Structure-property relationships of photofunctional diiridium(ii) complexes with tetracationic charge and an unsupported ir–ir bond

ABSTRACT In contrast to the extensively studied dirhodium(II) complexes and iridium(III) complexes, neutral or dicationic dinuclear iridium(II) complexes with an unsupported ligand are

underdeveloped. Here, a series of tetracationic dinuclear iridium(II) complexes, featuring the unsupported Ir(II)–Ir(II) single bond with long bond distances (2.8942(4)–2.9731(4) Å), are

synthesized and structurally characterized. Interestingly, compared to the previous unsupported neutral or dicationic diiridium(II) complexes, our DFT and high-level DLPNO-CCSD(T) results

found the largest binding energy in these tetracationic complexes even with the long Ir(II)–Ir(II) bond. Our study further reveals that London dispersion interactions enhance the stability

cooperatively and significantly to overcome the strong electrostatic repulsion between two half dicationic metal fragments. This class of complexes also exhibit photoluminescence in solution

and solid states, which, to our knowledge, represents the first example of this unsupported dinuclear iridium(II) system. In addition, their photoreactivity involving the generation of

iridium(II) radical monomer from homolytic cleavage was also explored. The experimental results of photophysical and photochemical behaviours were also correlated with computational studies.

SIMILAR CONTENT BEING VIEWED BY OTHERS PHOTOREDOX-ACTIVE CR(0) LUMINOPHORES FEATURING PHOTOPHYSICAL PROPERTIES COMPETITIVE WITH RU(II) AND OS(II) COMPLEXES Article Open access 14 August

2023 DESIGN, SYNTHESIS AND VISIBLE-LIGHT-INDUCED NON-RADICAL REACTIONS OF DUAL-FUNCTIONAL RH CATALYSTS Article 30 March 2023 AN OPEN-SHELL IR(II)/IR(IV) REDOX COUPLE OUTPERFORMS AN

IR(I)/IR(III) PAIR IN OLEFIN ISOMERIZATION Article 20 January 2025 INTRODUCTION The most common oxidation state of iridium complexes is +3; while those of iridium(II) complexes of d7

electronic configuration with radical character are rare probably because of their low air- and moisture-stabilities1,2,3. One way to stabilize the iridium(II) complexes is through the

formation of a Ir(II)–Ir(II) bond, leading to the pairing up of two individual radicals in the bonding orbital. The Ir(II)–Ir(II) bonds in such dinuclear iridium(II) complexes are usually

supported and stabilized by bridging ligands4,5,6,7,8,9,10,11. Whereas, diiridium(II) complexes with an unsupported Ir(II)–Ir(II) bond are much less explored and the examples with

structurally characterized are even more scarce12,13,14,15,16,17,18,19,20,21,22,23. In all reported complexes, the unsupported iridium(II) metal centres are found to coordinate with anionic

ligands leading to the overall formal charge of +2 or 0 (neutral) (Fig. 1). The nature of low formal charge should facilitate the formation of these diiridium(II) complexes with reduced

electrostatic repulsion between two half metal fragments. On the other hand, all reported examples with structural characterization were found to exist as only one entity without any

derivatives, which precludes systematic study for the understanding of their structure-property relationships, presumably due to challenging synthesis of stable diiridium(II) complexes. In

contrast, the isoelectronic dirhodium(II) compounds have been well known and extensively studied for the wide range of applications, such as catalysis24,25,26,27,28,29,30,31,32,33, antitumor

metallopharmaceuticals34,35,36,37, phototherapeutic agents38,39,40, photochemistry41,42,43,44,45 and design of supramolecular arrays46,47,48. The photophysical properties of polypyridine or

cyclometalated iridium(III) system have also received tremendous attentions. In the past two decades, diversified potential applications49,50,51,52 of the luminescent iridium(III) complexes

have been exploited because of their various advantages, such as wide colour-tunability, less thermally accessible 3d–d state, synthetic versatility and, photo- and chemical-stabilities. In

sharp contrast, the photophysical and photochemical studies of unsupported diiridium(II) system are unknown from the limited examples. The exploration and exploitation of such photophysical

and photochemical behaviours for the underdeveloped diiridium(II) complexes could open up an avenue for the development of new photofunctional materials. Therefore, synthesis and

modification of series of diiridium(II) complexes are crucial and urged for the systematic study. Herein, we report the synthesis and structural characterization of a series of tetracationic

dinuclear iridium(II) complexes, [Ir(II)(N^N^N)(CO)(PPh3)]2[X]4 (1–3) [N^N^N = 4,4′,4′′-tri-_tert_-butyl-2,2′,6′,2′′-terpyridine (_t_Bu3-terpy), 2,2′,6′,2′′-terpyridine (terpy) and

2,6-bis(_N_-_n_butylbenzimidazol-2'-yl)pyridine (bzimpy); X = OTf– or BF4–], featuring an unsupported and long Ir(II)–Ir(II) single bond for the first time (Fig. 1). Remarkably,

state-of-the-art DFT and DLPNO-CCSD(T) studies revealed that two dicationic Ir(II) fragments are significantly stabilized by considerable London dispersion interactions in these

tetracationic diiridium(II) complexes 1–3. Such non-covalent interactions are responsible for the computed exceptionally largest Ir(II)–Ir(II) binding energy in 1–3, even though they have a 

relatively long Ir(II)–Ir(II) bond. It is noteworthy that all of them are found to exhibit photoluminescence in various media, as the first example of the unsupported Ir(II) system. Their

electrochemical and photophysical behaviours with different pincer ligands were determined and correlated with the electronic structures obtained from computational studies. RESULTS AND

DISCUSSION DESIGN AND SYNTHESIS Reaction of [IrCl(PPh3)2(CO)] with AgX (X = OTf– or BF4–), followed by treatment with the N^N^N pincer ligand in THF or MeCN at room temperature for 3 days

afforded complexes 1–3 in 52–62% yield (Fig. 2). It is noteworthy that excess Ag(I) ion was added to serve as halide abstraction agent to remove the chloro group in the iridium(I) starting

material, and as the oxidizing agent to generate the desired complexes. After addition of the pincer ligand into the pale yellow filtrate from the reaction mixture of [IrCl(PPh3)2(CO)] with

AgX, greenish black solution was immediately formed. Such dark colour species was identified as [Ir(N^N^N)(CO)]+, based on the observation of [Ir(_t_Bu3-terpy)(CO)]+ at m/z = 622.23950

