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Article

Unpredicted Concentration-Dependent Sensory Properties of Pyrene-Containing NBN-Doped Polycyclic Aromatic Hydrocarbons

by
Hang Xiao
1,2,†,
Tao Li
1,2,†,
Xiao-Li Sun
1,*,
Wen-Ming Wan
2,3,*,
Hongli Bao
2,
Qingrong Qian
1 and
Qinghua Chen
1
1
Fujian Key Laboratory of Pollution Control & Resource Reuse, Engineering Research Center of Polymer Green Recycling of Ministry of Education, College of Environmental Science and Engineering, Fujian Normal University, Fuzhou 350007, China
2
State Key Laboratory of Structural Chemistry, Key Laboratory of Coal to Ethylene Glycol and Its ReLated Technology, Center for Excellence in Molecular Synthesis, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, 155 West Yangqiao Road, Fuzhou 350002, China
3
State Key Laboratory of Molecular Engineering of Polymers, Fudan University, Shanghai 200438, China
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Molecules 2022, 27(1), 327; https://doi.org/10.3390/molecules27010327
Submission received: 17 November 2021 / Revised: 20 December 2021 / Accepted: 30 December 2021 / Published: 5 January 2022
(This article belongs to the Special Issue Selected Papers from the 3rd Chinese Chemical Society Conference on Boron Sciences)
Browse Figures
Versions Notes

Abstract

:
Pyrene molecules containing NBN-doped polycyclic aromatic hydrocarbons (PAHs) have been synthesized by a simple and efficient intermolecular dehydration reaction between 1-pyrenylboronic acid and aromatic diamine. Pyrene-B (o-phenylenediamine) with a five-membered NBN ring and pyrene-B (1,8-diaminonaphthalene) with a six-membered NBN ring show differing luminescence. Pyrene-B (o-phenylenediamine) shows concentration-dependent luminescence and enhanced emission after grinding at solid state. Pyrene-B (1,8-diaminonaphthalene) exhibits a turn-on type luminescence upon fluoride ion addition at lower concentration, as well as concentration-dependent stability. Further potential applications of Pyrene-B (o-phenylenediamine) on artificial light-harvesting film were demonstrated by using commercial NiR dye as acceptor.

Graphical Abstract

1. Introduction

As a dopant, boron has received exceptional attention because of its unique photophysical and redox properties [1,2,3,4,5]. Boron-doped π-systems have received special attentions because of their desirable and potential optical, electronic and sensory properties [6,7,8,9]. Particularly, B-N substitutions in benzene and other cyclic hydrocarbons have been an active and productive field of study for more than 50 years. Many BN-containing organic compounds have been synthesized and applied in pharmacology, electronic materials, and nanoscience [10,11,12,13,14]. Compared with the corresponding all-carbon analogues, organic π-conjugated compounds with a novel BN bond usually have distinct optoelectronic properties/advantages due to the empty p-orbital of the boron center [15,16,17]. Therefore, the replacement of the C=C bond by isoelectronic and isosteric BN units has emerged as a viable strategy to produce functional materials [18,19,20,21,22]. Considerable progress has been made on the comprehensive synthesis of BN- and BNB-doped π-systems with outstanding photophysical properties by pioneering researchers such as Dewar, White, Ashe, Liu, Braunschweig, Schäfer and Jäkle, etc. [23,24,25,26,27,28,29,30,31,32]. However, these outstanding BN- and BNB-doped π-systems suffer from synthesis methods involving rigorous reaction conditions (e.g., air and/or moisture free), multiple steps and unsatisfied total yield [33,34,35,36,37,38].
Recently, NBN units have been incorporated into PAHs, zigzag-edged graphene nanoribbons and organic–inorganic hybrid polymers with the aid of electrophilic aromatic borylation [39,40,41]. In 2019, we reported a simple and efficient synthesis of NBN-doped conjugated diazaborinines by a catalyst-free intermolecular dehydration reaction, and a series of aggregation-induced emissive luminogens have been designed [42]. Nonetheless, the research on the NBN-doped π-conjugated compounds is still very rare. Further investigations on the photophysical and sensory properties of these easily synthesized NBN-doped π-systems will easily expand the functionality and property libraries of BN-doped conjugated compounds, and is therefore highly desirable.
Due to the empty p-orbital of the boron center, boron-doped π-systems also exhibit poor stability, and special molecular designs are required to achieve good stability, such as chemically introducing bulky protection groups. Demonstrating a physically simple method for stabilizing boron-doped π-systems is therefore highly desirable and still very challenging. Meanwhile, when boron-doped π-systems are used for fluoride-ion detection, it is mostly accompanied with turn-off type luminescence disappearance. As is known, there are many factors for achieving luminescence disappearance, which will cause detection interference of fluoride ion with a false report. To realize turn-on type luminescence appearance is an advanced technique in the detection of fluoride ion and is therefore highly desirable [43,44,45,46].
Herein, we demonstrate two pyrene-containing NBN-doped PAHs via a simple synthetic method through efficient intermolecular dehydration between boronic acid and diamine moieties. Their aromaticity, luminescence and sensory properties were investigated. It was found that a physical concentration strategy is a simple method to stabilize boron-doped π-systems.

