s (Fig. 4a), consistent with molecular dynamics simulations that showed a reduced proportion of dimers as the decrease in 4F concentration (Fig. S23).”
Quote in the paperSubstantial claim - Findingown data
The fluorescence brightness of 4F NP1s is decreased by an order of magnitude compared with unimolecular 4F in tetrahydrofuran (1.79 × 10^3 M−1 cm−1 vs. 1.09 × 10^4 M−1 cm−1).
“Correspondingly, the fluorescence brightness of 4F NP1s decreased by an order of magnitude compared to unimolecular 4F in THF (1.79 × 103 M−1 cm−1 vs. 1.09 × 104 M−1cm−1)”
Quote in the paperSubstantial claim - Findingown data
4F nanoparticles exhibit superior photostability compared with indocyanine green.
“Moreover, 4F NPs exhibited superior photostability compared to ICG (Fig. S21).”
Quote in the paperNot a substantial claim
- Findingown data
Spectral decomposition in Fig. 2g shows distinct absorption peaks corresponding to monomers (~760 nm) and dimers (~840 nm).
“This assignment is supported by the spectral decomposition in Fig. 2g which shows distinct absorption peaks corresponding to monomers (~760 nm) and dimers (~840 nm).”
Quote in the paperSubstantial claim - Findingown data
When the water fraction in THF/H2O mixed solutions is ≤10%, both absorption and photoluminescence spectra of 4F exhibit a similar lineshape to 4F in pure tetrahydrofuran, indicating a unimolecular nature.
“When the fraction of water (fw) in THF/H2O mixed solutions was ≤10%, both the absorption and PL spectra exhibited a similar lineshape to that of 4F in pure THF, indicating a unimolecular nature (Fig. S16).”
Quote in the paperSubstantial claim - Findingown data
Molecular dynamics simulation confirms the coexistence of multiple dimer architectures alongside monomers.
“Molecular dynamics simulation confirmed the coexistence of multiple dimer architectures alongside monomers (Fig. 2e, f; Fig. S17).”
Quote in the paperSubstantial claim - Findingown data
Spectral decomposition reveals bi-component fluorescence from 4F NP1s, with distinct emission peaks corresponding to monomers (~940 nm) and dimers (~1050 nm).
“Spectral decomposition further reveals the bi-component fluorescence from 4F NP1s (Fig. 2h), with distinct emission peaks corresponding to monomers (~940 nm) and dimers (~1050 nm).”
Quote in the paperSubstantial claim - Findingown data
4F in tetrahydrofuran exhibits a molar extinction coefficient at 808 nm of 6.4 × 10^4 M−1 cm−1.
“In tetrahydrofuran (THF) solution, 4F exhibits robust NIR absorption (ε808 nm = 6.4 × 104 M−1 cm−1, Fig. 2a, Fig. S9)”
Quote in the paperNot a substantial claim - Findingown data
The fluorescence of long-preserved 4F nanoparticles exhibits minimal variations in intensity and spectral lineshape, confirming outstanding optical stability.
“The fluorescence of long-preserved 4F NPs exhibit minimal variations in intensity and spectral lineshape (Fig. S22), further confirming their outstanding optical stability.”
Quote in the paperNot a substantial claim - Findingown data
4F NP3s exhibit noticeably decreased dimer-associated absorption around 840 nm and emission around 1050 nm.
“In contrast, 4F NP3s exhibited a noticeably decreased dimer-associated absorption around 840 nm and emission around 1050 nm (Fig. 4a, b).”
Quote in the paperSubstantial claim - Findingown data
In the NIR-IIb window (1500 nm LP), 4F NP3s provided clear visualization of blood vessels with significantly reduced background noise and remarkable contrast compared with the less distinct vessels seen in the conventional NIR-II region (980 and 1300 nm LP filters).
“Impressively, in the NIR-IIb window (1500 nm LP), 4F NP3s provided clear visualization of blood vessels with significantly reduced background noise, offering remarkable contrast compared to the less distinct vessels observed in the conventional NIR-II region (980 and 1300 nm LP filters).”
Quote in the paperSubstantial claim - Findingown data
4F NP3s satisfy the requirements of high fluorescence brightness and photostability for effective clinical imaging.
“For effective clinical imaging, fluorophores must exhibit high fluorescence brightness and photostability, which are all satisfied by 4F NP3s.”
Quote in the paperSubstantial claim - Findingown data
The brightness of 4F NP3s is approximately 5-times greater than that of indocyanine green (1560 M−1 cm−1).
“Notably, the brightness of 4F NP3s is also ~5-times greater than that of ICG (1560 M−1 cm−1), repressing the top-level NIR-II fluorescence brightness.”
Quote in the paperSubstantial claim - Findingown data
Even after 36 hours post-injection, the fluorescence signals at the tumor sites diminished but maintained satisfactory brightness.
“Even after 36 hours post-injection, the fluorescence signals at the tumor sites diminished but maintained satisfactory brightness, highlighting the potential of 4F NP3s as a long-term NIR-II fluorescence imaging probe for deep-seated tumor navigation (Fig. 5d).”
Quote in the paperSubstantial claim - Findingown data
4F NP3s exhibit negligible cytotoxicity in MC3T3-E1 cells even at concentrations up to 100 μg mL−1.
“4F NP3s exhibit negligible cytotoxicity even at high concentrations up to 100 μg mL−1, indicating excellent in vitro biocompatibility (Fig. S24).”
Quote in the paperSubstantial claim - Findingown data
Ultrafast spectroscopy indicates decelerated intermolecular nonradiative decay in 4F NP2s and 4F NP3s, reflected by extended time constants from 0.49 ps to 0.98 ps.
“The representative kinetic curves within the GSB region indicate a decelerated interNR decay in 4F NP2s and 4F NP3s, reflected by extended time constants from 0.49 ps to 0.98 ps (Fig. 4d, Table S5).”
Quote in the paperSubstantial claim - Findingown data
Full width at half-maximum measurements of hind-limb vessels were 0.49, 0.30, and 0.25 mm for 980, 1300, and 1500 nm LP filters, respectively.
“High-magnification imaging of hind-limb vessels provided detailed anatomical information, with full width at half-maxima (FWHM) measurements of 0.49, 0.30, and 0.25 mm for 980, 1300, and 1500 nm LP, respectively, demonstrating the superior resolution afforded by NIR-IIb imaging (Fig. 5b).”
Quote in the paperSubstantial claim - Findingown data
Dimer emission exhibits an extended lifetime, increasing from 9.4 ps to 11.6 ps.
“Concurrently, the dimer emission exhibited an extended lifetime, increasing from 9.4 ps to 11.6 ps.”
Quote in the paperSubstantial claim - Findingown data
4F NP2s and 4F NP3s exhibit enhanced photoluminescence quantum yields, increasing from 2.6% for 4F NP1s to 2.9% and 7.5%, respectively.
“As expected, 4F NP2s and 4F NP3s exhibited enhanced ΦPL, increasing from 2.6% for 4F NP1s to 2.9% and 7.5%, respectively (Fig. 4c, Fig S11, Table S3).”
Quote in the paperSubstantial claim - Findingown data
Molecular dynamics simulations show a reduced proportion of dimers as the 4F concentration decreases.
“consistent with molecular dynamics simulations that showed a reduced proportion of dimers as the decrease in 4F concentration (Fig. S23).”
Quote in the paperSubstantial claim - Findingown data
After intravenous injection, 4F NP3s primarily accumulated in the liver and spleen.
“NIR-II imaging revealed that the nanoparticles primarily accumulated in the liver and spleen, suggesting a metabolic pathway via the hepatobiliary system (Fig. S26).”