(calc. for [C28H35IrN3O]+ as 622.24039) in high-resolution mass spectrum (HRMS) during the formation of 1 (Supplementary Fig. S1). Interestingly, upon prolonged stirring, the iridium(I)

species was further oxidized to form the desired diiridium(II) complex and red solution with dark red suspension was obtained. Non-covalent Ir(I)–Ir(I)53,54 and π–π interactions are

suggested to facilitate the dimerization by holding the molecules into close proximity in the solution. Complexes 1–3 are stable toward air and moisture in the solid state. In dry and

degassed CD3CN or (CD3)2SO solution of 1–3, no observable change from their 1H NMR spectra was found for at least 24 h. Because of the highly charged nature, their solubilities are good in

polar CH3CN and DMSO solvents, whereas only slightly to moderately soluble in CHCl3 and insoluble in toluene. Complexes 1–3 were fully characterized by 1H, 13C{1H} and 31P{1H} NMR

spectrometry, HRMS, IR spectroscopy and satisfactory elemental analysis (Supplementary Figs. S2–S24). 19F{1H} NMR spectrum of 1' was also record to show the signal at _δ_ = –151.16 ppm

for the BF4– anon (Supplementary Fig. S12). The 1H NMR spectra of 1 and 1' (Fig. 2) in CD3CN at room temperature show broad peaks for the pyridyl signals (Supplementary Figs. S2 and

S9), whereas only sharp peaks were observed for those of 2 and 3 under the same conditions (Supplementary Figs. S15 and S20). It is attributable to the restricted rotation between two half

units in 1 resulting from the presence of bulky _tert_-butyl groups. These signals can be restored into sharp peaks in other solvents, such as CDCl3 or (CD3)2SO (Supplementary Figs. S5 and

S6), indicating the freely rotation about the Ir–Ir bond in such media. Their IR spectra show an absorption peak at 2035-2060 cm-1, assignable to the ν(C ≡ O) stretching frequency. STRUCTURE

AND BONDING The molecular structures of 1–3 were determined by X-ray crystallography. Their structural data, selected bond distances and angles are summarized in Supplementary Tables

S1–S12. This class of complexes represent the first structural characterized example of tetracationic diiridium(II) system without any bridging ligands. As depicted in Fig. 3a–c, all the

complex cations consist of two [Ir(II)(N^N^N)(CO)(PPh3)]2+ fragments in a head-to-tail arrangement and connected by an unsupported Ir(II)–Ir(II) single bond. Each iridium(II) metal centre is

coordinated with one N^N^N pincer and one CO ligands on the equatorial plane, while the PPh3 ligand and another iridium(II) metal centre are bound in the axial position to exhibit a

distorted octahedral geometry. In all cases, four counter-anions of OTf– (or BF4–) are positioned around the corresponding complex cation (Supplementary Fig. S25). It is noteworthy that an

interesting structural feature of these complexes is generally the longer Ir(II)–Ir(II) bond distance (1, 2.8942(4) Å; 2, 2.9421(9) Å; 3, 2.9731(4) Å), compared to the previously reported

unsupported neutral or dicationic diiridium(II) complexes (2.66–2.84 Å)12,13,14,15,16,17,18,19,20,21,22,23. The shortest Ir–Ir bond was observed in 1 even with bulky _tert_-butyl groups,

whereas the longest one was found in 3 with the larger π-conjugated pincer ligand of bzimpy. By changing the counter-anion from OTf– to BF4– in 1' as shown in Supplementary Fig. S25,

the complex cation exhibited similar structural features with elongation of the Ir–Ir bond (2.9135(5) Å). The change in this Ir–Ir bond length is ascribed to the different non-covalent

interaction between the complex cation and counter anions in crystal packing. The C ≡ O bond distances of 1.121(8)–1.135(4) Å are in the typical range of transition metal complexes. In 1,

the peripheral pyridine rings of _t_Bu3-terpy are found to tile from the central pyridine group with the interplanar angles of 10.674(67)–13.455(59)°, attributable to the mutual repulsion

from bulky _tert_-butyl groups. On the other hand, such deviation from coplanarity in the pincer ligand is diminished in 2 and 3 with the interplanar angles of 4.496(252)–5.383(258)° and

4.430(94)–4.507(102)°, respectively. The interplanar distances between the peripheral rings of pincer ligands on two half units are 3.2050(20)–3.2738(21) Å (1), 3.0761(71)–3.1702(77) Å (2)

and 3.1890(36)–3.1981(37) Å (3), indicating the presence of π–π interactions. In addition, two phenyl rings on the axial PPh3 ligand are arranged in a parallel way to the pincer ligand with

small tilted angles and short distances for the better π–π stacking (Fig. 3d–f). DFT (including M06-L, M06, B3LYP-D3, PBE0-D3 and MN15 methods) and high-level DLPNO-CCSD(T)

calculations55,56,57,58,59,60,61,62 were performed to examine the unusual tetracationic Ir(II) complexes 1–3 with unsupported long Ir(II)–Ir(II) bond. In addition, three model complexes

(4–6), other previously reported complexes with unsupported metal–metal bond, including ten Ir(II)–Ir(II), one Rh(II)–Rh(II) and one Au(II)–Au(II) complexes (A–L), were also examined for

comparison (Fig. 4)12,13,14,15,16,17,18,19,20,21,22,23,63,64. Despite the computed Ir–Ir bonds of 1–3 (2.94–2.99 Å) are generally longer, the present system was surprisingly computed to have

a larger binding free energy (ΔGsoln: _ca_. −49 kcal/mol by the SMD M06-L//M06-L method), compared to A–J (ΔGsoln: _ca_. −24 to −39 kcal/mol), K (ΔGsoln: −44 kcal/mol) and L (ΔGsoln: −35 

kcal/mol), as shown in Fig. 4. Such energetic trend was qualitatively supported by different DFT and high-level DLPNO-CCSD(T) methods (Supplementary Fig. S26 and Supplementary Table S13). It

is noteworthy that the diiridium(II) complexes 1–3 were found to have such large binding energies, even though they have smaller electron density (ρ) and positive electron density (∇2ρ)

values65,66,67,68,69 (Supplementary Table S13). Our computational study clearly manifests that the bonding features (a longer bond distance with a larger binding energy) for the

tetracationic complexes 1–3 are unprecedented. In order to further unravel the bonding features of 1–3, distortion/interaction analysis70 was employed and these results showed that the large

