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Article

Synthetic Exploration of Bis(phenolate) Aza-BODIPYs and Heavier Group 13 Chelates

by
Aiden M. Lane
1,
Ny T. C. Luong
1,
Jordan C. Kelly
2,
Martin J. Neal
2,
Jeremiah Jamrom
2,
Aaron J. Bloomfield
2,
Paul A. Lummis
2,
Thomas D. Montgomery
2,* and
Daniel T. Chase
1,*
1
Department of Chemistry and Biochemistry, St. Mary’s College of Maryland, St. Mary’s City, MD 20686, USA
2
Department of Chemistry and Biochemistry, Duquesne University, Pittsburg, PA 15282, USA
*
Authors to whom correspondence should be addressed.
Molecules 2022, 27(23), 8256; https://doi.org/10.3390/molecules27238256
Submission received: 27 October 2022 / Revised: 21 November 2022 / Accepted: 24 November 2022 / Published: 26 November 2022
(This article belongs to the Special Issue The Chemistry of BODIPY Today)
Browse Figures
Versions Notes

Abstract

:
A series of boron, aluminum, gallium, and indium chelates containing the underexplored bis(phenolate) aza-dipyrromethene (aza-DIPY) core were prepared. These compounds were found to possess near-infrared absorption and emission profiles in the 710 to 770 nm domain and exhibit quantum yield values up to 14%. X-ray diffraction analysis revealed that heavier group 13 bis(phenolate) aza-DIPY chelates possessed octahedral geometries with either THF or pyridine groups occupying the axial positions as opposed to the tetrahedral geometry of the boron chelate.

Graphical Abstract

1. Introduction

Since its resurgence nearly two decades ago, the aza-dipyrromethene (aza-DIPY) core (A, Figure 1) has received significant attention due to its intense absorbing and emitting profile in the near-infrared (NIR) region which makes them exciting candidates for application in both the physical and biological sciences [1,2,3,4]. From the perspective of effectively modulating these profiles, boron difluoride chelates of the aza-DIPY core (aza-BODIPYs, (B) represent the majority of literature examples as numerous strategies are known to push absorption and emission maxima beyond 800 nm [5,6,7,8,9,10].
In conjunction with our prior work functionalizing aza-BODIPYs through the direct incorporation of nitro groups [11], we became interested with the bis(phenolate) aza-DIPY core structure (C), having ortho-functionalized phenolic groups present on the proximal rings. Motivation for this core structure stemmed from the previous work done by Burgess and others which demonstrated that bis(phenolate) aza-BODIPYs can achieve absorption and emission maxima upwards of 780 nm [12,13,14,15,16,17,18]. Additionally, very recent work by Sauvé and coworkers detailed that the addition of phenylacetylene groups on the 2- and 6-positions of the bis(phenolate) aza-BODIPY core can further shift absorption and emission maxima past 820 nm [19].
The structurally related bis(phenolate) dipyrromethene core (D), whose boron chelates were also originally reported by Burgess and coworkers [20], represents a secondary source of inspiration as numerous elements beyond boron have also been chelated to afford a diverse array of compounds with interesting structural and photophysical properties. For example, Nabeshima and coworkers explored the insertion of heavier Group 13 centers (Al, Ga, In, E) and found that such complexes were able to serve as efficient luminescent sensors to both alkaline earth and transition metals [21,22,23]. Further work by their group also considered the insertion of Group 14 and 15 centers which yielded chelates that incorporate both bent and linear oxygen bonds and serve as zwitterionic NIR pH sensors [24,25,26,27]. Significant work on inserting transition metal centers into the bis(phenolate) DIPY core has also been performed. For example, Nozaki and coworkers explored Group 4 and heavier Group 14 (Ti, Zr, Ge, Sn, F) DIPY chelates as catalysts for the copolymerization of epoxides with carbon dioxide [28]. Work by Thomas and others have also demonstrated that DIPY chelates containing Mn can serve as catalysts for olefin epoxidations [29,30,31]. Furthermore, numerous reports have indicated that both mid- and late-transition metal DIPY chelates can exhibit both innocent and non-innocent redox properties [32,33,34,35]. Indeed, a recent 2019 report by Kadish and coworkers [36] directly suggested that such behavior with bis(phenolate) DIPYs may very well serve as an analogy for the well-known corrole macrocycle which has received significant attention in its own right over the past three decades. This analogy is also the subject of a very recent review by Paolesse and coworkers [37].
To the best of our knowledge, no chelates outside of boron that contain the bis(phenolate) aza-DIPY core structure are currently known to the literature. Given the likely structural properties that such chelates will share with their DIPY congeners in addition to their expected NIR traits, further research is of clear interest. Here, we disclose the synthesis of a series of aza-BODIPY (1a-b), aza-ALDIPY (2a-b), aza-GADIPY (3a-b), and aza-INDIPY (4a-b) complexes. This series of compounds lays the groundwork for a thorough investigation of this comparatively underexplored class of molecules and validates their expected structural and spectral properties. In addition to their 1H, 11B, 13C and HRMS data, we also report the X-ray structures of 1a, 2a-b, 3a-b, and 4a-b which unambiguously confirm their structural identities. Finally, the computational and photophysical properties of 1a-b, 2a-b, 3a-b, and 4a-b are discussed and compared.

2. Results and Discussion

2.1. Synthesis and Structural Characterization

The synthesis of bis(phenolate) aza-MDIPYs 1a-b, 2a-b, 3a-b, and 4a-b follows the well-established procedures previously outlined by Burgess [18] and Nabeshima [23] as depicted in Scheme 1. Bis(phenolate) aza-DIPY core structures 7a-b, containing para-functionalized methyl- and methoxyphenyl groups, were specifically chosen as they possess relatively similar electron donating capabilities and will likely exhibit the most bathochromically shifted absorption and emission spectra based on prior work by ourselves and others [11,12,13,14,15,16,17,18]. The first step involves subjecting known chalcones 5a-b to a Henry reaction with nitromethane to give compounds 6a-b in excellent yields (>95%). Next, 6a-b are reacted with an excess of ammonium acetate in refluxing 1-butanol to generate bis(phenolate) aza-DIPYs 7a-b in moderate yields (37–63%).
To form bis(phenolate) aza-BODIPYs, the final step involves subjecting 7a-b to a BF3·OEt2/DIPEA mixture in refluxing THF, forming 1a-b in moderate yields (45–52%) as depicted in Scheme 2. To generate heavier Group 13 derivatives, 1.5 equivalents of either Al(acac)3, Ga(acac)3, or In(acac)3 were added to the core in refluxing pyridine to form the corresponding bis(phenolate) aza-ALDIPYs (2a-b), aza-GADIPYs (3a-b), and aza-INDIPYs (4a-b), respectively, in good yields (65–72%).
All reactions were monitored through observation of a characteristic upfield shift of the pyrrolic 1H signal correlating to the 2- and 6-positions of the bis(phenolate) aza-DIPY core. Additionally, boron chelations were followed through the expected appearance of a 11B singlet between −3.5 and −2.5 ppm. For aluminum, gallium, and indium chelations, we observed the appearance of pyridine signals in an approximate 2:1 ratio with respect to the bis(phenolate) aza-DIPY core, implying the inclusion of two axially bound pyridine units to the metal center, completing their expected octahedral geometries.

2.2. Crystallography

Single crystals of bis(phenolate) aza-BODIPY 1a were obtained through the slow vapor diffusion of a THF solution of 1a with n-pentane. Analysis of the diffraction data unambiguously confirms the structural identity of 1a and its expected tetrahedral boron center (Figure 2). To accommodate this coordination geometry, both phenolic rings exhibit significant flexing as demonstrated by torsion angles of −22.23(9)° and −24.41(4)° along C2–C1–C9–C14 and C6–C5–C15–C20, respectively.
Single crystals of bis(phenolate) aza-ALDIPY 2a were obtained through layering n-hexane in a 1:1 pyridine:toluene solution followed by slow evaporation. As seen in Figure 3, two pyridine groups are bound axially to the Al center, giving a nearly linear angle of 176.55(7)° along the N4–Al1–N5 axis. The Al center also fits within the plane of the bis(phenolate) aza-DIPY core and we observe the phenolic rings puckering slightly inwards, resulting in an interplanar angle of 3.31(8)°. These structural trends are similarly found with the diffraction data of 2b, 3a-b, and 4a-b (see the Supporting Information for full details). Interestingly, when THF was used as a coordinating solvent instead of pyridine, single crystals of bis(phenolate) aza-INDIPY 4a’ were obtained through layering n-decane over a saturated THF solution. As seen in Figure 4, 4a’ incorporates two identical octahedral aza-INDIPY cores that are dimerized together forming a central four-membered ring that contains an In2O2 moiety (In1-O2: 2.141 Å; In1-O2’: 2.224 Å). The axially bound THF groups (omitted for clarity, see Supporting Information) are also moderately bent out of linearity as evidenced from the 163.81(12)° angle along the O3–In1–O2’ axis. There is also significant twisting (17.44(3)°) between the axially bound phenolic group and the aza-DIPY core to accommodate dimerization which also explains the discrete In-O bond lengths.

2.3. Computational Measurements

To better understand the photophysical properties of 1a-b, 2a-b, 3a-b¸and 4a-b, density functional theory (DFT) calculations were performed [38,39]. All data are given in Table 1 with the frontier molecular orbitals of 1a, 2a, 3a, and 4a displayed in Figure 5 (see the Supporting Information for full details). Using the experimentally determined crystal structure of 2a as a reference, the computed ground state geometries were found to be in excellent agreement using the B3LYP functional with Dunning’s jul-cc-pVDZ basis set [40]. The jul-cc-pVDZ basis set was selected due to its good performance in a variety of systems [41] and in our prior studies, we found it gave the best balance of accuracy and computational cost for functionalized DIPYs [11]. With the optimized structures in hand, TD-DFT calculations using B3LYP/jul-cc-pVDZ for 1a-b, 2a-b, and 3a-b with MeOH as the implicit solvent [42,43] were performed; for 4a-b, B3LYP/LanL2DZ was used for both geometry optimization and TD-DFT calculations to accommodate the In nuclei [44,45]. Overall, our computations generated theoretical λabs values that closely matched their experimental values with deviations below 5%; the sole exception to this was bis(phenolate) aza-BODIPY 1a which exhibited a deviation of 9.1%.
As seen in Figure 5, both methyl and methoxy-functionalized bis(phenolate) aza-MDIPYs possess little orbital density on the distal arenes which suggests that such functionalization bears little influence. Instead, the majority of HOMO and LUMO density resides on the aza-DIPY core, resulting in the expected π-π* transitions. Furthermore, little to no orbital density was found on the metal centers which agrees with numerous aza-DIPY studies performed previously [12,13,14,15,16,17,18,46,47]. Perhaps the greatest difference between the frontier molecular orbital plots of these compounds involves the LUMO+1 orbital as 1a-b has orbital density spread throughout the proximal rings and aza-DIPY core while 2a-b, 3a-b, and 4a-b have orbital density exclusively on the axially bound pyridines. These structures were also visualized in the DIPY plane, with the images included in the SI.

2.4. Photophysical Properties

2.4.1. Electronic Absorption Spectra

The absorption spectra for 1a-b, 2a-b, 3a-b and 4a-b in DMSO are shown in Figure 6 and listed in Table 1. As expected with most aza-BODIPYs, all compounds exhibited intense absorption maxima between 715–735 nm with extinction coefficients between 30,000 and 52,000 M−1 cm−1. Also present are smaller absorption maxima located at the 650 nm, 450 nm, and 325 nm ranges. Interestingly, 1a-b exhibit bathochromically shifted absorptions in the 525 nm range as compared to 2a-b, 3a-b, and 4a-b which give them a purple hue compared to the green color that the remaining complexes possess. As predicted by the frontier molecular orbital plots mentioned above, para-functionalization on the distal positions of the bis(phenolate) aza-DIPY core had little effect on the absorption maxima which was similarly observed by Burgess and coworkers regarding aza-BODIPYs [18]. The general trend was found to be B > Ga > Al > In with bis(phenolate) aza-BODIPYs 1a-b exhibiting the most bathochromically shifted absorption spectra which fits well with prior observations found by Nabeshima and co-workers [23].

2.4.2. Electronic Emission Spectra

The emission spectra for 1a-b, 2a-b, 3a-b and 4a-b in DMSO are shown in Figure 7 and listed in Table 1. Unlike the absorption data, the general emission trend stands at Ga > Al > B > In with bis(phenolate) aza-GADIPYs 2a-b exhibiting the most bathochromically shifted spectra. As found with the observations originally made by both Nabeshima and Burgess [18,23], methyl functionalized derivatives exhibited bathochromically shifted emission maxima when compared to their methoxy functionalized derivatives. With respect to Stokes shifts, the general trend stands at Ga > In > Al > B; this observation is reasoned to be due to the difference between the octahedral geometry of 2a-b, 3a-b, and 4a-b compared to the tetrahedral geometry of 1a-b. Quantum yields for 1a-b, 2a-b, 3a-b, and 4a-b were also measured in MeOH using an internal integrating sphere and their values are given in Table 1. It was found that quantum yields increased from 1a-b to 2a-b but then decreased as a function of increasing metal size.

3. Materials and Methods

3.1. General Considerations

Unless otherwise noted, solvents and reagents were purchased from either Thermo Fisher or Sigma Aldrich and used as received. Flash chromatography was performed using P60 silica purchased from SiliCycle. THF was distilled from sodium/benzophenone under a nitrogen atmosphere. Bis(phenolate) aza-BODIPY 7b and their precursors, 5b and 6b, were synthesized by their previously reported methods [18,23].
NMR spectra were recorded using a JEOL JMN-ECSZ400R 400 MHz (1H: 399.78 MHz; 13C: 100.52 MHz) spectrometer at room temperature. Chemical shifts (δ) are expressed in ppm relative to the residual chloroform (1H: 7.27 ppm; 13C: 77.2 ppm) or DMSO-d6 (1H: 2.50 ppm; 13C: 39.5 ppm) in solution. Coupling constants are expressed in hertz. UV-Visible spectra were recorded on a Cary 100 UV-Vis spectrometer. Fluorescence spectra were recorded on a PTI HORIBA QM-40 spectrofluorometer and quantum yields were obtained using a KSPHERE petite integrating sphere. Single crystal XRD measurements were collected from a Bruker Smart Apex II CCD diffractometer using graphite-monochromated Mo-K (λα = 0.71073 Å) radiation. Molecular crystal structure images were processed through CrystalMaker. HRMS-ESI measurements were taken on an Agilent 6530 high resolution quadrupole time of flight spectrometer (QTOF) utilizing an Agilent 1100 liquid chromatography system with model G1212A binary pump and G1367 autosampler. Samples were introduced via direct injection rather than isolating species with column chromatography to monitor changing levels of starting material as well as any potential side reactions which were ionized using a Dual Agilent Jet Stream G1958-66268 electrospray ionization source. Immediately prior to sample introduction, the QTOF was calibrated in the 50–1700 mass range for the 4 GHz high resolution mode. A mobile phase of HPLC acetone was utilized to reduce instrument noise related to the solvent and to ensure the analyte would stay in solution until ionized. Acetone was utilized as a needle wash to reduce contamination of samples. Samples were analyzed in the positive mode with a dragging gas temperature of 300 °C, a drying gas flow rate of 8 L/min, a nebulizer pressure of 35 psi, a sheath gas temperature of 350 °C, a sheath gas flow rate of 11 L/min, and a capillary voltage of 3500 V.

3.2. Synthesis and Characterization

3.2.1. 1,4-Product 6a

Chalcone 5a (6.00 g, 25.2 mmol) was dissolved in EtOH (150 mL) where diethylamine (13.0 mL, 126 mmol) and nitromethane (6.80 mL, 126 mmol) were added and the reaction mixture was heated to reflux and allowed to stir overnight. Upon cooling, the resulting mixture was evaporated to dryness and 1,4-product 6a (7.17 g, 95%) was obtained as a tan brown oil. 1H NMR (CDCl3): δ 11.99 (s, 1H), 7.73 (dd, J = 1.6, 7.2 Hz, 1H), 7.48 (dt, J = 1.6, 7.6 Hz, 1H), 7.17 (m, 4H), 6.98 (d, J = 9.2 Hz), 6.91 (t, J = 8.4 Hz), 4.74 (m, 1H), 4.68 (m, 1H), 4.20 (quintet, 1H), 3.48 (m, 2H), 2.33 (s, 3H). 13C NMR (CDCl3): δ 202.9, 162.7, 138.0, 137.0, 135.7, 130.0, 129.7, 127.4, 119.3, 119.2, 118.9, 79.9, 41.3, 39.0, 21.3. HRMS (ESI) for C17H17NO4 [M + Na]+: calcd 322.1050, found 322.1090.

3.2.2. 1,4-Product 6b

Chalcone 5b (5.00 g, 19.7 mmol) was dissolved in EtOH (150 mL) where diethylamine (10.1 mL, 98.3 mmol) and nitromethane (5.26 mL, 98.3 mmol) were added and the reaction mixture was heated to reflux and allowed to stir overnight. Upon cooling, the resulting mixture was evaporated to dryness and 1,4-product 6b (6.03 g, 97%) was obtained as a tan brown oil. The compound’s 1H NMR spectrum matched the known spectrum [18].

3.2.3. Bis(phenolate) Aza-DIPY 7a

1,4–Product 6a (5.00 g, 16.7 mmol) and ammonium acetate (40.0 g, 519 mmol) were dissolved in 1-butanol (75 mL). The reaction mixture was heated to reflux and allowed to stir overnight. Upon cooling to room temperature, the resulting precipitate was collected over filter paper, washed with H2O (200 mL) and EtOH (200 mL), and the solid was allowed to dry in the oven at 85 °C to obtain 7a (1.57 g, 37%) as a brown iridescent solid. 1H NMR (DMSO-d6): δ 8.09 (d, J = 7.6 Hz, 2H), 7.97 (d, J = 8.0 Hz, 4H), 7.70 (s, 2H), 7.38 (dt, J = 1.6, 7.6 Hz, 2H), 7.27 (d, J = 8.0 Hz, 4H), 7.12 (d, J = 8.0 Hz, 2H), 7.03 (t, J = 7.6 Hz, 2H), 2.40 (s, 6H). Due to insolubility, a 13C NMR spectrum could not be obtained. HRMS (ESI) for C34H27N3O2 [M + H]+: calcd 510.2176, found 510.2169.

3.2.4. Bis(phenolate) Aza-DIPY 7b

1,4–Product 6b (5.00 g, 15.9 mmol) and ammonium acetate (40.0 g, 519 mmol) were dissolved in 1-butanol (75 mL). The reaction mixture was heated to reflux and allowed to stir overnight. Upon cooling to room temperature, the resulting precipitate was collected over filter paper, washed with H2O (200 mL) and EtOH (200 mL), and the solid was allowed to dry in the oven at 85 °C to obtain 7b (1.60 g, 37%) as a brown iridescent solid. The compound’s 1H NMR spectrum matched the known spectrum [18].

3.2.5. Bis(phenolate) Aza-BODIPY 1a

To a degassed (30 min) solution of THF, bis(phenolate) aza-DIPY 7a (0.050 g, 0.098 mmol) was added along with N,N-diisopropylethylamine (0.26 mL, 1.5 mmol). BF3·OEt2 (0.24 mL, 2.0 mmol) was added carefully and the mixture was allowed to stir at reflux overnight. After completion by NMR, the mixture was evaporated to dryness and subsequently chromatographed on silica (CH2Cl2) to afford the appropriate bis(phenolate) aza-BODIPY 1a (0.023 g, 45%) as an iridescent green powder. 1H NMR (DMSO-d6): δ 8.14 (d, J = 8.0 Hz, 4H), 8.09 (d, J = 8.0 Hz, 2H), 7.82 (s, 2H), 7.48 (t, J = 8.0 Hz, 2H), 7.39 (d, J = 8.0 Hz, 4H), 7.20 (t, J = 8.4 Hz, 2H), 6.99 (d, J = 8.0 Hz, 2H), 2.41 (s, 6H). 13C NMR (DMSO–d6): δ 155.4, 149.5, 144.0, 141.2, 139.7, 133.9, 129.7, 129.1, 128.7, 127.3, 121.3, 119.7, 118.4, 113.9, 21.1. 11B NMR (DMSO–d6): δ -3.36. HRMS (ESI) for C34H24BN3O2 [M + EtOH + NH4]+: calcd 581.2178, found 581.2717.

3.2.6. Bis(phenolate) Aza-BODIPY 1b

To a degassed (30 min) solution of THF, bis(phenolate) aza-DIPY 7b (0.050 g, 0.092 mmol) was added along with N,N-diisopropylethylamine (0.24 mL, 1.4 mmol). BF3·OEt2 (0.23 mL, 1.8 mmol) was added carefully and the mixture was allowed to stir at reflux overnight. After completion by NMR, the mixture was evaporated to dryness and subsequently chromatographed on silica (CH2Cl2) to afford the appropriate bis(phenolate) aza-BODIPY 1b (0.023 g, 52%) as an iridescent green powder. The compound’s 1H NMR spectrum matched the known spectrum [18].

3.2.7. Bis(phenolate) Aza-ALDIPY 2a

To a solution of pyridine (15 mL), bis(phenolate) aza-DIPY 7a (0.150 g, 0.294 mmol) and Al(acac)3 (0.146 g, 0.441 mmol) were added and the mixture was heated to reflux overnight. Upon cooling to room temperature, hexanes (30 mL) was added to the mixture and cooled to 0 °C. Once cold, the resulting precipitate was collected over filter paper, washed with additional hexanes (30 mL) and evaporated from dryness to afford 2a (0.212 g, 72%) as a dark green solid. 1H NMR (DMSO-d6): δ 8.58 (m, 4H), 7.97 (d, J = 8.0 Hz), 7.78 (m, 2H), 7.70 (dd, J = 2.0, 8.2 Hz, 2H), 7.38 (m, 4H), 7.37 (s, 2H), 7.23 (d, J = 8.0 Hz), 7.11 (dt, J = 0.8, 7.8 Hz, 2H), 6.69 (dd, J = 0.8, 7.8 Hz, 2H), 2.38 (s, 6H). 13C NMR (DMSO-d6): δ 163.8, 156.5, 149.6, 147.0, 140.3, 136.8, 136.1, 131.5, 131.3, 128.6, 128.0, 123.9, 121.0, 119.1, 115.2, 114.2, 20.9. HRMS (ESI) for C34H24AlN3O2 [M + 3H]+: calcd 536.1913, found 536.1911.

3.2.8. Bis(phenolate) Aza-ALDIPY 2b

To a solution of pyridine (15 mL), bis(phenolate) aza-DIPY 7b (0.150 g, 0.277 mmol) and Al(acac)3 (0.124 g, 0.415 mmol) were added and the mixture was heated to reflux overnight. Upon cooling to room temperature, hexanes (30 mL) was added to the mixture and cooled to 0 °C. Once cold, the resulting precipitate was collected over filter paper, washed with additional hexanes (30 mL) and evaporated from dryness to afford 1b (0.134 g, 67%) as a dark green solid. 1H NMR (DMSO-d6): δ 8.57 (m, 4H), 8.00 (d, J = 8.8 Hz, 4H), 7.78 (m, 2H), 7.69 (dd, J = 1.2, 7.8Hz, 2H), 7.39 (m, 4H), 7.32 (s, 2H), 7.10 (dt, J = 1.2, 7.8 Hz, 2H), 6.99 (d, J = 8.8 Hz, 4H), 6.68 (d, J = 8.0 Hz, 2H), 6.56 (t, J = 8.0 Hz, 2H), 3.83 (s, 6H). 13C NMR (DMSO-d6): δ 163.8, 158.9, 156.5, 149.7, 149.9, 140.2, 139.2, 131.5, 130.1, 128.1, 126.8, 123.9, 121.1, 119.2, 115.2, 113.6, 55.2. HRMS (ESI) for C34H24AlN3O4 [M + 4H]+: calcd 569.1890, found 569.1899.

3.2.9. Bis(phenolate) Aza-GADIPY 3a

To a solution of pyridine (15 mL), bis(phenolate) aza-DIPY 7a (0.150 g, 0.294 mmol) and Ga(acac)3 (0.162 g, 0.441 mmol) were added and the mixture was heated to reflux overnight. Upon cooling to room temperature, hexanes (30 mL) was added to the mixture and cooled to 0 °C. Once cold, the resulting precipitate was collected over filter paper, washed with additional hexanes (30 mL) and evaporated from dryness to afford 3a (0.156 g, 72%) as a dark green solid. 1H NMR (DMSO-d6): δ 8.57 (m, 2H), 7.97 (d, J = 8.0 Hz, 4H), 7.79 (m, 2H), 7.74 (dt, J = 2.0, 8.2 Hz, 2H), 7.46 (s, 2H), 7.39 (m, 4H), 7.24 (d, J = 8.0 Hz, 4H), 7.12 (dt, J = 2.0, 7.2 Hz, 2H), 6.73 (dd, J = 1.2, 8.2 Hz, 2H), 6.59 (dt, 1.2, 7.4 Hz, 2H), 2.39 (s, 6H). 13C NMR (DMSO-d6): δ 165.8, 157.0, 149.6, 146.3, 140.4, 137.1, 136.2, 131.6, 131.1, 128.8, 128.7, 128.6, 123.9, 121.9, 117.7, 115.4, 114.4, 21.0. HRMS (ESI) for C34H24GaN3O2 [M + 3H]+: calcd 578.1354, found 578.1347.

3.2.10. Bis(phenolate) Aza-GADIPY 3b

To a solution of pyridine (15 mL), bis(phenolate) aza-DIPY 7b (0.150 g, 0.277 mmol) and Ga(acac)3 (0.152 g, 0.415 mmol) were added and the mixture was heated to reflux overnight. Upon cooling to room temperature, hexanes (30 mL) was added to the mixture and cooled to 0 °C. Once cold, the resulting precipitate was collected over filter paper, washed with additional hexanes (30 mL) and evaporated from dryness to afford 3b (0.151 g, 71%) as a dark green solid. 1H NMR (DMSO-d6): δ 8.57 (m, 4H), 8.00 (d, J = 9.2 Hz, 4H), 7.79 (m, 2H), 7.73 (dt, J = 1.2, 8.2 Hz, 2H), 7.39 (m, 6H), 7.11 (dt, J = 1.6, 7.8 Hz, 2H), 7.00 (d, J = 9.2 Hz, 4H), 6.73 (d, J = 8.0 Hz, 2H), 6.58 (t, J = 8.0 Hz, 2H), 3.84 (s, 6H). 13C NMR (DMSO-d6): δ 165.8, 159.1, 157.0, 149.6, 146.2, 140.3, 136.3, 136.2, 131.6, 130.2, 128.6, 126.5, 124.0, 121.9, 117.8, 115.4, 113.7, 113.6, 55.2. HRMS (ESI) for C34H24GaN3O4 [M + 3H]+: calcd 610.1252, found 610.1278.

3.2.11. Bis(phenolate) Aza-INDIPY 4a

To a solution of pyridine (15 mL), bis(phenolate) aza-DIPY 7a (0.150 g, 0.294 mmol) and In(acac)3 (0.182 g, 0.441 mmol) were added and the mixture was heated to reflux overnight. Upon cooling to room temperature, hexanes (30 mL) was added to the mixture and cooled to 0 °C. Once cold, the resulting precipitate was collected over filter paper, washed with additional hexanes (30 mL) and evaporated from dryness to afford 4a (0.149 g, 65%) as a dark green solid. 1H NMR (DMSO–d6): δ 8.57 (m, 4H), 7.94 (d, J = 8.4 Hz, 4H), 7.84 (dd, J = 1.6, 8.0 Hz, 2H), 7.79 (m, 2H), 7.59 (s, 2H), 7.38 (m, 4H), 7.23 (d, J = 8.0 Hz, 4H), 7.14 (dt, J = 1.6, 7.6 Hz, 2H), 6.78 (d, J = 8.0 Hz, 2H), 6.61 (dt, J = 0.8, 7.4 Hz, 2H), 2.39 (s, 6H). 13C NMR (DMSO–d6): δ 167.2, 158.7, 149.6, 146.0, 141.6, 137.1, 136.2, 131.3, 131.2, 129.9, 129.0, 128.7, 123.9, 123.2, 118.4, 116.0, 115.4, 21.0. HRMS (ESI) for C34H24InN3O2 [M + 3H]+: calcd 624.1137, found 624.1128.

3.2.12. Bis(phenolate) Aza-INDIPY 4b

To a solution of pyridine (15 mL), bis(phenolate) aza-DIPY 7b (0.150 g, 0.277 mmol) and In(acac)3 (0.171 g, 0.415 mmol) were added and the mixture was heated to reflux overnight. Upon cooling to room temperature, hexanes (30 mL) was added to the mixture and cooled to 0 °C. Once cold, the resulting precipitate was collected over filter paper, washed with additional hexanes (30 mL) and evaporated from dryness to afford 4b (0.157 g, 70%) as a dark green solid. 1H NMR (DMSO-d6): δ 8.57 (m, 4H), 7.98 (d, J = 8.0 Hz, 4H), 7.83 (dd, J = 1.6, 8.0 Hz, 2H), 7.79 (m, 2H), 7.53 (s, 2H), 7.38 (m, 4H), 7.13 (dt, J = 1.6, 7.6 Hz, 2H), 6.99 (d, J = 8.8 Hz, 4H), 6.78 (dd, J = 0.8, 8.0 Hz, 2H), 6.61 (dt, J = 0.8, 7.6 Hz, 2H), 3.84 (s, 6H). 13C NMR (DMSO-d6): δ 167.2, 159.1, 158.6, 149.6, 145.9, 141.4, 136.2, 131.2, 130.5, 129.8, 126.7, 123.9, 123.2, 118.5, 115.4, 115.2, 113.6, 55.2. HRMS (ESI) for C34H24InN3O4 [M + 2H]+: calcd 655.0957, found 655.0953.

4. Conclusions

The synthesis and characterization of stable NIR absorbing and emitting bis(phenolate) aza-BODIPYs 1a-b, aza-ALDIPYs 2a-b, aza-GADIPYs, 3a-b, and aza-INDIPYs 4a-b are reported. Single crystal X-ray diffraction data was able to elucidate that heavier group 13 analogues are able to exist as octahedral complexes that can support either THF or pyridine groups as coordinating ligands. Combined, these experimental results lead to the conclusion that the bis(phenolate) aza-DIPY core is a viable choice for chelating elements beyond boron. Future work will explore the structural consequences of chelating the bis(phenolate) aza-DIPY core to both main group and transition metals.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules27238256/s1, Figures S1–S8: molecular orbital plots of 1a-b, 2a-b, 3a-b, and 4a-b, Figures S9–S16: single crystal X-ray diffraction analyses of 1a, 2a-b, 3a-b, 4a-b, and 4a’, Tables S1 and S2: UV-Vis calculations with TD-DFT computations, Tables S3–S6: crystallographic structure data for 1a, 2a-b, 3a-b, 4a-b, and 4a’, cartesian coordinates of 1a, 2a-b, 3a-b, and 4a-b, NMR spectra of 1a, 2a-b, 3a-b, 4a-b, and 4a’. Data structures for 1a, 2a-b, 3a-b, 4a-b, and 4a’ were deposited in the Cambridge Crystallographic Data Center (CCDC) under the deposit numbers 2168300-2168305, 21903914, and 2215010 and can be obtained free of charge via http://www.ccdc.cam.ac.uk.

Author Contributions

A.M.L. and N.T.C.L. performed the synthesis and characterization of all compounds. J.C.K. performed X-ray diffraction work. M.J.N. performed computational analysis. J.J. performed all HRMS work. A.J.B., P.A.L., T.D.M., and D.T.C. supervised the experiments performed and wrote the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the American Chemical Society Petroleum Research Fund (ACS-PRF 61563-UR3) and the National Science Foundation (CHE-1726824, CHE-1950585).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples of all compounds are available from the authors at request.

References

  1. Ge, Y.; O’Shea, D.F. Azadipyrromethenes: From traditional dye chemistry to leading edge applications. Chem. Soc. Rev. 2015, 45, 3846–3864. [Google Scholar] [CrossRef] [PubMed]
  2. Shi, Z.; Han, X.; Hu, W.; Bai, H.; Peng, B.; Ji, L.; Fan, Q.; Li, L.; Hwuang, W. Bioapplications of small molecule Aza-BODIPY: From rational structural design to in vivo investigations. Chem. Soc. Rev. 2020, 49, 7533–7567. [Google Scholar] [CrossRef]
  3. Shamova, L.I.; Zatsikha, Y.V.; Nemykin, V.N. Synthesis pathways for the preparation of the BODIPY analogues: Aza-BODIPYs, BOPHYs, and some other pyrrole-based acyclic chromophores. Chem. Soc. Rev. 2021, 50, 1569–1593. [Google Scholar] [CrossRef] [PubMed]
  4. Pascal, S.; David, S.; Andraud, C.; Maury, O. Near-infrared dyes for two-photon absorption in the short-wavelength infrared: Strategies toward optical power limiting. Chem. Soc. Rev. 2021, 50, 6613–6658. [Google Scholar] [CrossRef] [PubMed]
  5. Bellier, Q.; Pégaz, S.; Aronica, C.; Le Guennic, B.; Andraud, C.; Maury, O. Near-infrared nitrofluorene substituted aza-boron-dipyrromethene dyes. Org. Lett. 2011, 13, 22–25. [Google Scholar] [CrossRef] [PubMed]
  6. Gao, L.; Senevirathna, W.; Sauvé, G. Azadipyrromethene-based conjugated oligomers with near-IR absorption and high electron affinity. Org. Lett. 2011, 13, 5354–5357. [Google Scholar] [CrossRef] [PubMed]
  7. Sheng, W.; Zheng, Y.-Q.; Wu, Q.; Wu, Y.; Yu, C.; Jiao, L.; Hao, E.; Wang, J.-Y.; Pei, J. Synthesis, properties, and semiconducting characteristics of BF2 complexes of β,β-bisphenanthrene-fused azadipyrromethenes. Org. Lett. 2017, 19, 2893–2896. [Google Scholar] [CrossRef] [PubMed]
  8. Sheng, W.; Wu, Y.; Yu, C.; Bobadova-Parvanova, P.; Hao, E.; Jiao, L. Synthesis, crystal structure, and the deep near-infrared absorption/emission of bright azaBODIPY-based organic fluorophores. Org. Lett. 2018, 20, 2620–2623. [Google Scholar] [CrossRef] [PubMed]
  9. Sheng, W.; Chang, F.; Wu, Q.; Hao, E.; Jiao, L.; Wang, J.-Y.; Pei, J. Synthesis and semiconducting characteristics of the BF2 complexes of bisbenzothiophene-fused azadipyrromethenes. Org. Lett. 2020, 22, 185–189. [Google Scholar] [CrossRef]
  10. David, S.; Chang, H.-J.; Lopes, C.; Brännlund, C.; Le Guennic, B.; Berginc, G.; Van Stryland, E.; Bondar, M.V.; Hagan, D.; Jacquemin, D.; et al. Benzothiadiazole-substituted aza-BODIPY dyes: Two-photon absorption enhancement for improved optical limiting performances in the short-wave IR range. Chem. Eur. J. 2021, 27, 3517–3525. [Google Scholar] [CrossRef]
  11. Zarcone, S.R.; Yarbrough, H.J.; Neal, M.J.; Kelly, J.C.; Kaczynski, K.L.; Bloomfield, A.J.; Bowers, G.M.; Montgomery, T.D.; Chase, D.T. Synthesis and photophysical properties of nitrated aza-BODIPYs. New. J. Chem. 2022, 46, 4483–4496. [Google Scholar] [CrossRef]
  12. Kovtun, Y.P.; Yakubovskiy, V.P.; Shandura, M.P. Azadipyrromethene dye with a fully chelated boron atom. Chem. Heterocycl. Compd. 2008, 44, 1298–1299. [Google Scholar] [CrossRef]
  13. Leblebici, S.Y.; Catane, L.; Barclay, D.E.; Olson, T.; Chen, T.L.; Ma, B. Near-infrared azadipyrromethenes as electron donor for efficient planar heterojunction organic solar cells. ACS Appl. Mater. Interfaces 2011, 3, 4469–4474. [Google Scholar] [CrossRef]
  14. Ma, X.; Jiang, X.; Zhang, S.; Huang, X.; Cheng, Y.; Zhu, C. Near-infrared emission on novel bent-core V-shaped conjugated polymers based on the B,O-chelated azadipyrromethene structure. Polym. Chem. 2013, 4, 4396–4404. [Google Scholar] [CrossRef]
  15. Zatsikha, Y.V.; Blesener, T.S.; Goff, P.C.; Healy, A.T.; Swedin, R.K.; Herbet, D.E.; Rohde, G.T.; Chanwanno, K.; Ziegler, C.J.; Belosludov, R.V.; et al. 1,7-Dipyrene-containing aza-BODIPYs: Are pyrene groups effective ligands to promote and direct complex formation with common nanocarbon materials? J. Phys. Chem. C 2018, 122, 27893–27916. [Google Scholar] [CrossRef]
  16. Wang, Y.; Xiao, F.; Shao, T.; Jin, G. A near-infrared zadipyrromethene dye: Photophysical properties under different acidity conditions. Inorg. Chem. Commun. 2020, 116, 107942. [Google Scholar] [CrossRef]
  17. Mori, R.; Asakura, M.; Kobayashi, Y.; Mashimo, H.; Roppongi, M.; Ito, S. Synthesis of π-conjugated asymmetric aza-BODIPYs via nitrosobicyclopyrroles. Tetrahedron Lett. 2022, 96, 153759. [Google Scholar] [CrossRef]
  18. Loudet, A.; Bandichor, R.; Burgess, K.; Palma, A.; McDonnel, S.O.; Hall, M.J.; O’Shea, D.F. B,O-Chelated azadipyrromethenes as near-IR probes. Org. Lett. 2008, 21, 4771–4774. [Google Scholar]
  19. Jimenez, J.C.; Zhou, Z.; Rheingold, A.L.; Parker, S.M.; Sauvé, G. Tuning the properties of azadipyrromethene-based near-infrared dyes using intramolecular BO chelation and peripheral substitutions. Inorg. Chem. 2021, 60, 13320–13331. [Google Scholar] [CrossRef]
  20. Kim, H.; Burghart, A.; Welch, M.B.; Reibenspies, J.; Burgess, K. Synthesis and spectroscopic properties of a new 4-bora-3a,4a-diaza-s-indacene (BODIPY) dye. Chem. Commun. 1999, 35, 1889–1990. [Google Scholar] [CrossRef]
  21. Ikeda, C.; Ueda, S.; Nabeshima, T. Aluminum complexes of N2O2-type dipyrrins: The first hetero-nuclear complexes of metallo-dipyrrins with high fluorescence quantum yields. Chem. Commun. 2009, 45, 2544–2546. [Google Scholar] [CrossRef]
  22. Saikawa, M.; Daicho, M.; Nakamura, T.; Uchida, J.; Yamamura, M.; Nabeshima, T. Synthesis of a new family of ionophores based on aluminum-dipyrrin complexes (ALDIPYs) and their strong recognition of alkaline earth ions. Chem. Commun. 2016, 52, 4014–4017. [Google Scholar] [CrossRef] [PubMed]
  23. Sumiyoshi, A.; Chiba, Y.; Matsuoka, R.; Noda, T.; Nabeshima, T. Efficient luminescent properties and cation recognition ability of heavy group 13 element complexes of N2O2- and N2O4-type dipyrrins. Dalton Trans. 2019, 48, 13169–13175. [Google Scholar] [CrossRef]
  24. Sakamoto, N.; Ikeda, C.; Yamamura, M.; Nabeshima, T. Structural interconversion and regulation of optical properties of stable hypercoordinate dipyrrin-silicon complexes. J. Am. Chem. Soc. 2011, 133, 4726–4729. [Google Scholar] [CrossRef]
  25. Yamamura, M.; Takizawa, H.; Sakamoto, N.; Nabeshima, T. Monomeric and dimeric red/NIR-fluorescence dipyrrin-germanium complexes: Facile monomer-dimer interconversion driven by acid/base reactions. Tetrahedron Lett. 2013, 54, 7049–7052. [Google Scholar] [CrossRef]
  26. Yamamura, M.; Albrecht, M.; Albrecht, M.; Nishimura, Y.; Arai, T.; Nabeshima, T. Red/near-infrared luminescence tuning of group-14 element complexes of dipyrrins based on a central atom. Inorg. Chem. 2014, 53, 1355–1360. [Google Scholar] [CrossRef] [PubMed]
  27. Yamamura, M.; Takizawa, H.; Nabeshima, T. Zweitterionic N2O2-type protonated dipyrrin bearing a phosphonate anionic moiety as a pH-responsive fluorescence indicator. Org. Lett. 2015, 17, 3114–3117. [Google Scholar] [CrossRef]
  28. Nakano, K.; Kobayashi, K.; Nozaki, K. Tetravalent metal complexes as a new family of catalysts for copolymerization of epoxides with carbon dioxide. J. Am. Chem. Soc. 2011, 133, 10720–10723. [Google Scholar] [CrossRef]
  29. Rausaria, S.; Kamadulski, A.; Rath, N.P.; Bryant, L.; Chen, Z.; Salvemini, D.; Neumann, W.L. Manganese(III) complexes of bis(hydroxyphenyl)dipyrromethenes are potent orally active peroxynitrite scavengers. J. Am. Chem. Soc. 2011, 133, 4200–4203. [Google Scholar] [CrossRef] [Green Version]
  30. El Ghachtouli, S.; Wójcik, K.; Copey, L.; Szydlo, F.; Framery, E.; Goux-Henry, C.; Billon, L.; Charlot, M.-F.; Guillot, R.; Andrioletti, B.; et al. Dipyrrinphenol-Mn(III) complex: Synthesis, electrochemistry, spectroscopic characterization and reactvity. Dalton Trans. 2011, 40, 9090–9093. [Google Scholar] [CrossRef]
  31. Lecarme, L.; Chiang, L.; Moutet, J.; Leconte, N.; Philouze, C.; Jarjayes, O.; Storr, T.; Thomas, F. The structure of a one-electron oxidized Mn(III)-bis(phenolate)dipyrrin radical complex and oxidation catalysis control via ligand-centered redox activity. Dalton Trans. 2016, 45, 16325–16334. [Google Scholar] [CrossRef] [PubMed]
  32. Kochem, A.; Chiang, L.; Baptiste, B.; Philouze, C.; Leconte, N.; Jarjayes, O.; Storr, T.; Thomas, F. Ligand-centered redox activity of cobalt(II) and nickel(II) bis(phenolate)-dipyrrin complexes. Chem. Eur. J. 2012, 18, 14590–14593. [Google Scholar] [CrossRef] [PubMed]
  33. Yamamura, M.; Takizawa, H.; Gobo, Y.; Nabeshima, T. Stable neutral radicals of planar N2O2-type dipyrrin platinum complexes: Hybrid radicals of the delocalized organic π-orbital and platinum d-orbital. Dalton Trans. 2016, 45, 6834–6838. [Google Scholar] [CrossRef] [PubMed]
  34. Moutet, J.; Philouze, C.; du Moulinet d’Hardemare, A.; Leconte, N.; Thomas, F. Ni(II) complexes of the redox-active bis(2-aminophenyl)dipyrrin: Structural, spectroscopic, and theoretical characterization of three members of an electron transfer series. Inorg. Chem. 2017, 56, 6380–6392. [Google Scholar] [CrossRef]
  35. Kunert, R.; Philouze, C.; Jarjayes, O.; Thomas, F. Stable M(II)-radicals and nickel(III) complexes of a bis(phenol) N-heterocyclic carbene chelated to group 10 metal ions. Inorg. Chem. 2019, 58, 8030–8044. [Google Scholar] [CrossRef]
  36. Shan, W.; Desbois, N.; Pacquelet, S.; Brandès, S.; Rousselin, Y.; Conradie, J.; Ghosh, A.; Gros, C.P.; Kadish, K.M. Ligand noninnocence in cobalt dipyrrin-bisphenols: Spectroscopic, electrochemical, and theoretical insights indicating an emerging analogy with corroles. Inorg. Chem. 2019, 58, 7677–7689. [Google Scholar] [CrossRef]
  37. Di Natale, C.; Gros, C.P.; Paolesse, R. Corroles at work: A small macrocycle for great applications. Chem. Soc. Rev. 2022, 51, 1277–1335. [Google Scholar] [CrossRef]
  38. Verma, P.; Truhlar, D.G. Status and Challenges of Density Functional Theory. Trends Chem. 2020, 2, 302–318. [Google Scholar] [CrossRef]
  39. Frisch, M.J.; Trucks, G.W.; Schlegel, H.B.; Scuseria, G.E.; Robb, M.A.; Cheeseman, J.R.; Scalmani, G.; Barone, V.; Petersson, G.A.; Nakatsuji, H.; et al. Gaussian 16; Revision C.01; Gaussian, Inc.: Wallingford, CT, USA, 2016. [Google Scholar]
  40. Dunning, T.H., Jr. Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen. J. Chem. Phys. 1989, 90, 1007–1023. [Google Scholar] [CrossRef]
  41. Papajak, E.; Zheng, J.; Xu, X.; Leverentz, H.R.; Truhlar, D.G. Perspectives on Basis Sets Beautiful: Seasonal plantings of diffuse basis functions. J. Chem. Theory Comput. 2011, 7, 3027–3034. [Google Scholar] [CrossRef] [PubMed]
  42. Miertus, S.; Scrocco, E.; Tomasi, J. Electrostatic interaction of a solute with a continuum. A direct utilization of AB initio molecular potentials for the prevision of solvent effects. Chem. Phys. 1981, 55, 117–129. [Google Scholar] [CrossRef]
  43. Menucci, B. Polarizable continuum model. Wiley Interdiscip. Rev. Comput. Mol. Sci. 2012, 2, 386–404. [Google Scholar] [CrossRef]
  44. Wadt, W.R.; Hay, P.J. Ab initio effective core potentials for molecular calculations. Potentials for main group elements Na to Bi. J. Chem. Phys. 1985, 82, 284–298. [Google Scholar] [CrossRef]
  45. Hay, P.J.; Wadt, W.R. Ab initio effective core potentials for molecular calculations. Potentials for K to Au including the outermost core orbitals. J. Chem. Phys. 1985, 82, 298–310. [Google Scholar] [CrossRef]
  46. Teets, T.S.; Updegraff III, J.B.; Esswein, A.J.; Gray, T.G. Three-coordinate, phosphine-ligated azadipyrromethene complexes to univalent group 11 metals. Inorg. Chem. 2009, 48, 8134–8144. [Google Scholar] [CrossRef]
  47. Deligonul, N.; Gray, T.G. Azadipyrromethene complexes of d8 metal centers: Rhodium(I), iridium(I), palladium(II), and platinum(II). Inorg. Chem. 2013, 52, 13048–13057. [Google Scholar] [CrossRef]
Molecules 27 08256 g001 550
Figure 1. Aza-DIPY (A), aza-BODIPY (B), bis(phenolate) aza-DIPY (C), bis(phenolate) DIPY (D), bis(phenolate) DIPY main group chelates (E) and bis(phenolate) transition metal chelates (F).
Figure 1. Aza-DIPY (A), aza-BODIPY (B), bis(phenolate) aza-DIPY (C), bis(phenolate) DIPY (D), bis(phenolate) DIPY main group chelates (E) and bis(phenolate) transition metal chelates (F).
Molecules 27 08256 g001
Molecules 27 08256 sch001 550
Scheme 1. Synthesis of bis(phenolate) aza-DIPY cores 7a-b.
Scheme 1. Synthesis of bis(phenolate) aza-DIPY cores 7a-b.
Molecules 27 08256 sch001
Molecules 27 08256 sch002 550
Scheme 2. Synthesis of bis(phenolate) aza-BODIPYs 1a-b, aza-ALDIPYs 2a-b, aza-GADIPYs 3a-b, and aza-INDIPYs 4a-b.
Scheme 2. Synthesis of bis(phenolate) aza-BODIPYs 1a-b, aza-ALDIPYs 2a-b, aza-GADIPYs 3a-b, and aza-INDIPYs 4a-b.
Molecules 27 08256 sch002
Molecules 27 08256 g002 550
Figure 2. Molecular structure of 1a. Ellipsoids are drawn at the 40% probability level. Hydrogen atoms have been removed for clarity.
Figure 2. Molecular structure of 1a. Ellipsoids are drawn at the 40% probability level. Hydrogen atoms have been removed for clarity.
Molecules 27 08256 g002
Molecules 27 08256 g003 550
Figure 3. Molecular structure of 2a. Ellipsoids are drawn at the 40% probability level. Hydrogen atoms have been removed for clarity.
Figure 3. Molecular structure of 2a. Ellipsoids are drawn at the 40% probability level. Hydrogen atoms have been removed for clarity.
Molecules 27 08256 g003
Molecules 27 08256 g004 550
Figure 4. Molecular structure of 4a’. Ellipsoids are drawn at the 40% probability level. Axial THF groups and hydrogen atoms have been removed for clarity.
Figure 4. Molecular structure of 4a’. Ellipsoids are drawn at the 40% probability level. Axial THF groups and hydrogen atoms have been removed for clarity.
Molecules 27 08256 g004
Molecules 27 08256 g005 550
Figure 5. HOMO-1, HOMO, LUMO, and LUMO+1 plots of 1a, 2a, 3a, and 4a. Calculations were performed at the B3LYP/jul-cc-pVDZ level of theory for 1a, 2a, and 3a and the B3LYP/LanL2DZ level of theory for 4a with MeOH as the implicit solvent for all compounds.
Figure 5. HOMO-1, HOMO, LUMO, and LUMO+1 plots of 1a, 2a, 3a, and 4a. Calculations were performed at the B3LYP/jul-cc-pVDZ level of theory for 1a, 2a, and 3a and the B3LYP/LanL2DZ level of theory for 4a with MeOH as the implicit solvent for all compounds.
Molecules 27 08256 g005
Molecules 27 08256 g006 550
Figure 6. Absorption spectra of 1a-b, 2a-b, 3a-b, and 4a-b in DMSO. All spectra are recorded at a concentration of 10 μM.
Figure 6. Absorption spectra of 1a-b, 2a-b, 3a-b, and 4a-b in DMSO. All spectra are recorded at a concentration of 10 μM.
Molecules 27 08256 g006
Molecules 27 08256 g007 550
Figure 7. Emission spectra of 1a-b, 2a-b, 3a-b, and 4a-b in DMSO. All spectra are recorded at a concentration of 10 μM. λabs was used as the excitation wavelength for λem.
Figure 7. Emission spectra of 1a-b, 2a-b, 3a-b, and 4a-b in DMSO. All spectra are recorded at a concentration of 10 μM. λabs was used as the excitation wavelength for λem.
Molecules 27 08256 g007
Table
Table 1. Photophyiscal and computational data for bis(phenolate) aza-DIPYs 1a-b, 2a-b, 3a-b, and 4a-b.
Table 1. Photophyiscal and computational data for bis(phenolate) aza-DIPYs 1a-b, 2a-b, 3a-b, and 4a-b.
Photophysical aComputational d
Compoundλabslog εEgap bλem cSS c (nm)SS c (cm−1)ΦcEHOMOELUMOEGapλGap
1a7284.501.717471935013.7−5.56−3.661.90652
1b7324.471.70751193458.8−5.21−3.431.78695
2a7314.481.70766356257.5−5.00−3.201.80689
2b7284.561.71762346137.0−4.97−3.171.80689
3a7344.581.69774407046.1−5.01−3.211.80688
3b7324.711.70770386748.4−4.98−3.171.81688
4a7144.671.74752387080.3−5.01−3.141.87661
4b7134.451.74746376200.7−4.983.111.87665
a Spectra were obtained in MeOH at 10 μM. Wavelengths are in nm. b Optical HOMO/LUMO gap was determined at λabs. c λabs was used as the excitation wavelength for λem. Stokes shifts (SS) are measured in both nm and cm−1. Quantum yields are measured using an internal integrating sphere in ambient air at room temperature and are reported in %. d Calculations were performed using B3LYP/jul-cc-pVDZ for 1a-b, 2a-b, and 3a-b with MeOH as implicit solvent; B3LYP/LanL2DZ was used for 4a-b with MeOH as implicit solvent.
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Lane, A.M.; Luong, N.T.C.; Kelly, J.C.; Neal, M.J.; Jamrom, J.; Bloomfield, A.J.; Lummis, P.A.; Montgomery, T.D.; Chase, D.T. Synthetic Exploration of Bis(phenolate) Aza-BODIPYs and Heavier Group 13 Chelates. Molecules 2022, 27, 8256. https://doi.org/10.3390/molecules27238256

AMA Style

Lane AM, Luong NTC, Kelly JC, Neal MJ, Jamrom J, Bloomfield AJ, Lummis PA, Montgomery TD, Chase DT. Synthetic Exploration of Bis(phenolate) Aza-BODIPYs and Heavier Group 13 Chelates. Molecules. 2022; 27(23):8256. https://doi.org/10.3390/molecules27238256

Chicago/Turabian Style

Lane, Aiden M., Ny T. C. Luong, Jordan C. Kelly, Martin J. Neal, Jeremiah Jamrom, Aaron J. Bloomfield, Paul A. Lummis, Thomas D. Montgomery, and Daniel T. Chase. 2022. "Synthetic Exploration of Bis(phenolate) Aza-BODIPYs and Heavier Group 13 Chelates" Molecules 27, no. 23: 8256. https://doi.org/10.3390/molecules27238256

APA Style

Lane, A. M., Luong, N. T. C., Kelly, J. C., Neal, M. J., Jamrom, J., Bloomfield, A. J., Lummis, P. A., Montgomery, T. D., & Chase, D. T. (2022). Synthetic Exploration of Bis(phenolate) Aza-BODIPYs and Heavier Group 13 Chelates. Molecules, 27(23), 8256. https://doi.org/10.3390/molecules27238256

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