2. Results and Discussion

2.1. Fabrication and Aromaticity of NBN-Doped PAHs

To verify the physical concentration strategy to stabilize boron-doped π-systems, the pyrene moiety was molecularly designed in the NBN-doped PAHs specifically, as shown in Scheme 1. Through one-step intermolecular dehydration between 1-pyrenylboronic acid and o-phenylenediamine or 1,8-diaminonaphthalene in tetrahydrofuran (THF), pyrene-B (1,2-diaminobenzene) (Py-NBN-Ph) with a five-membered NBN ring and pyrene-B (1,8-diaminonaphthalene) (Py-NBN-Naphth) with a six-membered NBN ring were synthesized with a yield of 94% and 95%, respectively. Their successful synthesis was verified by the disappearance of B(OH)2 protons at ~8.02 ppm and NH2 protons at ~4.37 ppm of 1,2-diaminobenzene and ~5.45 ppm of 1,8-diaminonaphthalene, and by the appearance of NBN protons at ~9.37 ppm of Py-NBN-Ph and ~8.54 ppm of Py-NBN-Naphth in the 1H nuclear magnetic resonance (NMR) spectra (Figures S1 and S2). The FI-IR spectra in Figure S4 also confirmed the chemical structure of Py-NBN-Ph and Py-NBN-Naphth. Stable NBN ring formation, strong N- > B dative bonding and hydrogen bonding interactions between B(OH)2 and NH2 lead to the success of this catalyst-free dehydration with high yield. Meanwhile, as shown in Figure S3, the temperature at 5% weight loss (Td5%) of Py-NBN-Ph was 218.3 °C and the Td5% of Py-NBN-Naphth was 345.5 °C, which indicates that the solid power of NBN-doped PAHs has good thermal stability.
Due to the isoelectronic and isosteric characterization between the B-N and the C=C bond, five- and six-membered NBN rings in Py-NBN-Ph and Py-NBN-Naphth are congeneric to aromatic pyrrole and pyridine, respectively. The aromaticity investigations were therefore carried out via an ab initio method and the nucleus-independent chemical shift (NICS) values were calculated at the GIAO-B3LYP/6-311+G(2d,p) level of the theory at distances of 0.0 Å (A(0) and B(0)) and 1.0 Å (A(1) and B(1)) from each ring system, as well as from the center of the bicyclic systems (Center(1)) in the perpendicular direction, as shown in Figure 1. All rings of Py-NBN-Ph showed negative NICS values, indicating its aromaticity. But Py-NBN-Naphth exhibited positive NICS values for the NBN ring and negative values for other rings and the center, which indicates an anti-aromatic NICS characteristic of NBN ring. The different aromaticity characteristics can be verified by comparing the electron orbits of these two NBN rings. As shown in Figure 1, the number of π-electrons of the five-membered NBN ring in Py-NBN-Ph is 6, indicating an aromaticity characteristic. On the other hand, the number of π-electrons in the six-membered NBN ring of Py-NBN-Naphth is 7 and the extra electron occupies the lowest anti-bonding molecular orbitals, which violates the Hückel rule and results in anti-aromaticity [46,47,48]. Therefore, the five-membered NBN ring in Py-NBN-Ph and six-membered NBN ring in Py-NBN-Naphth exhibit totally different aromaticity. The electronic distribution of HOMO and LUMO orbitals of Py-NBN-Ph and Py-NBN-Naphth was calculated and shown in Figure S9 and Table S3.
The NH proton in BN and NBN isostere is more acidic than the CH analogues, and could engage in to H-bonding interactions. Thus, Py-NBN-Ph and Py-NBN-Naphth could act as H-bonding donors. We investigated the H-bonding complex between them and pyridine by 1H NMR. Upon addition of increasing amount of pyridine (up to 20 equiv) to a solution of Py-NBN-Ph in C6D6, a downfield shift from 6.08 ppm to 6.62 ppm of the H (e) proton was observed, as shown in Figure S10A and Figure 2A. This indicates that H-bonding formation occurs between the H atom of -NH in NBN ring and the N atom of the pyridine. The same phenomenon was obtained by titrating Py-NBN-Naphth (c0 = 8.152 × 10−3 M) with pyridine (up to 20 equiv) in C6D6, and a downfield shift from 5.38 ppm to 6.21 ppm of the H (f) proton was observed, as shown in Figure S10B and Figure 2B. H-bonded complexes of pyridine·Py-NBN-Ph, pyridine·Py-NBN-Naphth were formed, proving the good H-bonding capabilities of the NBN functional group. These findings provide a new idea for the application of NBN-doped PAHs in supramolecular chemistry.

2.2. Luminescent Properties of NBN-Doped PAHs

Boron-doped π-systems are widely utilized as luminogens and sensors accompanied with luminescence changes attributed to the empty p-orbital of the boron center in π-systems. As is known, pyrene is a well-investigated luminescent material [49,50,51]. Therefore, the luminescent behaviour of pyrene-containing NBN-doped PAHs was investigated. The absorption spectra of Py-NBN-Ph and Py-NBN-Naphth were similar and shown in Figure S5. Interestingly, Py-NBN-Ph and Py-NBN-Naphth exhibited totally different luminescent properties in solution, as shown in Figure 1. Py-NBN-Ph showed a strong cyan fluorescence, with a maximum emission wavelength of 460 nm in solution. By contrast, Py-NBN-Naphth was nonemissive both in solution (such as in THF, methanol) and at a solid state, which may have been caused by the antiaromaticity-type NICS values and the extra electron on the lowest anti-bonding molecular orbitals of the NBN ring. These results indicate that pyrene-containing NBN-doped PAHs exhibits aromaticity-dependent luminescence, and the difference in luminescence derives from the significant differences in aromaticity mentioned above. Meanwhile, Py-NBN-Ph is weakly emissive at a solid state due to the aggregation-caused quenching (ACQ) effect, as shown in Figure S6 [52,53]. Interestingly, it exhibited grinding enhanced emission behavior. As shown in Figure 3, Py-NBN-Ph showed strong blue emission after grinding, exhibiting amorphization-induced emission behavior, which conforms to reports in the literature on pyrene-containing material [54].

2.3. Fluoride Ion Detection

Another interesting aspect is the aromaticity and concentration-dependent sensory properties of these pyrene-containing NBN-doped PAHs. The utilization of these two materials for fluoride ion detection was carried out, and different phenomena were exhibited (Figure 4, Figure 5 and Figure S7). For Py-NBN-Ph, it was highly emissive at 460 nm with a cyan color in THF (1 mg/mL). With the addition of tetrabutylammonium fluoride (TBAF) to three equivalents, the luminescent intensity decreased by 85%. The emission was almost quenched, and fell to less than 5% intensity when 6 equivalent fluoride ions were added. Further addition of water caused the recovery of cyan emission and then a shift to a blue color, as shown in Figure 4A. The whole process was verified by 1H NMR titrations in Figure 4B, where NBN unit changed to pyrene-BF2 with the addition of fluoride ion and then to pyrene-B(OH)2 with the addition of water. Py-NBN-Ph exhibited a turn-off type luminescence in the fluoride ion detection.
In comparison, for Py-NBN-Naphth, 1 mg/mL solution in THF showed no changes with the addition of fluoride ion or water, which can be verified from photo images in Figure 5A. The 1 mg/mL solution of Py-NBN-Naphth in THF was stable with fluoride ion, and its 1H and 11B NMR spectra before and after the addition of fluoride ion exhibited no changes, as shown in Figure S8. In addition, the Py-NBN-Naphth solution was stable at 1 mg/mL, even with the addition of concentrated HCl (11.8 mol/L) solution, which was verified by 1H spectra without any changes. However, when the concentration of Py-NBN-Naphth decreased to 0.1 mg/mL, it exhibited a turn-on type luminescence upon the addition of fluoride ion. Although the 0.1 mg/mL solution of Py-NBN-Naphth was non-emissive, the emission appeared and its strength increased with the addition of fluoride ion, as shown in Figure 5A,B. The 0.5 mg/mL solution of Py-NBN-Naphth also showed a turn-on type luminescence when 1.0 equivalent fluoride ion was added. All these results indicate that stability and sensory properties of Py-NBN-Naphth depend on its concentration. To investigate the mechanism for these concentration-dependent properties, its single crystal structures were revealed. As shown in Figure 5C–E, the boron center is embedded by pyrene and naphthalene cycles, and there are weak intermolecular B···H interactions with a distance of 3.1 Å as well. Based on the existence of an embedding effect and intermolecular B···H interactions, we assume that they protect the boron center from fluoride ion and acid when the concentration is high, while these embedding effects and weak interactions can be ignored at lower concentration, resulting in the concentration-dependent stability and sensory properties.

2.4. Artificial Light-Harvesting Film

To demonstrate the applications of pyrene-containing NBN-doped PAHs, the artificial light-harvesting film was prepared with Py-NBN-Ph as donor and nile red (NiR) as acceptor, because the absorption of the NiR acceptor overlaps with the emission of the Py-NBN-Ph donor [55,56,57,58]. The artificial light-harvesting films were prepared with different Py-NBN-Ph/NiR ratios. As shown in Figure 6B, the luminescent intensity at 621 nm assigned to the NiR acceptor increased with the increase of the NiR ratio, and the luminescent intensity at 448 nm assigned to the Py-NBN-Ph donor decreased under the excitation at 381 nm, indicating successful energy transfer from Py-NBN-Ph at an excited state (Py-NBN-Ph*) to NiR at a ground state. The energy transfer can be further verified by comparing the luminescent intensities of different control experiments (Figure 6C). In the absence of Py-NBN-Ph, the NiR acceptor emits weakly, with low luminescent intensity (black line in Figure 6C). The Py-NBN-Ph donor without NiR emits at 448 nm under the excitation at 381 nm, as the red line in Figure 6C shows. In the presence of Py-NBN-Ph (Py-NBN-Ph/NiR ratio of 100/1), the energy transfer between the Py-NBN-Ph donor and the NiR acceptor occurs with the decrease in the luminescent intensity of Py-NBN-Ph and the increase in the luminescent intensity of NiR.
The photophysical process of this artificial light-harvesting film is therefore illustrated in Figure 6A. When the artificial light-harvesting film absorbs the photo energy at 381 nm, the Py-NBN-Ph donor at the ground state will be excited to the excited state as Py-NBN-Ph*, which is supposed to return to the ground state radiatively with emission at 448 nm. In the presence of NiR, the Py-NBN-Ph* transfers energy to the NiR molecules at the ground state, resulting in the formation of NiR* at an excited state. Finally, the NiR* molecules radiatively return to the ground state with an emission at 621 nm.

3. Materials and Methods

3.1. Materials

1-pyrenylboronic acid, 1,2-phenylenediamine, 1,8-diaminonaphthalene, THF and TBAF were purchased from Aladdin (China) and used without further purification. THF was distilled from sodium/benzophenone prior to use. Ultra-pure water treated by a water purification system was used. All other reagents and solvents were purchased as analytical grade from Energy Chemical (China) and used without further purification.

3.2. Synthetic Procedures

3.2.1. Synthesis of Py-NBN-Ph

1-pyrenylboronic acid (0.246 g, 1 mmol) and 1,2-phenylenediamine (0.108 g, 1 mmol) were dissolved in THF (10 mL), and the reaction solution was heated from room temperature to 80 °C to reflux and continued for 12 h under nitrogen protection. The reaction was stopped and cooled, then the solution was concentrated by a rotary evaporator under reduced pressure and the crude product was purified by column chromatography on silica gel (petroleum ether: ethyl acetate = 10:1) to yield Py-NBN-Ph. 1H NMR (600 MHz, DMSO-d6) δ (ppm) 6.89 (dd, J = 4.8, 4.92 Hz, 2H, -C6H4), 7.20 (dd, J = 4.86, 4.92 Hz, 2H, -C6H4), 9.37 (s, 2H, -NH). 11B NMR (600MHz, DMSO-d6) δ (ppm) 28.21.

3.2.2. Synthesis of Py-NBN-Naphth

Py-NBN-Naphth was prepared by a similar procedure as the above, except using 1,8-diaminonaphthalene (0.158 g, 1 mmol) instead of 1,2-phenylenediamine. 1H NMR (600 MHz, DMSO-d6) δ (ppm) 6.62(d, J = 10.98 Hz, 1H, -C6H4), 7.03 (d, J = 12.3 Hz, 1H, -C6H4), 7.17 (t, J = 23.34 Hz, 2H, -C6H4), 8.54 (s, 2H, -NH). 11B NMR (600MHz, DMSO-d6) δ (ppm) 30.22.

3.2.3. Ab Initio Calculations

All the molecules were fully optimized by density functional theory (DFT) methods with the B3LYP hybrid functional and the 6-311+G(d,p) basis set implemented in the Gaussian 09 package (Gaussian, Inc., Wallingford, CT, USA). The values of nucleus-independent chemical shift (NICS) were simulated with the gauge-independent atomic orbital (GIAO) method. The environment layer was treated with the universal force field (UFF). All the atoms were allowed to relax on the ground.

