Development of fluorinated benzils and bisbenzils as room-temperature phosphorescent molecules

Pure organic phosphorescent molecules are attractive alternatives to transition-metal-complex-based phosphores for biomedical and technological applications owing to their abundance and nontoxicity. This article discloses the design, synthesis, and photophysical properties of fluorinated benzil and bisbenzil derivatives as potential pure organic room-temperature phosphorescent molecules. These compounds were separately converted from the corresponding fluorinated bistolanes via PdCl2-catalyzed oxidation by dimethyl sulfoxide, while nonfluorinated bistolane provided the corresponding bisbenzil derivatives exclusively in a similar manner. Intensive investigations of the photophysical properties of the benzil and bisbenzil derivatives in toluene at 25 °C showed both fluorescence with a photoluminescence (PL) band at a maximum wavelength (λPL) of around 400 nm and phosphorescence with a PL band at a λPL of around 560 nm. Interestingly, intersystem crossing effectively caused fluorinated benzils to emit phosphorescence, which may arise from immediate spin-orbit coupling involving the 1(n, π)→3(π, π) transition, unlike the case of fluorinated or nonfluorinated bisbenzil analogues. These findings offer a useful guide for developing novel pure organic room-temperature phosphorescent materials.


Introduction
The development of organic light-emitting molecules is recognized as one of the most important studies because of the broad application of these compounds as fluorescence probes, bio-imaging materials, and biosensors in biomedical diagnostics [1][2][3][4] and as organic light-emitting diodes in the technological field [5][6][7][8]. Among the organic light-emitting molecules de- veloped thus far, extended π-conjugated compounds (e.g., pyrenes and perylenes) emit fluorescence, which is a radiative deactivation process from the lowest singlet (S 1 ) excited state to the ground (S 0 ) state [9]. Interestingly, for such π-conjugated molecules, suitable structural modifications can switch the radiative S 1 →S 0 process to another radiative deactivation process from the triplet (T 1 ) excited state to S 0 via an S 1 →T 1 intersystem crossing (ISC), resulting in the emission of phosphorescence [9].
Phosphorescent molecules generate two excitons (i.e., 25% S 1 excitons and 75% T 1 excitons) by application of an electric field, which is well known for organic light-emitting diodes. S 1 excitons are converted to T 1 excitons via an ISC process, finally achieving an excellent light-emitting efficiency (up to 100%) [10]. Therefore, extensive investigations to develop phosphorescent molecules have been performed thus far [11][12][13].
It has been established that transition metal complexes containing a heavy atom can promote ISC (e.g., Ru [14], Ir [15,16], Pt [17], and Au [18][19][20][21]) ( Figure 1A), and this offers a molecular design approach for phosphorescence emission. However, it is becoming necessary to explore alternatives to rare metals because of the latter's scarcity and toxicity. Owing to recent considerable efforts, several molecular designs have been proposed as alternatives, particularly the use of pure organic phosphorescent molecules [22].
As a powerful tool to develop novel pure organic phosphorescent molecules, we envisioned the structural modification of the carbon-carbon triple (C≡C) bond in fluorinated bistolane 1 via oxidation to form the corresponding benzil 2 and/or bisbenzil 3 derivatives ( Figure 2B). A literature review reveals that bisbenzil-type analogues have not received much attention, despite several publications on benzil-type phosphorescent molecules [25,26,32]. In this study, therefore, we examined the synthesis of novel benzil-and bisbenzil-type molecules via oxidation of fluorinated and nonfluorinated bistolane derivatives and evaluated their photophysical properties in detail.