binding energy is mainly attributed to the considerable interaction energy (Supplementary Fig. S27a). Interestingly, a much larger interaction energy plays the key role of the largest

binding energy determined in 1 (ΔEint,soln: _ca_. −91 kcal/mol), relative to 2 and 3 (_ca_. −65 to −68 kcal/mol). While, entropy effect favors 3 >1, which reduces their binding

free-energy difference. Empirical dispersion (e.g. D3 contribution for B3LYP method) correction61 (Supplementary Fig. S27b and Supplementary Table S14) and non-covalent interactions (NCIs)

analysis71 further demonstrated that London dispersion (Fig. 5a for 1 and Supplementary Fig. S28a for 2 and 3), including π–π interactions among the two pincer ligands and the four OTf–

counterions, play one of the key roles in their high binding energies. These interactions can also be visualized by the bond-critical-points (BCPs) from the results of the quantum theory of

atoms in molecules (QTAIM) method72,73. (Fig. 5b for 1 and Supplementary Fig. S28b for 2 and 3). In this connection, a longer Ir–Ir bond distance (3.08 Å) and much smaller binding energy

(ΔGsoln: _ca_. −26.4 kcal/mol) were also computed for model complex 5, in which a smaller and less conjugated tridentate pincer ligand with smaller dispersion stabilization was adopted. This

result is in agreement with other previous computational studies suggesting the importance of London dispersion in some metal complexes74,75,76,77,78,79,80,81. As shown in Supplementary

Table S14, both metal–metal82 and non-covalent interactions among the tridentate pincer ligands and counterions should be generally the critical factors in stabilizing the rare Ir(II)–Ir(II)

bond and rendering the unusually large binding energies for tetracationic complexes 1–3 by conquering unfavorable and strong electrostatic repulsions. PHOTOPHYSICAL AND ELECTROCHEMICAL

BEHAVIOURS The photophysical and electrochemical behaviours of 1–3 have been investigated and the data are summarized in Table 1. Their UV-vis absorption spectra of 1–3 in CH3CN are also

depicted in Fig. 6. In addition to the intraligand (IL) π–π* absorptions of N^N^N pincer ligand at 343 and 385 nm, the UV-Vis absorption spectra exhibit a low-energy absorption band at

493–553 nm. Our TD-DFT (CPCM TD-B3LYP-D3//M06-L) calculations18 suggested that the low-energy absorption is mainly ascribed to metal–metal bond-to-ligand charge transfer (MMLCT) dσ(Ir–Ir) → 

π*(N^N^N ligand) transition with some mixing of dσ(Ir–Ir) → dσ*(Ir–Ir) character (Supplementary Figs. S29–S31). Such an assignment is also consistent with the computed composition of the

donor/highest occupied molecular orbital (Ir–Ir, 31–37%; P, 18–23%; N^N^N ligand, 15–18%) and the acceptor/lowest unoccupied orbital (Ir–Ir, 13–18%; P, 1–2%; N^N^N ligand, 62–80%) for 1–3 by

the M06-L method (Table 2). Figure 5a also shows the schematic frontier molecular orbital (FMO) diagram of the ground-state metal complexes, illustrating the key MOs involved in the

lowest-lying electronic transition of the MMLCT character. Interestingly, this absorption band in 1 with electron-rich _tert_-buty groups exhibited a slight red-shift, relative to 2. The

change in the pincer ligand was found to vary the energy levels of HOMO and LUMO at the same time, as revealed from the potentials for the first oxidation and reduction (vide infra). In view

of this, the MMLCT absorption energy could not simply correlate to the π* orbital energy level by subtle modification in the pincer ligand. For complex 3 with substantial lower-lying π*

orbital in bzimpy ligand, this absorption band was found to shift to lower energy significantly. Despite of this, our TD-DFT calculations also suggested the red-shift absorption trend of the

two key low-lying transitions from 1 to 3 (1: 377 and 496 nm; 3: 398 and 540 nm; Supplementary Tables S15–S17). This result further supports the assignment of such low-energy absorption

band as MMLCT transition based on the substantial lower-lying π* orbital energy level of bzimpy ligand in 3 (540 nm), relative to 1 (496 nm) with terpyridine ligand. Upon excitation at λex 

> 450 nm on their MMLCT absorption bands, 1–3 were found to exhibit orange-red luminescence at 620–678 nm in degassed CH3CN solution at 298 K (Fig. 6). To the best of our knowledge, this

is the first example of unsupported diiridium(II) systems showing luminescence. Their excitation bands from the excitation spectra in degassed CH3CN solution were found to resemble to the

corresponding low-energy absorption bands (Supplementary Fig. S32). In addition, the luminescence intensity of 1 diminishes to around 50% as in aerated CH3CN solution. Collectively, together

with the large Stokes shift, such luminescence of 1–3 is assigned to be originated from the triplet metal–metal bond-to-ligand charge transfer (3MMLCT), with some mixing of dσ(Ir–Ir) → 

dσ*(Ir–Ir) character, as shown in Fig. 7b. This assignment is also qualitatively consistent with the spin density of the optimized triplet structure and emission transition for 31 by the

M06-L and TD-B3LYP-D3//M06-L methods, respectively (Supplementary Figs. S33–S36). Similar to the low-energy absorption bands, the luminescence energy of 3 (678 nm) is lower than those of 1

(620 nm) and 2 (650 nm), which further supports the nature of 3MMLCT origin. Qualitatively, our CPCM TD-B3LYP-D3//M06-L (including effect of spin-orbital coupling) calculations83,84,85 also

supported the observed red-shift luminescence of 3 for the assignment of 3MMLCT excited state (1: ~611 nm vs. 3: ~644 nm; Supplementary Tables S18–S20). It is noteworthy that the UV-vis

absorption and luminescence spectra of 1' (Supplementary Fig. S37) with the counter anion of BF4– showed essentially the same spectra as in 1, indicative of insignificant influence from

its counter anion in the solution state. The luminescence quantum yield (Φlum) of 1–3 (1, 4.99 × 10–4; 1', 4.86 × 10–4; 2, 2.62 × 10–4; 3, 0.85 × 10–4) were obtained in degassed CH3CN.

