Aggregation-induced emission (AIE) is a photophysical phenomenon correlated closely with the excited-state intramolecular motions. Although AIE has attracted increasing attention due to the significant applications in biomedical and optoelectronics, an in-depth understanding of the excited-state intramolecular motion has yet to be fully developed. Here we found the non-aromatic annulene derivative of cyclooctatetrathiophene shows typical AIE phenomenon in spite of its rotor-free structure. The underlying mechanism is investigated through photoluminescence spectra, time-resolved absorption spectra, theoretical calculations, circular dichroism as well as by pressure-dependent fluorescent spectra etc., which indicate that the aromaticity reversal from ground state to the excited state serves as a driving force for inducing the excited-state intramolecular vibration, leading to the AIE phenomenon. Therefore, aromaticity reversal is demonstrated as a reliable strategy to develop vibrational AIE systems. This work also provides a new viewpoint to understand the excited-state intramolecular motion behavior of lumiongens.
The utilization of microscopic molecular motion to design macroscopic materials is receiving gradually more attention as it not only affords versatile functional materials but also broadens the fundamental understanding of dynamic molecular systems1,2. In this regard, scientists have made great achievements with fascinating concepts and materials such as in making molecular machines (e.g., molecular motors, molecular switches, and molecular shuttles), stimuli-responsive polymers and smart fluorescent materials etc. were all well proposed and developed3,4,5,6,7,8,9,10. Among them, molecular motion responsive fluorescent materials have attracted much attention due to their wide applications in biological systems, materials science and membrane chemistry7,8,9,10,11. While unlike the other molecular motion responsive systems such as molecular motors that rely on controlling and promoting the molecular motion to attain specific functionality, fluorescent systems generally need the suppression of molecular motion to generate a strong fluorescence12,13. A concept that has attracted increasing attention in this context is the development of aggregation-induced emission (AIE)12. Typical AIE systems show quenched emission in the solution state since the dynamic intramolecular motion accelerates the non-radiative decay process of the excited state12,13,14,15, while in the solid state the restriction of intramolecular rotation (RIR) and intramolecular vibration (RIV) suppresses the non-radiative decay and thus generate a high-fluorescence quantum efficiency12. So far, AIE systems based on RIR have been deeply investigated both mechanistically and in practice, based on which versatile solid-state fluorescent materials and stimuli-responsive fluorescent probes were developed12,13,14,15,16. However, molecular systems based on RIV are still rather limited in variety due to the unclear molecular design and the intrinsic difficulty in regulating the vibrational magnitude than the rotation magnitude, although vibrations are more general than rotation as a motion mode17,18. Additionally, an in-depth understanding of the excited-state molecular motion behavior and elucidation of the origin of the molecular motion are yet to be explored.
In general, most of the developed luminogens are based on aromatic compounds since they hold better electron conjugation and are more stable thermodynamically than the appropriate non-aromatic systems19,20,21,22,23. However, aromatic compounds generally show suppressed molecular motion via superior electron conjugation, which makes their vibrational/rotational degrees of freedom and torsional space rather limited for further tuning. In this regard, the annulene system with non-aromaticity shows a large magnitude of vibration upon photoexcitation, which provides a suitable platform for studying the influence of vibrational behavior on the exciton relaxation24,25,26. According to the aromaticity reversal theory proposed by Baird in 1972 (Baird’s rule)27,28,29,30, the aromaticity (antiaromaticity) of annulenes in the triplet excited-state (T1) is reversed to that in the ground state. In other words, annulenes with [4n + 2] π electrons show aromatic character in the ground state but antiaromatic character in the excited state. Similarly, annulenes with [4n] π electrons exhibit antiaromatic character in the ground state but aromatic feature in the excited state. This theory later has been found also applicable to the singlet excited state (S1)31,32,33,34,35,36,37. Since the aromaticity reversal will result in a change of molecular conformation, the excited-state aromaticity reversal can possibly serve as a driving force to induce a large amplitude conformation flip to quench the emission and the suppression of which theoretically can light up the emission, leading to the generation of a new type of AIE system.
Cyclooctotetraene (COT) is a prototype molecule of non-aromatic annulenes32,33,34,35. Recently, versatile aromatics/heteroaromatics fused COT systems have been developed with some of them are suitable candidates to explore excited-state aromaticity reversal29,38,39,40,41,42,43,44,45. For instance, Itoh and colleagues29 energetically quantified Baird’s aromaticity via investigation of the inversion of photoexcited cyclooctatetrathiophene (COTh) derivatives. Hada et al. monitored the dynamic structural change of thiazole fused COT with liquid crystal character induced by excited-state aromaticity reversal38. Although these COT derivatives show active conformation flip after photoexcitation, their luminescent properties have not been investigated, which inspired us to explore the possibility of using COT derivatives to construct vibrational AIE system and unveil the relationship among the aromaticity reversal, molecular motion, and luminescent properties.
In this work, we investigate the luminescent behavior of COTh and its derivatives by photoluminescence (PL) spectra, time-resolved absorption spectra, theoretical calculations, circular dichroism (CD), and circular polarized luminescence (CPL) spectroscopy, as well as pressure-dependent fluorescent spectra. COThs are demonstrated to be a unique vibrational AIE system (Fig. 1). Furthermore, the relationship between the AIE property and the excited-state aromaticity reversal is elucidated. The results here indicate that the aromaticity reversal from ground state to the excited state serves as a driving force for the structural vibrational behavior of COThs, leading to their AIE phenomenon. Furthermore, because of the chirality and the enhanced emission of COThs in aggregates and solid state, some of its derivatives exhibit CPL and microbial imaging capability. Aromaticity reversal thus is demonstrated as a reliable strategy to develop new AIE systems. Furthermore, the extensive application platform of AIE materials also provides a new outlet for utilizing Baird’s rule to develop luminescent functional materials.
Results and discussion
Molecular synthesis and characterization
The molecular structures involved have been presented in Fig. 2. Their synthetic routes are shown in the Supplementary Figs. 1 and 2. In general, COTh and COTh-tetramethylsilane (TMS) and COTh-Ph were synthesized according to literature methods46,47. COTh-Py was synthesized by using a SN2 reaction of 1 and pyridine at room temperature that gave a yield of 57%. While 1 was produced through the SN2 reaction between 2 and 1,6-dibromohexane (yield: 52%). The demethoxy derivative of 3 can generate 2 in a yield of 62%. 3 was synthesized by Suzuki coupling between brominated COTh and 4-methoxy phenylboronic acid efficiently with a yield of 70%. The new compounds have been characterized by 1H NMR, 13C NMR, and high-resolution mass spectroscopies with satisfied results (Supplementary Figs. 2−13).
The optical properties of COTh and COTh-TMS were first investigated using ultraviolet (UV)–visible (Vis) and photoluminescence (PL) spectra (Fig. 3 and Supplementary Figs. 14−16). COTh showed a strong absorption peak at 280 nm and a weak shoulder peak at around 340 nm, which could be assigned to a ππ* and nπ* transition, respectively. COTh-TMS shows slightly redder absorption wavelengths than that of COTh (310 nm, shoulder: 350 nm) due to the TMS substitution. In the film state, both the absorption of COTh and COTh-TMS show a slight red-shift, possibly due to the enhanced intermolecular interaction and/or molecular planarization. Interestingly, COTh-TMS exhibited AIE activity with dim emission in dilute solution but bright green emission in the solid state (ΦF: photoluminescence quantum yield, ΦF, soln, = 0.7%, ΦF, solid, = 10%, determined by using a calibrated integrating sphere) as shown in Fig. 3. The AIE characteristic was also confirmed by studying its PL behaviors in acetone/water mixtures with different water fractions (fw) (Supplementary Fig. 15). At a low fw, the mixture exhibited negligible PL emission, while at a high fw, the PL intensities became very strong due to the formation of aggregates. According to the RIM mechanism proposed by Tang and co-workers12, the non-emissive characteristic of COTh-TMS possibly is ascribed to its active intramolecular motion in the solution state. We thus measured its PL spectra at room temperature and 77 k because the molecular motion can be greatly suppressed at 77 k (Supplementary Fig. 16). COTh-TMS is dimly emissive at room temperature but brightly emissive at 77 k, suggesting that molecular motion possibly plays a key role for the AIE phenomenon. Initially, we assume that the TMS group possibly works as rotors to promote the non-radiative decay process, resulting in the AIE phenomenon of COTh-TMS. However, further investigation indicates COTh, an analog of COTh-TMS without TMS group also shows a typical AIE property (ΦF, soln, = 0.4%, ΦF, solid, = 11%). This suggests that the molecular backbone vibration rather than the rotation of the TMS group plays a predominant role for the AIE phenomenon of the COTh system, although the TMS rotation may contribute to the increased AIE effect of COTh-TMS with a larger αAIE value than that of COTh (Supplementary Fig. 15).