Synthesis
This study was initiated with the synthesis of fluorinated bisbenzil derivatives. The PdCl 2 -catalyzed oxidation of the C≡C bonds in 1 by dimethyl sulfoxide (DMSO) was performed according to a previously reported procedure (Scheme 1) [33,34]. The methoxy-substituted fluorinated bistolane 1a was prepared from commercially available 4-ethynylanisole in four facile steps. Interestingly, stirring 1a in DMSO solution in the presence of 30 mol % of PdCl 2 at 140 °C for 17 h produced two products (56% yield for the more polar product and 37% yield for the less polar product) after purification with column chromatography. Spectroscopic analyses (i.e., 1 H, 19 F, and 13 C nuclear magnetic resonance (NMR) spectroscopy, infrared spectroscopy, and high-resolution mass spectrometry) successfully identified the more polar product as the half-oxidized benzil 2a and the less polar one as the fully oxidized bisbenzil 3a. Fluorinated bistolane 1b, bearing a hexyloxy chain, also underwent PdCl 2 -catalyzed C≡C oxidation to give rise to the corresponding benzil 2b and bisbenzil 3b in 28% and 21% yield, respectively. When nonfluorinated bistolane 1c was used as the substrate, the corresponding bisbenzil 3c was obtained in 40% yield as the major product together with an inseparable mixture.
The proposed mechanism of Pd(II)-catalyzed C≡C oxidation is illustrated in Scheme 2 [33]: The catalytic cycle starts with the coordination of the electron-rich C≡C bond to the electron-deficient divalent Pd center, forming the corresponding π-complex (Int-A). Int-A smoothly undergoes nucleophilic attack by the oxygen atom in DMSO to construct a cationic vinyl-palladium(II) species (Int-B). Further nucleophilic attack of another DMSO molecule against Int-B, followed by elimination of dimethyl sulfide, furnishes a cationic intermediate (Int-C).
Finally, immediate elimination of dimethyl sulfide and the Pd(II) catalyst gives rise to the corresponding benzil 2, after which the eliminated Pd(II) catalyst is recycled to provide the oxidation products. The fully oxidized bisbenzil 3 is generated after further Pd(II)-catalyzed C≡C oxidation of the halfoxidized benzil 2 via the same catalytic cycle.
Considering the proposed reaction mechanism, the successful isolation of the half-oxidized benzil derivatives 2a and 2b from the oxidation of fluorinated bistolanes 1a and 1b, respectively, may be due to the decreased reactivity of the C≡C bond toward Pd(II)-catalyzed C≡C oxidation caused by the adjacent electrondeficient fluorinated aromatic ring. To confirm the electronwithdrawing effect of this fluorinated aromatic ring, the electronic charge at the adjacent C≡C bond was calculated by density functional theory (DFT) using the Gaussian 16 (Revision B.01) software package [35]. As typical examples, the molecular geometries of 1a and 1c were optimized at the CAM-B3LYP/6-31+G(d) level of theory. The absence of any imaginary frequency in the vibrational analysis proved that the calculated structures are the minima. Figure 3 shows the calculated Mulliken charge distributions of fluorinated 1a and nonfluorinated 1c.
The sp-hybridized carbon adjacent to the fluorinated aromatic ring of 1a has a significant positive Mulliken charge (+0.472), while that adjacent to the nonfluorinated aromatic ring of 1c has a negative charge (−0.304). This clearly indicates that the fluo-