The decrease in Φlum from 1 to 3 with lower luminescence energy is probably due to the effect arising from the energy gap law. It is noteworthy that very short luminescence lifetimes (τ1 = 

55-63 ps; τ2 = 291–389 ps) were revealed in degassed CH3CN or in solid state 298 K (Table 2 and Supplementary Figs. S38–S39). Such short luminescence lifetime and low Φlum could be realized

by intersystem crossing back to the ground state from the triplet-state minimum, which could facilitate non-radiative decay pathway with a low-energy barrier at their minimum crossing point

(MECP)86 as suggested from our DFT calculations for 1 (Supplementary Fig. S40). In addition, photogeneration of radical monomer as a competing process is also responsible for the rapid

deactivation process for the 3MMLCT excited state (vide infra). On the other hand, 1–3 were also found to exhibit photoluminescence at 632–673 nm in the solid state at 298 K (Supplementary

Fig. S41a), while the corresponding luminescence at 77 K showed a blue-shift energy at 610–648 nm with narrower band shape (Supplementary Fig. S41b). It is interesting to note that the

emission energies of 1' in solid state at room temperature and 77 K are found to be higher than those of 1 (Supplementary Fig. S42). This could be rationalized by the lower-lying HOMO

in 1' resulting from the longer Ir–Ir bond, which was observed from their crystal structures. Since the LUMOs of 1 and 1' are predominantly of π* orbital of the same terpyridine

ligand, larger HOMO-LUMO energy gap in 1' could give rise to higher emission energy in solid state. The electrochemical behaviours of 1–3 were also studied by cyclic voltammetry in

CH3CN (0.1 M _n_Bu4NPF6) at 298 K (Table 1 and Supplementary Fig. S43). The oxidative scan showed an irreversible anodic wave (1, +1.80 V; 2, +1.90 V; 3, +1.73 V) (_vs_. SCE), attributed to

the Ir(II) metal centre oxidation with some mixing of PPh3 ligand. The less positive potential for this oxidation in 1, relative to 2, is ascribed to the more electron-rich Ir(II) metal

centre, through the incorporation of terpyridine ligand with electron-donating _tert-_butyl groups. Upon reductive scan, an irreversible cathodic wave at –0.26 V to –0.40 V (_vs_. SCE) was

observed, which is reasonably assigned as the reduction on the terpyridine ligand with some σ*(Ir(II)–Ir(II)) character. The reduction potentials of these cathodic waves (1, –0.26 V; 2,

–0.30 V; 3, –0.40 V) are in agreement with the π* orbital energy level of the pincer ligand. Compared to 1 and 2, the smallest potential difference between the potentials for oxidation and

reduction in 3 is well correlated with the observation of the smallest MMLCT absorption energy. The essentially irreversible nature of this reduction process is probably due to dissociation

of the diiridium(II) framework, resulting from the population of σ*(Ir(II)–Ir(II)) orbital. In 1, an additional anodic peak at –0.16 V is only emerged after the first reduction scan beyond

–0.40 V (Supplementary Fig. S43a), indicative of the oxidation of the decomposed product. Similar to the photophysical properties, the observation of almost the same reduction potentials for

the reduction and oxidation of 1' (Supplementary Fig. S44) and 1, indicated the insignificant effect from the change of counter anion in solution state. PHOTOREACTIVITY In connection

with the unprecedentedly high binding energy by our DFT calculations, 1–3 were found to be inert towards O2, H2O, as well as Br2 and I2 in CH3CN solution. In view of the corresponding

bonding(Ir–Ir) and anti-bonding(Ir–Ir) characters in their donor and acceptor orbitals (Fig. 7), the Ir–Ir bond cleavage resulting from photoexcitation would be anticipated to generate the

respective radical monomer [Ir(N^N^N)(CO)(PPh3)]2+•20. As shown in Fig. 8, such photoreactivity behaviour was realized by the UV-vis spectral changes of 1–3 in CH3CN solution upon

photoirradiation at the region of the MMLCT absorption band (Fig. 8a). By keeping the absorbance of 1–3 the same at 500 nm for the photoirradiation, the absorbance changes with time were

monitored and their relative photostabilities could be qualified as 1 < 2 < 3 (Fig. 8b). The higher photostability would be envisioned for the complex with the computed smaller

contribution from Ir(II) metal centre for the donor and acceptor orbitals (Table 2), which is in line with the experimental results of their relative photostabilities. The vanishment of the

MMLCT absorption bands suggests that the photogenerated radical monomers would repel from each other to avoid the radical-radical coupling for the backward formation of the diiridium(II)

complex. The photostability of 1' was also found to be similar to that of 1, suggesting that the influence of counter anion is insignificant in the solution state. Electron paramagnetic

resonance (EPR) spectroscopy is a suitable technique to probe the formation of radical monomer upon photoirradiation. The EPR spectra of 1–3 in CH3CN at 100 K after photoirradiation for 5 

min in solution state are depicted in Fig. 9. The EPR spectra clearly indicate that the photogenerated species are of S = 1/2 paramagnetic nature with typical axial symmetry87,88. On the

basis of the _g_-tensor values (gz > gx,gy > 2) suggestive of a compressed octahedral structure88, [Ir(N^N^N)(CO)(PPh3)(CH3CN)]2+• species is likely generated arising from readily

occupation of the vacant site in 5-coordinated [Ir(N^N^N)(CO)(PPh3)]2+• by a CH3CN solvent molecule. It is noteworthy that no corresponding EPR signal would be observed for1–3 in the absence

of photoirradiation, which further supports the formation of radical being orginated from the photocleavage process. According to the isolobal analogy, the d7 five-coordinate [11/2]2+•

species upon photocleavage is isolobal to CH3• radical with similar reactivity towards Br2 or I2 (Fig. 10a). Interestingly, mononuclear iridium(III) complexes,

[Ir(_t_Bu3-terpy)(CO)(PPh3)X]2+ [X = Br, 7 (yield = 83%); I, 8 (yield = 78%)] were afforded from the reactions of 1 with X2 under photoirradiation at room temperature (Fig. 10b). Such

photoreactions are possibly triggered from the photo-induced cleavage of the Ir–Ir bond in 1 because the related reactions were not observed in the dark. Based on the photoreactivity and EPR

studies, generation of a reactive radical monomer is suggested for these reactions. Although the excited-state potential for the oxidation process of 1III/II* (–0.45 V _vs_. SCE) is

comparable or sufficient for the reduction of Br2 (+0.47 V) or I2 (+0.26 V), the very short excited-state lifetime should unfavour this bimolecular photo-induced electron-transfer process

from the 3MMLCT excited state. Attempts have been made to trap the radical species by a common spin trapping agent, TEMPO. Surprisingly, an unprecedented complex 9,

[Ir(_t_Bu3-terpy)(PPh3){HNC(CH3)}2C(CN)]2+ (86%), was isolated from the reaction of 1 with TEMPO upon photoirradiation (Fig. 10c). Uncommon trimerization of acetonitrile is ascribed to the

formation of the chelating ligand, {HNC(CH3)}2C(CN), and the proposed mechanism is suggested in Supplementary Fig. S45. It is noteworthy that this reaction cannot occur in the dark or by

replacing TEMPO with potassium _tert_-butoxide. These results indicate that this reaction should involve the photogeneration of radical monomer and could not be initiated by simple

deprotonation of acetonitrile. One related example about trimethylgallium-induced trimerization of acetonitrile was also reported in the presence of halide ions at 60 °C89. No related

trapped species could be isolated from the reaction of 1 with other radical trapping reagents, butylated hydroxytoluene (BHT) and diphenylethylene (DPE). All the products 7–9 from these

photoreactions were fully characterized by 1H, 13C{1H} and 31P{1H} NMR spectroscopy, HRMS, IR spectroscopy and satisfactory elemental analysis (Supplementary Figs. S46–S60). Their molecular

structures were also confirmed by X-ray crystallography, as shown in Fig. 10d. Their structural data, selected bond distances and angles are summarized in Supplementary Tables S21–S29.

CONCLUSIONS We report a series of tetracationic diiridium(II) complexes with an unsupported and long Ir(II)–Ir(II) bond for the first time. Our systematic computational study unveils that

they possess the largest binding (dimerization) energy than the other related diiridium(II) complexes with the shorter metal–metal bond. Significant non-covalent London dispersion

interactions were realized to overcome the considerable electrostatic repulsion between the two corresponding dicationic metal fragments. Moreover, these complexes were found to exhibit

photo-luminescence in both solution and solid states, as the first example of luminescent unsupported diiridium(II) system. Photoreactions, including an interesting trimerization of

acetonitrile, initiated from the generation of radical monomer were also explored. Experimental and computational studies on a series of unsupported diiridium(II) complexes were investigated

for the understanding of their electronic structures. Tuning of photophysical and photoreactivity properties of these dirridium(II) complexes was achieved by changing the pincer ligands in

this study. Further research for the improvement of photoluminescence efficiency or exploration of other possible photoactivated radical mediated reactions by variation of different ligands

is ongoing. This work provides the first systematic study of a series of unsupported diiridium(II) system to open up an avenue for the fundamental understanding about the structural, bonding

and photofunctional properties of these rare complexes. METHOD EXPERIMENTAL AND COMPUTATIONAL DETAILS See Supplementary Methods in the Supplementary Information. ANALYTICAL DATA INCLUDING

1H, 13C{1H} AND 31P{1H} NMR SPECTROSCOPY, HRMS, IR SPECTROMETRY See Figs. S1–S24 and Figs. 46–60 in the Supplementary Information. COMPUTAIONAL RESULTS See Tables S13–S20 and Tables S30–S48

in the Supplementary Information. GENERAL PROCEDURES Unless otherwise noted, all experiments were performed under an atmosphere of nitrogen with the rigid exclusion of air and moisture using

standard Schlenk or cannula techniques, or in a glovebox. SYNTHESIS. PREPARATION OF [IR(II)(_T_BU3-TERPY)(CO)(PPH3)]2[OTF]4 (1) AgOTf (56 mg, 218 μmol) was added to [IrCl(CO)(PPh3)2] (80 

mg, 102 μmol) in dry and degassed THF (15 mL). The mixture was allowed to stir for 1 h at room temperature, and then the filtrate was transferred in a dropwise fashion to a solution of

4,4′,4″-tri-_tert_-butyl-2,2′:6′,2″-terpyridine (42 mg, 103 μmol) in THF (15 mL). The resulting solution was allowed to stir for 72 h at room temperature in the absence of light, after

which, the red suspension was filtered and washed with multiple portions of tetrahydrofuran (20 mL) to give a red solid mixed with metallic Ag. The mixture was dissolved in a minimum amount

of CH3CN to give a deep red solution. Recrystallization by the slow diffusion of diethyl ether to the filtrate gave 1 as red crystals (77 mg, 62%). 1H NMR (400 MHz, CD3CN, 298 K): _δ_ 8.74

(br, 4H, _t_Bu3-terpy C_H_), 8.31 (br, 4H, _t_Bu3-terpy C_H_), 7.65 (br, 4H, _t_Bu3-terpy C_H_), 7.45 (t, _J_ = 7.5 Hz, 6H, PPh3 C_H_), 7.16 (t, _J_ = 7.8 Hz, 12H, PPh3 C_H_), 6.69 (m, 16H,

_t_Bu3-terpy and PPh3 C_H_), 1.74 (s, 18H, _t_Bu3-terpy CH3), 1.35 ppm (s, 36H, _t_Bu3-terpy CH3). 13C{1H} NMR (100 MHz, CD3CN, 298 K): _δ_ 171.6 (_C_O), 169.2, 166.7, 155.8, 155.2, 152.3,

133.5, 133.4, 131.0, 130.9, 128.2, 127.7, 127.2, 124.3, 124.0, 123.8, 123.7, 120.6 (aromatic _C_ and _C_H), 38.3, 36.9 (_C_Me3), 31.0, 30.5 ppm (_C_H3). 31P{1H} NMR (162 MHz, CD3CN, 298 K):

_δ_ −14.2 ppm (_P_Ph3). IR (KBr disk): _v_ = 2060 cm−1 (_v_(C ≡ O)), 1155 cm−1 (_v_(S = O)). HRMS (ESI). Calcd for C95H100F9Ir2N6O11P2S3 ([M − OTf]+): m/z 2215.5197. Found: m/z 2215.5212.