Single crystal analysis and theoretical calculation
To gain insight into the details of the AIE phenomenon of COTh and its derivatives, we analyzed their crystal structures (Supplementary Figs. 17−19)46,47. COTh and its derivatives examined all showed non-coplanar and saddle-type conformations, which avoid strong intermolecular π–π interactions that are detrimental for the luminescence to take place12. Furthermore, multiple intermolecular C−H…π and S…π interactions exist in the crystals, which help to rigidify the molecular conformation and are beneficial for the solid state emission to occur12,18. It is worthy to note that the non-coplanar and saddle-type conformations of COTh are similar to that of COT, which implys vibrational molecular motion possibly occur for COTh upon photoexcitation due to lack of aromaticity stabilization32,33,34. To better understand the influence of the molecular motion on the AIE phenomenon of COTh, theoretical calculations were carried out for the ground state (S0) at the DFT/B3LYP/SV(P) level and for the first excited singlet state (S1) at TDDFT/B3LYP/SV(P) level, respectively, for the COTh molecule in both the gas phase and in its crystal state (Table 1, Fig. 4, Supplementary Figs. 20−21, and Supplementary Table 1−4)48. In Table 1 and Supplementary Table 1, we present selected major geometrical stuctural parameters of the ground (S0) and singlet excited state (S1) for the COTh molecule, as well as the corresponding X-ray crystal structure data for comparison. The optimized geometry of COTh at the S0 minimum in the solid state is consistent with the crystal structure. This confirms the reliability of the QM/MM method at the B3LYP/SV(P) level and the general Amber force field49. It is clear that the isolated COTh molecule is more flexible than the molecule in a cluster, and this is reflected by the structral differences between S0 and S1 for the representative dihedral angles in Table 1. The torsional angles ΘI–II and ΘII–III are 22.82° and 24.22° in the gas phase, far larger than those in the solid state of 12.78° and 12.96°. Additionally, the torsional angle between the neighboring thienyl rings are decreased in the excited state, indicating a better planarity of the central large ring V. These results suggest that the four wings of COTh undergoes an up-down molecular motion from S0 to S1, supporting the existence of a vibrational motion behavior. The electron density contours of HOMO and LUMO of COTh at their side and top views are shown in Fig. 4b and Supplementary Fig. 20, respectively. The HOMO is of π character, while LUMO is of π* character. Both the HOMO and LUMO delocalized in the whole molecule. In addition, the transition between the HOMO and LUMO plays a significant contribution (>99%) for the singlet excited state (Supplementary Table 2). The AIE effect of the COTh molecule was explicitly confirmed by theoretically calculation results for the radiative rate (kr), the non-radiative rate (kic) and the fluorescence quantum yield (ηF), (Supplementary Table 3). It was demonstrated that the fluorescence quantum yield of COTh in the solid state is three orders of magnitude larger than that in the isolated state, because of the significant enhancement of kr and decrease of kic. The increase of the kr in the solid state should be attributed to the larger oscillator strength (f) and larger adiabatic excitation energy (Supplementary Table 3). More importantly, the kic of COTh in the solid state was two orders of magnitude smaller than that of the isolated molecule. The reorganization energy of the solid state is much smaller than that in the gas phase and is a key factor influencing the value of the kic. We further projected the reorganization energy into the internal coordinates to explicitly partition the total reorganization energy into bond lengths, bond angles and dihedral angles of the COTh molecule in both the gas phase and in the solid state. As shown in Supplementary Table 4, the major differences in the reorganization energies between the gas phase and the solid state should be due to the dihedral angles, which corresponds to the low-frequency normal modes (Fig. 4c). Thus, the low-frequency vibrational motion plays a significant role for the AIE phenomenon of COTh system.
The excited-state conformation reversal
Circular dichroism (CD) spectroscopy can be used to monitor the stereo conformation change of a chiral compound50,51. Since COTh is conformationally chiral, we did the chiral resolution of rac-COTh via preparative chiral HPLC (Supplementary Figs. 22−24) and investigated the dynamical change of the chiral properties in the excited state using CD spectroscopy (Fig. 5 and Supplementary Figs. 25−27). It is worthy to note that this experiment is exact the same measurements performed previously by Itoh and colleagues, in which they investigated the conformation change of 2-methylthiphene fused COT, a structural ananlogue of COTh, via CD spectroscopy. The stereo conformations of the two enantiomers were confirmed by their single crystal structures (Supplementary Table 5, Table 6, and Supplementary Fig. 25). The two enantiomers show strong CD signals, which are mirror symmetrical. Interestingly, the CD signals of the two enantiomers in freshly distilled tetrahydrofuran (THF) solutions gradually decreased upon UV irradiation and totally racemized after 14 min UV irradiation. As a contrast, without UV irradiation, the CD signals are almost unchanged. These results indicate that in the solution state, the two enantiomers of COTh can transform with each other through ring inversion upon excitation, which is consistent with its up-down molecular vibrational behavior. We then measured their CD spectra in the solid state upon UV irradiation under the same conditions with same irradiation time and the results indicate that the CD signals show almost no change, suggesting that the conformation inversion was suppressed in the solid state. The CD data suggest that the up-down conformation inversion behavior is the main molecular motion active for COThs, which should play a key role for the AIE phenomenon. Based on the chiral property and enhanced PL of COTh in the solid state, we then explored the CPL property of the crystal of the enantiomers of COTh, and both of the enantiomers exhibit obvious CPL signals with the gCPL values around 10−3, and the CPL signals of the crystals also show almost no change under same UV irradiation as the CD experiments, which should be ascribed the restricted conformation inversion in the solid state (Supplementary Figs. 28 and 29).
In comparison with typical AIEgens that generally show intramolecular rotation behavior, the large magnitude of the up-down conformation inversion of COTh molecules is kind of unique. According to a previous study about Baird’s aromaticity, the excited-state aromaticity reversal can lead to this large magnitude of up-down conformation inversion25,26. Indeed, the pioneering work by Itoh and colleagues29 and Hada et al.38 indicated methyl substituted COTh derivatives underwent a large magnitude of up-down conformation inversion upon photoexcitation. Therefore, the up-down ring inversion of COTh is ascribed to the aromaticity reversal from the ground state to excited state. By analyzing the geometric structures at the minima and at transition state of COTh in both the ground and excited states via Gaussian 09 at the (TD)DFT/B3LYP/6–31G** level, we indeed found that, in contrast to the ground state, both the structures at the global minima and transition states on potential energy surface of the excited state of COTh exhibited a more planar conformation and a diminished bond length difference between the single and double bonds, which matched well with its aromatic character at the excited state (Supplementary Figs. 30 and 31). Furthermore, nucleus-independent chemical shift (NICS) and anisotropy of the induced current density (ACID) are commonly utilized methods to evaluate the aromaticity of the molecules, negative NICS value, and clockwise ring current usually suggest the aromaticity while positive NICS value and counterclockwise ring current indicate the antiaromaticity. Here, we also performed the NICS the ACID calculations, the NICSzz scan of COTh, perpendicular to its central 8-member ring, demonstrate positive and negative minima for the transition states at S0 and T1 states respectively, which is consistent with the ground-state antiaromaticity and excited-state aromaticity characteristic of COTh (Supplementary Fig. 32). Furthermore, ACID for the transition state structures in the S0 and T1 states show counterclockwise and clockwise ring current, which also supports the ground-state antiaromaticity and excited-state aromaticity characteristic of COTh (Supplementary Fig. 33).
Ultrafast optical spectroscopy gives a wealth of information on the photophysical properties and dynamical processes of the excited state. This enables us to investigate the excited state relaxation behavior of COTh52,53. The femtosecond transient-absorption (fs-TA) spectra of COTh obtained after 267 nm excitation in acetonitrile with a time delay up to 59 ps are shown in Fig. 6a−c. As presented in Fig. 6a, an absorption band at 450 nm emerged whose intensity increases with a delay time from 682 fs to 1.1 ps. In the later delay times, the band at 450 nm decays from 1.1 ps to 59 ps. The kinetics at 450 nm could be fitted satisfactorily by a two-exponential function with time constants of 0.1 ps and 4.9 ps, respectively. The first time constant (0.1 ps) originates from the internal conversion (IC) process from Sn to S1 while the second time constant (4.9 ps) is assigned to the IC process from S1 to S0, corresponding to the ring inversion process. Therefore, the ring inversion process is very rapid. In the thin film state, a similar transition from Sn to S1 and S1 to S0 were observed. However, the kinetics at 470 nm affords three time constants, with two shorter ones (0.4 ps and 57.7 ps) corresponding to the IC process and a longer one (687 ps), which suggests a radiative decay. Therefore, both non-radiative decay and radiative decay processes coexist in the film state, which is in accordance with its not very high-fluorescence quantum yield. These data suggest that COTh has a very rapid molecular deformation in the solution state, resulting in a non-emissive property. While in the solid state, the molecular deformation was partially suppressed, which leads to the observed enhanced emission.
Proposed sketch of the AIE mechanism of COTh
To illustrate the AIE mechanism of COTh and the relationship between the AIE phenomenon and aromaticity reversal, a hypothetical diagrammatic sketch that fits the data is shown in Supplementary Fig. 34. Supplementary Table 7 gives the criteria to judge the involved concepts such as aromaticity, antiaromaticity, and non-aromaticity. In general, the chiral COTh in the solution state adopts a tub-like conformation in the ground state due to its non-aromatic characteristic, which will exceed a quick molecular deformation after excitation to approach the planar/quasi-planar aromatic state (transition state) according to Baird’s rule. The planar/quasi-planar excited state relaxed to the ground state within picosecond timescale, in which the molecular conformation is almost unchanged. As the planar conformation of COTh in the ground state is antiaromatic, it will further relax to the non-aromatic tub-like conformation quickly to avoid the destabilization of antiaromaticity. The molecular deformation of the planar excited state has two pathways, e.g., go up and go down, consequently, the racemization occurred. It is also worthy to note that the racemization also possibly occurs in the excited state, where the two minimum energy structures (MES) adjacent the transition state can overcome the energy barrier to transform with each other and result in the racemization. In that case, the exciton relaxation possibly proceeds via the MES besides the planar transition state. No matter in which pathway, the whole conformation flip and exciton relaxation process occur within picoseconds, corresponding to the non-radiative decay of the exciton, the emission was thus quenched (Supplementary Fig. 34a). However, in the solid state, the energy barrier for conformation change is large enough to restrict the molecular deformation process, the radiative decay pathway was thus opened, resulting in the enhanced emission in the solid state (Supplementary Fig. 34b).
Pressure-dependent fluorescent spectroscopy
As the molecular deformation of the luminogen correlates with their luminescence behavior, the luminescence of COTh upon hydrostatic pressure was thus investigated by using diamond anvil cell (DAC) equipment (Fig. 7)54,55. Indeed, with the external pressure gradually increased from 0 atm to 7 GPa, the emission color and spectra of the crystal underwent a blue-shift with the emission intensity becoming dimmer. Upon releasing the pressure to initial state, the emission could almost completely recover to the original position, corresponding to the molecular deformation and recovery. Geometry optimization upon varying pressures indicates that under high pressure, the intermolecular distance become smaller and the molecular conformation tends to more twisted (Supplementary Figs. 35 and 36). The smaller intermolecular distance suggests stronger intermolecular interaction, which caused the quenching of the emission under high pressure, while the more twisted structure should be responsible for the emission to blue-shift.
To confirm whether the AIE character of COTh could be extended to other COTh systems, we also synthesized other derivatives by phenyl and methoxyphenyl substitution and all of the prepared derivatives show AIE activity (Supplementary Figs. 37 and 38). In particular, COTh-Py is water-soluble with weak emission in water solution but bright yellow emission in its aggregation state, enabling it to become a suitable candidate for a wash-free bio-imaging application. We further explored the microbial imaging ability of COTh-Py since its positive charge is inclined to interact with the negative charge on the surface of microbial, which would restrict the vibration of the four arms of COTh-Py and thus light up the emission56. As shown in Supplementary Fig. 39, COTh-Py can stain E. coli and P. chrysogenum by a wash-free method with low background, suggesting its great potential in microbial detection.
COThs, a new family of non-aromatic annulene-based luminescent molecules has been developed and demonstrated to be a unique vibrational AIE system. The aromaticity reversal triggered intramolecular motion has been demonstrated experimentally and theoretically to play a key role for the AIE phenomenon of COTh system. This new AIE system not only enriched the AIE family, but also provided a reliable strategy for the design of vibrational AIE systems. Additionally, based on the chiral and AIE properties of the COTh system, CPL and microbial imaging application were explored. To the best of our knowledge, this is the first time that the AIE phenomenon has been considered from the viewpoint of aromaticity inversion, which fundamentally helps understanding the excited-state relaxation of luminescent molecules. Furthermore, the extensive application platform of AIE materials also provides a new outlet for utilizing Barid’s rule to develop luminescent functional materials.
All chemicals were commercially available and used as supplied without further purification. Deuterated solvents were purchased from J&K. 3,3′-bithiophene was purchased from Derthon Optoelectronic Materials Science Technology Co., Ltd. Tetrahydrofuran (THF) was dried by distillation using sodium as drying agent and benzophenone as indicator. The 1H and 13C NMR spectra were recorded on a Bruker ARX 400 MHz and Bruker Biospin GmbH 600 MHz NMR spectrometer using the deuterated solvent as the lock and TMS (δ = 0) as internal reference. Mass spectra and High-resolution mass spectra (HRMS) were obtained on a Finnigan MAT TSQ 7000 Mass Spectrometer System operated in a MALDI-TOF mode. Absorption spectra were measured on a Milton Roy Spectronic 3000 Array spectrophotometer. Steady-state photoluminescence (PL) spectra were recorded on a Perkin-Elmer spectrofluorometer LS 55. Quantum yield was determined by a Quanta-φ integrating sphere. Circular dichroism (CD) measurements were carried out on an Applied Photophysics Chirascan Plus spectropolarimeter. Circularly polarized luminescence (CPL) spectra of the solid was recorded on JASCO CPL-300 at room temperature.
High-pressure experiment was carried out using Sapphire-anvil cell. The culet diameter of the sapphire anvils was 0.6 mm, while copper gasket was preindented to a thickness of 0.17 mm, and center hole of 0.24 mm was drilled for the single crystal. A ruby chip was inserted into the sample compartment for in situ pressure calibration according to the R1 ruby fluorescence method. Silicone oil was used as the pressure-transmitting medium. The hydrostatic pressure on the single crystal was determined through monitoring the widths and separation of the R1 and R2 lines. The PL measurement under high pressure was performed on a QuantaMaster 40 spectrometer in the reflection mode. The 380 nm line of a xenon lamp with a power of 60 W was used as the excitation source. The fluorescence images of the single crystal under visible light and 380 nm UV light were taken by putting the Sapphire-anvil cell (SAC) containing the sample on a Nikon fluorescence microscope. All experiments were conducted at room temperature.
