Extracurricular laboratory:new discovery of 4411-80-7

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The iridium(III) dihydride complexes [Ir(H)2(L1)(6,6?-bi-2-picoline)]BArF (5; L1 = (S)-1-[2-(2-adamantan-2-yl-4,5-dihydrooxazol-4-yl)-ethyl]-3-(2,6-diisopropylphenyl)-1,2-dihydroimidazol-2-ylidene, BArF = tetrakis[3,5-bis(trifluoromethyl)phenyl]borate) and [Ir(H)2(L2)(6,6?-bi-2-picoline)]BArF (6; L2 = (R)-2-((di-tert-butylphosphanyl)methyl)-4-phenyl-4,5-dihydrooxazole) were prepared from the corresponding [Ir(COD)(L)]BArF precursors by treatment with 6,6?-bi-2-picoline under H2 and characterized by 2D NMR spectroscopy and X-ray diffraction. In solution, the N,P complex 6 exists as two isomeric dihydride species (6a and 6b) that are in rapid equilibrium at room temperature. Furthermore, the X-ray structures for [Ir(COD)(L1)]BArF (1) and [Ir(COD)(L2)]BArF (2) are reported. The structural comparison of the solid-state structures of the iridium(I) precursor 1 and the iridium(III) dihydride complex 5 revealed a significant change in the backbone geometry of the C,N ligand. The original U-shaped conformation of the ligand switches to an S-shaped conformation, and therefore, the substituent in the oxazoline ring occupies different quadrants in the iridium coordination sphere. Notable in this context is the finding that a similar switch in the ligand backbone was observed for the C,N iridium(III) dihydride olefin species 3 ([Ir(H)2[(E)-1-methyl-4-(1-phenylprop-1-en-2-yl)benzene-D5](L1)]BArF), which represents a catalytically competent intermediate.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Recommanded Product: 6,6′-Dimethyl-2,2′-bipyridine, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 4411-80-7

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI