Closo- or nido-carborane diphosphane as responsible for strong thermochromism or time activated delayed fluorescence (TADF) in [Cu(N^N)(P^P)]0/+

Closo-orNido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)]0/+ Adrián Alconchel, Olga Crespo,*Pilar García-Orduna, and M. Concepción Gimeno* Cite This: Inorg. Chem. 2021, 60, 18521−18528 Read Online ACCESS Metrics & More Article Recommendations * sıSupporting Information ABSTRACT: Ortho-closo or ortho-nido-carborane-diphosphanes have been selected to prepare the heteroleptic cationic or neutral [Cu(N^N){(PPh2)2C2B10H10}]PF6(1) and [Cu(N^N){(PPh2)2C2B9H10}] (2) [N^N = 2-(4-thiazolyl)benzimidazole], respectively. Complexes 1and 2display very different emissive behavior. Neutral complex 2exhibits TADF (time activated delayed fluorescence) which has been studied both as powder and PMMA composite with similar ΔE(S1−T1), τ(T1), and τ(S1) in both phases. Cationic complex 1displays a much lower quantum yield than 2and does not show TADF, but it exhibits a significant thermochromic luminescence, and its emission is very dependent on the medium. Theoretical studies show that metal−ligand (M− diphosphane) to ligand (L′, diimine) transitions, MLL′CT, are responsible of the transitions which originate the emissive properties, but with very different contribution of the copper center, carborane cluster, and diphosphane phenyl rings for 1and 2. ■INTRODUCTION The synthesis and study of heteroleptic copper complexes [Cu(N^N)(P^P)]n(n= 0, 1) represents a growing field in the study of emissive coordination complexes. 1−12 One evident reason is the use of a cheaper metal (Cu) compared to those widely selected for the design of phosphors for emissive devices, such as Ir, Pt, or Au. Another relevant reason is related to their composition, which combines a diimine and a diphosphane. Substitution of a mostly planar diimine by a nonplanar ligand, a diphosphane, in the heteroleptic species diminishes the flattening distortion of the tetrahedral geometry in the excited state, compared with the homoleptic bis- (diimine) copper complexes. This flattening distortion enables quenching mechanisms of the luminescence. ISC (intersystem crossing) should be increased by avoiding flattening distortion. As a consequence, in these systems, phosphorescence and TADF (time activated delayed fluorescence) 13 should be favored. Both emissive mechanisms lead to an increment in the number of useful transitions for an emissive device. These facts have prompted an important effort in the synthesis and study of heteroleptic copper complexes [Cu- (N^N)(P^P)]0/+ for which the emission energies mostly lie in the yellow-green region. Among them, neutral complexes are still scarcely represented, 14−18 and some of them exhibit TADF. 19 Studies of composites are growing, 20−25 also including those in which these derivatives are tested in OLED devices, 26,27 revealing the potential of these systems. Carborane diphosphanes are rigid electron-withdrawing ligands. Their rigidity could avoid flattening distortion, and the electron-withdrawing characteristics could affect the copper diamine bond, as the electron density at copper would be diminished, due to the electron-withdrawing effect of the carborane ligand, compared with other diphosphanes. Copper [Cu(N^N)(dppnc)][dppnc−= (7,8-(PPh2)2-1,2C2B9H10)−] complexes have been reported with different substituted phenanthroline diimine ligands. 14,28,29 These complexes exhibit TADF, and some of them have been tested as dopants in the design of OLEDs. The influence of the partial degradation of the carborane cage in these properties has not been analyzed. We have previously reported that the nido nature of the carborane diphosphane plays a relevant role in the luminescent properties in three coordinated group 11 complexes. 30,31 Thus, we wonder if partial degradation of the carborane cage could also play such a key role in the TADF behavior of heteroleptic four coordinated copper derivatives. In addition, as most of the reported works display analysis of TADF for powder samples, Received: October 5, 2021 Published: November 23, 2021 Articlepubs.acs.org/IC © 2021 The Authors. Published by American Chemical Society 18521 https://doi.org/10.1021/acs.inorgchem.1c03092 Inorg. Chem. 2021, 60, 18521−18528 Downloaded via CSIC on February 17, 2022 at 10:22:00 (UTC). See https://pubs.acs.org/sharingguidelines for options on how to legitimately share published articles. our aim is also to compare τ(S1), τ(T1) (lifetime values of the first excited singlet and triplet, respectively) and ΔE(S1−T1) (energy gap between the first excited singlet and triplet) in solid and PMMA films at 5% wt. Here we report on the synthesis of two copper complexes with the diimine ligand 2-(4-thiazolyl)benzimidazole (N^N) and ortho-carborane diphosphanes: the cationic compound [Cu(N^N)(dppcc)]PF61with the closo-diphosphane (PPh2)21,2-C2B10H10 (dppcc) and the neutral complex [Cu(N^N)- (dppnc)] (2) with the nido-diphosphane [7,8-(PPh2)2-7,8C2B9H10]−(dppnc), which display very different emissive behaviors. The emissive TADF behavior of 2has been studied both as solid powder and as PMMA composite material. ■DISCUSSION Synthesis and Characterization. Reaction of [Cu- (CH3CN)4]PF6with the carborane diphosphane 1,2-(PPh2)21,2-C2B10H10 and further addition of 2-(4-thiazolyl)- benzimidazole (N^N) affords a cationic (1) or neutral (2) copper(I) complex (Scheme 1) depending on the solvent (dichloromethane or ethanol), respectively. Complexes 1and 2have been characterized by NMR spectroscopy, showing a unique resonance for the 31P{1H} NMR spectra. A broad signal at −2 ppm in the 1H NMR spectrum, corresponding to the bridging H hydrogen, proves the partial degradation of the carborane cage in 2. The crystal structure of compound 1has been elucidated by X-ray crystal diffraction (Figure 1). The copper center displays a distorted tetrahedral environment due to the small bite angles of both chelating ligands, N2−Cu−N1 81.60(13)°,P2− Cu−P3 98.18(4)°, with the one with the N^N ligand being narrower. The angle between N1−Cu−N2 and P2−Cu−P3 planes is 82.70°. Unexpectedly, the X-ray diffraction analysis of one crystal obtained from slow diffusion of n-hexane over an acetone solution of 2leads to the structure shown in Figure 2, which corresponds to [Cu(N^N)(Odppnc)] (3a) [Odppnc = (1- (OPPh2)-2-(PPh2)-1,2-C2B9H10)−]. The copper atom in 3a is coordinated to the two nitrogen atoms of the diimine, one phosphorus atom of the nido-diphosphane, and an oxygen atom resulting from the oxidation of the diphosphane. The bond distances for the oxidized diphosphane are Cu1−O1 2.165(4) Å and Cu1−P1 2.1665(13) Å, with the latter shorter than the Cu−P distances found in complex 1.Cu−P distances in other [Cu(N^N)(dppnc)] complexes are also shorter than those found in 1, which points out to a stronger Cu−P bond with nido-carborane diphosphanes, probably due to the additional electronic density in the carborane backbone, compared with that of the closo-carborane diphosphane. Cu− N distances in 1may also be compared with that found in [Cu(N^N)(dppnc)], but a general trend is not so clear. Further attempts to crystallize complex 2in the absence of oxygen, under an argon atmosphere, or in a different solvent were unsuccessful. However, it was possible to obtain crystals of a different solvate of the oxidized compound under air. Analysis by X-ray studies of a crystal obtained by slow diffusion of hexane over a dichloromethane solution of 2afforded the crystal structure of a different isomer of 3a (3b), which crystallizes with dichloromethane as solvent. These results show that partial oxidation seems to be accessible for 2and different isomers may be obtained. In isomer 3a,the benzimidazole unit of the N^N ligand is oriented opposite to the open face of the carborane cage, whereas in 3b the thiazole ring of the N^N ligand is oriented opposite to the open face of the carborane cage, as shown in Figure 2. Both isomers display very similar bond lengths and angles. Oxidation and partial degradation of the closo-diphosphane through reaction with H2O2has been reported. 32 Oxidation of dppcc has been also observed in the synthesis of copper(II), nickel(II), and zinc(II) complexes during degradation process in refluxing ethanol; 33 nevertheless, it has not been described Scheme 1. Synthetic Routes for Complexes 1 and 2 Figure 1. ORTEP diagram of the cation of compound 1. Ellipsoids represent 50% probability. Hydrogen atoms have been omitted for the sake of clarity. Bond distances (Å) and angles (deg): Cu−P2 2.2242(11), Cu−P3 2.2398(11), Cu−N1 2.073(3), Cu−N2 2.057(3), N2−Cu−N1 81.60(13), P2−Cu−P3 98.18(4). Figure 2. ORTEP diagram of the isomers of compound 3. Ellipsoids represent 50% probability. Hydrogen atoms have been omitted for the sake of clarity. Bond distances (Å) and angles (deg): 3a (acetone solvate) [Cu1−O1 2.165(4), Cu1−P1 2.1665(13), Cu1−N1 2.162(4), Cu1−N2 2.020(4), N2−Cu1−N1 80.20(16)]; 3b (dichloromethane solvate) [Cu1−O1 2.234(4), Cu1−P1 2.1759(14), Cu1−N1 2.050(4), Cu1−N2 2.148(4), N2−Cu1−N1 80.26(17)]. Inorganic Chemistry pubs.acs.org/IC Article https://doi.org/10.1021/acs.inorgchem.1c03092 Inorg. Chem. 2021, 60, 18521−18528 18522 during the synthesis and characterization of the copper complexes [Cu{(PR2)2C2B9H10}(PPh3)] (R = Ph, iPr), which were also carried out in refluxing ethanol, 31 nor during the synthesis of the copper complexes [Cu(N^N)- (dppnc)], 28,29 analogous to 2. These facts point to an oxidation of 2during the crystallization process. We have carried out the corresponding studies in order to confirm this point. The 31P{1H} NMR spectrum of a solution of the crystals grown in acetone shows two main signals at 16.7 and 36.8 ppm, one at higher field corresponding to the lack of oxidized phosphorus atom and the other to the oxidized one. In addition, a weak signal at a 33.5 ppm appears, which could correspond to the compound with two oxidized phosphorus atoms (see SI). We also recorded the 31P{1H} NMR spectrum of 2after months of its preparation, at low temperature, and two signals, at 13 and 17 ppm, are observed, which would correspond to two nonoxidized and no equivalent phosphorus atoms (see SI). Furthermore, we have also recorded the 31P{1H} NMR spectrum of a solution of 2after 24 h of its preparation, and no oxidation product has been observed (see SI). These data prove that the emissive properties described below for 2, not only in the solid state and as a film composite, but also in solution, correspond to the tetracoordinated derivative [Cu(N^N)(dppnc)] (2) and not to the isomers of 3. As oxidation of 2seems to be accessible, but not complete, as 2is still present in the reaction mixture, we tried a total transformation of 2by bubbling pure oxygen through a solution of 2in dichloromethane and some drops of hexane for one night. However, the 31P{1H} NMR spectrum shows that the result of the reaction is a mixture of 2and the oxidized product 3(probably a mixture of isomers) (see SI). Unsuitable crystals of 2for X-ray measurements were obtained from these mixtures. Thus, synthesis of pure 3or any of the isomers, as a pure product, is not easy and represents the subject of further work. From the data above, it seems that the presence of atmospheric oxygen is enough for the formation of the isomers of 3, although only part of 2is oxidized. We propose that the transformation of 2in the oxidized 3isomers may take place through a dissociative or associative pathway in solution, which are shown in Scheme 2, although we have not detected the corresponding intermedia. In the dissociative pathway, compound 2would dissociate in solution to afford Aor B (Scheme 2). The oxidation of the uncoordinated phosphorus atom could lead to intermediate Cthat can further coordinate to the copper center to give 3. Alternatively, the associative pathway would take place through the simultaneous formation of one oxygen copper bond and breaking of the Cu−P bond through D, leading to the formation of 3. These processes are in equilibria from which mixtures of 2and 3are obtained. This oxidation has not been detected for compound 1 bearing the analogous closo-carborane-diphosphane, nor has it been reported for three or four other coordinated copper(I) complexes with the anionic nido-carborane-diphosphane. Emission of Powder Samples. Powder samples of complexes 1and 2are luminescent upon excitation at about 400 nm (Table 1 and SI). The emissive behavior of complex 1 in the solid state (powder) shows a strong thermochromism. At room temperature, a band is observed in the red region, whereas the emission is blue-shifted at 77 K, and a greenyellow emission is observed. Rigidochromic effects have been claimed as responsible for the blue shift of emissions upon cooling. 25 The opposite trend is observed for compound 2, which displays emission in the green-yellow region showing a small red shift (11 nm) upon cooling. An increment of the lifetime is observed for both complexes upon cooling. This increment is much higher for 2(from 25 to 2900 μs). The shift to lower energies of the emission maximum and the increment of the lifetime upon cooling point to TADF behavior for 2. Thus, we have studied lifetime vs temperature for 2with the aim of analyzing TADF behavior. By fitting the observed τat different temperatures to eq 1 (KB= Boltzmann constant) using the least-squares fitting method (Figure 3), the calculated values are τ(S1) = 0.34 μs, τ(T1) = 2.92 ms, and ΔE(S1−T1) = 925 cm−1. ()() 3e 3e EKT EKT (S T)/ 1 (T) 1 (S ) (S T)/ 11 B 11 11 B τ =+ + ττ −Δ − −Δ − (1) Crystals of 3are brightly emissive. As discussed above, further efforts are needed in order to obtain isomers of 3as pure samples which would allow characterization of their emissive properties. Emission of PMMA Films. As mentioned above, we have checked by NMR that the compound used for luminescence studies, not only in the solid state, but also as film composite and in solution, corresponds to the tetracoordinated derivative [Cu(N^N)(dppnc)] (2) and not to isomers of 3, as no signal corresponding to the presence of 3is observed in the 31P{1H} NMR spectrum of a sample of 2after months of its Scheme 2. Formation of 3 from 2 Considering Cu−P Previous Dissociation or Not Table 1. Emissive Properties of Complexes 1 and 2 conditions λem b λex b Φ c τ d Compound 1 film 540 360, 395(sh) <1 powder, RT 700 450 <1 41.5 (0.991) powder, 77 K 542 400 336.8 (0.982) frozen soln a 450 270 1044.9 (0.999) Compound 2 film 542 395 10 23.0 (0.998) powder, RT 547 455 16 25.8 (0.999) powder, 77 K 558 335, 423 2932.3 (0.996) frozen soln a 530 315, 395 3885.5 (0.998) a 10−3M acetone solution. b λem, emission maxima; λex, excitation maxima (in nm). sh = shoulder. c In %; λex = 395 nm. d In μs(χ2). The studies have been carried out using the λem and λex maxima. Inorganic Chemistry pubs.acs.org/IC Article https://doi.org/10.1021/acs.inorgchem.1c03092 Inorg. Chem. 2021, 60, 18521−18528 18523 preparation. During frozen solution measurements and film preparation, formation of 3is also discarded, because no signal corresponding to the presence of 3is observed in the 31P{1H} NMR spectrum of a solution of 2after more than 1 day from the preparation of the solution, which represents a longer period from that employed for luminescence measurements and film preparation. Composites of both complexes as PMMA films at 5 wt % lead to emissions in the green region. Representation of the lifetime at different temperatures and fitting to eq 1 for the composite of compound 2leads to ΔE(S1−T1) = 1027 cm−1, τ(S1) = 0.39 μs, and τ(T1) = 2.91 ms (Figure 4). The powder value for the ΔE(S1−T1) gap is a bit smaller than in the less rigid PMMA film but does not show a significant difference. The results are summarized in Figure 5. Prompt fluorescence is not observed as the ISC process is very fast (ps). 19 ΔE(S1− T1) values for 2are in the range considered for practical use of TADF 19 and may be compared with those calculated for similar [Cu(N^N)(dppnc)] compounds using the same method, which range from 741 to 1195 cm−1. 28 We can conclude that the change of a phenanthroline diimine ligand by the N^N ligand does not lead to a significant decrease in the ΔE(S1−T1) gap. Quantum yields of powder and PMMA films at 5 wt % of complex 2are 16% and 10%, respectively, whereas those for complex 1are about 1%. Values observed for 2are in between those reported for [Cu(N^N)(dppnc)] complexes, 19,20 which range between ca. 5% and 32% in film and 4% and 39% in powder samples. After removing the excitation light, from the emission spectra, the CIE 1931 coordinates have been obtained (SI). A noticeable point is the different emission energy observed at room temperature for the composite and powder samples of 1. Powder samples (red emissive) display an important blue shift compared with the PMMA composites at 5 wt % (weakly yellow emissive). Emission in Frozen Solutions. UV−vis spectra have been recorded for complexes 1and 2, as well as for the ligands N^N and dppcc (see SI). The diphosphane dppcc displays an intense band at 273 nm. Intense bands at about 300 nm and a shoulder at about 310 nm are observed for the N^N ligand as well as for complexes 1and 2. In addition to this intense band, compound 1displays a shoulder at 347 nm and a weak band centered at 393 nm. Thus, absorption of compound 2 resembles that of the N^N ligand, whereas that of 1displays additional bands, probably related to charge transfer transitions. No emission has been observed for 1and 2in 10−3M acetone or dichloromethane solutions at room temperature. Frozen acetone glasses are highly emissive. Their maxima are blue-shifted, compared with the values for powder samples of PMMA composites at 5 wt % and display blue (1) or green (2) emission. Figures 6 and 7summarize the emissive color of complexes 1or 2, respectively, depending on the aggregation state. Figure 3. Temperature dependence of the emission lifetime of complex 2in the solid state with fitting values using eq 1. Figure 4. Temperature dependence of the emission lifetime of PMMA film at 5 wt % of complex 2with fitting values using eq 1. Figure 5. Energy level diagram for 2showing data calculated from eq 1as well as τ(DF) (thermal activated delayed fluorescence lifetime) and kr(radiative constant) values. Figure 6. Compound 1under UV (360 nm) light in the solid state at room temperature (a) and 77 K (b), as a frozen acetone solution (c), and in PMMA film (d). Figure 7. Compound 2under UV (360 nm) light in the solid state at room temperature (a), as a frozen acetone solution (b), and in PMMA film (c). Inorganic Chemistry pubs.acs.org/IC Article https://doi.org/10.1021/acs.inorgchem.1c03092 Inorg. Chem. 2021, 60, 18521−18528 18524 These data reveal that the emissive behavior of the cationic tetracoordinated complex 1is highly dependent on temperature and aggregation state. Compound 1follows the expected rule as a blue shift of the emission is observed upon cooling the solid powder. Different explanations for the blue shift upon cooling in the same media have been attributed to rigidochromism, 34 but also to emissions from different excited states. These excited states exhibit different distortions from the ideal tetrahedral geometry. 35 The explanation for the modification of the emission energy with the media is more complicated. Some literature studies attribute the red shift seen when changing from the solid powder to the film to an expected structural relaxation, 26 but this red shift, as observed for compound 1and other complexes reported in the literature, may not be considered a general trend. 19 Thus, other factors may be important. ■THEORETICAL STUDIES In order to get insight into the different emissive behaviors of 1 and 2, TD-DFT calculations were carried out for both complexes. The X-ray atomic coordinates were used in the case of compound 1as a starting point. Comparisons of the copper environment in the crystal structure and optimized geometry are shown in Table 2. Longer Cu−P, but shorter Cu−N, distances are observed in the optimized geometry. Chelate angles are diminished in the optimized structure. As a result, distortion from the tetrahedral geometry is increased in the optimized structure, as may be shown by the αangle. At the ground-state geometry, the excitation energies were calculated, being the only contribution to the S0→S1 transition (Table 3) corresponding to the HOMO−LUMO orbitals. The HOMO (Figure 8) is built mostly by contributions of the copper atom (32%), the phosphorus (30%), and phenyl rings (22%) of the carborane diphosphane ligand (simple contributions), with an almost negligible contribution of the N^N ligand. In the LUMO (Figure 8), all of the electronic density is distributed thought the N^N ligand. Thus, the origin of the absorption leading to the emission seems to be a metal− ligand(diphosphane) (ML) to the N^N ligand (L′) charge transfer transition (MLL′CT). HOMO to LUMO and HOMO−1 to LUMO contribute to the S0→T1transition (Table 3). Geometry parameters for the optimized structure of 2are shown in Table 2. For compound 2, transitions S0→Sn(n= 1−3, Table 3) involve HOMO−1, HOMO, LUMO, and LUMO+1 at the ground-state geometry. The electronic density of both HOMO and HOMO−1(Figure 9) is mainly located in the copper center and carborane backbone with an additional contribution of the phosphorus of the nido-diphosphane. The contribution of the copper atom represents 22% and 9% in HOMO−1 and HOMO, respectively. That of the carborane backbone represents 33% and 60% in HOMO−1 and HOMO, respectively, and that of the phosphorus atoms of the diphosphane 26% and 14% in HOMO−1 and HOMO, respectively. The LUMO and LUMO+1 are mainly located in the N^N ligand (Figure 8). Thus, the electronic transition may also be described as metal−ligand(diphosphane) (ML) to the N^N ligand (L′) charge transfer transition (MLL′CT), but important differences, when compared with compound 1, are found related to (i) the contribution of the nido-carborane skeleton, negligible in 1, (ii) the lesser contribution of the copper atom found for 2, and (iii) contribution of the phenyl rings of the carborane diphosphane found in 1, negligible in 2. HOMO to LUMO and HOMO−1 to LUMO contribute to the S0→T1transition (Table 3). Theoretical studies reported on other [Cu(N^N)(dppnc)] complexes [N∧N = neocuproine, 1,10-phenanthroline, or functionalized neocuproine], 28,29 for which TADF has been Table 2. Selection of Bond Distances (Å) and Angles (°)in 1 and 2 Cu−PCu−NN−Cu−NP−Cu−Pα a Compound 1 X-ray data 2.2398 2.073 81.60 98.18 82.70 2.2242 2.057 optimized 2.3548 2.236 78.76 95.88 75.84 2.3528 2.105 Compound 2 optimized 2.357 2.216 78.10 90.57 78.02 2.326 2.139 a α= angle between N−Cu−N and P−Cu−P planes. Table 3. Calculated Transitions for 1 and 2 λex a Transition (f) Orbitals λ b 1450 S0→S1(0.006) 194 (HOMO) →195 (LUMO) 409 S0→T1194 (HOMO) →195 (LUMO) 451 193 (HOMO−1) →195 (LUMO) 2455 S0→S1(0.0047) 191 (HOMO−1) →193 (LUMO) 614 192 (HOMO) →193 (LUMO) S0→S2(0.0017) 191 (HOMO −1) →193 (LUMO) 532 192 (HOMO) →193 (LUMO) S0→S3(0.0420) 191 (HOMO−1) →194 (LUMO+1) 438 192 (HOMO) →194 (LUMO+1) S0→T1191 (HOMO−1) →193 (LUMO) 631 192 (HOMO) →193 (LUMO a λex = excitation maximum in the solid state (nm). b λ= calculated values (nm). Figure 8. HOMO and LUMO calculated molecular orbitals for compound 1. Inorganic Chemistry pubs.acs.org/IC Article https://doi.org/10.1021/acs.inorgchem.1c03092 Inorg. Chem. 2021, 60, 18521−18528 18525 proposed, have attributed the origin of the emissions to MLCT or MLCT mixed with LL′CT transitions. These studies have revealed no contribution or negligible representation of the carborane skeleton of the dppnc ligand in the orbitals mainly responsible of the excitation transitions leading to emission. In all these complexes with the nido-diphosphane, the dppnc− contribution of the phenyl rings of the diphosphane 28,29 seems to be less important than in 1with the closo-diphosphane dppcc, for which TADF has not been found. Further work is needed in order to extend this effect as a general rule when comparing similar complexes with the closo (dppcc) and nido (dppnc−) diphosphanes. ■CONCLUSION The presence of an anionic nido-diphosphane (dppnc−) or the neutral closo-diphosphane (dppcc) in the tetracoordinated [Cu(N^N)(P^P)]n(n= 0, 1) complexes represents the key factor for the tuning of the emissive properties. The neutral compound [Cu(N^N)(dppnc)] exhibits TADF and singlet and triplet lifetimes; in addition, the ΔE(S1−T1) is almost unmodified from the solid to PMMA composites at 5% wt. The cationic complex [Cu(N^N)(dppcc)]PF6exhibits a strong thermochromic behavior. Its emissive excited state is highly dependent on the medium and temperature, displaying emissions which span from the red (solid at room temperature) to yellow (solid at 77 K) and blue (frozen acetone solution). It does not exhibit TADF. Charge transfer (copper to diimine) transitions have been claimed as responsible for the emissive behavior of many complexes of stoichiometry [Cu(N^N)(P^P)]0/+. More specifically, for different complexes with phenanthroline type N∧N ligands and nidocarborane diphosphanes, theoretical calculations lead to such a conclusion (in some cases with some mixed ligand to ligand charge transfer (LLCT) character). 28,29 Previously reported studies for similar complexes with the nido-diphosphane may conclude that changes in the diimine lead to different emission energies and quantum yields. In addition, steric effects avoiding distortion in the excited state have been claimed as very relevant in the emissive behavior of [Cu(N∧N)(P∧P)]0/+ compounds and, thus, in the design of TADF materials. Complexes 1and 2do not show significant differences in their steric hindrance, with this being the unique modification that is related to the partial degradation of the carborane cage. These results point to electronic effects as another relevant factor in controlling their luminescence behavior and more specifically TADF emission. For complexes 1and 2, the nature of the diphosphane represents the unique difference. The electronwithdrawing effect of carborane is supposed to be diminished in the mononegative nido-carborane-diphosphane, compared with the neutral closo-carborane-diphosphane. Deeper understanding of the relevance of the concrete effect of these electronic differences between the closo and nido clusters is needed, but theoretical studies on 1and 2reveal that MLL′CT transitions are responsible for the transitions related to the excitations leading to luminescence with the main differences regarding a lesser contribution of the copper center in compound 2with the nido-diphosphane; the contribution of the diphosphane skeleton (carborane cage) found in 2is not relevant in 1with the closo-diphosphane, and the important contribution of the orbitals of the phenyl rings of the diphosphane is found in 1, which is not present or is negligible in 2, as in other previously reported complexes with the nidodiphosphane. ■EXPERIMENTAL SECTION Instrumentation. NMR spectra were carried out in a Bruker AV 400 or 300 in CDCl3if solvent is not specified, and chemical shifts (ppm) are reported relative to the solvent peaks of the deuterated solvent. 36 Steady-state photoluminescence spectra were recorded with a Jobin-Yvon Horiba Fluorolog FL-3-11. Lifetime measurements were recorded with a Fluoromax phosphorimeter accessory containing a UV xenon pulsed flash tube. Multichannel scaling (MSC) has been used as the measuring method. Data were fitted to monoexponential functions, and the corresponding fitting curves are included in the SI. An OptistatDN Oxford variable temperature liquid nitrogen cryostat has been used for lifetime studies at different temperatures and a liquid nitrogen dewar assembly for steady-state studies at 77 K. Quantum yields were measured by the absolute method using a Hamamatsu Quantaurus-QY C11347 compact one-box absolute quantum yield measurement system. Quartz tubes were used for the measurement of solid samples. For film preparation, ca. 4 mg of compound and ca. 76 mg of PMMA were dissolved in 1 mL of CH2Cl2in order to obtain films which contain about at 5 wt % of the copper compound. The mixture was sonicated for 15−20 min. Films were prepared by drop casting the resulting solution. Two or three films of each complex were prepared as well as two or three reference samples. Each sample was measured using each reference in order to prove the reproducibility of the results. Crystallography. Crystals suitable for X-ray studies were obtained by diffusion of n-hexane over a solution of the corresponding compound in dichloromethane (1,3b) or acetone (3a). Crystals were mounted in inert oil on a glass fiber and transferred to the cold gas stream of a SMART APEX (1,3a) or mounted on a MiTeGen Crystal micromount and transferred to the cold gas stream of a Bruker D8 VENTURE (3b)diffractometer. Data were collected using monochromated Mo Kαradiation (λ= 0.71073 Å), with scan type ω. Absorption corrections based on multiple scans were applied with the program SADABS; 37 for 3b, numerical absorption corrections based on crystal face indexing have been performed. The structures were Figure 9. HOMO−1, HOMO, LUMO, and LUMO+1 calculated molecular orbitals for compound 2. Inorganic Chemistry pubs.acs.org/IC Article https://doi.org/10.1021/acs.inorgchem.1c03092 Inorg. Chem. 2021, 60, 18521−18528 18526 refined on F2using the program SHELXL-2018. 38 All non-hydrogen atoms were refined anisotropically. Hydrogen atoms were included using a riding model. CCDC depositions 2076381 (1), 2076380 (3a), and 2088767 (3b) contain the supplementary crystallographic data. These data can be obtained free of charge by The Cambridge Crystallography Data Center. Theoretical Studies. The Gaussian 09 program was used in order to carry out the DTF calculations. Geometry optimizations were performed on the ground state using the hybrid B3LYP functional and the basis sets def2-SVP (for C, S, and H atoms), 7 def2-TZVP (for P, N, and O atoms), and LANL2DZ for the copper atom. 28,29 For the copper atom, the corresponding associated pseudopotential to LANL2DZ was applied. Synthesis. The synthetic procedures were carried out under an Ar atmosphere, using Schlenk techniques. Dry degassed solvents were used. The starting materials [Cu(CH3CN)4]PF6and N^N [2-(4thiazolyl)benzimidazole] are commercially available and were used as received. The diphosphane 1,2-(PPh2)2-1,2-C2B10H10 was prepared using a published procedure. 39 Synthesis of [Cu(N^N)(dppnc)]PF6(1). To a solution of [Cu- (CH3CN)4](PF6) (0.1 mmol, 37.2 mg) in dichloromethane was added [1,2-(PPh2)2-1,2-C2B10H10] (0.1 mmol, 51.3 mg). The mixture was stirred for 30 min, and 2-(4-thiazolyl)benzimidazole (0.1 mmol, 20.8 mg) was added. The mixture was stirred for 1 h. Then, it was evaporated to a minimum volume. Addition of n-hexane led to the precipitation of 1as a pale yellow solid, which was filtered and dried under vacuum. Yield: 87.2 mg, 94.5%. Q-TOF: m/z777 (34.3%) [M −PF6]. 1H NMR (400 MHz, acetone-d6,25°C): δ= 12.95 (s, 1H), 9.58 (s, 1H), 8.87 (s, 1H), 7.96−7.72 (m, 10H), 7.70−7.39 (m, 14H), 3−0.6 (m, 10H) ppm. 31P{1H} NMR (121 MHz, acetone-d6,25°C): δ= 13.5 ppm. Synthesis of [Cu(N^N)(dppnc)] (2). To a solution of [Cu- (CH3CN)4](PF6) (0.1 mmol, 37.2 mg) in ethanol was added 1,2- (PPh2)2-1,2-C2B10H10 (0.1 mmol, 51.3 mg). The mixture was stirred for 30 min, and 2-(4-thiazolyl)benzimidazole (0.1 mmol, 20.8 mg) was added. The mixture was refluxed for 1 h. Concentration of the solution led to precipitation of a solid which was filtered and dried under vacuum. Yield: 52.9 mg, 69%. Q-TOF: m/z789.22 (5.4%) [M + Na]. 1H NMR (400 MHz, acetone-d6,25°C): δ= 12.95 (s, 1H), 8.58 (s, 1H), 7.91−7.09 (m, 20H, Ph; 5H, N^N), 3−0.6 (m, 10H), −1.85 (s, br, 1H) ppm. 31P{1H} NMR (121 MHz, acetone-d6,25 °C): δ= 16.6 ppm. ■ASSOCIATED CONTENT * sıSupporting Information The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acs.inorgchem.1c03092. Additional details of the emissive properties and theoretical studies (PDF) Coordinates of the optimized structures (XYZ) Accession Codes CCDC 2076380−2076381 and 2088767 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/data_request/ cif, or by emailing [email protected],orby contacting The Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033. ■AUTHOR INFORMATION Corresponding Authors Olga Crespo −Departamento de Química Inorgánica, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), Universidad de Zaragoza-CSIC, E-50009 Zaragoza, Spain; orcid.org/0000-0001-9522-5840; Email: [email protected] M. Concepción Gimeno −Departamento de Química Inorgánica, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), Universidad de Zaragoza-CSIC, E50009 Zaragoza, Spain; orcid.org/0000-0003-05530695; Email: [email protected] Authors Adrián Alconchel −Departamento de Química Inorgánica, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), Universidad de Zaragoza-CSIC, E-50009 Zaragoza, Spain Pilar García-Orduna−Departamento de Química Inorgánica, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), Universidad de Zaragoza-CSIC, E-50009 Zaragoza, Spain Complete contact information is available at: https://pubs.acs.org/10.1021/acs.inorgchem.1c03092 Notes The authors declare no competing financial interest. ■ACKNOWLEDGMENTS We thank Dr. Enrique Onate, from the Departamento de Química Inorgánica, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), Universidad de Zaragoza-CSIC, for his kind guidance with the theoretical studies, and for his supervision, explanations, and fruitful discussions. The authors also thank the Agencia Estatal de Investigación PID2019104379RB-C21/AEI/10.13039/50110001103 and DGA-FSE (E07_20R) for financial support and to the Centro de Supercomputación de Galicia (CESGA) for providing access to the Finish Terrae supercomputer. A.A. appreciates the predoctoral contract award BES-2017-082997. ■REFERENCES (1) Holler, M.; Delavaux-Nicot, B.; Nierengarten, J.-F. Topological and Steric Constrains to Stabilize Heteroleptic Coper(I) Complexes Combining Phenanthroline Ligands and Phosphines. Chem. - Eur. J. 2019,25, 4543−4550. (2) Zhang, Y.; Schulz, M.; Wachtler, M.; Karnahl, M.; Dietzek, B. Heteroleptic diamine-diphosphine Cu(I) complexes as an alternative towards noble-metal based photosensitizers: Design strategies, photophysical properties and perspective applications. Coord. Chem. Rev. 2018,356, 127−146. (3) Liu, Y.; Yiu, S.-C.; Ho, C.-L.; Wong, W.-L. Recent advances in copper complexes for electrical/light energy conversion. Coord. Chem. 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Chem. 1963,2, 1107−1110. ■NOTE ADDED AFTER ASAP PUBLICATION This paper was published ASAP on November 23, 2021 with errors in Schemes 1 and 2 and the abstract graphic. The corrected version was reposted on December 6, 2021. Inorganic Chemistry pubs.acs.org/IC Article https://doi.org/10.1021/acs.inorgchem.1c03092 Inorg. Chem. 2021, 60, 18521−18528 18528