Quote in the paperNot a substantial claim - Findingreasoning
Reducing the dimer population leads to the development of ultrabright 4F NP3s.
“Building on this finding, reducing the dimer population leads to the development of ultrabright 4F NP3s, which enable high-resolution imaging of vascular blood vessels and deep-seated osteosarcoma.”
Quote in the paperSubstantial claim - Findingown data
In whole-body fluorescence angiography of mice, the spatial resolution of 4F NP3s notably outperformed that of ICG.
“The imaging results revealed that the spatial resolution of 4F NP3s notably outperformed that of ICG (Fig. S25).”
Quote in the paperSubstantial claim - Interpretationown data
The absorption and emission of 4F originate primarily from its extensive π-conjugation rather than from a conventional charge-transfer state.
“This is consistent with the minimal solvation effect (Fig. S14), indicating that the absorption and emission of 4F originate primarily from its extensive π-conjugation, rather than from the conventional charge-transfer (CT) state typically observed in traditional D-A NIR-II fluorophores33.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [33] Li, M. Y. et al. Near-infrared-II fluorophore with inverted dependence of fluorescence quantum yield on polarity as potent phototheranostics for fluorescence-image-guided phototherapy of tumors. Adv. Mater. 35, 2209647 (2023). source
Not checked in the free run.
- Interpretationown data
The planar architecture of 4F is attributed to an intramolecular noncovalent S···O conformational lock.
“The interaction region indicator attributes the planar architecture of 4F to an intramolecular noncovalent S···O conformational lock (Fig. 2c)34–36.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [34] Yang, K. et al. Alkoxy-functionalized bithiophene/thiazoles: versatile building blocks for high-performance organic and polymeric semiconductors. Acc. Mater. Res. 4, 237–250 (2023). source
Not checked in the free run.
- cites [35] Wang, X. Y. et al. Unlocking the NIR-II AIEgen for high brightness through intramolecular electrostatic locking. Angew. Chem. Int. Ed. 63, e202404142 (2024). source
Not checked in the free run.
- cites [36] Huang, H. et al. Organic and polymeric semiconductors enhanced by noncovalent conformational locks. Chem. Rev. 117, 10291–10318 (2017). source
Not checked in the free run.
- Interpretationown data
The close intermolecular distance (~3 Å) of dimers within nanoparticles facilitates intense π-π interaction, indicating strong nonradiative decay.
“Moreover, the close intermolecular distance (~3Å) of dimers within NPs facilitates the intense π-π interaction (Figs. 2f; S17), indicating strong nonradiative decay.”
Quote in the paperSubstantial claim - Interpretationreasoning
These two processes, especially intermolecular nonradiative decay, are more competitive than those of monomers, resulting in significantly reduced emission.
“Notably, these two processes, especially interNR, are more competitive than that of monomers, resulting in significantly reduced emission.”
Quote in the paperSubstantial claim - Interpretationreasoning
Further improvement in NIR-II brightness is principally achievable if aggregation-caused quenching can be significantly alleviated.
“Thus, further improvement in NIR-II brightness is principally achievable if ACQ can be significantly alleviated.”
Quote in the paperSubstantial claim - Interpretationown data
The 4.6 ps component in 4F is ascribed to intramolecular nonradiative decay.
“The 4.6 ps component in 4F is ascribed to intramolecular NR decay.”
Quote in the paperSubstantial claim - Premisecitation
Donor-acceptor engineering leads to weak absorption at long wavelengths.
“Worse still, D-A engineering leads to weak absorption in the long wavelengths20.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [20] Zhang, Q. S. et al. Bright and stable NIR-II J-aggregated AIE dibodipy-based fluorescent probe for dynamic in vivo bioimaging. Angew. Chem. Int. Ed. 60, 3967–3973 (2021). source
Not checked in the free run.
- Interpretationown data
The reduced emission in 4F aggregates essentially arises from the predominant population of dimers with weak emission and intense intermolecular nonradiative decay features.
“Based on these findings, we recognize that the reduced emission in 4F aggregates essentially arises from the predominant population of dimers with weak emission and intense interNR decay features.”
Quote in the paperSubstantial claim - Interpretationreasoning
The reduced emission observed in 4F aggregates is primarily due to the predominant population of dimers with weak emissive properties.
“Together, these results suggest that the reduced emission observed in 4F aggregates is primarily due to the predominant population of dimers with weak emissive properties.”
Quote in the paperSubstantial claim - Interpretationreasoning
The femtosecond component suggests a deactivation preference over all other decay pathways within 4F NP1s, highlighting an intense intermolecular nonradiative decay that reduces emission.
“Notably, this femtosecond component suggests a deactivation preference over all other decay pathways within 4F NP1s, highlighting an intense interNR decay that reduces emission39,40.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [39] Miao, X. F. et al. Excimer-mediated ultrafast intermolecular nonradiative decay enables giant photothermal performance for optimized phototheranostic. Adv. Mater. 35, 2301739 (2023). source
Not checked in the free run.
- cites [40] Liang, Y. Y. et al. Alkyl-doping enables significant suppression of conformational relaxation and intermolecular nonradiative decay for improved near-infrared fluorescence imaging. Angew. Chem. Int. Ed. 63, e202408861 (2024). source
Not checked in the free run.
- Interpretationreasoning
The long-lived component of 134 ps for 4F and 179 ps for 4F nanoparticles is attributed to monomer fluorescence, due to consistency with the fluorescence lifetime.
“The long-lived component of 134 ps for 4F and 179 ps for 4F NPs are attributed to monomer fluorescence, due to their consistency with the fluorescence lifetime (vide infra).”
Quote in the paperSubstantial claim - Interpretationreasoning
Reducing the dimer population through a nanoengineering strategy is principally applicable to creating bright NIR-II fluorophores.
“Therefore, reducing the dimer population through a nanoengineering strategy is principally applicable to creating bright NIR-II fluorophores.”
Quote in the paperSubstantial claim- Rests on an assumption: Aggregation-caused quenching typically arises from fluorophore aggregation, which brings molecules into close contact and facilitates nonradiative energy loss via intermolecular interactions.
- Interpretationown data
The longer-wavelength absorption around 850 nm and emission around 1050 nm are assigned to the dimer.
“We thus assign the longer-wavelength absorption of around 850 nm and emission of around 1050 nm to the dimer.”
Quote in the paperSubstantial claim - Premisecitation
Most available NIR-II fluorophores are prone to aggregation-caused quenching in practical applications, which typically reduces photoluminescence quantum yields to below 2%.
“However, these NIR-II fluorophores are prone to aggregation-caused quenching (ACQ) in practical applications16–19, which typically reduces ΦPL values to below 2% (Table S1).”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [16] Zhu, Y. L. et al. The balance effect of π-π electronic coupling on NIR-II emission and photodynamic properties of highly hydrophobic conjugated photosensitizers. Adv. Sci. 11, 2307569 (2024). source
Not checked in the free run.
- cites [17] Ma, S. Q. et al. Organic molecular aggregates: from aggregation structure to emission property. Aggregate 2, e96 (2021). source
Not checked in the free run.
- cites [18] Qi, J. et al. Gathering brings strength: how organic aggregates boost disease phototheranostics. Aggregate 2, 95–113 (2021). source
Not checked in the free run.
- cites [19] Barman, D. et al. Review on recent trends and prospects in π-conjugated luminescent aggregates for biomedical applications. Aggregate 3, e172 (2022). source
Not checked in the free run.
- Premisereasoning
Most available NIR-II fluorophores have unsatisfactory NIR-II brightness, typically below 1000 M−1 cm−1.