Elemental analyses calcd for C100H106F12Ir2N8O14P2S4 (1·2CH3CN), found (calcd): C, 49.17 (49.09); H, 4.47 (4.37); N, 4.65 (4.58). PREPARATION OF [IR(II)(_T_BU3-TERPY)(CO)(PPH3)]2[BF4]4

(1') This complex was prepared as red crystals from AgBF4 (42 mg, 218 μmol), [IrCl(CO)(PPh3)2] (80 mg, 102 μmol) and 4,4′,4″-tri-_tert_-butyl-2,2′:6′,2″-terpyridine (42 mg, 103 μmol) in

THF using the same procedure reported for 1: yield 65 mg (60%). X-ray-quality crystals were obtained by the slow diffusion of diethyl ether to the filtrate at room temperature. 1H NMR (400 

MHz, CD3CN, 298 K): _δ_ 8.71 (br, 4H, _t_Bu3-terpy CH), 8.30 (br, 4H, _t_Bu3-terpy CH), 7.60 (br, 4H, _t_Bu3-terpy C_H_), 7.44 (t, _J_ = 7.6 Hz, 6H, PPh3 CH), 7.17 (t, _J_ = 7.6 Hz, 12H,

PPh3 CH), 6.71 (dd, _J1_ = 12.8, _J2_ = 6.4 Hz, 12H, PPh3 C_H_), 6.63 (br, 4H, _t_Bu3-terpy CH), 1.73 (s, 18H, _t_Bu3-terpy CH3), 1.35 ppm (s, 36H, _t_Bu3-terpy CH3). 13C{1H} NMR (100 MHz,

CD3CN, 298 K): _δ_ 171.8 (_C_O), 169.5, 166.9, 155.5, 155.2, 152.2, 133.5, 133.4, 133.3, 131.0, 130.9, 128.0, 124.4, 124.1, 123.9 (aromatic _C_ and CH), 38.2, 36.8 (_C_Me3), 31.0, 30.5 ppm

(CH3). 31P{1H} NMR (162 MHz, CD3CN, 298 K): _δ_ −13.7 ppm (_P_Ph3). 19F{1H} NMR (376 MHz, CD3CN, 298 K): _δ_ −151.16 ppm (B_F_4–). IR (KBr disk): _v_ = 2056 cm−1 (_v_(C ≡ O)). HRMS (ESI).

Calcd for C92H100B3F12Ir2N6O2P2 ([M – BF4]+): m/z 2029.6724. Found: m/z 2029.6755. Elemental analyses calcd for C92H100B4F16Ir2N6O2P2 (1'), found (calcd): C, 52.01 (52.23); H, 4.88

(4.76); N, 4.04 (3.97). PREPARATION OF [IR(II)(TERPYRIDINE)(CO)(PPH3)]2[OTF]4 (2) AgOTf (56 mg, 218 μmol) was added to [IrCl(CO)(PPh3)2] (80 mg, 102 μmol) in dry and degassed CH3CN (15 mL).

The mixture was allowed to stir for 1 h at room temperature, and then the filtrate was transferred in a dropwise fashion to a solution of 2, 2':6',2''-terpyridine (24 mg,

103 μmol) in CH3CN (15 mL). The resulting solution was allowed to stir for 7 days at room temperature in the absence of light, after which, the deep brown suspension was filtered and the

filtrate was concentrated to 2 mL. Recrystallization by the slow diffusion of diethyl ether to the filtrate gave 2 as leaf-shaped brown crystals (59 mg, 55%). 1H NMR (400 MHz, CD3CN, 298 K):

_δ_ 8.35 (d, _J_ = 5.6 Hz, 4H, terpyridine CH), 8.31 (t, _J_ = 8.2 Hz, 2H, terpyridine CH), 8.02 (t, _J_ = 8.0 Hz, 4H, terpyridine CH), 7.90 (d, _J_ = 8.2 Hz, 4H, terpyridine CH), 7.79 (d,

_J_ = 8.0 Hz, 4H, terpyridine CH), 7.46 (t, _J_ = 7.5 Hz, 6H, PPh3 CH), 7.38 (t, _J_ = 6.1 Hz, 4H, terpyridine CH), 7.18 (t, _J_ = 7.9 Hz, 12H, PPh3 CH), 6.72 ppm (m, 12H, PPh3 CH). 13C{1H}

NMR (100 MHz, CD3CN, 298 K): _δ_ 173.1 (CO), 156.9, 154.1, 150.6, 143.2, 143.0, 133.9, 133.3, 133.2, 133.1, 131.2, 131.1, 128.5, 127.6, 123.8, 123.5, 123.2, 123.0, 120.6 ppm (aromatic _C_

and CH). 31P{1H} NMR (162 MHz, CD3CN, 298 K): _δ_ −12.3 ppm (PPh3). IR (KBr disk): _v_ = 2060 cm−1 (_v_(C ≡ O)), 1157 cm−1 (_v_(S = O)). HRMS (ESI). Calcd for C71H52F9Ir2N6O11P2S3

([M–OTf]+): m/z 1879.1441. Found: m/z 1879.1433. Elemental analyses calcd for C72H56F12Ir2N6O16P2S4 (2·2H2O), found (calcd): C, 41.38 (41.90); H, 2.83 (2.73); N, 4.19 (4.07). PREPARATION OF

[IR(II)(_N_-BU2BZIMB)(CO)(PPH3)]2[OTF]4 (3) This complex was prepared as deep red crystals from AgOTf (56 mg, 218 μmol), [IrCl(CO)(PPh3)2] (80 mg, 102 μmol) and

2,2′-(1,3-phenylene)bis[1-butyl-1_H_-benzimidazole] (44 mg, 103 μmol) (_n_-Bu2bzimb) in THF using the same procedure reported for 1: yield 71 mg (58%). X-ray-quality crystals were obtained

by the slow diffusion of diethyl ether to the filtrate at room temperature. 1H NMR (400 MHz, CD3CN, 298 K): _δ_ 8.92 (t, _J_ = 8.2 Hz, 2H, _n_-Bu2bzimb CH), 8.55 (d, _J_ = 8.3 Hz, 4H,

_n_-Bu2bzimb CH), 7.53 (d, _J_ = 7.3 Hz, 4H, _n_-Bu2bzimb CH), 7.46 (d, _J_ = 7.3 Hz, 4H, _n_-Bu2bzimb CH), 7.27 (m, 10H, _n_-Bu2bzimb and PPh3 CH), 6.90 (m, 16H, _n_-Bu2bzimb and PPh3 CH),

6.36 (dd, _J1_ = 12.8, _J2_ = 6.4 Hz, 12H, PPh3 CH), 6.63 (s, 18H, _t_Bu3-terpy CH3), 4.41 (m, 4H, NCH2CH2CH2CH3), 4.16 (m, 4H, NC_H_2CH2CH2CH3), 1.57 (m, 16H, NCH2C_H_2C_H_2CH3), 1.12 ppm

(t, _J_ = 6.8 Hz, 12H, NCH2CH2CH2CH3). 13C{1H} NMR (100 MHz, CD3CN, 298 K): _δ_ 173.0 (_C_O), 147.8, 145.6, 144.7, 137.9, 134.9, 133.9, 133.4, 133.3, 130.3, 130.2, 129.3, 128.5, 123.8,