Prior to bacteria imaging, a single colony of bacteria on solid culture medium [Luria broth (LB) for E. coli] was transferred to 50 mL of the liquid culture medium and grown at 37 °C for 12–16 h. The concentrations of bacteria were determined by measuring the optical density at 600 nm (OD600) and then 109 colony forming unit (CFU) of bacteria was transferred to a 1.5 mL EP tube. Bacteria was harvested by centrifuging at 10,000 rpm for 5 min. After removal of the supernatant, 1 mL PBS was added into the EP tube to wash the bacteria, then the bacteria were collected by centrifuging at 10,000 rpm for 5 min again. After removal of the supertant, 1 mL 50 µM dye solution in PBS was added into the EP tube. After dispersing with a vortex, the bacteria were incubated at room temperature for 60 min. To take fluorescence images, about 10 µL of the stained bacteria solution was transferred to a glass slide and then covered by a coverslip. The image was collected using a 100x objective. The bacteria was imaged under a Confocal microscope (Zeiss LSM 710) using 405 nm excitation wavelength.
Prior to fungi imaging, Penicillium chrysogenum was cultured on Malt Extract Agar for 7 days at 28 °C. Gently scrape the surface growth from the culture of the test organism using an inoculating wire. Putting the spore into a sterile container of sterile water, vigorously shaking the flask or sonicate to liberate the spores from the fruiting bodies and to break the spore clumps. Remove large mycelial fragments and clumps of agar. The spore suspension was store at 4 °C. Twenty microliters 1 mM dye stock solution was added into 980 µL P. chrysogenum spore suspension and incubated at room temperature for 3 h. To take fluorescence images, about 10 µL of the stained bacteria solution was transferred to a glass slide and then covered by a coverslip. The image was collected using a 100x objective. The fungus was imaged under a Confocal microscope (Zeiss LSM 710) using 405 nm excitation wavelength.
All relevant data that support the findings of this study are available from the corresponding authors upon reasonable request.
Iamsaard, S. et al. Conversion of light into macroscopic helical motion. Nat. Chem. 6, 229 (2014).
Lv, J. -a et al. Photocontrol of fluid slugs in liquid crystal polymer microactuators. Nature 537, 179 (2016).
Kassem, S. et al. Artificial molecular motors. Chem. Soc. Rev. 46, 2592–2621 (2017).
Erbas-Cakmak, S., Leigh, D. A., McTernan, C. T. & Nussbaumer, A. L. Artificial molecular machines. Chem. Rev. 115, 10081–10206 (2015).
Stoddart, J. F. Mechanically interlocked molecules (mims)—molecular shuttles, switches, and machines (nobel lecture). Angew. Chem. Inter. Ed. 56, 11094–11125 (2017).
Jean-Pierre, S. From chemical topology to molecular machines (Nobel lecture). Angew. Chem. Int. Ed. 56, 11080–11093 (2017).
Qian, H. et al. Suppression of Kasha’s rule as a mechanism for fluorescent molecular rotors and aggregation-induced emission. Nat. Chem. 9, 83–87 (2016).
Dong, J. et al. Ultrathin two-dimensional porous organic nanosheets with molecular rotors for chemical sensing. Nat. Commun. 8, 1142 (2017).
Chen, W. et al. Snapshotting the excited-state planarization of chemically locked N,N′-disubstituted dihydrodibenzo[a,c]phenazines. J. Am. Chem. Soc. 139, 1636–1644 (2017).
Zhang, Z. et al. Tuning the conformation and color of conjugated polyheterocyclic skeletons by installing ortho-methyl groups. Angew. Chem. Inter. Ed. 57, 9880–9884 (2018).
Jin, M., Chung, T. S., Seki, T., Ito, H. & Garcia-Garibay, M. A. Phosphorescence control mediated by molecular rotation and aurophilic interactions in amphidynamic crystals of 1,4-bis[tri-(p-fluorophenyl)phosphane-gold(I) -ethynyl]benzene. J. Am. Chem. Soc. 139, 18115–18121 (2017).
Mei, J. et al. Aggregation-induced emission: the whole is more brilliant than the parts. Adv. Mater. 26, 5429–5479 (2014).
Feng, G. & Liu, B. Aggregation-induced emission (AIE) dots: emerging theranostic nanolights. ACC Chem. Res. 51, 1404–1414 (2018).
Shao, A. et al. Far-red and near-IR AIE-active fluorescent organic nanoprobes with enhanced tumor-targeting efficacy: shape-specific effects. Angew. Chem. Inter. Ed. 54, 7275–7280 (2015).
Yoshii, R., Hirose, A., Tanaka, K. & Chujo, Y. Boron diiminate with aggregation-induced emission and crystallization-induced emission-enhancement characteristics. Chem. Eur. J. 20, 8320–8324 (2014).
Zhan, C., You, X., Zhang, G. & Zhang, D. Bio-/chemosensors and imaging with aggregation-induced emission luminogens. Chem. Rec. 16, 2142–2160 (2016).
Leung, N. L. C. et al. Restriction of intramolecular motions: the general mechanism behind aggregation-induced emission. Chem. Eur. J. 20, 15349–15353 (2014).
Gu, Y. et al. Exploration of biocompatible AIEgens from natural resources. Chem. Sci. 9, 6497–6502 (2018).
Cyrański, M. K. Energetic aspects of cyclic Pi-electron delocalization: evaluation of the methods of estimating aromatic stabilization energies. Chem. Rev. 105, 3773–3811 (2005).
Krygowski, T. M. & Cyrański, M. K. Structural aspects of aromaticity. Chem. Rev. 101, 1385–1420 (2001).
Zhu, C. et al. Stabilization of anti-aromatic and strained five-membered rings with a transition metal. Nat. Chem. 5, 698 (2013).
Sturala, J. et al. Excited-state aromatic interactions in the aggregation-induced emission of molecular rotors. J. Am. Chem. Soc. 139, 17882–17889 (2017).
Yin, X. et al. A reversible single-molecule switch based on activated antiaromaticity. Sci. Adv. 3, eaao2615 (2017).
Yuan, C. et al. A π-conjugated system with flexibility and rigidity that shows environment-dependent RGB luminescence. J. Am. Chem. Soc. 135, 8842–8845 (2013).
Rosenberg, M., Dahlstrand, C., Kilså, K. & Ottosson, H. Excited state aromaticity and antiaromaticity: opportunities for photophysical and photochemical rationalizations. Chem. Rev. 114, 5379–5425 (2014).
Oh, J. et al. Unraveling excited-singlet-state aromaticity via vibrational. Anal. Chem. 3, 870–880 (2017).
Baird, N. C. Quantum organic photochemistry. II. Resonance and aromaticity in the lowest 3 π-π* state of cyclic hydrocarbons. J. Am. Chem. Soc. 94, 4941–4948 (1972).
Ottosson, H. Exciting excited-state aromaticity. Nat. Chem. 4, 969 (2012).
Ueda, M. et al. Energetics of Baird aromaticity supported by inversion of photoexcited chiral [4n]annulene derivatives. Nat. Commun. 8, 346 (2017).
Karadakov, P. B. Ground- and excited-state aromaticity and antiaromaticity in benzene and cyclobutadiene. J. Phys. Chem. A 112, 7303–7309 (2008).
Sung, Y. M. et al. Reversal of Hückel (anti)aromaticity in the lowest triplet states of hexaphyrins and spectroscopic evidence for Baird’s rule. Nat. Chem. 7, 418 (2015).
Feixas, F., Vandenbussche, J., Bultinck, P., Matito, E. & Solà, M. Electron delocalization and aromaticity in low-lying excited states of archetypal organic compounds. Phys. Chem. Chem. Phys. 13, 20690–20703 (2011).
Karadakov, P. B. Aromaticity and antiaromaticity in the low-lying electronic states of cyclooctatetraene. J. Phys. Chem. A 112, 12707–12713 (2008).
Gogonea, V., Schleyer, Pv. R. & Schreiner, P. R. Consequences of triplet aromaticity in 4nπ-electron annulenes: calculation of magnetic shieldings for open-shell species. Angew. Chem. Inter. Ed. 37, 1945–1948 (1998).
Nishinaga, T., Ohmae, T. & Iyoda, M. Recent studies on the aromaticity and antiaromaticity of planar cyclooctatetraene. Symmetry 2, 76–97 (2010).
Liu, C. et al. Macrocyclic polyradicaloids with unusual super-ring structure and global aromaticity. Chem 4, 1586–1595 (2018).
Lu, X. et al. Global aromaticity in macrocyclic cyclopenta-fused tetraphenanthrenylene tetraradicaloid and its charged species. Angew. Chem. Inter. Ed. 57, 13052–13056 (2018).
Hada, M. et al. Structural monitoring of the onset of excited-state aromaticity in a liquid crystal phase. J. Am. Chem. Soc. 139, 15792–15800 (2017).
Mouri, K., Saito, S., Hisaki, I. & Yamaguchi, S. Thermal 8π electrocyclic reaction of heteroarene tetramers: new efficient access to π-extended cyclooctatetraenes. Chem. Sci. 4, 4465–4469 (2013).
Mouri, K., Saito, S. & Yamaguchi, S. Highly flexible π-expanded cyclooctatetraenes: cyclic thiazole tetramers with head-to-tail connection. Angew. Chem. Inter. Ed. 51, 5971–5975 (2012).
