Near-infrared phosphorescence in a ruthenium(<sc>ii</sc>) complex equipped with a pyridyl-1,2-azaborine ligand

被引:0
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作者
Pompei, Matteo [1 ]
Monti, Filippo [2 ]
Sambri, Letizia [1 ]
Armaroli, Nicola [2 ]
Baschieri, Andrea [2 ]
机构
[1] Univ Bologna, Dept Ind Chem Toso Montanari, Via Piero Gobetti 85, I-40129 Bologna, Italy
[2] Natl Res Council Italy CNR, Inst Organ Synth & Photoreact ISOF, Via Piero Gobetti 101, I-40129 Bologna, Italy
关键词
SET MODEL CHEMISTRY; TRICARBONYLCHROMIUM COMPLEXES; DENSITY FUNCTIONALS; HYDROGEN STORAGE; QUANTUM YIELDS; TOTAL ENERGIES; AZABORINE; RING; 1,2-DIHYDRO-1,2-AZABORINES; HETEROCYCLES;
D O I
10.1039/d4dt03115f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The 4-methyl-2-(pyridin-2-yl)-2,1-borazaronaphthalene molecule Hazab-py has been successfully used, for the first time, as a ligand in a ruthenium(ii) polypyridine complex A (with the formula [Ru(dtbbpy)2(azab-py)]+, where dtbbpy = 4,4 '-di-tert-butyl-2,2 '-bipyridine). This compound was characterized by NMR spectroscopy and high-resolution mass spectrometry (MS), and its electrochemical and photophysical properties were fully investigated and compared to those of its homoleptic analogue [Ru(dtbbpy)3]2+ (B), an archetypical mono-cationic cyclometalated complex C (with the formula [Ru(dtbbpy)2(ppy)]+, where Hppy = 2-phenylpyridine), and the more structurally similar analogue [Ru(dtbbpy)2(naft-py)]+ (D), where the B-N unit of the azaborine ligand is replaced by a standard C 00000000 00000000 00000000 00000000 11111111 00000000 11111111 00000000 00000000 00000000 C one, resulting in the 2-(naphthalen-2-yl)pyridine ligand (Hnaft-py). The presence of the novel 1,2-azaborine ligand induces a 0.51 V decrease in the redox gap of complex A, compared to that of B, leading to electrochemical and photophysical properties that resemble those of C and D. Accordingly, the azaborine complex displays an emission band extending up to the near infrared region of the spectrum (with the maximum at 765 nm in room-temperature acetonitrile solution), arising from a triplet metal-to-ligand charge-transfer (3MLCT) state. As in the case of other mono-cationic cyclometalated ruthenium(ii) complexes, A shows modest photoluminescence quantum yields (PLQYs), but higher PLQYs when compared to those of its direct CC analogue D (e.g., PLQY = 0.6 vs. 0.1% in a PMMA matrix at 298 K). Density functional theory (DFT) calculations were used to provide complete rationalization of the electronic properties of all the complexes and to identify lower-lying metal-centred triplets (3MC), responsible for the low PLQYs of such an azaborine-based ruthenium(ii) complex.
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页码:1633 / 1645
页数:13
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