123.0, 122.8, 122.5, 120.6, 116.4, 114.7 (aromatic _C_ and CH), 47.8 (N_C_H2CH2CH2CH3), 33.4 (NCH2_C_H2CH2CH3), 20.5 (NCH2CH2_C_H2CH3), 13.9 ppm (NCH2CH2CH2_C_H3). 31P{1H} NMR (162 MHz,

CD3CN, 298 K): _δ_ −11.0 ppm (_P_Ph3). IR (KBr disk): _v_ = 2035 cm−1 (_v_(C ≡ O)), 1157 cm−1 (_v_(S = O)). HRMS (ESI). Calcd for C95H88F9Ir2N10O11P2S3 ([M–OTf]+): m/z 2259.4381. Found: m/z

2259.4390. Elemental analyses calcd for C96H88F12Ir2N10O14P2S4 (3), found (calcd): C, 47.68 (47.88); H, 3.86 (3.68); N, 5.80 (5.82). PHOTOCHEMICAL REACTION OF 1. PREPARATION OF

[IR(III)(_T_BU3-TERPY)(CO)(PPH3)BR][OTF]2 (7) Bromine (7 mg, 42 μmol) was added to 1 (66 mg, 28 μmol) in dry and degassed CH3CN (15 mL). The mixture was allowed to stir for 12 h at room

temperature upon irradiation of light, giving a brown solution which was then concentrated to 2 mL. Recrystallization by the slow diffusion of diethyl ether to the concentrated solution gave

7 as yellow crystals (55 mg, 78%). 1H NMR (400 MHz, CD3CN, 298 K): _δ_ 8.89 (d, _J_ = 6.2 Hz, 2H, _t_Bu3-terpy CH), 8.39 (s, 2H, _t_Bu3-terpy CH), 8.21 (d, _J_ = 2.1 Hz, 2H, _t_Bu3-terpy

CH), 7.62 (m, 5H, _t_Bu3-terpy and PPh3 CH), 7.37 (m, 6H, PPh3 CH), 7.14 (m, 6H, PPh3 CH), 1.61 (s, 9H, _t_Bu3-terpy CH3), 1.41 ppm (s, 18H, _t_Bu3-terpy CH3). 13C{1H} NMR (100 MHz, CD3CN,

298 K): _δ_ 171.4 (_C_O), 169.5, 161.9, 161.8, 157.4, 156.8, 153.7, 134.6, 134.5, 134.2, 134.1, 131.2, 131.0, 129.0, 126.6, 125.6, 123.8, 123.5, 122.9, 120.6 (aromatic _C_ and CH), 38.4,

37.2 (_C_Me3), 30.7, 30.2 ppm (CH3). 31P{1H} NMR (162 MHz, CD3CN, 298 K): _δ_ −8.0 ppm (_P_Ph3). IR (KBr disk): _v_ = 2102 cm−1 (_v_(C ≡ O)), 1157 cm−1 (_v_(S = O)). HRMS (ESI). Calcd for

C46H50BrIrN3OP ([M − 2OTf]2+): m/z 481.6247. Found: m/z 481.6233. Elemental analyses calcd for C50H53BrF6IrN4O7PS2 (7·CH3CN), found (calcd): C, 45.97 (46.08); H, 4.22 (4.10); N, 4.09 (4.30).

PREPARATION OF [IR(III)(_T_BU3-TERPY)(CO)(PPH3)I][OTF]2 (8) This complex was prepared as yellow crystals from iodine (11 mg, 42 μmol) and 1 (66 mg, 28 μmol) in CH3CN using the same

procedure reported for 7: yield 61 mg (83%). X-ray-quality crystals were obtained by the slow diffusion of diethyl ether to the concentrated solution at room temperature. 1H NMR (400 MHz,

CD3CN, 298 K): _δ_ 8.90 (d, _J_ = 6.2 Hz, 2H, _t_Bu3-terpy CH), 8.39 (s, 2H, _t_Bu3-terpy CH), 8.21 (d, _J_ = 2.1 Hz, 2H, _t_Bu3-terpy CH), 7.62 (m, 5H, _t_Bu3-terpy and PPh3 CH), 7.36 (m,

6H, PPh3 CH), 7.13 (m, 6H, PPh3 CH), 1.62 (s, 9H, _t_Bu3-terpy CH3), 1.41 ppm (s, 18H, _t_Bu3-terpy CH3). 13C{1H} NMR (100 MHz, CD3CN, 298 K): _δ_ 171.1 (_C_O), 169.4, 162.3, 157.8, 157.0,

153.7, 134.5, 134.2, 134.1, 131.2, 131.1, 129.0, 126.6, 125.7, 123.8, 123.2, 122.6, 120.6 (aromatic _C_ and CH), 38.4, 37.2 (_C_Me3), 30.7, 30.2 ppm (CH3). 31P{1H} NMR (162 MHz, CD3CN, 298 

K): _δ_ −9.4 ppm (_P_Ph3). IR (KBr disk): _v_ = 2112 cm−1 (_v_(C ≡ O)), 1155 cm−1 (_v_(S = O)). HRMS (ESI). Calcd for C47H50F3IrIN3O4PS ([M–OTf]+): m/z 1160.1880. Found: m/z 1160.1893.

Elemental analyses calcd for C48H50F6IrIN3O7PS2 (8), found (calcd): C, 44.00 (44.04); H, 4.01 (3.85); N, 3.12 (3.21). PREPARATION OF [IR(III)(_T_BU3-TERPY)(HNC(CH3)C(CN)C(CH3)NH)(PPH3)]

[OTF]2 (9) TEMPO (13 mg, 83 μmol) was added to 1 (24 mg, 10 μmol) in dry and degassed CH3CN (3 mL). The mixture was allowed to stir for 72 h at room temperature upon irradiation of 355 nm Xe

lamp, giving a yellow solution which was then concentrated to 1 mL. Recrystallization by the slow diffusion of diethyl ether to the concentrated solution gave 9 as yellow crystals (22 mg,

86%). 1H NMR (400 MHz, CD3CN, 298 K): _δ_ 8.42 (d, _J_ = 6.1 Hz, 2H, _t_Bu3-terpy CH), 8.27 (s, 2H, _t_Bu3-terpy CH), 8.00 (d, _J_ = 2.0 Hz, 2H, _t_Bu3-terpy CH), 7.77 (br, 1H, N_H_), 7.64

