2016
DOI: 10.1021/acs.inorgchem.6b00527
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Asymmetric Synthesis of Enantiomerically Pure Mono- and Binuclear Bis(cyclometalated) Iridium(III) Complexes

Abstract: Chiral precursors Λ-[Ir(ppy)2(l-pro)] (Λ-L, where ppy is 2-phenylpyridine; pro is proline), Λ-[Ir(ppy)2(MeCN)2](PF6) (Λ-1), Δ-[Ir(ppy)2(d-pro)] (Δ-D), and Δ-[Ir(ppy)2(MeCN)2](PF6) (Δ-1) were synthesized from rac-[(Ir(ppy)2)2Cl2] and l-pro or d-pro by means of the auxiliary ligand strategy with 99% de values. The enantiopure mono complexes Λ/Δ-[Ir(ppy)2(L)](PF6) (L is 2,2'-bipyridine, Λ/Δ-2; L is 2,2'-dipyrimidine (dpm), Λ/Δ-3; L is 2,2'-bibenzimidazole (H2bbim), Λ/Δ-4) with 99% ee values and binuclear complexe… Show more

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Cited by 43 publications
(31 citation statements)
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“…Ir1 is coordinated by two phenylpyridine ligands with cis ‐metalated C atoms and trans ‐metalated N atoms. The Ir–N and Ir–C lengths are in accordance with the reported L 2 Ir(C^N) 2 complexes . The bond lengths Ir1–N5 (2.136[12] Å) and Ir1–N6 (2.185[13] Å) are slightly longer than those of Ir1–N2 (2.078[13] Å) and Ir1–N3 (2.056[13] Å), indicating that the carbon atoms on the phenylpyridine have strong trans effect .…”
Section: Resultssupporting
confidence: 86%
“…Ir1 is coordinated by two phenylpyridine ligands with cis ‐metalated C atoms and trans ‐metalated N atoms. The Ir–N and Ir–C lengths are in accordance with the reported L 2 Ir(C^N) 2 complexes . The bond lengths Ir1–N5 (2.136[12] Å) and Ir1–N6 (2.185[13] Å) are slightly longer than those of Ir1–N2 (2.078[13] Å) and Ir1–N3 (2.056[13] Å), indicating that the carbon atoms on the phenylpyridine have strong trans effect .…”
Section: Resultssupporting
confidence: 86%
“…This is complementary to using enantiomerically pure dichloro-bridged dimers, as reported for other systems. 49,52 Analogous to the mesityl-functionalised complex 11, the diastereomers rac 13 (stereochemistry confirmed by X-ray diffraction, Fig. 4) and meso 13 were easily separated.…”
Section: Dalton Transactions Papermentioning
confidence: 85%
“…, and [Ir(pq) 2 (bpy)](PF 6 ) were synthesized according to the literatures. [18][19][20][21] Column chromatography was performed with silica gel (300-400 mesh) under low light. Elemental (C, H, and N) analyses were carried out on an Elementar Vario EL analyzer.…”
Section: Materials and General Methodsmentioning
confidence: 99%