3.2.4. The Detection of TBAF

The THF solutions of Py-NBN-Ph and Py-NBN-Naphth with concentrations of 1 mg/mL, 0.5 mg/mL and 0.1 mg/mL were used to detect TBAF. The fluorescence spectra upon different amounts of TBAF addition were recorded.

3.2.5. Thin-Film Fabrication

The Py-NBN-Ph was dissolved in THF at a concentration of 10 mg/mL. Ten microliters of this solution was deposited on a quartz glass sheet. Then it was put in a Petri dish and left undisturbed until the solvent evaporated at room temperature.

3.3. Characterizations

NMR spectroscopy. The NMR measurements were performed on a Bruker Ascend TM ECZ600S spectrometer (Bruker, Rheinstetten, Germany) in DMSO-d6 using tetramethylsilane as an internal standard.
UV-vis absorption. The spectra were recorded in THF on a Shimadzu UV-2450 UV-Vis spectrophotometer (Shimadzu, Kyoto, Japan) at room temperature.
Fluorescence spectroscopy. The spectra were performed on a RF-5301pc fluorescence spectrophotometer (Shimadzu, Kyoto, Japan) in a quartz cuvette with a path length of 1 cm.
Fourier transform infrared (FT-IR) spectroscopy. FT-IR data were obtained from Bruker VERTEX 70 (Bruker, Rheinstetten, Germany). The spectra were recorded from an accumulation of 32 scans in the range of 4000~400 cm−1.

4. Conclusions

In summary, we demonstrated unpredicted concentration-dependent sensory properties of pyrene-containing NBN-doped PAHs via a simple synthetic method through efficient intermolecular dehydration between boronic acid and diamine moieties. Py-NBN-Ph with a five-membered NBN ring exhibits an aromaticity-type NICS characteristic with traditional ACQ luminescent properties and grinding enhanced emission at a solid state, while Py-NBN-Naphth with a six-membered NBN ring exhibits an antiaromaticity-type NICS characteristic without luminescence. Py-NBN-Naphth exhibits unpredicted concentration-dependent stability and turn-on type luminescent sensory properties towards fluoride ion. A further potential application of NBN-doped pyrene-containing PAH was demonstrated as well by using Py-NBN-Ph as donor and commercial NiR dye as acceptor. This work therefore opens up a new avenue for realizing the luminescent and sensory properties of boron-doped PAHs through a simple synthetic method, and also expands the property and application libraries of BN-doped π-systems.

Supplementary Materials

The following supporting information can be downloaded online, Figure S1: 1H (A), 13C (B) and 11B (C) NMR spectra of Py-NBN-Ph in DMSO-d6; Figure S2: 1H (A), 13C (B) and 11B (C) NMR spectra of Py-NBN-Naphth in DMSO-d6; Figure S3: The TGA curves of Py-NBN-Ph (A) and Py-NBN-Naphth (B); Figure S4: FT-IR spectra of Py-NBN-Ph (A) and Py-NBN-Naphth (B); Figure S5: The absorption spectra of Py-NBN-Ph (A) and Py-NBN-Naphth (B); Figure S6: Fluorescence properties of Py-NBN-Ph. (A) Emission spectra in THF mixtures with different concentration (excited at 384 nm); (B) Plot of relative emission intensity at 460 nm and the corresponding fluorescence diagram; (C) Photographic images of one drop of Py-NBN-Ph solution on thin-layer chromatography under UV lamp @ 365 nm; (D) Digital photos of Py-NBN-Ph (0.4 mg/mL) in H2O/THF mixtures with different H2O fractions (vol %) under UV lamp @ 365 nm (up) and under daylight (down); Figure S7: Fluoride ion detection of Py-NBN-Ph (1 mg/mL in THF). (A) Emission spectra with different amount of TBAF (excitation at 356 nm); (B) Plot of relative emission intensity at 460 nm with amounts of TBAF (excitation at 356 nm); (C) Emission spectra with further addition of water (excitation at 356 nm); Figure S8: The NMR spectra of Py-NBN-Naphth. (A) 1H NMR spectra and (B) 11B NMR spectra with and without TBAF; (C) 1H NMR spectra with and without DCl; Figure S9: The electronic distribution of HOMO and LUMO orbitals of Py-NBN-Ph and Py-NBN-Naphth; the electronic distribution of HOMO orbitals of Py-NBN-Ph (A), the electronic distribution of LUMO orbitals of Py-NBN-Ph (B), the electronic distribution of HOMO orbitals of Py-NBN-Naphth (C), the electronic distribution of LUMO orbitals of Py-NBN-Naphth (D); Figure S10: 1H NMR spectra of Py-NBN-Ph (A) and Py-NBN-Naphth (B) in C6D6. Table S1: The elemental analysis of Py-NBN-Ph and Py-NBN-Naphth; Table S2: Crystal data and structure refinement for NBN-doped pyrene-containing PAH with six-membered NBN ring; Table S3: The HOMO energy and LUMO energy of Py-NBN-Ph and Py-NBN-Naphth.

Author Contributions

Methodology, software, validation and formal analysis, H.X. and T.L.; writing—original draft preparation, X.-L.S. and W.-M.W.; writing—review and editing, W.-M.W., H.B., Q.Q. and Q.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Natural Science Foundation of China (grant number 21801251, 21971236 and 21871258), Natural Science Foundation of Fujian Province (grant number 2021J01199), the National Key R&D Program of China (grant number 2017YFA0700103), and the Haixi Institute of CAS (grant number CXZX-2017-P01).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding authors.

Conflicts of Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Sample Availability

Samples of the compounds are available from the authors.

References

  1. Vidal, F.; Lin, H.; Morales, C.; Jakle, F. Polysiloxane/Polystyrene Thermo-Responsive and Self-Healing Polymer Network via Lewis Acid-Lewis Base Pair Formation. Molecules 2018, 23, 405. [Google Scholar] [CrossRef] [Green Version]
  2. Lv, X.-H.; Li, S.-S.; Tian, C.-Y.; Yang, M.-M.; Li, C.; Zhou, Y.; Sun, X.-L.; Zhang, J.; Wan, W.-M. Borinic Acid Polymer: Simplified Synthesis and Enzymatic Biofuel Cell Application. Macromol. Rapid Commun. 2017, 38, 1600687. [Google Scholar] [CrossRef]
  3. Lv, X.-H.; Wang, X.-Y.; Zhou, Y.; Xu, H.; Wan, W.-M. Promoting water dissociation performance by borinic acid for the strong-acid/base-free hydrogen evolution reaction. Chem. Commun. 2019, 55, 9821–9824. [Google Scholar] [CrossRef] [PubMed]
  4. Ishibashi, J.S.A.; Marshall, J.L.; Mazière, A.; Lovinger, G.J.; Li, B.; Zakharov, L.N.; Dargelos, A.; Graciaa, A.; Chrostowska, A.; Liu, S.-Y. Two BN Isosteres of Anthracene: Synthesis and Characterization. J. Am. Chem. Soc. 2014, 136, 15414–15421. [Google Scholar] [CrossRef] [PubMed]
  5. Mellerup, S.K.; Wang, S. Boron-Based Stimuli Responsive Materials. Chem. Soc. Rev. 2019, 48, 3537–3549. [Google Scholar] [CrossRef] [PubMed]
  6. Neena, K.K.; Thilagar, P. Replacing the non-polarized C=C bond with an isoelectronic polarized B–N unit for the design and development of smart materials. J. Mater. Chem. C 2016, 4, 11465–11473. [Google Scholar] [CrossRef]
  7. Ren, Y.; Sezen, M.; Guo, F.; Jäkle, F.; Loo, Y.-L. [d]-Carbon-Carbon Double Bond Engineering in Diazaphos-phepines: A Pathway to Modulate the Chemical and Electronic Structures of Heteropines. Chem. Sci. 2016, 7, 4211–4219. [Google Scholar] [CrossRef] [Green Version]
  8. Sun, X.L.; Liu, D.M.; Lv, X.H.; Zhou, P.; Sun, M.; Wan, W.M. Thermo-responsive rheological behavior of borinic acid polymer in dilute solution. RSC Adv. 2016, 6, 83393–83398. [Google Scholar] [CrossRef]
  9. Wan, W.-M.; Li, S.-S.; Liu, D.-M.; Lv, X.-H.; Sun, X.-L. Synthesis of Electron-Deficient Borinic Acid Polymers with Multiresponsive Properties and Their Application in the Fluorescence Detection of Alizarin Red S and Electron-Rich 8-Hydroxyquinoline and Fluoride Ion: Substituent Effects. Macromolecules 2017, 50, 6872–6879. [Google Scholar] [CrossRef]
  10. Ayhan, O.; Eckert, T.; Plamper, F.A.; Helten, H. Poly(iminoborane)s: An Elusive Class of Main-Group Polymers? Angew. Chem. Int. Edit. 2016, 55, 13321–13325. [Google Scholar] [CrossRef]
  11. Lorenz, T.; Crumbach, M.; Eckert, T.; Lik, A.; Helten, H. Poly(p -phenylene iminoborane): A Boron-Nitrogen Analogue of Poly(p -phenylene vinylene). Angew. Chem. Int. Ed. 2017, 56, 2780–2784. [Google Scholar] [CrossRef]
  12. Wang, X.-Y.; Wang, J.-Y.; Pei, J. BN Heterosuperbenzenes: Synthesis and Properties. Chem. Eur. J. 2015, 21, 3528–3539. [Google Scholar] [CrossRef] [PubMed]
  13. Zhao, P.; Nettleton, D.O.; Karki, R.G.; Zécri, F.J.; Liu, S.-Y. Medicinal Chemistry Profiling of Monocyclic 1,2-Azaborines. ChemMedChem 2017, 12, 358–361. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Rudebusch, G.; Zakharov, L.N.; Liu, S. Rhodium-Catalyzed Boron Arylation of 1,2-Azaborines. Angew. Chem. Int. Ed. 2013, 52, 9316–9319. [Google Scholar] [CrossRef] [Green Version]
  15. Muñoz, A.D.O.; Escobedo-Morales, A.; Skakerzadeh, E.; Anota, E.C. Effect of homonuclear boron bonds in the adsorption of DNA nucleobases on boron nitride nanosheets. J. Mol. Liq. 2021, 322, 114951. [Google Scholar] [CrossRef]
  16. Juárez, A.R.; Ortiz-Chi, F.; Pino-Ríos, R.; Cárdenas-Jirón, G.; Villanueva, M.S.; Anota, E.C. The boron nitride (B116N124) fullerene: Stability and electronic properties from DFT simulations. Chem. Phys. Lett. 2020, 741, 137097. [Google Scholar] [CrossRef]
  17. Escobedo-Morales, A.; Tepech-Carrillo, L.; Bautista-Hernández, A.; Camacho-García, J.H.; Cortés-Arriagada, D.; Chigo-Anota, E. Effect of Chemical Order in the Structural Stability and Physicochemical Properties of B12N12 Fullerenes. Sci. Rep. 2019, 9, 1–11. [Google Scholar] [CrossRef]
  18. Mellerup, S.; Li, C.; Peng, T.; Wang, S. Regioselective Photoisomerization/C−C Bond Formation of Asymmetric B(ppy)(Mes)(Ar): The Role of the Aryl Groups on Boron. Angew. Chem. Int. Ed. 2017, 56, 6093–6097. [Google Scholar] [CrossRef]
  19. Shi, Y.-G.; Wang, J.-W.; Li, H.; Hu, G.-F.; Li, X.; Mellerup, S.K.; Wang, N.; Peng, T.; Wang, S. A simple multi-responsive system based on aldehyde functionalized amino-boranes. Chem. Sci. 2018, 9, 1902–1911. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Wei, H.P.; Liu, Y.L.; Gopalakrishna, T.Y.; Phan, H.; Huang, X.B.; Bao, L.P.; Guo, J.; Zhou, J.; Luo, S.L.; Wu, J.S.; et al. B-N-B Bond Embedded Phenalenyl and Its Anions. J. Am. Chem. Soc. 2017, 139, 15760–15767. [Google Scholar] [CrossRef] [PubMed]