(dd, _J1_ = 6.1, _J2_ = 2.1 Hz, 22H, _t_Bu3-terpy CH), 7.50 (m, 3H, PPh3 CH), 7.27 (m, 6H, PPh3 CH), 6.89 (m, 6H, PPh3 C_H_), 6.77 (br, 1H, N_H_), 2.57, (s, 3H, HNC(C_H_3)), 1.89 (s, 3H,

HNC(CH3)), 1.61 (s, 9H, _t_Bu3-terpy CH3), 1.39 ppm (s, 18H, _t_Bu3-terpy CH3). 13C{1H} NMR (100 MHz, CD3CN, 298 K): _δ_ 168.8, 167.9, 166.1, 165.8, 159.0, 156.6, 153.6, 134.0, 133.9, 133.7,

133.0, 130.5, 130.4, 126.9, 124.7, 124.2, 124.0, 123.7, 123.6, 120.6 (aromatic _C_ and CH, HN_C_(CH3)C(CN)_C_(CH3)NH), 122.1 (_C_N), 80.4 (_C_CN), 37.9, 36.8 (_C_Me3), 31.0, 30.4 (C(CH3)3),

28.3, 25.9 ppm (HNC(CH3)C(CN)C(CH3)NH). 31P{1H} NMR (162 MHz, CD3CN, 298 K): _δ_ −16.8 ppm (_P_Ph3). IR (KBr disk): _v_ = 2191 cm−1 (_v_(C ≡ N)), 1157 cm−1 (_v_(S = O)). HRMS (ESI). Calcd

for C53H57F6IrN6O6PS2 ([M − H]-): m/z 1275.3058. Found: m/z 1275.3064. Elemental analyses calcd for C53H58F6IrN6O6PS2 (9), found (calcd): C, 49.46 (49.87); H, 4.73 (4.58); N, 6.54 (6.58).

DATA AVAILABILITY Experimental and computational details can be accessed from Supplementary Methods in the Supplementary Information. Analytical data including 1H, 13C{1H} and 31P{1H} NMR

spectroscopy, HRMS, IR spectrometry can be obtained from Figs. S1–S24 and Figs. 46–60 in the Supplementary Information. Computaional results can be found from Tables S13–S20 and Tables

S30–S48 in the Supplementary Information. Cartesian coordinates from computational studies can be accessed from Supplementary Data 1 from this article. The X-ray crystallographic coordinates

for structures reported in this Article have been deposited at the Cambridge Crystallographic Data Centre (CCDC), under deposition number CCDC-2167632 (1), CCDC-2167633 (1'),

CCDC-2167634 (2), CCDC-2167635 (3), CCDC-2167638 (7), CCDC-2167636 (8), CCDC-2167637 (9). These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via

www.ccdc.cam.ac.uk/data_request/cif, or accessed from Supplementary Data 2–8 from this article. CHANGE HISTORY * _ 12 MAY 2025 A Correction to this paper has been published:

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_Organometallics_ 17, 4226–4231 (1998). Article  CAS  Google Scholar  Download references ACKNOWLEDGEMENTS K.M.-C.W. acknowledges the National Natural Science Foundation of China (22171126),

the Science, Technology and Innovation Commission of Shenzhen Municipality (JCYJ20210324104609025 and JCYJ20190809165411528), and the assistance of SUSTech Core Research Facilities. We

gratefully thank Dr. Z. Tang, Dr. Y.H. Yang and Mr. N. Qin for their help and discussions in EPR measurements. L.W.C. acknowledges the National Natural Science Foundation of China (21933003,

22193020 and 22193023), Shenzhen Nobel Prize Scientists Laboratory Project (C17783101) and Guangdong Provincial Key Laboratory of Catalysis (2020B121201002) as well as the Center for

Computational Science and Engineering at SUSTech and the CHEM high performance supercomputer cluster at department of chemistry, SUSTech. AUTHOR INFORMATION Author notes * These authors

contributed equally: Fangrui Zheng, Yuhong Yang. AUTHORS AND AFFILIATIONS * Department of Chemistry, Southern University of Science and Technology, 1088 Xueyuan Blvd., Shenzhen, 518055, P.R.

China Fangrui Zheng, Yuhong Yang, Siye Wu, Shunan Zhao, Yifan Zhu, Zeyin Yan, Lung Wa Chung & Keith Man-Chung Wong * Analysis and Testing Center, Shenzhen Technology University, 3002

Lantian Road, Shenzhen, 518118, P. R. China Fangrui Zheng * Shenzhen Institute for Quantum Science and Engineering, Southern University of Science and Technology, International Quantum

Academy (SIQA), and Shenzhen Branch, Hefei National Laboratory, Shenzhen Key Laboratory of Quantum Science and Engineering, Futian District, Shenzhen, 518055, China Huimin Su & Jun-Feng

Dai Authors * Fangrui Zheng View author publications You can also search for this author inPubMed Google Scholar * Yuhong Yang View author publications You can also search for this author

inPubMed Google Scholar * Siye Wu View author publications You can also search for this author inPubMed Google Scholar * Shunan Zhao View author publications You can also search for this

author inPubMed Google Scholar * Yifan Zhu View author publications You can also search for this author inPubMed Google Scholar * Huimin Su View author publications You can also search for

this author inPubMed Google Scholar * Jun-Feng Dai View author publications You can also search for this author inPubMed Google Scholar * Zeyin Yan View author publications You can also

search for this author inPubMed Google Scholar * Lung Wa Chung View author publications You can also search for this author inPubMed Google Scholar * Keith Man-Chung Wong View author

publications You can also search for this author inPubMed Google Scholar CONTRIBUTIONS K.M.-C.W. directed and conceived this project. F.Z., S.W., S.Z., Y.Z., H.S. and J.-F.D. conducted the

experiments. Y.Y., Z.Y. and L.W.C. did the theoretical works. All authors discussed the results and wrote the manuscript. L.W.C. and K.M.-C.W. performed data analysis and prepared the

manuscript. All authors have given approval to the final version of the manuscript. CORRESPONDING AUTHORS Correspondence to Lung Wa Chung or Keith Man-Chung Wong. ETHICS DECLARATIONS

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Structure-property relationships of photofunctional diiridium(II) complexes with tetracationic charge and an unsupported Ir–Ir bond. _Commun Chem_ 5, 159 (2022).

https://doi.org/10.1038/s42004-022-00775-4 Download citation * Received: 15 July 2022 * Accepted: 09 November 2022 * Published: 23 November 2022 * DOI:

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