“These limitations result in unsatisfactory NIR-II brightness for most available NIR-II fluorophores, with values typically below 1000 M−1 cm−1 (Table S1).”
Quote in the paperSubstantial claim - Interpretationreasoning
The noncovalent conformational lock of 4F addresses the challenges of traditional D-A type NIR-II fluorophores, which often possess twisted structures that result in weaker absorption at longer wavelengths.
“This noncovalent conformational lock addresses the challenges associated with traditional D-A type NIR-II fluorophores, which often possess twisted structures that result in weaker absorption at longer wavelengths.”
Quote in the paperSubstantial claim - Interpretationown data
These results reinforce the critical role of dimers in modulating NIR-II brightness from 4F aggregates.
“Together, these results reinforce the critical role of dimers in modulating NIR-II brightness from 4F aggregates.”
Quote in the paperSubstantial claim - Interpretationreasoning
The predominant population of dimers, characterized by weak emission and intense interNR decay, underlies the aggregation-caused quenching (ACQ) observed in 4F aggregates.
“Together, the predominant population of dimers, characterized by weak emission and intense interNR decay, underlies the ACQ observed in 4F aggregates.”
- Also stated in: § Discussion · boosted
“this study also proposes and validates that the predominant population of dimers, characterized by weak emission and intense interNR decay, underlies the ACQ observed in 4F aggregates.”
Quote in the paperSubstantial claim - Also stated in: § Discussion · boosted
- Interpretationreasoning
The time constants of 227 ps for 4F NP2s, 179 ps for 4F NP1s, and 134 ps for 4F are reasonably attributed to monomer fluorescence.
“Thus, the time constants of 227 ps for 4F NP2s, 179 ps for 4F NP1s, and 134 ps for 4F were reasonably attributed to monomer fluorescence.”
Quote in the paperSubstantial claim - Interpretationown data
The long-term colloidal and optical stability of 4F NP3s facilitates real-time and dynamic high-resolution imaging.
“Moreover, their long-term colloidal and optical stability facilitates real-time and dynamic high-resolution imaging (Fig. 5b, Fig. S19–22), which could revolutionize surgical procedures and therapeutic interventions.”
Quote in the paperSubstantial claim - Interpretationreasoning
The robust properties of 4F afford great potential for its clinical translation.
“These robust properties afford great potential for the clinical translation of 4F, although clinical and translational path is undeniably complex.”
Quote in the paperNot a substantial claim- Rests on an assumption: The osteosarcoma-bearing BALB/c nude mouse model represents deep-seated tumors for the purpose of assessing the clinical imaging potential of 4F NP3s.
- Interpretationown data
The inefficient intermolecular nonradiative decay and extended fluorescence lifetime from the dimer can be attributed to the increased intermolecular distance within the dimer, which creates significant space for monomer fluorescence.
“This inefficient interNR and extended fluorescence lifetime from the dimer can be attributed to the increased intermolecular distance within the dimer (Table S4), which creates significant space for monomer fluorescence.”
Quote in the paperSubstantial claim - Interpretationreasoning
The extensive π-conjugation and rigid structure of 4F contribute significantly to its high NIR-II photoluminescence quantum yield.
“Together, these features contribute significantly to the high NIR-II ΦPL for 4F.”
Quote in the paperSubstantial claim - Interpretationreasoning
The approach of reducing the dimer population introduces an innovative strategy for developing ultrabright organic π-conjugated materials even in aggregated states, which is unattainable in the traditional strategy.
“The success of this approach introduces an innovative strategy for the development of ultrabright organic π-conjugated materials even in aggregated states that is unattainable in traditional strategy.”
Quote in the paperSubstantial claim - Interpretationown data
4F NP3s are metabolized via the hepatobiliary system.
“NIR-II imaging revealed that the nanoparticles primarily accumulated in the liver and spleen, suggesting a metabolic pathway via the hepatobiliary system (Fig. S26).”
- Also stated in: § Discussion · hedged
“Biosafety analyses of 4 F NP3s indicate negligible long-term toxicity, with metabolism primarily via liver (Fig. S26, 27).”
Quote in the paperSubstantial claim - Also stated in: § Discussion · hedged
- Interpretationown data
4F NP3s have potential as a long-term NIR-II fluorescence imaging probe for deep-seated tumor navigation.
“Even after 36 hours post-injection, the fluorescence signals at the tumor sites diminished but maintained satisfactory brightness, highlighting the potential of 4F NP3s as a long-term NIR-II fluorescence imaging probe for deep-seated tumor navigation (Fig. 5d).”
Quote in the paperSubstantial claim- Rests on an assumption: The osteosarcoma-bearing BALB/c nude mouse model represents deep-seated tumors for the purpose of assessing the clinical imaging potential of 4F NP3s.
- Classified as probably not a substantial claim. 3
- May combine two claims. 41
- The quote only partly states this claim. 2
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown data4F NP2s (0.1 mg mL−1) and 4F NP3s (0.01 mg mL−1) with lower doping concentration exhibit slightly smaller hydrodynamic diameters of 40 nm and 30 nm, respectively, compared with 4F NP1s (1 mg mL−1).
“The resulting 4F NP2s (4F: 0.1 mg mL−1) and 4F NP3s (4F: 0.01 mg mL−1) with lower doping concentration exhibit slightly smaller hydrodynamic diameters of 40 nm and 30 nm (Fig. S15), respectively, compared to 4F NP1s (4F: 1 mg mL−1).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataKinetic curves within the ground-state bleaching region around 765 nm reveal three components with time constants of 0.43, 7.73, and 179 ps for 4F NP1s, compared with two components of 4.6 and 134 ps for 4F in tetrahydrofuran.
“The representative kinetic curves within the GSB region around 765 nm reveal three components with time constants of 0.43, 7.73, and 179 ps for 4F NP1s, compared to two components of 4.6 and 134 ps for 4F in THF (Fig. 3c, Table. S5).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown data4F NP1s show a significant decrease in fluorescence, with photoluminescence quantum yield decreasing from 17.1% to 2.6%.
“In contrast, 4F NP1s show a significant decrease in fluorescence, with ΦPL dramatically decreasing from 17.1% to 2.6% (Figs. 2b, S11, Table S3).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown data4F NP2s display an absorption spectrum similar to that of 4F NP1s, with distinct monomer and dimer peaks at 760 nm and 840 nm, respectively.
“4F NP2s displayed an absorption spectrum similar to that of 4F NP1s, with distinct monomer and dimer peaks at 760 nm and 840 nm (Fig. 4a), respectively.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown data4F NP1s present accelerated excited-state decay compared with 4F in tetrahydrofuran, consistent with reduced emission.
“As shown in Fig. 3a, b, the fs-TA mapping of 4F and 4F NP1s exhibits prominent ground state bleaching (GSB) signals around 750 nm, where 4F NP1s present accelerated excited state decay compared to 4F in THF, consistent with its reduced emission.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataAs the water fraction increases, the aggregation-associated emission around 1050 nm becomes more pronounced while the overall photoluminescence intensity of 4F gradually decreases.
“As the fw continued to increase, the aggregation-associated emission around 1050 nm became more pronounced, while the overall PL intensity of 4F gradually decreased (Figs. 2d, S16).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown data4F nanoparticles maintain a zeta potential of approximately −15 mV and show negligible changes in size over 15 days of storage, indicating good colloidal stability.
“These nanoparticles maintain a zeta potential of approximately −15 mV (Fig. S19) and show negligible changes in size over 15 days of storage (Fig. S20), indicating good colloidal stability41,42.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [41] Gu, Y. et al. Chlorination-mediated π-π stacking enhances the photodynamic properties of a NIR-II emitting photosensitizer with extended conjugation. Angew. Chem. Int. Ed. 62, e202303476 (2023). source
Not checked in the free run.
- cites [42] Li, D. et al. Photo-triggered cascade therapy: a NIR-II AIE luminogen collaborating with nitric oxide facilitates efficient collagen depletion for boosting pancreatic cancer phototheranostics. Adv. Mater. 36, 2306476 (2024). source
Not checked in the free run.
May combine two claims.
Findingown dataIn 4F NP1s, the weight of dimers significantly surpasses that of monomers (64.3% vs. 35.7%), indicating a predominant population of dimers.
“Notably, the weight of dimers significantly surpasses that of monomers (64.3% vs. 35.7%) in 4F NP1s, indicating a predominant population of dimers within 4F NP1s (Fig. 2h).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe accelerated radiative decay of dimers (7.7 ps) occurs at a rate nearly 30 times faster than that of monomers (179 ps), suggesting a deactivation preference in radiative pathways for dimers over monomers.
“In addition, the accelerated radiative decay of dimers (7.7 ps), occurring at a rate nearly 30 times faster than that of monomers (179 ps), also suggests a deactivation preference in radiative pathways for dimers over monomers.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataCompared with unimolecular 4F in tetrahydrofuran, 4F NP1s exhibit a pronounced redshift in absorption maximum and an increased molar extinction coefficient at 808 nm of 6.8 × 10^4 M−1 cm−1.
“Compared to unimolecular 4 F in THF, 4F NP1s exhibited a pronounced redshift in their absorption maximum and an increased ε at 808 nm of 6.8 × 104 M−1 cm−1 (Figs. 2a, S9).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataUpon increasing the water fraction to 20%, 4F displays a new red-shifted absorption peak around 850 nm and a photoluminescence peak around 1050 nm, corresponding to the spectral features of 4F NP1s.
“However, upon increasing the fw to 20%, 4F displayed a new, red-shifted absorption peak around 850 nm and a PL peak around 1050 nm, corresponding well to the spectral features of 4F NP1s (aggregates).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown data4F NP1s are uniform nanoparticles with a hydrodynamic diameter of 50 nm.
“Dynamic light scattering (DLS) and transmission electron microscopy (TEM) confirmed that the resulting nanoparticles were uniform, with a hydrodynamic diameter of 50 nm (Fig. S15).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe NIR-IIb region exhibited the highest signal-to-background ratio of 4.04, surpassing the SBRs of 1.71 and 2.75 for 980 and 1300 nm LP, respectively.
“Meanwhile, the NIR-IIb region exhibited the highest signal-to-background ratio (SBR) of 4.04, surpassing the SBRs of 1.71 and 2.75 for 980 and 1300 nm LP, respectively.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown data4F NP3s demonstrate superior fluorescence brightness of 7.1 × 10^3 M−1 cm−1, nearly maintaining the brightness of unimolecular 4F in tetrahydrofuran (10.9 × 10^3 M−1 cm−1) and being 4-times higher than that of 4F NP1s (1.8 × 10^3 M−1 cm−1).
“Collectively, 4F NP3s demonstrated superior fluorescence brightness of 7.1 × 103 M−1cm−1 (Fig. 4c), which nearly maintains the brightness of unimolecular 4F in THF (10.9 × 103 M−1cm−1) and is 4-times higher than that of 4F NP1s (1.8 × 103 M−1cm−1).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataIn osteosarcoma-bearing mice, distinct NIR-II fluorescence signals appeared at the tumor sites after 6 h post-administration, with signal intensity progressively increasing and peaking at 24 h.
“As shown in Fig. 5c, distinct NIR-II fluorescence signals were observed at the tumor sites after 6 h post-administration, with signal intensity progressively increasing and peaking at 24 hours.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataMultiple dimer architectures coexist alongside monomers of 4F within its aggregate, with the dimer population predominating.
“Our findings reveal the coexistence of multiple dimer architectures alongside monomers of 4F within its aggregate, with dimer population predominating.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataDimers of 4F exhibit significantly weaker emission and more intense intermolecular nonradiative (interNR) decay compared to monomers.
“Notably, dimers exhibit significantly weaker emission and more intense interNR compared to monomers.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataFemtosecond transient fluorescence spectroscopy measures the fluorescence lifetime of 4F NP3s as 435 ps, which aligns well with the long-lived component (496 ps) extracted by femtosecond transient absorption within ground-state bleaching regions.
“Femtosecond transient fluorescence spectroscopy measured the fluorescence lifetime of 4F NP3s as 435 ps (Fig. 4e), which aligns well with the long-lived component (496 ps) extracted by the fs-TA within GSB regions.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown data4F NP3s have an ultrahigh NIR-II brightness of 7125 M−1 cm−1, one of the highest levels of brightness among available NIR-II fluorophores.
“The ultrahigh NIR-II brightness (7125 M−1 cm−1) represents one of the highest levels of brightness among available NIR-II fluorophores (Table S1, 2), offering unprecedented potential in high-resolution visualization of vital structures such as blood vessels and malignant lesions (Fig. 5a, b).”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenThe 4F molecule features an intramolecular noncovalent S···O interaction that promotes a giant π-conjugation and a rigid molecular structure.
“The 4F molecule features an intramolecular noncovalent S···O interaction that promotes a giant π-conjugation and a rigid molecular structure.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataSmall vessels branching around the abdominal vessels were clearly distinguished in the NIR-IIb region, whereas no clear image could be obtained in the conventional NIR-II window.
“Importantly, small vessels branching around the abdominal vessels were clearly distinguished in the NIR-IIb region, whereas no clear image could be obtained in the conventional NIR-II window (Fig. 5a).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown data4F NP3s exhibit long-term colloidal and optical stability.
“Moreover, their long-term colloidal and optical stability facilitates real-time and dynamic high-resolution imaging (Fig. 5b, Fig. S19–22), which could revolutionize surgical procedures and therapeutic interventions.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe populations of monomer fluorescence increase from 9.6% to 20.2% as the dimer populations decrease, supporting the elevated photoluminescence quantum yield of 4F NP3s.
“Moreover, the populations of this monomer fluorescence increased from 9.6% to 20.2% as the dimer populations decreased (Table S5), supporting the elevated ΦPL of 4F NP3s.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe molar extinction coefficient is progressively enhanced from 6.8 × 10^4 to 7.2 × 10^4 and 9.5 × 10^4 M−1 cm−1 at 808 nm as aggregation decreases, with 4F NP3s exhibiting an ultrahigh molar extinction coefficient relative to unimolecular 4F.
“Moreover, ε was also progressively enhanced from 6.8 × 104 to 7.2 × 104 and 9.5 × 104 M−1cm−1 at 808 nm as aggregation decreased (Fig. S9), with 4F NP3s exhibiting an ultrahigh ε relative to unimolecular 4F (ε808nm = 6.4 × 104 M−1cm−1).”
Quote in the paperSubstantial claimThe quote only partly states this claim.
Findingown dataHematoxylin-eosin staining of the major organs 48 h post-injection showed no significant hydropic damage or necrotic lesions.
“Furthermore, hematoxylin–eosin (H&E) staining of the major organs showed no significant hydropic damage or necrotic lesions, indicating the good biosafety of 4F NP3s (Fig. S27).”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningWeak dimer emission, together with nonradiative deactivation priority over monomer, further reduces emission.
“This weak dimer emission, but having nonradiative deactivation priority over monomer, further reduces emission.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationConjugation extension can improve long-wavelength absorption but often shows ultralow photoluminescence quantum yield due to more pronounced aggregation-caused quenching and molecular motion.
