Matches in SemOpenAlex for { <https://semopenalex.org/work/W1972429552> ?p ?o ?g. }
- W1972429552 endingPage "2719" @default.
- W1972429552 startingPage "2711" @default.
- W1972429552 abstract "The reaction of the cyclometalated chloro-bridged iridium(III) dimer, [(ppy)2 Ir(μ-Cl)]2 (ppy – 2-phenyl pyridine) with N-aryl picolinamides (LH, LH–NO2, LH–CH3, LH–l, LH–F) resulted in the formation of neutral heteroleptic complexes [Ir(ppy)2L] (1), [Ir(ppy)2L–NO2](2), [Ir(ppy)2L–CH3](3), [Ir(ppy)2L–Cl](4) and [Ir(ppy)2L–F] (5). These complexes contain a six-coordinate iridium with a 2C, 4N coordination environment. The N-aryl picolinamide ligands are deprotonated during complexation and the resulting amidates bind to iridium in a chelating manner (N, N). Optical spectroscopic studies revealed that the complexes 1–5 exhibited intense π→π∗ absorptions in the ultraviolet region. In addition low energy transitions due to 1MLCT, 1LLCT and 3MLCT are also seen. The emission spectra of 1–5, upon excitation at 450 nm, show a single emission with a λmax around 513 nm. The lifetimes of this emission are in between 7.4 and 9.6 μs while the quantum yields are quite high and range from 0.2 to 0.5. Based on density functional theory (DFT) calculations on 1 and 3, the three highest occupied orbitals are composed of ligand π orbitals mixed with Ir-d orbitals while the three lowest unoccupied orbitals are mostly π orbitals of the ligands. From the time dependent DFT calculations it is revealed that the lowest energy electronic singlet and triplet excitations are a mixture of MLCT and LLCT." @default.
- W1972429552 created "2016-06-24" @default.
- W1972429552 creator A5008238569 @default.
- W1972429552 creator A5036410275 @default.
- W1972429552 creator A5053407756 @default.
- W1972429552 creator A5060043376 @default.
- W1972429552 creator A5086589401 @default.
- W1972429552 date "2011-07-01" @default.
- W1972429552 modified "2023-10-16" @default.
- W1972429552 title "Cyclometalated Ir(III) complexes containing N-aryl picolinamide ancillary ligands" @default.
- W1972429552 cites W1627110571 @default.
- W1972429552 cites W1966182479 @default.
- W1972429552 cites W1966282563 @default.
- W1972429552 cites W1968203733 @default.
- W1972429552 cites W1972964253 @default.
- W1972429552 cites W1979102452 @default.
- W1972429552 cites W1985695193 @default.
- W1972429552 cites W1987907156 @default.
- W1972429552 cites W1990425292 @default.
- W1972429552 cites W1990570667 @default.
- W1972429552 cites W1995794402 @default.
- W1972429552 cites W1996293877 @default.
- W1972429552 cites W1998464834 @default.
- W1972429552 cites W2000614287 @default.
- W1972429552 cites W2001823292 @default.
- W1972429552 cites W2002111447 @default.
- W1972429552 cites W2003155086 @default.
- W1972429552 cites W2007866726 @default.
- W1972429552 cites W2010111245 @default.
- W1972429552 cites W2010821434 @default.
- W1972429552 cites W2017012005 @default.
- W1972429552 cites W2017080534 @default.
- W1972429552 cites W2017743572 @default.
- W1972429552 cites W2017832858 @default.
- W1972429552 cites W2020736879 @default.
- W1972429552 cites W2021502908 @default.
- W1972429552 cites W2022573775 @default.
- W1972429552 cites W2023271753 @default.
- W1972429552 cites W2030051480 @default.
- W1972429552 cites W2031301453 @default.
- W1972429552 cites W2032341987 @default.
- W1972429552 cites W2033534524 @default.
- W1972429552 cites W2051036147 @default.
- W1972429552 cites W2052329392 @default.
- W1972429552 cites W2053334373 @default.
- W1972429552 cites W2054704030 @default.
- W1972429552 cites W2060813357 @default.
- W1972429552 cites W2062156448 @default.
- W1972429552 cites W2062224143 @default.
- W1972429552 cites W2064714065 @default.
- W1972429552 cites W2068617439 @default.
- W1972429552 cites W2071569358 @default.
- W1972429552 cites W2072515914 @default.
- W1972429552 cites W207396953 @default.
- W1972429552 cites W2073994997 @default.
- W1972429552 cites W2078801745 @default.
- W1972429552 cites W2081118530 @default.
- W1972429552 cites W2084766057 @default.
- W1972429552 cites W2085400086 @default.
- W1972429552 cites W2086021375 @default.
- W1972429552 cites W2086748759 @default.
- W1972429552 cites W2087593458 @default.
- W1972429552 cites W2091131480 @default.
- W1972429552 cites W2094027528 @default.
- W1972429552 cites W2094408698 @default.
- W1972429552 cites W2095917356 @default.
- W1972429552 cites W2104510081 @default.
- W1972429552 cites W2106824077 @default.
- W1972429552 cites W2106997539 @default.
- W1972429552 cites W2109043233 @default.
- W1972429552 cites W2111091421 @default.
- W1972429552 cites W2119249051 @default.
- W1972429552 cites W2119783360 @default.
- W1972429552 cites W2126301265 @default.
- W1972429552 cites W2143981217 @default.
- W1972429552 cites W2150315121 @default.
- W1972429552 cites W2151256381 @default.
- W1972429552 cites W2151704214 @default.
- W1972429552 cites W2157787898 @default.
- W1972429552 cites W2158422033 @default.
- W1972429552 cites W2172097676 @default.
- W1972429552 cites W2312715951 @default.
- W1972429552 cites W2326781119 @default.
- W1972429552 cites W2878404963 @default.
- W1972429552 cites W2950135852 @default.
- W1972429552 cites W3136132297 @default.
- W1972429552 cites W3138308008 @default.
- W1972429552 cites W4232565521 @default.
- W1972429552 cites W4249293795 @default.
- W1972429552 cites W4385795638 @default.
- W1972429552 doi "https://doi.org/10.1016/j.jorganchem.2011.04.011" @default.
- W1972429552 hasPublicationYear "2011" @default.
- W1972429552 type Work @default.
- W1972429552 sameAs 1972429552 @default.
- W1972429552 citedByCount "10" @default.
- W1972429552 countsByYear W19724295522012 @default.
- W1972429552 countsByYear W19724295522013 @default.
- W1972429552 countsByYear W19724295522014 @default.