Photophysical behavior
Our interest was then directed toward the photophysical properties of benzil and bisbenzil derivatives, which were freshly purified by column chromatography (eluent: hexane/EtOAc = 5:1 for benzil and 10:1 for bisbenzil) and subsequently recrystallized from hexane. The sample solution concentrations in toluene were 1.0 × 10 −5 and 1.0 × 10 −3 M for the absorption and photoluminescence (PL) measurements, respectively, and the absorption and PL spectra are shown in Figure 4. The photophysical data obtained from these measurements are summarized in Table 1.
The main electronic transition with a relatively large oscillator strength (f) in both 2a and 3a is the highest occupied molecular orbital (HOMO)→lowest unoccupied molecular orbital (LUMO) transition. Focusing on the orbital distribution, the HOMO lobe of 2a covers the entire molecule, while the LUMO lobe is localized at the tolane moiety. In the case of 3a, the HOMO lobe is localized at the methoxy-substituted benzene ring, while the LUMO lobe is localized at the central benzene ring. Accordingly, it can be concluded that the absorption bands at the short-wavelength region (around 290-315 nm) stems from the π-π* transition. The TD-DFT calculation also reveals that n-π* transitions (e.g., HOMO-2→LUMO for 2a and HOMO-3→LUMO for 3a) have small values of f; thus, the small absorption band at around 400 nm can be safely attributed to an n-π* transition.
Upon irradiation of the toluene solutions of benzil derivatives 2a and 2b with a 350 nm UV light, three PL bands at 395, 507, and 563 nm, along with a shoulder signal at around 406 nm, are observed ( Figure 4A and 4B). The bisbenzil derivatives, i.e., 3a-c, also show similar PL behavior to the aforementioned benzil analogues: four PL bands with λ PL of 393-397, 406-412, 514-517, and 551-569 nm are observed. To gain more information about the PL process in benzils and bisbenzils, the PL spectra of the toluene solutions (1.0 × 10 −3 M) were acquired after bubbling with N 2 or O 2 gas for 30 min. In general, an O 2 -saturated environment strongly deactivates the triplet states; thus, PL emission stems only from fluorescence. On the other hand, elimination of O 2 gas from a solution by bubbling with an inert gas (N 2 or Ar) allows the triplet states to survive for a long lifetime, which possibly leads to a phosphorescence emission. Hence, the elimination of O 2 gas from solutions by N 2 gas bubbling (or addition of O 2 gas in solutions) can judge the presence of phosphorescence, as well as the assignment of PL bands. The obtained PL spectra are superimposed on the PL spectra of a pristine sample (Figure 4). Upon bubbling the solution with N 2 gas for 30 min, a dramatic enhancement of the PL intensities of benzils 2a and 2b at λ PL = 563 nm is observed. The PL intensities of bisbenzils 3a-c at the long-wavelength region between 551 and 569 nm also increase, although the increment rates are not as high as those of 2a and 2b. On the contrary, bubbling the toluene solutions of benzil or bisbenzil derivatives with O 2 gas causes the intensity of the long-wavelength PL band to decrease compared with that of the pristine solution, while the other remaining PL bands in the short-wavelength region do not change. Judging from the PL behavior under N 2 or O 2 flow conditions, the PL bands at the shortwavelength region around 395 nm and long-wavelength region around 560 nm can be safely considered fluorescence via radiative deactivation from the S 1 excited state to the S 0 state and phosphorescence via electronic transition from the T 1 excited state to the S 0 state, respectively. Accordingly, fluorinated benzils and bisbenzils show room-temperature phosphorescence in the solution state.
To understand the effects of structural modification (i.e., the benzil structure with a tolane vs bisbenzil moiety) and incorporation of fluorine atoms on the phosphorescence, the ratio between the peak intensities at ≈395 and ≈560 nm (I 560 /I 395 ) was quantitatively calculated, and the results are summarized in Additionally, the quantum yields (Φ PL ) of the PL bands in the range of 350-600 nm were acquired using an absolute quantum yield measurement system with a calibrated integrating sphere. All samples have a low Φ PL of less than 0.02 (Table 1), meaning that most of the excited states of all samples deactivate nonradiatively. At the moment, we cannot certify the origin of the low Φ PL in terms of the molecular properties, for instance, the main pathway of nonradiative deactivation. Experiments are currently being conducted to better understand the photophysical mechanisms of the excited-state dynamics of these benzil and bisbenzil derivatives.

Conclusion
In this article, we described the design and synthesis of benzilor bisbenzil-based room-temperature phosphorescent molecules via a simple oxidation protocol for fluorescent bistolane derivatives. Nonfluorinated bistolane derivatives exclusively gave the corresponding products with a bisbenzil scaffold, whereas the fluorinated bistolane derivatives generated not only mono-oxidized benzil derivatives bearing a fluorinated tolane scaffold, but also the corresponding bis-oxidized bisbenzil derivatives. Based on theoretical calculations, the selective formation of the fluorinated analogues stemmed from the slight modulation of the charge distribution at the alkyne moiety of the reactant induced by the electron-withdrawing fluorine atoms. Evaluation of the photophysical behavior of the benzils and bisbenzils through several PL measurements under N 2 and O 2 flow conditions probed the successful room-temperature phosphorescence of the compounds in toluene solution. A fuller understanding of the excited-state dynamics of these benzil and bisbenzil derivatives will assist the development of environmentally benign, pure organic phosphorescent materials.

Supporting Information File 1
Experimental preocedures, NMR spectra and Cartesian coordinates.

Funding
The following sources of funding are acknowledged: Japan Society for the Promotion of Science (JSPS) KAKENHI Grantin-Aid for Scientific Research (C) (Grant No. JP18K05262) and the AIST Nanocharacterization Facility (ANCF) platform as part of a program of the "Nanotechnology Platform" of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan.