Matches in SemOpenAlex for { <https://semopenalex.org/work/W4383875341> ?p ?o ?g. }
- W4383875341 endingPage "11341" @default.
- W4383875341 startingPage "11325" @default.
- W4383875341 abstract "We report on a facile method for the optical resolution of cyclometalated iridium(III) (Ir(III)) complexes via diastereomers formed with chiral auxiliaries. The racemic carboxylic acids of Ir(III) complexes (fac-4 (fac-Ir(ppyCO2H)3 (ppy: 2-phenylpyridine)), fac-6 (fac-Ir(tpyCO2H)3 (tpy: 2-(4'-tolyl)pyridine)), and fac-13 (fac-Ir(mpiqCO2H)3 (mpiq: 1-(4'-methylphenyl)isoquinoline))) were converted into the diastereomers, Δ- and Λ-forms of fac-9 (from fac-6), fac-10 (from fac-4), fac-11 (from fac-6), and fac-14 (from fac-13), respectively, by the condensation with (1R,2R)-1,2-diaminocyclohexane or (1R,2R)-2-aminocyclohexanol. The resulting diastereomers were separated by HPLC (with a nonchiral column) or silica gel column chromatography, and their absolute stereochemistry was determined by X-ray single-crystal structure analysis and CD (circular dichroism) spectra. Spectra of all diastereomers of the Ir(III) complexes are reported. Hydrolysis of the ester moieties of Δ- and Λ-forms of fac-10, fac-11, and fac-14 gave both enantiomers of the corresponding carboxylic acid derivatives in the optically pure forms, Δ-fac and Λ-fac-4, -6, and -13, respectively." @default.
- W4383875341 created "2023-07-12" @default.
- W4383875341 creator A5014198802 @default.
- W4383875341 creator A5016789715 @default.
- W4383875341 creator A5027301360 @default.
- W4383875341 creator A5029676343 @default.
- W4383875341 creator A5031507015 @default.
- W4383875341 creator A5035723665 @default.
- W4383875341 creator A5047599576 @default.
- W4383875341 creator A5054844732 @default.
- W4383875341 creator A5064992165 @default.
- W4383875341 date "2023-07-11" @default.
- W4383875341 modified "2023-10-01" @default.
- W4383875341 title "Optical Resolution of Carboxylic Acid Derivatives of Homoleptic Cyclometalated Iridium(III) Complexes via Diastereomers Formed with Chiral Auxiliaries" @default.
- W4383875341 cites W1440631406 @default.
- W4383875341 cites W1512388082 @default.
- W4383875341 cites W1657433554 @default.
- W4383875341 cites W1672706895 @default.
- W4383875341 cites W1968621300 @default.
- W4383875341 cites W1974717099 @default.
- W4383875341 cites W1976726008 @default.
- W4383875341 cites W1995976722 @default.
- W4383875341 cites W1996293877 @default.
- W4383875341 cites W1998596780 @default.
- W4383875341 cites W1998928990 @default.
- W4383875341 cites W2006195089 @default.
- W4383875341 cites W2011032033 @default.
- W4383875341 cites W2012213924 @default.
- W4383875341 cites W2013481481 @default.
- W4383875341 cites W2015826183 @default.
- W4383875341 cites W2017588171 @default.
- W4383875341 cites W2022396615 @default.
- W4383875341 cites W2022573775 @default.
- W4383875341 cites W2026875674 @default.
- W4383875341 cites W2027246322 @default.
- W4383875341 cites W2027389851 @default.
- W4383875341 cites W2033499737 @default.
- W4383875341 cites W2033534524 @default.
- W4383875341 cites W2035757873 @default.
- W4383875341 cites W2041084364 @default.
- W4383875341 cites W2042812106 @default.
- W4383875341 cites W2046018892 @default.
- W4383875341 cites W2047001506 @default.
- W4383875341 cites W2047865529 @default.
- W4383875341 cites W2048160294 @default.
- W4383875341 cites W2050190659 @default.
- W4383875341 cites W2052093022 @default.
- W4383875341 cites W2052329392 @default.
- W4383875341 cites W2057775919 @default.
- W4383875341 cites W2059511412 @default.
- W4383875341 cites W2062349797 @default.
- W4383875341 cites W2066255247 @default.
- W4383875341 cites W2066774243 @default.
- W4383875341 cites W2071065914 @default.
- W4383875341 cites W2104516185 @default.
- W4383875341 cites W2104696739 @default.
- W4383875341 cites W2105005637 @default.
- W4383875341 cites W2119783360 @default.
- W4383875341 cites W2129070049 @default.
- W4383875341 cites W2132539085 @default.
- W4383875341 cites W2143817553 @default.
- W4383875341 cites W2149352862 @default.
- W4383875341 cites W2156492711 @default.
- W4383875341 cites W2158422033 @default.
- W4383875341 cites W2168779636 @default.
- W4383875341 cites W2179552369 @default.
- W4383875341 cites W2284199874 @default.
- W4383875341 cites W2315213594 @default.
- W4383875341 cites W2317168270 @default.
- W4383875341 cites W2317637174 @default.
- W4383875341 cites W2319182059 @default.
- W4383875341 cites W2324281570 @default.
- W4383875341 cites W2328520826 @default.
- W4383875341 cites W2329914044 @default.
- W4383875341 cites W2333429831 @default.
- W4383875341 cites W2333723157 @default.
- W4383875341 cites W2401276562 @default.
- W4383875341 cites W2401746232 @default.
- W4383875341 cites W2416000321 @default.
- W4383875341 cites W2419268321 @default.
- W4383875341 cites W2436176790 @default.
- W4383875341 cites W2463890439 @default.
- W4383875341 cites W2464470593 @default.
- W4383875341 cites W2465194626 @default.
- W4383875341 cites W2514805672 @default.
- W4383875341 cites W2516466373 @default.
- W4383875341 cites W2519398776 @default.
- W4383875341 cites W2522229560 @default.
- W4383875341 cites W2551186060 @default.
- W4383875341 cites W2554992892 @default.
- W4383875341 cites W2558654750 @default.
- W4383875341 cites W2560438053 @default.
- W4383875341 cites W2566922150 @default.
- W4383875341 cites W2575244367 @default.
- W4383875341 cites W2598734643 @default.
- W4383875341 cites W2604555249 @default.
- W4383875341 cites W2605114720 @default.
- W4383875341 cites W2606680753 @default.