  21. Xu, S.M.; Mikulas, T.C.; Zakharov, L.N.; Dixon, D.A.; Liu, S.Y. Boron-Substituted 1,3-Dihydro-1,3-azaborines: Synthesis, Structure, and Evaluation of Aromaticity. Angew. Chem. Int. Edit. 2013, 52, 7527–7531. [Google Scholar] [CrossRef] [Green Version]
  22. Liu, X.G.; Zhang, Y.Z.; Li, B.; Zakharov, L.N.; Vasiliu, M.; Dixon, D.A.; Liu, S.Y. A Modular Synthetic Approach to Monocyclic 1,4-Azaborines. Angew. Chem. Int. Edit. 2016, 55, 8333–8337. [Google Scholar] [CrossRef] [PubMed]
  23. Braunschweig, H.; Damme, A.; Jimenez-Halla, J.O.C.; Pfaffinger, B.; Radacki, K.; Wolf, J. Metal-Mediated Synthesis of 1,4-Di-tert-butyl-1,4-azaborine. Angew. Chem. Int. Edit. 2012, 51, 10034–10037. [Google Scholar] [CrossRef] [PubMed]
  24. Campbell, P.G.; Marwitz, A.J.V.; Liu, S.-Y. Recent Advances in Azaborine Chemistry. Angew. Chem. Int. Edit. 2012, 51, 6074–6092. [Google Scholar] [CrossRef] [PubMed]
  25. Tasseroul, J.; Lorenzo-Garcia, M.M.; Dosso, J.; Simon, F.; Velari, S.; De Vita, A.; Tecilla, P.; Bonifazi, D. Probing Peripheral H-Bonding Functionalities in BN-Doped Polycyclic Aromatic Hydrocarbons. J. Org. Chem. 2020, 85, 3454–3464. [Google Scholar] [CrossRef]
  26. Liu, K.; Lalancette, R.A.; Jäkle, F. Tuning the Structure and Electronic Properties of B–N Fused Dipyri-dylanthracene and Implications on the Self-Sensitized Reactivity with Singlet Oxygen. J. Am. Chem. Soc. 2019, 141, 7453–7462. [Google Scholar] [CrossRef]
  27. Liu, Z.Q.; Marder, T.B. B-N versus C-C: How Similar are They? Angew. Chem. Int. Edit. 2008, 47, 242–244. [Google Scholar] [CrossRef]
  28. Wan, W.M.; Baggett, A.W.; Cheng, F.; Lin, H.; Liu, S.Y.; Jakle, F. Synthesis by Free Radical Polymerization and Properties of BN-polystyrene and BN-poly(vinylbiphenyl). Chem. Commun. 2016, 52, 13616–13619. [Google Scholar] [CrossRef]
  29. Xu, S.; Zakharov, L.N.; Liu, S.-Y. A 1,3-Dihydro-1,3-azaborine Debuts. J. Am. Chem. Soc. 2011, 133, 20152–20155. [Google Scholar] [CrossRef] [Green Version]
  30. Zhang, W.; Li, G.; Xu, L.; Zhuo, Y.; Wan, W.; Yan, N.; He, G. 9,10-Azaboraphenanthrene-containing small molecules and conjugated polymers: Synthesis and their application in chemodosimeters for the ratiometric detection of fluoride ions. Chem. Sci. 2018, 9, 4444–4450. [Google Scholar] [CrossRef] [Green Version]
  31. Alahmadi, A.F.; Lalancette, R.A.; Jäkle, F. Highly Luminescent Ladderized Fluorene Copolymers Based on B–N Lewis Pair Functionalization. Macromol. Rapid Commun. 2018, 39, e1800456. [Google Scholar] [CrossRef]
  32. Liu, K.; Lalancette, R.A.; Jäkle, F. B–N Lewis Pair Functionalization of Anthracene: Structural Dynamics, Optoelectronic Properties, and O2 Sensitization. J. Am. Chem. Soc. 2017, 139, 18170–18173. [Google Scholar] [CrossRef] [PubMed]
  33. Araneda, J.F.; Neue, B.; Piers, W.E. Enforced Planarity: A Strategy for Stable Boron-Containing π-Conjugated Materials. Angew. Chem. Int. Edit. 2012, 51, 9977–9979. [Google Scholar] [CrossRef] [PubMed]
  34. Huang, J.; Li, Y. BN Embedded Polycyclic π-Conjugated Systems: Synthesis, Optoelectronic Properties, and Photovoltaic Applications. Front. Chem. 2018, 6, 341. [Google Scholar] [CrossRef] [PubMed]
  35. Li, G.; Zhao, Y.; Li, J.; Cao, J.; Zhu, J.; Sun, X.W.; Zhang, Q. Synthesis, Characterization, Physical Properties, and OLED Application of Single BN-Fused Perylene Diimide. J. Org. Chem. 2015, 80, 196–203. [Google Scholar] [CrossRef]
  36. Lu, J.S.; Ko, S.B.; Walters, N.R.; Kang, Y.; Sauriol, F.; Wang, S.N. Formation of Azaborines by Photoelimi-nation of B,N-Heterocyclic Compounds. Angew. Chem. Int. Edit. 2013, 52, 4544–4548. [Google Scholar] [CrossRef]
  37. Wang, S.N.; Yuan, K.; Hu, M.F.; Wang, X.; Peng, T.; Wang, N.; Li, Q.S. Cleavage of Unstrained C-C Bonds in Acenes by Boron and Light: Transformation of Naphthalene into Benzoborepin. Angew. Chem. Int. Edit. 2018, 57, 1073–1077. [Google Scholar] [CrossRef]
  38. Zhou, Z.; Wakamiya, A.; Kushida, T.; Yamaguchi, S. Planarized Triarylboranes: Stabilization by Structural Constraint and Their Plane-to-Bowl Conversion. J. Am. Chem. Soc. 2012, 134, 4529–4532. [Google Scholar] [CrossRef]
  39. Wang, X.; Zhang, F.; Schellhammer, K.S.; Machata, P.; Ortmann, F.; Cuniberti, G.; Fu, Y.; Hunger, J.; Tang, R.; Popov, A.A.; et al. Synthesis of NBN-Type Zigzag-Edged Polycyclic Aromatic Hydrocarbons: 1,9-Diaza-9a-boraphenalene as a Structural Motif. J. Am. Chem. Soc. 2016, 138, 11606–11615. [Google Scholar] [CrossRef]
  40. Yang, D.-T.; Nakamura, T.; He, Z.; Wang, X.; Wakamiya, A.; Peng, T.; Wang, S. Doping Polycyclic Arenes with Nitrogen–Boron–Nitrogen (NBN) Units. Org. Lett. 2018, 20, 6741–6745. [Google Scholar] [CrossRef]
  41. Lorenz, T.; Lik, A.; Plamper, F.A.; Helten, H. Dehydrocoupling and Silazane Cleavage Routes to Organic-Inorganic Hybrid Polymers with NBN Units in the Main Chain. Angew. Chem. Int. Edit. 2016, 55, 7236–7241. [Google Scholar] [CrossRef]
  42. Wan, W.-M.; Tian, D.; Jing, Y.-N.; Zhang, X.-Y.; Wu, W.; Ren, H.; Bao, H.-L. NBN-Doped Conjugated Polycyclic Aromatic Hydrocarbons as an AIEgen Class for Extremely Sensitive Detection of Explosives. Angew. Chem. Int. Edit. 2018, 57, 15510–15516. [Google Scholar] [CrossRef]
  43. Peng, H.Q.; Niu, L.Y.; Chen, Y.Z.; Wu, L.Z.; Tung, C.H.; Yang, Q.Z. Biological Applications of Supramolecular Assemblies Designed for Excitation Energy Transfer. Chem. Rev. 2015, 115, 7502–7542. [Google Scholar] [CrossRef] [PubMed]
  44. Cheng, F.; Bonder, E.M.; Jakle, F. Electron-Deficient Triaryl borane Block Copolymers: Synthesis by Con-trolled Free Radical Polymerization and Application in the Detection of Fluoride Ions. J. Am. Chem. Soc. 2013, 135, 17286–17289. [Google Scholar] [CrossRef] [PubMed]
  45. Davies, G.H.M.; Molander, G.A. Synthesis of Functionalized 1,3,2-Benzodiazaborole Cores Using Bench-Stable Components. J. Org. Chem. 2016, 81, 3771–3779. [Google Scholar] [CrossRef]
  46. Hudson, Z.; Wang, S. Impact of Donor−Acceptor Geometry and Metal Chelation on Photophysical Properties and Applications of Triarylboranes. Acc. Chem. Res. 2009, 42, 1584–1596. [Google Scholar] [CrossRef] [PubMed]
  47. Makedonas, C.; Mitsopoulou, C.A. The Relationship Between Aromaticity and Charge-Transfer Transitions: A Combined Study of Square-Planar Metal Complexes Based on DFT, NMR and Nucleus-Independent Chemical Shifts. Eur. J. Inorg. Chem. 2006, 2006, 2460–2468. [Google Scholar] [CrossRef]
  48. Chan, T.L.; Xie, Z. Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles. Chem. Sci. 2018, 9, 2284–2289. [Google Scholar] [CrossRef] [Green Version]
  49. Long, S.; Miao, L.; Li, R.; Deng, F.; Qiao, Q.; Liu, X.; Yan, A.; Xu, Z. Rapid Identification of Bacteria by Mem-brane-Responsive Aggregation of a Pyrene Derivative. ACS Sens. 2019, 4, 281–285. [Google Scholar] [CrossRef]
  50. Aratani, N.; Yamada, H.; Mei, P.; Kurosaki, R.; Matsumoto, A. One-Pot Synthesis of a Cyclic Pyrene Octamer from Two Bifunctionalized Pyrene Monomers. Synthesis 2020, 53, 344–347. [Google Scholar]
  51. Orita, A.; Watanabe, H.; Nakajima, K.; Ekuni, K.; Edagawa, R.; Akagi, Y.; Okuda, Y.; Wakamatsu, K. Custom-Made Pyrene Photocatalyst-Promoted Desulfonylation of Arylethenyl Sulfones Using Green-Light-Emitting Diodes. Synthesis 2021, 53, 2984–2994. [Google Scholar] [CrossRef]
  52. Shen, Q.; Liu, H.; Peng, Y.; Zheng, J.; Wu, J. Visualization of the self-healing process by directly observing the evolution of fluorescence intensity. Polym. Chem. 2021, 12, 494–500. [Google Scholar] [CrossRef]
  53. Wu, B.Y.; Le, X.X.; Jian, Y.K.; Lu, W.; Yang, Z.Y.; Zheng, Z.K.; Theato, P.; Zhang, J.W.; Zhang, A.; Chen, T. pH and Thermo Dual-Responsive Fluorescent Hydrogel Actuator. Macromol. Rapid Commun. 2019, 40, e1800648. [Google Scholar] [CrossRef] [PubMed]
  54. Su, M.; Jing, Y.N.; Bao, H.L.; Wan, W.M. Triarylmethanolation as A Aersatile Strategy for the Conversion of PAHs into Amorphization-Induced Emission Luminogens for Extremely Sensitive Explosive Detection and Fabrication of Artificial Light-Harvesting Systems. Mater. Chem. Front. 2020, 4, 2435–2442. [Google Scholar] [CrossRef]
  55. Sun, X.-L.; Liu, N.-M.; Tian, D.; Zhang, X.-Y.; Wu, W.; Wan, W.-M. The introduction of the Barbier reaction into polymer chemistry. Nat. Commun. 2017, 8, 1210. [Google Scholar] [CrossRef] [Green Version]
  56. Jing, Y.N.; Li, S.S.; Su, M.; Bao, H.; Wan, W.M. Barbier Hyperbranching Polymerization-Induced Emission toward Facile Fabrication of White LED and Light Harvesting Film. J. Am. Chem. Soc. 2019, 141, 16839–16848. [Google Scholar] [CrossRef]
  57. Li, S.-S.; Jing, Y.-N.; Bao, H.; Wan, W.-M. Exploitation of Monofunctional Carbonyl Resources by Barbier Polymerization for Materials with Polymerization-Induced Emission. Cell Rep. Phys. Sci. 2020, 1, 100116. [Google Scholar] [CrossRef]
  58. Li, S.S.; Zhu, N.B.; Jing, Y.N.; Li, Y.J.; Bao, H.L.; Wan, W.M. Barbier Self-Condensing Ketyl Polymerization-Induced Emission: A Polarity Reversal Approach to Reversed Polymerizability. iScience 2020, 23, 58. [Google Scholar] [CrossRef]
