Luminescent Behavior of Liquid–Crystalline Gold(I) Complexes Bearing a Carbazole Moiety: Effects of Substituent Bulkiness

Abstract

Organometallic materials that exhibit white luminescence in condensed phases are of considerable interest for lighting and display applications. Herein, new carbazole-based Au(I) complexes containing an isocyanide group and a long pentyl chain were synthesized. The complex with an unsubstituted carbazole moiety exhibited a white emission at room temperature as well as nematic liquid crystalline behavior. Color tunability from white to blue was achieved when bulkier substituents were introduced at the 3 and 6 positions of the carbazole moiety. Furthermore, all complexes possessed long phosphorescence lifetimes in the crystal state. The proposed design framework provides new opportunities for practical applications using luminescent organometallic molecules.

1. Introduction

Luminescent molecules are of importance in both materials and life sciences [1,2,3]. In particular, white-light-emitting organometallic materials have attracted increasing attention owing to their potential applications in lighting devices and display media. However, the generation of white light commonly requires the simultaneous emission of the three primary RGB colors (red, green, and blue) or at least two complementary colors [4]. Moreover, achieving white room temperature phosphorescence (RTP) from a single molecule is highly challenging because the different radiation pathways involved in the emission process can affect each other [5].

Although most luminescent organometallic molecules exhibit efficient photoluminescence in dilute solutions, aggregation in condensed phases (e.g., crystals and solid films) typically results in partial or complete quenching of their luminescence. This phenomenon, known as aggregation-caused quenching (ACQ), is common in organometallic molecules with π-electron systems and prevents their practical use. Owing to the essential contribution of molecular aggregation to luminescence properties, aggregated structures play an important role in luminescence behavior [5,6,7,8,9,10]. Liquid crystals (LCs) are a unique class of soft materials that flow like liquids and possess a long-range orientational order similar to that of crystals [7,11,12,13,14]. LCs have the potential to control the aggregated structure of luminescent materials. Moreover, the material properties and aggregated structures of LC molecules can be influenced by various external stimuli. The molecular skeleton of an LC molecule generally consists of a rod-like rigid core and flexible chains, such as alkoxy and alkyl chains. Various aggregation-induced emission (AIE)-active LC systems have been developed [15,16].

Au(I) complexes show very interesting behavior because of their metallophilic d¹⁰–d¹⁰ interactions. The emission observed in Au(I) complexes results from an interatomic Au–Au interaction; thus, Au(I) complexes exhibit the luminescence mainly from their aggregates and have been known as the AIE-active material. The Au–Au interaction as well as the luminescence behavior can be tuned via not only modification of the chemical structure around Au atoms but also by controlling the aggregated structures [5]. For instance, previously synthesized Au(I) complexes with isocyanides and phenylacetylene ligands exhibited interesting AIE properties [16]. Furthermore, our group reported a biphenyl ring system with an LC phase, where luminescence was observed in both the crystal and LC phases [14].

Carbazole-based luminescent materials are valuable candidates for photoelectronic devices. Carbazole units are suitable building blocks for functional materials in organometallic light-emitting diodes because of their high triplet energy and good thermal stability [17]. Herein, we developed a carbazole-based Au(I) complex with a flexible pentyl isocyanide group. This complex shows a white emission at room temperature (rt) along with a nematic (N) LC phase. Color tunability from white (Cbz-H) to blue (Cbz-t-Bu) was also realized by changing the substituents at the 3 and 6 positions of the carbazole moiety.

2. Materials and Methods

2.1. Materials

Compound 1-R was prepared by following the reported procedure [18]. Complexes Cbz-H, Cbz-Br, and Cbz-t-Bu were prepared via a one-step synthetic route using compounds 1-R. The reagents and solvents used for the synthesis were obtained from commercial sources and used without further purification. ¹H and ¹³C NMR spectra were recorded using a JEOL ECS-400 spectrometer (JEOL, Tokyo, Japan) (400 MHz for ¹H and 100 MHz for ¹³C) in CDCl₃ (Figures S1–S3 for ¹H NMR, Figures S4–S6 for ¹³C NMR). Chemical shifts are reported in parts per million (ppm), using the residual ¹H or ¹³C in the NMR solvent as an internal reference. IR spectra were obtained using the KBr disk method with a FT/IR-4100 spectrometer (JASCO, Tokyo, Japan), and all spectra are reported in wavenumbers (cm⁻¹). Elemental analysis (C, H, and N) was performed using a Micro Corder JM10 analyzer (J-Science, Tokyo, Japan). Electrospray ionization mass spectrometry (ESI-MS) was carried out using a Bruker micrOTOF II instrument (JEOL, Tokyo, Japan).

2.1.1. Synthesis of Cbz-H

Compound 1-H (0.30 g, 1.5 mmol) and (tht) AuCl (tht: tetrahydrothiophene) (0.47 g, 1.5 mmol) were dissolved in 10 mL of CH₂Cl₂. Then, a methanol (10 mL) solution of CH₃COONa (0.61 g, 7.2 mmol) was added dropwise, and the resulting mixture was stirred for 2 h at rt. Subsequently, 1-pentyl isocyanide (0.071 g, 0.73 mmol) in CH₂Cl₂ (7 mL) was added and the mixture was stirred for a further 1 h at rt. The reaction mixture was then filtered through Celite and evaporated under vacuum. The crude product was purified by silica gel column chromatography using CH₂Cl₂ as the mobile phase and then recrystallized in a CH₂Cl₂/n-hexane mixed solvent system (1:2, v/v) to obtain 0.28 g, 0.57 mmol of the title complex as white crystal in 78% yield, mp 156 °C. ¹H NMR (400 MHz, CDCl₃, δ): 8.06–8.04 (d, J = 7.5 Hz, 2H, ArH), 7.56–7.54 (dd, J = 7.5 Hz, 2H, ArH), 7.44 (d, J = 7.5 Hz, 2H, ArH), 7.25–7.20 (m, J = 7.5 Hz, 2H, ArH), 5.15–5.12 (s, 2H, ArNCH), 3.52–3.49 (t, 2H, NCH), 1.73 (s, J = 7.1 Hz, 2H, CH₂), 1.36–1.2 (m, J = 7.1 Hz, 2H, CH₂), 0.95–0.87 (t, J = 8 Hz 3H, CH₃). ¹³C NMR (400 MHz, CDCl₃, δ): 140.04 (9-C in carbazole), 125.78 (2,7-C in carbazole), 123.09 (Au–C$\equiv$N), 120.23 (3,6-C in carbazole), 119.10 (4-C in carbazole), 114.84 (4-C in carbazole), 109.29 (1,8-C in carbazole), 77.13 (Au–C$\equiv$C), 43.83 (N–CH₂), 33.44 (N–CH₂ in carbazole), 28.22 (NCH₂CH₂), 27.56 (NCH₂CH₂CH₂), 21.71 (CH₂CH₃), 13.79 (CH₂CH₃).

FTIR (KBr, cm⁻¹): 3049, 2953, 2248, 1460. ESI-MS m/z: [M + H]⁺ calcd for C₂₁H₂₁AuN₂, 499.14; found, 499.11. Anal calcd for C₂₁H₂₁AuN₂: C, 50.61; H, 4.25; Au, 39.52; N, 5.62; found: C, 50.43; H, 4.12; N, 5.51.

2.1.2. Synthesis of Cbz-Br

The same procedure was followed using 1-Br for the synthesis of Cbz-Br to obtain the title complex as a white solid in 84% yield, mp 168 °C. ¹H NMR (400 MHz, CDCl₃, δ): 8.11–8.10 (d, J = 7.5 Hz, 2H, ArH), 7.56–7.53 (dd, J = 7.5 Hz, 2H, ArH), 7.44–7.42 (d, J = 7.5 Hz, 2H, ArH), 5.09 (s, 2H, ArNCH), 3.56–3.52 (s, 2H, NCH), 1.76 (s, J = 7.1 Hz, 2H, CH₂), 1.39–1.32 (m, J = 7.1 Hz, 2H, CH₂), 0.92–0.89 (t, J = 8 Hz 3H, CH₃). ¹³C NMR (400 MHz, CDCl₃, δ): 139.05 (9-C in carbazole), 129.13 (2,7–C in carbazole), 123.84 (Au–C$\equiv$N), 123.17 (3,6-C–Br in carbazole), 115.72 (4-C in carbazole), 112.34 (4-C in carbazole), 111.13 (1,8-C in carbazole), 77.11 (Au–C$\equiv$C), 40.01 (N–CH₂), 33.79 (N–CH₂ in carbazole), 33.41 (NCH₂CH₂), 27.77 (NCH₂CH₂CH₂), 21.75 (CH₂CH₃), 13.80 (CH₂CH₃). FTIR (KBr, cm⁻¹): 3073, 2957, 2245, 1472, 645. ESI-MS m/z: [M]⁺ calcd for C₂₁H₁₉AuBr₂N₂, 653.96; found, 653.46. Anal calcd for C₂₁H₁₉AuBr₂N₂: C, 38.44; H, 2.92; Au, 30.02; N, 4.27; Br, 24.35 found: C, 38.27; H, 2.79; N, 4.21.

2.1.3. Synthesis of Cbz-t-Bu

The same procedure was followed using 1-t-Bu for the synthesis of Cbz-t-Bu to obtain the title complex as white solid in 81% yield, mp 190 °C. ¹H NMR (400 MHz, CDCl₃, δ): 8.04 (d, J = 7.5 Hz, 2H, ArH), 7.50–7.47 (t, J = 7.5 Hz, 2H, ArH), 7.45–7.42 (d, J = 7.5 Hz, 2H, ArH), 5.09 (s, 2H, ArNCH), 3.43–3.40 (t, 2H, NCH), 1.53 (s, J = 7.1 Hz,2H, CH₂), 1.42 (s, 18H, CH₃), 1.29–1.28 (m, J = 7.1 Hz, 4H, CH₂), 0.87 (t, J = 8 Hz 3H, CH₃). ¹³C NMR (400 MHz, CDCl₃, δ): 141.72 (C(CH₃)₃), 138.60 (9-C in carbazole), 123.42 (Au–C$\equiv$N), 122.98 (2,7-C in carbazole), 116.17 (4-C in carbazole), 114.45 (4a-C in carbazole), 108.59 (1,8-C in carbazole), 77.12 (Au–C$\equiv$C), 43.86 (N–CH₂), 34.74 (N–CH₂ in carbazole), 33.41 (NCH₂CH₂), 32.16 (C(CH₃)₃), 27.61 (NCH₂CH₂CH₂), 21.729 (CH₂CH₃), 13.79 (CH₂CH₃). FTIR (KBr, cm⁻¹): 3044, 2953, 2245, 1477. ESI-MS m/z: [M + H]⁺ calcd for C₂₉H₃₇AuN₂, 611.27; found, 611.26. Anal calcd for C₂₉H₃₇AuN₂: C, 57.05; H, 6.11; Au, 32.26; N, 4.59; found: C, 56.94; H, 6.05; N, 4.37.

2.2. X-ray Crystallography

A single crystal was prepared via slow evaporation in a mixed solvent system (CH₂Cl₂/n-hexane). The obtained crystal was mounted on a glass fiber. The omega scanning technique was applied to collect the reflection data using a Bruker D8 goniometer (Bruker, Millerica, MA, USA) with monochromatized MoKα radiation (λ = 0.71075 Å). To estimate the actual crystal structure of the synthesized materials, measurements were performed at ambient temperature (296 K). The initial structure of the unit cell was determined via a direct method using APEX2. The structural model was refined by the full-matrix least-squares method using SHELXL-2014/6. All calculations were performed using the SHELXL software [19,20]. The crystallographic data for the synthesized compounds are summarized in the Supplementary Materials, and the indexed data were deposited in the Cambridge Crystallographic Data Centre (CCDC) database (CCDC 2160379 for Cbz-H). These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html accessed on 21 March 2022 (or from the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; Fax: [phone]; E-mail: [email protected]).

2.3. Phase Transition Behavior

LC behavior as well as the melting points of the complexes were observed via polarized optical microscopy (POM) using an Olympus BX51 (Tokyo, Japan) microscope equipped with a hot stage (Instec HCS302 hot stage with an mK1000 controller). To assess the thermochemical stability, thermogravimetric–differential thermal analysis (TG/DTA) was carried out using a DTG-60AH instrument (Shimadzu, Kyoto, Japan) at a heating rate of 5.0 °C min⁻¹ in air. The thermodynamic parameters were determined via differential scanning calorimetry (DSC; SII X-DSC7000, Tokyo, Japan) at a scanning rate of 3.0 °C min⁻¹.

2.4. Photophysical Properties

UV–Vis absorption spectra were recorded on a JASCO V-550 (JASCO, Tokyo, Japan) absorption spectrometer, and steady-state photoluminescence spectra were recorded on a Hitachi F-7000 fluorescence spectrometer (Hitachi, Tokyo, Japan) with an R928 photomultiplier (Hamamatsu Photonics, Hamamatsu, Japan) as the detector. Photoluminescence lifetimes were measured at various excitation wavelengths using a Quantaurus-Tau photoluminescence lifetime measurement system (C1136-21, Hamamatsu Photonics, Hamamatsu, Japan).

3. Results and Discussion

3.1. Synthesis and Characterization of Complex Cbz-R

Complex Cbz-R were synthesized according to the synthetic route shown in Figure 1. After purification, all complexes were characterized via ¹H NMR spectroscopy, mass spectrometry, and elemental analysis. All the analytical data (presented in the Materials and Methods section) confirmed that the desired products were obtained.

Complex Cbz-H furnished single crystals suitable for X-ray crystallography via a slow evaporation technique using the mixed solvent system; however, suitable single crystals were not obtained for other complexes. To determine the molecular structure of Cbz-H, single-crystal X-ray diffraction (XRD) was performed at room temperature. The obtained crystal structure is shown in Figure 2. The corresponding crystallographic data and key structural parameters are summarized in Tables S1 and S2, respectively. According to the crystal structure, Cbz-H belongs to the triclinic space group Pī. The C1–Au–C2 bond angle is ~180° [21], and molecular packing gives a Au–Au bond distance of 6.4 Å, which suggests the absence of aurophilic interactions between the molecules. We have previously reported the structure of a similar Au(I) complex that has less-hindered 4-ethynylbiphenyl and alkyl isocyanide ligands [14]. This complex also crystallized in triclinic space group Pī, and the C1–Au–C2 bond angles were the same as in Cbz-H, i.e., ~180°; however, the intermolecular Au–Au distance was 3.46 Å, which confirms the presence of intermolecular aurophilic interactions in the crystal. The longer intermolecular distance between Au atoms in Cbz-H is due to the bulkier carbazolylmethyl unit. Additionally, the face of the carbazole moiety is orthogonal to the C1–Au–C2 axis. We consider that this orthogonal structure of the bulky carbazole moiety resulted in the longer intermolecular Au–Au distance in the Cbz-H complex.

3.2. Thermal Behavior of Complex Cbz-R

The thermal stability of complex Cbz-R was analyzed using TG/DTA measurements (Figure S7). The thermal decomposition temperature (T_dec) is defined as the temperature at which 5% weight loss occurs [22,23]. The TG/DTA thermograms show that all of the synthesized complexes are thermally stable up to 170–220 °C. The 12–15% weight loss observed near T_dec can be attributed to the loss of the isocyanide moieties. The second weight loss may be due to the removal of the propargyl moiety. The amount of residual ash obtained at 600 °C corresponds to the percentage of gold(I) in the complex.

The thermodynamic behavior was evaluated using DSC and POM techniques. The DSC thermogram of Cbz-H suggests LC behavior during heating (Figure S8). To further investigate this behavior, POM images were collected to examine the optical texture of Cbz-H (Figure 3). A schlieren texture was obtained at 93 °C, which confirmed that the observed phase for Cbz-H is the N phase [14,16]. In the DSC thermogram, a small endothermic peak was observed at 73 °C during the heating process, and an isotropic phase was achieved at 118 °C. The N phase was observed between these temperatures. However, in the cooling process of the DSC thermograms, no exothermic peak was observed. Through POM observation, we confirmed that the phase transition from the isotropic liquid to the amorphous solid occurred at ~80 °C, and that once Cbz-H was melted, the complex did not exhibit crystalline and LC phases.

In contrast, no LC phases were observed for complexes Cbz-Br and Cbz-t-Bu at any temperature. In Cbz-Br and Cbz-t-Bu, the substituents attached at the 3 and 6 positions of the carbazole moiety are bulkier than H atoms (i.e., Br atoms or t-butyl groups). As the steric hindrance of these bulky substituents disturbs the LC alignment, only Cbz-H shows an LC phase [24,25,26].

3.3. Solution and Solid-State Photoluminescence Properties of Complex Cbz-R

The UV–vis absorption spectra of compounds Cbz-H, Cbz-Br, and Cbz-t-Bu were recorded in dilute CH₂Cl₂ solution. Cbz-H (2.1 × 10⁻⁵ mol L⁻¹), Cbz-Br (4.3 × 10⁻⁵ mol L⁻¹), and Cbz-t-Bu (3.3 × 10⁻⁵ mol L⁻¹) exhibited absorption bands at 293, 310, and 297 nm, respectively (Figure 4a), which may be attributable to a metal-to-ligand charge transfer (MLCT) transition or a ligand-based π–π* transition [5,27,28]. All complexes also showed smaller absorption peaks with a vibronic structure at 340–360 nm. This small absorption band is known as the n–π* transition of the carbazole unit. Additionally, it has also been reported that the absorption band at this wavelength originated from the transition from the alkynyl-to-isocyanide ligand-to-ligand charge transfer [29]. Thus, we can consider that both transitions are overlapped in this absorption band.

All complexes showed monomeric-type emissions with a vibronic structure at ~350 nm in dilute solutions (Figure 4b). Similar spectral shapes were observed at this wavelength in all complexes; however, in Cbz-t-Bu and Cbz-Br, the vibronic bands were slightly broadened. The emission peaks of Cbz-H and Cbz-t-Bu were observed at 375 and 380 nm, respectively, whereas that of Cbz-Br was slightly red-shifted to approximately 400 nm. Although the luminescence behaviors of all complexes were comparable in the dilute solution, significant differences were observed in the solid state.

The emission spectra of the complexes were obtained in the crystal state (Figure 5a). Each complex exhibited a peak in the region of 370–400 nm, which is similar to the emission peak in the solution state and can be considered a monomeric-type fluorescence emission. Furthermore, Cbz-Br and Cbz-t-Bu exhibited additional emission peaks at approximately 430 and 450 nm. Thus, the emission of these complexes in the crystal state is more structured than that in the crystal state and extends into the blue region. Furthermore, Cbz-Br exhibits a brighter blue emission than Cbz-t-Bu owing to the heavy-atom effect [30]. In contrast, the emission of Cbz-H covers the entire spectral range, including a prominent peak at approximately 550 nm due to crystallization-induced phosphorescence [31,32,33]. Consequently, Cbz-H shows a white emission. As shown by the CIE plot (Figure 5b), Cbz-H, Cbz-Br, and Cbz-t-Bu show white, bluish-white, and bluish emissions, respectively. Thus, color tunability from white to blue was successfully achieved by changing the substituents at the 3 and 6 positions of the carbazole moiety. The color tunability of these complexes can be attributed to the introduction of bulky substituents, which inhibits free rotation of the luminophore.

To further clarify the photophysical properties of these complexes, the lifetimes and luminescence quantum yields were measured in the crystal state at room temperature (Figure S13–S15, Table S3). The decay profiles were well-fitted using a biexponential function. In all complexes, it was confirmed that the emission band at <400 nm was fluorescence due to the S₁–S₀ transition. In Cbz-H, the emission at 450 nm decayed on a nanosecond timescale, indicating that the emission bands in this wavelength region can be also assigned to fluorescence emitted from a higher excited state (S_n). In contrast, the emission at 550 nm contains a component with a lifetime of the microsecond timescale, suggesting that a part of this band can be attributed to phosphorescence. Interestingly, in Cbz-Br, emissions at 450 nm and 550 nm decayed on a microsecond timescale, and both emission bands can be attributed to phosphorescence due to the heavy-atom effects of the Br atoms. In Cbz-t-Bu, contrary to Cbz-H, phosphorescence was observed at 450 nm; however, fluorescence mainly contributed to the emission at 550 nm. In the Cbz-t-Bu crystal, we consider that phosphorescence from monomers of the complex was observed at 450 nm, and that fluorescence from the aggregates, i.e., excimer-type fluorescence, was observed at ~550 nm.

As shown in Table S3, the complexes had luminescence quantum yields (Φ) of 0.34–2.3% in the crystal state, even at room temperature in air. The excitation spectra of the crystals (Figure S9) revealed an excitation band at shorter wavelengths (320–340 nm), which is assigned to the S₀–S_n transition. The excitation spectra of all complexes showed an additional band at longer wavelengths (380–430 nm). We previously reported that similar Au(I) complexes with ethynyl and isocyanide ligands showed an efficient direct S₀–T_n transition owing to aggregation; that is, the S₀–T_n transition is enhanced by not only the heavy-atom effect but also the aggregation of Au(I) complexes. Thus, we conclude that the longer-wavelength band in the excitation spectra can be assigned to a spin-forbidden direct S₀–T_n transition. Because the spin-forbidden transition occurs efficiently, the complexes show intense RTP in crystals under ambient conditions [14,34].

The photoluminescence of Cbz-H in the LC phase was also examined to determine the effects of the phase structure on luminescence behavior (Figure S10). The emission intensity levels were recorded at various temperatures. The emission intensity gradually decreased upon heating from rt to the LC phase, which indicates that a nonradiative decay was promoted by thermal motion of the Au(I) complex [14,16,22]. The emission intensity was recovered in the cooling process; however, it still remained lower than that of the original crystal before heating. This behavior is attributed to the crystal size dependence of the aggregation-enhanced spin-forbidden transition [14,34].

To obtain further insight into the luminescence properties, photophysical studies were performed in a mixed water–tetrahydrofuran (THF) system with various volume fractions of water. As all compounds showed good solubility in THF and very poor solubility in water, increasing the volume fraction of water induced aggregation. As shown in Figure S11, when the water concentration increased, the luminescence intensity decreased because of molecular aggregation. These results demonstrate that complexes of Cbz-R exhibit ACQ behavior [7]. In the case of Cbz-H, the same spectral shape was observed in the mixed solvent with a high water fraction as that in pure THF; namely, the spectral shape of aggregates in the mixed solvent was different from those in the crystal and LC, as shown in Figure S10. The results suggest that Cbz-H formed aggregates with different aggregate structures from the crystal, and that the luminescence behavior of this complex is sensitive to its aggregated structure, although no change in the spectral shape was observed via crystal-to-LC phase transition.

4. Conclusions

Color tunability was observed for carbazole-based Au(I) complexes, with a color change from white to blue occurring as the steric bulkiness of the carbazole moiety increased. Furthermore, all complexes showed phosphorescence in the crystal state. Notably, complex Cbz-H showed an N phase along with a white emission at room temperature. However, no LC phases were observed for Cbz-Br and Cbz-t-Bu. These findings suggest a new approach for designing luminescent materials.

Author Contributions

Conceptualization, O.T. and G.P.; methodology, K.S.; formal analysis, K.S.; investigation, K.S.; writing—original draft preparation, K.S.; writing—review and editing, O.T. and G.P.; supervision, O.T. and G.P.; project administration, O.T.; funding acquisition, O.T. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in the article and Supplementary Materials.

Conflicts of Interest

The authors declare no conflict of interest.

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Figure 1. Molecular structure and synthetic route for complex Cbz-R: (i) (tht) AuCl/CH2Cl2, CH3COONa/MeOH; (ii) 1-pentyl isocyanide.

Figure 2. Molecular structure (a) and molecular packing structure (b) of complex Cbz-H determined via single-crystal X-ray diffraction at rt (gray, C; blue, N; yellow, Au; white, H).

Figure 3. Optical texture of Cbz-H observed via polarized optical microscopy at 93 °C during the first heating process (scanning rate: 3.0 °C min−1).

Figure 4. (a) UV–Vis absorption spectra of complex Cbz-R in CH2Cl2 solution: [Cbz-H], 2.1 × 10−5 mol L−1; [Cbz-Br], 4.3 × 10−5 mol L−1; [Cbz-t-Bu], 3.3 × 10−5 mol L−1. (b) Normalized emission spectra of complex Cbz-R in CH2Cl2 solution: [Cbz-H], 2.1 × 10−5 mol L−1, λex = 293 nm; [Cbz-Br], 4.3 × 10−5 mol L−1, λex = 300 nm; [Cbz-t-Bu], 3.3 × 10−5 mol L−1, λex = 297 nm.

Figure 5. (a) Solid-state emission spectra (λex = 300 nm) of complex Cbz-R (orange, Cbz-H; green, Cbz-Br; blue, Cbz-t-Bu). (b) CIE plot for the luminescence of complex Cbz-R in the crystal state.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/cryst12060810/s1: Figure S1: ¹H NMR spectra of complex Cbz-H. Figure S2: ¹H NMR spectra of complex Cbz-Br. Figure S3: ¹H NMR spectra of complex Cbz-t-Bu. Figure S4: ¹³C NMR spectra of complex Cbz-H. Figure S5: ¹³C NMR spectra of complex Cbz-Br. Figure S6: ¹³C NMR spectra of complex Cbz-t-Bu. Table S1: Crystallographic data of complex Cbz-H. Table S2: Optimized bond parameters for Cbz-H. Figure S7: TG/DTA thermograms of complex Cbz-R. Figure S8: DSC thermogram of complex Cbz-H. Table S3: Photoluminescence decay parameters of complex Cbz-R. Figure S9: Excitation spectra of complex Cbz-R in solid state. Figure S10: Solid-state emission spectra of complex Cbz-H after first heating and cooling. Figure S11: Emission spectra of complex Cbz-R in THF–water mixture. Figure S12: Emission spectra of complex Cbz-R in CH₂Cl₂ before and after degassing. Figures S13–S15: Photoluminescence decay profile of complex Cbz-R.

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