“In contrast, conjugation extension can improve long-wavelength absorption but often shows ultralow ΦPL due to more pronounced ACQ and molecular motion21.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [21] Su, Y. B. et al. NIR-II bioimaging of small organic molecule. Biomaterials 271, 120717 (2021). source
Not checked in the free run.
May combine two claims.
Interpretationown dataThe intense long-wavelength absorption and emission of 4F arise from extensive π-conjugation in its fully planar backbone, with negligible torsion (<0.4°) in both S0 and S1 states.
“The intense long-wavelength absorption and emission arise from the extensive π-conjugation in the fully planar backbone of 4F, with negligible torsion (<0.4˚) in both S0 and S1 states (Fig. 2c, Fig. S12).”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataThe femtosecond component of 0.43 ps observed in 4F NP1s corresponds to intermolecular nonradiative decay from dimers, while the 7.7 ps component is attributed to dimer emission.
“The femtosecond component of 0.43 ps observed in 4F NP1s corresponds to interNR decay from dimers, while the 7.7 ps component is attributed to dimer emission.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataUpon photoexcitation, both monomers and dimers reach the excited state; dimers primarily return to the ground state through ultrafast intermolecular nonradiative decay and, to a lesser extent, through radiative decay.
“Upon photoexcitation, both monomers and dimers reach the excited state. Dimers primarily return to the ground state through ultrafast interNR and, to a lesser extent, through radiative decay.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningThe distinctive conformational lock of 4F supports the planar conformation necessary for intense long-wavelength absorption and emission and induces a rigid structure that significantly inhibits nonradiative energy loss through molecular motions.
“Notably, this distinctive conformational lock not only supports the planar conformation necessary for intense long-wavelength absorption and emission but also induces a rigid structure that significantly inhibits nonradiative energy loss through molecular motions.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataIn 4F aggregates, the formation of dimers generates new near-infrared absorption peaks around 840 nm and induces a further redshift of the original monomer absorption peak.
“In 4F aggregates, the formation of dimers not only generates new near-infrared absorption peaks around 840 nm but also induces a further redshift of the original monomer absorption peak.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningThe absence of the femtosecond component in diluted tetrahydrofuran solutions rules out structural relaxation and reinforces the assignment of the femtosecond component to dimer.
“Therefore, the absence of the femtosecond component in these solutions rules out the possibility of structural relaxation, reinforcing the assignment of femtosecond component to dimer.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationRing-fused NIR-II fluorophores undergo severe aggregation-caused quenching, with photoluminescence quantum yield decreasing from 15.1% in the unimolecular state to 2.1% in the aggregated state.
“However, these ring-fused NIR-II fluorophores also undergo severe ACQ, showing a dramatic decrease in ΦPL from 15.1% in unimolecular state to 2.1% in practical application (aggregated state)31.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [31] Yuan, Y. et al. Molecular programming of NIR-IIb-Emissive semiconducting small molecules for in vivo high-contrast bioimaging beyond 1500 nm. Adv. Mater. 34, 2201263 (2022). source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFemtosecond transient fluorescence spectroscopy could not measure the fluorescence lifetimes for 4F NP2s, 4F NP1s, and 4F due to its detection limit of approximately 300 ps.
“Unfortunately, our femtosecond transient fluorescence spectroscopy could not measure the fluorescence lifetimes for 4F NP2s, 4F NP1s, and 4F due to its detection limit (~300 ps).”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningThe extensive π-conjugation of 4F facilitates both intense absorption and high photoluminescence quantum yield, while its rigid structure minimizes nonradiative energy loss from molecular motions such as conformational dynamics.
“The extensive π-conjugation facilitates both intense absorption and high ΦPL, while the rigid structure minimizes nonradiative energy loss by molecular motions such as conformational dynamics.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationreasoning4F NP3s enable high-resolution imaging of vascular blood vessels and deep-seated osteosarcoma.
“Building on this finding, reducing the dimer population leads to the development of ultrabright 4F NP3s, which enable high-resolution imaging of vascular blood vessels and deep-seated osteosarcoma.”
Quote in the paperSubstantial claim- Rests on an assumption: The osteosarcoma-bearing BALB/c nude mouse model represents deep-seated tumors for the purpose of assessing the clinical imaging potential of 4F NP3s.
May combine two claims. The quote only partly states this claim.
Interpretationown data4F NP3s enable high-performance in vivo NIR-II fluorescence imaging with superior signal-to-background ratio and sharp resolution.
“These findings demonstrate high-performance fluorescence imaging in vivo with superior SBR using 4F NP3s.”
- Also stated in: § High-performance NIR-II fluorescence imaging in vivo · boosted
“Overall, 4F NP3s demonstrate high-performance NIR-IIb angiography with sharp resolution and excellent potential as tumor navigation contrasts for phototheranostic applications.”
Quote in the paperSubstantial claim- Also stated in: § High-performance NIR-II fluorescence imaging in vivo · boosted
May combine two claims.
Interpretationown dataThese phenomena suggest successful regulation of dimer population in alleviating aggregation-caused quenching, thereby improving the NIR-II brightness of 4F aggregates.
“These phenomena suggest the successful regulation of dimer population in alleviating ACQ, thereby improving the NIR-II brightness of 4F aggregates.”
Quote in the paperSubstantial claim- Rests on an assumption: Aggregation-caused quenching typically arises from fluorophore aggregation, which brings molecules into close contact and facilitates nonradiative energy loss via intermolecular interactions.
May combine two claims.
InterpretationreasoningDimers with extended intermolecular distances not only preserve intense long-wavelength absorption but also alleviate the long-standing aggregation-caused quenching issue, offering insights for designing brighter fluorophores beyond NIR-II fluorescence imaging applications.
“Dimers with extended intermolecular distances not only preserve the intense long-wavelength absorption but also alleviate the long-standing ACQ issue, offering valuable insights for designing brighter fluorophores beyond NIR-II fluorescence imaging applications.”
Quote in the paperSubstantial claim- Rests on an assumption: Aggregation-caused quenching typically arises from fluorophore aggregation, which brings molecules into close contact and facilitates nonradiative energy loss via intermolecular interactions.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenAll animal studies were performed following the Guide for the Institutional Animal Care and Use Committee and under a protocol approved by the Animal Health and Use Committee of Northwestern Polytechnical University.
“All the animal studies were performed following the Guide for the Institutional Animal Care and Use Committee and the protocol approved by the Animal Health and Use Committee of Northwestern Polytechnical University.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown data4F NP3s have good biosafety, with negligible long-term toxicity.
“Furthermore, hematoxylin–eosin (H&E) staining of the major organs showed no significant hydropic damage or necrotic lesions, indicating the good biosafety of 4F NP3s (Fig. S27).”
- Also stated in: § Discussion · hedged
“Biosafety analyses of 4 F NP3s indicate negligible long-term toxicity, with metabolism primarily via liver (Fig. S26, 27).”
Quote in the paperSubstantial claim- Also stated in: § Discussion · hedged
May combine two claims.
Interpretationown data4F NP3s can achieve deep penetration imaging and effectively accumulate in the tumor region through the enhanced permeability and retention (EPR) effect.
“These results indicate that 4F NP3s can achieve deep penetration imaging and effectively accumulate in the tumor region through the enhanced permeability and retention (EPR) effect.”
Quote in the paperSubstantial claim- Rests on an assumption: The intensity of the NIR-II fluorescence signal at the tumor site reflects the amount of 4F NP3s accumulated there.
- Rests on an assumption: The osteosarcoma-bearing BALB/c nude mouse model represents deep-seated tumors for the purpose of assessing the clinical imaging potential of 4F NP3s.
The paper relies on this without support.
The exact nature and role of aggregates in aggregation-caused quenching remain poorly understood.
“Unfortunately, the exact nature and role of these aggregates remain poorly understood.”
The paper relies on this without support.
Aggregation-caused quenching typically arises from fluorophore aggregation, which brings molecules into close contact and facilitates nonradiative energy loss via intermolecular interactions.
“ACQ typically arises from fluorophore aggregation, which brings molecules into close contact, facilitating nonradiative energy loss via intermolecular interactions.”
The paper relies on this without support.
The intensity of the NIR-II fluorescence signal at the tumor site reflects the amount of 4F NP3s accumulated there.
“These results indicate that 4F NP3s can achieve deep penetration imaging and effectively accumulate in the tumor region through the enhanced permeability and retention (EPR) effect.”
The paper relies on this without support.
The osteosarcoma-bearing BALB/c nude mouse model represents deep-seated tumors for the purpose of assessing the clinical imaging potential of 4F NP3s.
“4F NP3s further demonstrate its potential in deep-seated tumor imaging using an osteosarcoma-bearing BALB/c nude mouse mode45.”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
NP3 dimer population matches the previously reported NP1 value
MajorThe paper describes a reduction to 64.3% dimers in NP3s, but earlier assigns 64.3% dimers to NP1s. As stated, those values do not show a reduction from NP1s to NP3s.
“Spectral decomposition revealed a reduced dimer population from 73.5% to 64.3% in 4F NP3s (Fig. 4a)”
“Notably, the weight of dimers significantly surpasses that of monomers (64.3% vs. 35.7%) in 4F NP1s, indicating a predominant population of dimers within 4F NP1s (Fig. 2h).”
Reported decay-rate comparison is nearly 30-fold instead of 23-fold
MinorFor decay time constants of 7.7 ps and 179 ps, the rate ratio is 179/7.7 ≈ 23.25, not nearly 30.
Reported 30 · recomputed 23.246753
“the accelerated radiative decay of dimers (7.7 ps), occurring at a rate nearly 30 times faster than that of monomers (179 ps)”
Angiography filter wavelength differs between sections
MinorThe results describe a 1000 nm long-pass filter for the angiography experiment, while the methods specify a 980 nm long-pass filter.
“The whole-body fluorescence angiography was performed using an InGaAs detector equipped with different long wavelength pass filters (1000, 1300, and 1500 nm) (Fig. 5a).”
“In vivo NIR-II fluorescence imaging was performed using a NIR-II imaging system (Wuhan Grand-imaging Technology Co., Ltd) under 808 nm photoexcitation, equipped with LP 980 nm, LP 1300 nm, LP 1500 nm filters.”
Cites
Aggregation-Induced Emission: Together We Shine, United We Soar!
Mei, J., Leung, N. L. C., Kwok, R. T. K., Lam, J. W. Y., & Tang, B. Z. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00263 · Cited by 8,270 · see citing works
Advanced Fluorescence Imaging Technology in the Near-Infrared-II Window for Biomedical Applications
Li, C., Chen, G., Zhang, Y., Wu, F., & Wang, Q. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c07022 · Cited by 1,037 · see citing works
Multifunctional in vivo vascular imaging using near-infrared II fluorescence
Hong, G., Lee, J. C., Robinson, J. T., Raaz, U., Xie, L., Huang, N. F., Cooke, J. P., & Dai, H. (2012) · Nature Medicine · doi:10.1038/nm.2995 · Cited by 995 · see citing works
Organic and Polymeric Semiconductors Enhanced by Noncovalent Conformational Locks
Huang, H., Yang, L., Facchetti, A., & Marks, T. J. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00084 · Cited by 804 · see citing works
Molecular Engineering of NIR‐II Fluorophores for Improved Biomedical Detection
Lei, Z., & Zhang, F. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202007040 · Cited by 690 · see citing works
In vivo NIR-II fluorescence imaging for biology and medicine
Wang, F., Zhong, Y., Bruns, O., Liang, Y., & Dai, H. (2024) · Nature Photonics · doi:10.1038/s41566-024-01391-5 · Cited by 564 · see citing works
Donor Engineering for NIR-II Molecular Fluorophores with Enhanced Fluorescent Performance
Yang, Q., Hu, Z., Zhu, S., Ma, R., Ma, H., Ma, Z., Wan, H., Zhu, T., Jiang, Z., Liu, W., et al. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.7b10334 · Cited by 554 · see citing works
Liu, Y., Li, Y., Koo, S., Sun, Y., Liu, Y., Liu, X., Pan, Y., Zhang, Z., Du, M., Lu, S., et al. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00553 · Cited by 544 · see citing works
Self-citationUltrafast Spectroscopy: State of the Art and Open Challenges
Maiuri, M., Garavelli, M., & Cerullo, G. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.9b10533 · Cited by 460 · see citing works
Perfecting and extending the near-infrared imaging window
Feng, Z., Tang, T., Wu, T., Yu, X., Zhang, Y., Wang, M., Zheng, J., Ying, Y., Chen, S., Zhou, J., et al. (2021) · Light: Science & Applications · doi:10.1038/s41377-021-00628-0 · Cited by 394 · see citing works
Organic molecular aggregates: From aggregation structure to emission property
Ma, S., Du, S., Pan, G., Dai, S., Xu, B., & Tian, W. (2021) · Aggregate · doi:10.1002/agt2.96 · Cited by 387 · see citing works
The fast-growing field of photo-driven theranostics based on aggregation-induced emission
Zhang, Z., Kang, M., Tan, H., Song, N., Li, M., Xiao, P., Yan, D., Zhang, L., Wang, D., & Tang, B. Z. (2022) · Chemical Society Reviews · doi:10.1039/d1cs01138c · Cited by 374 · see citing works
The Chemistry of Organic Contrast Agents in the NIR‐II Window
Mu, J., Xiao, M. W., Shi, Y., Geng, X., Li, H., Yin, Y., & Chen, X. S. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202114722 · Cited by 319 · see citing works
Shen, H., Sun, F., Zhu, X., Zhang, J., Ou, X., Zhang, J., Xu, C., Sung, H. H. Y., Williams, I. D., Chen, S., et al. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.2c07443 · Cited by 292 · see citing works
Self-citationGathering brings strength: How organic aggregates boost disease phototheranostics
Qi, J., Ou, H., Liu, Q., & Ding, D. (2021) · Aggregate · doi:10.1002/agt2.25 · Cited by 284 · see citing works
Liu, S., Ou, H., Li, Y., Zhang, H., Liu, J., Lu, X., Kwok, R. T. K., Lam, J. W. Y., Ding, D., & Tang, B. Z. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c07193 · Cited by 277 · see citing works
NIR-II bioimaging of small organic molecule
Su, Y., Yu, B., Wang, S., Cong, H., & Shen, Y. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.120717 · Cited by 251 · see citing works
Zhang, Q., Yu, P., Fan, Y., Sun, C., He, H., Liu, X., Lu, L., Zhao, M., Zhang, H., & Zhang, F. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202012427 · Cited by 216 · see citing works
Rational Design of High Brightness NIR-II Organic Dyes with S-D-A-D-S Structure
Yang, Q., Ma, H., Liang, Y., & Dai, H. (2021) · Accounts of Materials Research · doi:10.1021/accountsmr.0c00114 · Cited by 188 · see citing works
Biophotonic probes for bio-detection and imaging
Pan, T., Lu, D., Xin, H., & Li, B. (2021) · Light Science & Applications · doi:10.1038/s41377-021-00561-2 · Cited by 156 · see citing works
Tian, R., Ma, H., Yang, Q., Wan, H., Zhu, S., Chandra, S., Sun, H., Kiesewetter, D. O., Niu, G., Liang, Y., et al. (2018) · Chemical Science · doi:10.1039/c8sc03751e · Cited by 151 · see citing works
Feng, Z., Li, Y., Chen, S., Li, J., Wu, T., Ying, Y., Zheng, J., Zhang, Y., Zhang, J., Fan, X., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-40728-6 · Cited by 146 · see citing works
Self-citationManipulating the Dynamics of Dark Excited States in Organic Materials for Phototheranostics
Hu, W., Prasad, P. N., & Huang, W. (2021) · Accounts of Chemical Research · doi:10.1021/acs.accounts.0c00688 · Cited by 141 · cited 1× · see citing works
“Femtosecond transient absorption (fs-TA) spectra provided experimental evidence of the weak emission and intense inter NR decay from dimers in 4F NP1s 37,38 .”