Molecules 27 00327 sch001 550
Scheme 1. The preparation of NBN-doped pyrene-containing PAHs (A) Py-NBN-Ph (B) Py-NBN-Naphth through intermolecular dehydration between boronic acid and diamine moieties.
Scheme 1. The preparation of NBN-doped pyrene-containing PAHs (A) Py-NBN-Ph (B) Py-NBN-Naphth through intermolecular dehydration between boronic acid and diamine moieties.
Molecules 27 00327 sch001
Molecules 27 00327 g001 550
Figure 1. Electron orbital of NBN-doped PAHs, corresponding to the NICS calculation model and NICS values. The photographs in the upper right corner are fluorescent images of Py-NBN-Ph (up) and Py-NBN-Naphth (down) in THF solution (0.1 mg/mL) under the UV light.
Figure 1. Electron orbital of NBN-doped PAHs, corresponding to the NICS calculation model and NICS values. The photographs in the upper right corner are fluorescent images of Py-NBN-Ph (up) and Py-NBN-Naphth (down) in THF solution (0.1 mg/mL) under the UV light.
Molecules 27 00327 g001
Molecules 27 00327 g002 550
Figure 2. 1H-NMR titration of (A) Py-NBN-Ph (c0 = 1.572 × 10−3 M) and (B) Py-NBN-Naphth (c0 = 8.152 × 10−3 M) with pyridine in C6D6 at 298 K.
Figure 2. 1H-NMR titration of (A) Py-NBN-Ph (c0 = 1.572 × 10−3 M) and (B) Py-NBN-Naphth (c0 = 8.152 × 10−3 M) with pyridine in C6D6 at 298 K.
Molecules 27 00327 g002
Molecules 27 00327 g003 550
Figure 3. (A) Digital images of Py-NBN-Ph at a solid state and after grinding (under sunlight and UV light at 365 nm); (B) Emission spectra at a solid state before and after grinding (excited at 398 nm).
Figure 3. (A) Digital images of Py-NBN-Ph at a solid state and after grinding (under sunlight and UV light at 365 nm); (B) Emission spectra at a solid state before and after grinding (excited at 398 nm).
Molecules 27 00327 g003
Molecules 27 00327 g004 550
Figure 4. (A) Emission changes of Py-NBN-Ph solution after adding TBAF and water; (B) 1H NMR spectra of Py-NBN-Ph in DMSO-d6 (a), after the addition of 1.0 equal of TBAF (b), and followed by the addition of 15 μL of D2O (c).
Figure 4. (A) Emission changes of Py-NBN-Ph solution after adding TBAF and water; (B) 1H NMR spectra of Py-NBN-Ph in DMSO-d6 (a), after the addition of 1.0 equal of TBAF (b), and followed by the addition of 15 μL of D2O (c).
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Molecules 27 00327 g005 550
Figure 5. The responsive behaviors of Py-NBN-Naphth. (A) Schematic diagram with the addition of fluoride ion at different concentrations; (B) Emission spectra with the addition of different amounts of TBAF; (C–E) Single-crystal structures.
Figure 5. The responsive behaviors of Py-NBN-Naphth. (A) Schematic diagram with the addition of fluoride ion at different concentrations; (B) Emission spectra with the addition of different amounts of TBAF; (C–E) Single-crystal structures.
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Molecules 27 00327 g006 550
Figure 6. Artificial light-harvesting application of Py-NBN-Ph. (A) Schematic diagram of light-harvesting application, Py-NBN-Ph is the ground state molecule and Py-NBN-Ph* is the excited state molecule; (B) Emission spectra of light-harvesting films with different Py-NBN-Ph/NiR ratios; (C) Emission spectra of NiR, Py-NBN-Ph and Py-NBN-Ph/NiR (100:1).
Figure 6. Artificial light-harvesting application of Py-NBN-Ph. (A) Schematic diagram of light-harvesting application, Py-NBN-Ph is the ground state molecule and Py-NBN-Ph* is the excited state molecule; (B) Emission spectra of light-harvesting films with different Py-NBN-Ph/NiR ratios; (C) Emission spectra of NiR, Py-NBN-Ph and Py-NBN-Ph/NiR (100:1).
Molecules 27 00327 g006
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Xiao, H.; Li, T.; Sun, X.-L.; Wan, W.-M.; Bao, H.; Qian, Q.; Chen, Q. Unpredicted Concentration-Dependent Sensory Properties of Pyrene-Containing NBN-Doped Polycyclic Aromatic Hydrocarbons. Molecules 2022, 27, 327. https://doi.org/10.3390/molecules27010327

AMA Style

Xiao H, Li T, Sun X-L, Wan W-M, Bao H, Qian Q, Chen Q. Unpredicted Concentration-Dependent Sensory Properties of Pyrene-Containing NBN-Doped Polycyclic Aromatic Hydrocarbons. Molecules. 2022; 27(1):327. https://doi.org/10.3390/molecules27010327

Chicago/Turabian Style

Xiao, Hang, Tao Li, Xiao-Li Sun, Wen-Ming Wan, Hongli Bao, Qingrong Qian, and Qinghua Chen. 2022. "Unpredicted Concentration-Dependent Sensory Properties of Pyrene-Containing NBN-Doped Polycyclic Aromatic Hydrocarbons" Molecules 27, no. 1: 327. https://doi.org/10.3390/molecules27010327

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