Marsella, M. J., Reid, R. J., Estassi, S. & Wang, L.-S. Tetra[2,3-thienylene]: a building block for single-molecule electromechanical actuators. J. Am. Chem. Soc. 124, 12507–12510 (2002).
Marsella, M. J., Kim, I. T. & Tham, F. Toward conjugated double helical ladder polymers: cyclooctatetrathiophene as a highly versatile double helical scaffold. J. Am. Chem. Soc. 122, 974–975 (2000).
Zhang, S. et al. Thiophene-based double helices: syntheses, X-ray structures, and chiroptical properties. J. Am. Chem. Soc. 138, 10002–10010 (2016).
Hau, C. -K. et al. Thermotropic liquid crystals based on 1,8,9,16-tetrasubstituted tetraphenylenes and their structure–property relationship studies. Chem. Sci. 2, 1068–1075 (2011).
Han, J.-W., Li, X. & Wong, H. N. C. Our expedition in eight-membered ring compounds: from planar dehydrocyclooctenes to tub-shaped chiral tetraphenylenes. Chem. Rec. 15, 107–131 (2015).
Wang, Y. et al. Derivation of saddle shaped cyclooctatetrathiophene: increasing conjugation and fabricating pentamer. Tetrahedron 70, 631–636 (2014).
Wang, Y. et al. Efficient synthesis of trimethylsilyl-substituted dithieno[2,3-b:3′,2′-d]thiophene, tetra[2,3-thienylene] and hexa[2,3-thienylene] from substituted [3,3′]bithiophenyl. Synlett 2007, 2390–2394 (2007).
Furche, F. et al. Turbomole. Wiley Interdiscip. Rev.: Comput. Mol. Sci. 4, 91–100 (2014).
Wang, J., Wolf, R. M., Caldwell, J. W., Kollman, P. A. & Case, D. A. Development and testing of a general amber force field. J. Comput. Chem. 25, 1157–1174 (2004).
Li, W. et al. Enantiospecific photoresponse of sterically hindered diarylethenes for chiroptical switches and photomemories. Sci. Rep. 5, 9186 (2015).
Zhang, H. et al. In situ monitoring of molecular aggregation using circular dichroism. Nat. Commun. 9, 4961 (2018).
Chan, K. T. et al. The interplay between fluorescence and phosphorescence with luminescent gold(i) and gold(iii) complexes bearing heterocyclic arylacetylide ligands. Chem. Sci. 8, 2352–2364 (2017).
Du, L. et al. Direct detection of the open-shell singlet phenyloxenium ion: an atom-centered diradical reacts as an electrophile. J. Am. Chem. Soc. 139, 15054–15059 (2017).
Yang, Z. et al. Recent advances in mechano-responsive luminescence of tetraphenylethylene derivatives with aggregation-induced emission properties. Mater. Chem. Front. 2, 861–890 (2018).
Qi, Q. et al. Remarkable turn-on and color-tuned piezochromic luminescence: mechanically switching intramolecular charge transfer in molecular crystals. Adv. Funct. Mater. 25, 4005–4010 (2015).
Li, Y. et al. A bifunctional aggregation-induced emission luminogen for monitoring and killing of multidrug-resistant bacteria. Adv. Funct. Mater. 28, 1804632 (2018).
This work was supported by the National Science Foundation of China (51622305 and 21788102), the Innovation and Technology Commission (ITC-CNERC14SC01 and ITS/254/17), the Research Grants Council of Hong Kong (16305015, 16308016, A-HKUST605/16, C2014–15G, and C6009–17G), the PCSIRT (IRT13023) and the Shenzhen Science and Technology Program (JCYJ20160229205601482 and JCYJ20160509170535223), the UGC Special Equipment Grant (SEG-HKU-07) as well as the University of Hong Kong Development Fund 2013–2014 project New Ultrafast Spectroscopy Experiments for Shared Facilities
The authors declare no competing interests.
Peer review information: Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work. Peer reviewer reports are available.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Zhao, Z., Zheng, X., Du, L. et al. Non-aromatic annulene-based aggregation-induced emission system via aromaticity reversal process. Nat Commun 10, 2952 (2019). https://doi.org/10.1038/s41467-019-10818-5
Exploration of photophysics and presence of Long singlet exciton diffusion length in dibenz[a,h]anthracene nanoaggregates
Journal of Photochemistry and Photobiology A: Chemistry (2020)
TrAC Trends in Analytical Chemistry (2020)
Visualization and Manipulation of Molecular Motion in the Solid State through Photoinduced Clusteroluminescence
The Journal of Physical Chemistry Letters (2019)
The butterfly effect in bisfluorenylidene-based dihydroacenes: aggregation induced emission and spin switching
Chemical Science (2019)
The Journal of Physical Chemistry Letters (2019)