Self-citationMeng, X., Pang, X., Zhang, K., Gong, C., Yang, J., Dong, H., & Zhang, X. (2022) · Small · doi:10.1002/smll.202202035 · Cited by 135 · see citing works
Ma, Z., Zhang, M., Yue, J., Alcazar, C. A., Zhong, Y., Doyle, T. C., Dai, H., & Huang, N. F. (2018) · Advanced Functional Materials · doi:10.1002/adfm.201803417 · Cited by 134 · see citing works
Liu, S., Chen, R., Zhang, J., Li, Y., He, M., Fan, X., Zhang, H., Lu, X., Kwok, R. T. K., Lin, H., et al. (2020) · ACS Nano · doi:10.1021/acsnano.0c07527 · Cited by 129 · see citing works
Self-citationYang, S., Zhang, J., Zhang, Z., Zhang, R., Ou, X., Xu, W., Kang, M., Li, X., Yan, D., Kwok, R. T. K., et al. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c08627 · Cited by 128 · see citing works
Self-citationWang, L., Li, N., Wang, W., Mei, A., Shao, J., Wang, W., & Dong, X. (2024) · ACS Nano · doi:10.1021/acsnano.3c12316 · Cited by 127 · see citing works
Thiophene π‐Bridge Manipulation of NIR‐II AIEgens for Multimodal Tumor Phototheranostics
Gui, Y., Wang, Y., Wang, D., Qin, Y., Song, G., Yan, D., Tang, B. Z., & Wang, D. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202318609 · Cited by 114 · see citing works
Barman, D., Narang, K., Parui, R., Zehra, N., Khatun, M. N., Adil, L. R., & Iyer, P. K. (2022) · Aggregate · doi:10.1002/agt2.172 · Cited by 113 · cited 1× · see citing works
“However, these NIR-II fl uorophores are prone to aggregation-caused quenching (ACQ) in practical applications 16 – 19 , which typically reduces Φ PL values to below 2% (Table S1).”
Propylenedioxy Thiophene Donor to Achieve NIR-II Molecular Fluorophores with Enhanced Brightness
Ma, H., Liu, C., Hu, Z., Yu, P., Zhu, X., Ma, R., Sun, Z., Zhang, C.-H., Sun, H., Zhu, S., et al. (2020) · Chemistry of Materials · doi:10.1021/acs.chemmater.9b05159 · Cited by 110 · see citing works
Gu, Y., Lai, H., Chen, Z., Zhu, Y., Sun, Z., Lai, X., Wang, H., Wei, Z., Chen, L., Huang, L., et al. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202303476 · Cited by 101 · see citing works
Yuan, Y., Feng, Z., Li, S., Huang, Z., Wan, Y., Cao, C., Lin, S., Wu, L., Zhou, J., Liao, L., et al. (2022) · Advanced Materials · doi:10.1002/adma.202201263 · Cited by 99 · see citing works
Bright short-wavelength infrared organic light-emitting devices
Xie, Y., Liu, W., Deng, W., Wu, H., Wang, W., Si, Y., Zhan, X., Gao, C., Chen, X., Wu, H., et al. (2022) · Nature Photonics · doi:10.1038/s41566-022-01069-w · Cited by 98 · see citing works
Chen, Y., Chen, S., Yu, H., Wang, Y., Cui, M., Wang, P., Sun, P., & Ji, M. (2022) · Advanced Healthcare Materials · doi:10.1002/adhm.202201158 · Cited by 95 · see citing works
Li, D., Chen, X., Dai, W., Jin, Q., Wang, D., Ji, J., & Tang, B. Z. (2023) · Advanced Materials · doi:10.1002/adma.202306476 · Cited by 95 · see citing works
Li, D., Qu, C., Liu, Q., Wu, Y., Hu, X., Qian, K., Chang, B., He, S., Yuan, Y., Li, Y., et al. (2019) · Advanced Functional Materials · doi:10.1002/adfm.201906343 · Cited by 94 · see citing works
Yang, K., Chen, Z., Wang, Y., & Guo, X. (2023) · Accounts of Materials Research · doi:10.1021/accountsmr.2c00237 · Cited by 72 · see citing works
Li, M., Lu, Z., Zhang, J., Chen, L., Tang, X., Jiang, Q., Hu, Q., Li, L., Liu, J., & Huang, W. (2023) · Advanced Materials · doi:10.1002/adma.202209647 · Cited by 56 · see citing works
Self-citationMiao, X., Yao, W., Chen, R., Jia, M., Ren, C., Zhao, H., He, T., Fan, Q., & Hu, W. (2023) · Advanced Materials · doi:10.1002/adma.202301739 · Cited by 55 · see citing works
Self-citationMa, F., Jia, Q., Deng, Z., Wang, B., Zhang, S., Jiang, J., Xing, G., Wang, Z., Qiu, Z., Zhao, Z., et al. (2024) · ACS Nano · doi:10.1021/acsnano.3c11078 · Cited by 49 · see citing works
Unlocking the NIR‐II AIEgen for High Brightness through Intramolecular Electrostatic Locking
Wang, X., Yang, X., Jiang, G., Hu, Z., Liao, T., Wang, G., Zhang, X., He, X., Zhang, J., Zhang, J., et al. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202404142 · Cited by 44 · see citing works
Self-citationZhu, Y., Lai, H., Gu, Y., Wei, Z., Chen, L., Lai, X., Han, L., Tan, P., Pu, M., Xiao, F., et al. (2024) · Advanced Science · doi:10.1002/advs.202307569 · Cited by 36 · see citing works
High brightness NIR-II nanofluorophores based on fused-ring acceptor molecules
Zhu, X., Liu, C., Hu, Z., Liu, H., Wang, J., Wang, Y., Wang, X., Ma, R., Zhang, X., Sun, H., et al. (2020) · Nano Research · doi:10.1007/s12274-020-2901-y · Cited by 34 · see citing works
Liang, Y., Pan, Y., Chen, L., Li, P., Xu, M., Zhou, H., Lu, X., Hu, W., Yin, C., & Fan, Q. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202408861 · Cited by 22 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Organic photosensitizers: from molecular design to phototheranostics
Zhang, T. Y., Qu, X., Shao, J., & Dong, X. (2025) · Chemical Society Reviews · doi:10.1039/d5cs00599j · Cited by 148 · see citing works
Zhang, X., Yang, L., Jia, M., Chen, R. Q., Zhang, H., Yao, S., Bai, R., Tian, Y., Chen, B., Li, J., et al. (2025) · Advanced Materials · doi:10.1002/adma.202513693 · Cited by 21 · see citing works
Self-citationOrganic small-molecule NIR-II fluorophores for tumor phototheranostics
Xiang, D., Wang, Z., Zheng, H., Tang, Y., & Li, Q. (2026) · Light: Science & Applications · doi:10.1038/s41377-026-02212-w · Cited by 22 · see citing works
“Among the diverse optical imaging modalities, fl uorescence imaging within the near-infrared II (NIR-II, 1000 – 1700 nm) window represents a major leap forward compared with those operating in the visible (400 – 700 nm) and near-infrared I (NIR-I, 700 – 1000 nm) regions 34 – 37 .”
Advanced second near-infrared fluorophores for bioapplications
Bai, Q., Yang, Q., Liu, Y., Li, A., Yin, X.-B., & Wu, S. (2025) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2025.217146 · Cited by 14 · see citing works
High-contrast mechanochromic luminescent material with enhanced blue-shift emission
Wu, Z., Du, N., Liu, J., Gong, M., & Wang, G. (2025) · Dyes and Pigments · doi:10.1016/j.dyepig.2025.113295 · Cited by 7 · see citing works
Development of quick, sensitive method for pea variety selection
Kong, L., He, W., Zhao, F., Chen, X., Zhang, R., Bin, Z., Zhao, Z., & Tang, B. Z. (2025) · Matter · doi:10.1016/j.matt.2025.102259 · Cited by 4 · see citing works
Fluorescent J-Aggregates in the NIR-II Window: Unlocking Frontiers in Biomedical Imaging
Wei, X., & Chen, W. (2026) · Chemical & Biomedical Imaging · doi:10.1021/cbmi.5c00232 · Cited by 4 · see citing works
Gao, Z., Lin, J., Yang, G., Shen, H., Shi, J., Han, N., Li, B., Zhang, H., Zhu, S., & Wang, M. (2026) · ACS Nano · doi:10.1021/acsnano.6c04422 · Cited by 3 · see citing works
Chen, C., Guo, K., Ren, L., Xue, T., Zhang, F., & Li, Z. (2025) · Chemical Engineering Journal · doi:10.1016/j.cej.2025.165050 · Cited by 3 · see citing works
Dendritic NIR‐II Cyanines Enable Deep Imaging and Precise Surgery
He, B., Wang, Z., Sun, Y., Piao, Y., Dong, C., Shen, Y., & Zhou, Z. (2025) · Small · doi:10.1002/smll.202509826 · Cited by 2 · see citing works
Li, J., Zhang, Y., Wang, T., Ta, X., Zhang, Y., Kong, F., Hu, B., Zhao, L., & Che, G. (2025) · Results in Surfaces and Interfaces · doi:10.1016/j.rsurfi.2025.100673 · Cited by 1 · see citing works
Xunwen, 张. Z., Yaowei, 申. S., Wen, 李. L., Dalong, 马. M., Jie, 刘. L., & Wei, 黄. H. (2025) · Chinese Journal of Lasers · doi:10.3788/cjl251135
Wenbo, 胡. H., Yonghui, 潘. P., & Xiaofei, 苗. M. (2025) · Chinese Journal of Lasers · doi:10.3788/cjl251131
Xinxin, 熊. X., Chi, 张. Z., Zhong, 杜. D., Jun, 李. L., & Nuernisha, 努. A. (2025) · Chinese Journal of Lasers · doi:10.3788/cjl251119
Chen, P., Liu, C., Wang, X., Qi, C., Zhang, W., Yu, Z., Lan, Y.-S., Li, C., Sun, P., & Fan, Q. (2026) · ChemNanoMat · doi:10.1002/cnma.202500522
Self-citationEngineering J-Aggregated Organic Dyes for Enhanced Phototheranostics
Zou, X., Li, N., & Zhao, N. (2026) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.6c03549
Yao, W., Yang, L., Chen, R., Yao, S., Zhang, H., Jia, M., Pan, Y., Bai, R., Yu, Z., Fan, Q., et al. (2026) · Light Science & Applications · doi:10.1038/s41377-026-02429-9
Self-citationInside-out and monitoring-assisted phototheranostics enabled by molecular–optoelectronic integration
Xu, G., Zhong, Y., Zhang, Y., Law, W., & Xu, Z. (2026) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2026.218424
Advances in polymer-based NIR-II fluorescent probes and their biomedical applications
Ahmad, A., Kanwal, M., Palaniyappan, N., Adnan, M., Fayaz, M., Pan, W., Akram, N., Rafiq, M., Rizwan, M., Yu, B., et al. (2026) · Sustainable materials and technologies · doi:10.1016/j.susmat.2026.e02197
An, L., Ou, C., An, H., Sun, H., Mou, X., Dong, X., & Cai, Y. (2026) · Materials Today Bio · doi:10.1016/j.mtbio.2026.103575
Zhang, Z., Lei, H., Yin, Z., Cheng, J. P., Zhao, L., Zhang, T., Chen, J., Li, T., Yang, D., & Chen, M. (2026) · Journal of Manufacturing Processes · doi:10.1016/j.jmapro.2026.08.035
Wang, A., Tao, Z., Chen, S., Zhan, R., Huang, W., Wang, W., Zhang, J., Ma, H., Zhang, W., & Tian, J. H. (2026) · Biomaterials · doi:10.1016/j.biomaterials.2026.124594
Self-citationAdvances in Organic Aggregates for Biomedical Phototheranostics
Fu, B., Peng, Y., & Cai, T. (2026) · MedComm – Biomaterials and Applications · doi:10.1002/mba2.70077
Miao, X., Jia, M., Yao, W., Chen, R., Lu, X., Wu, Z., Hu, W., & Fan, Q. (2026) · Science Advances · doi:10.1126/sciadv.aeh5112
Self-citationA NIR-II AIEgen with superior fluorescence and photothermal performance for precision theranostics
Zheng, H., Li, T., Sun, T., Xu, J., Wei, J., Zhang, S.-T., Wang, C., Wang, D., Lu, G., & Tang, B. Z. (2026) · Science Advances · doi:10.1126/sciadv.aeh5939
- Authors
- Miao, X., Jia, M., Weng, X., Zhang, J., Pan, Y., Zhao, H., Yu, Z., Fan, Q., & Hu, W.
- Affiliations
- Northwestern Polytechnical University (CN)
- Nanjing University of Posts and Telecommunications (CN)
- University of Cambridge (GB)
- Corresponding author
- Fan, Quli
- Hu, Wenbo
- Venue
- Light: Science & Applications
- Published
- 2025-03-04
- Volume
- 14
- Issue
- 1
- Pages
- 109-109
- ISSN
- 2047-7538 (ISSN-L)
- PMC
- PMC11880303
- OpenAlex
- W4408133384
- Semantic Scholar
- fcb5d5828af82ffe7d8e5a83189f0b37f2144c75
- Cited by
- 25
- References
- 45
- Citations by year
- 2026: 14 · 2025: 11
- FWCI
- 5.28
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Light Science & Applications (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Apollo (University of Cambridge) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation of China (62288102, 62175201, 52373142)
- Fundamental Research Funds for the Central Universities
- the open research fund of State Key Laboratory of Organic Electronics and Information Displays
- Topics
- Physical Sciences › Materials Science › Materials Chemistry › Luminescence and Fluorescent Materials
- Physical Sciences › Chemistry › Spectroscopy › Molecular Sensors and Ion Detection
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Photochemistry and Electron Transfer Studies
- Keywords
- NIR-II fluorescence, aggregation-caused quenching, vascular imaging, fluorescence imaging, molecular dynamics simulation, ultrafast spectroscopy
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-08.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-08.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review