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Isomeric Separations of Cyclometalated Iridium (III) Complexes Using the ACQUITY UPC2 System

Applications | 2012 | WatersInstrumentation
SFC
Industries
Materials Testing
Manufacturer
Waters

Summary

Importance of the Topic


Cyclometalated iridium complexes serve as key emitters in OLED technology due to high quantum yields and tunable color emission. Their performance depends on the purity and isomeric form: facial and meridional geometric isomers exhibit different photophysical properties, while heteroleptic complexes also show optical isomerism. Rapid, mild separations are vital to ensure material integrity and device reliability.

Objectives and Study Overview


The study aimed to develop and demonstrate fast and efficient supercritical fluid chromatography methods using the Waters ACQUITY UPC2 system for isomeric separation of two representative cyclometalated iridium(III) compounds: homoleptic tris(2-(2,4-difluorophenyl)pyridine)iridium(III) (Ir(Fppy)3) and heteroleptic bis(4,6-difluorophenyl)pyridinato-N,C2')picolinate iridium(III) (Flrpic). Both analytical and semi-preparative separations were evaluated to enhance purity assessment and facilitate preparative isolation under mild conditions.

Methodology and Instrumental Setup


All analytical separations were carried out on the Waters ACQUITY UPC2 system controlled by Empower 3 software, using BEH and 2-ethylpyridine stationary phases (3.0×100 mm, 1.7 µm). Preparative isolations employed the Waters Investigator SFC system with CHIRALPAK AS-H columns (4.6×150 mm, 5 µm) under isocratic conditions with isopropanol co-solvent. Key parameters included flow rates of 1.5–3.0 mL/min, back pressures of 1740–2175 psi, and temperatures of 40–50 °C. Samples, both untreated and heat-stressed, were dissolved in chloroform to assess thermal isomerization effects.

Main Results and Discussion


  • Rapid baseline resolution of facial and meridional isomers of Ir(Fppy)3 in under 5 min under mild SFC conditions, with heat stress demonstrating meridional-to-facial conversion.
  • Achiral UPC2 separation of Flrpic revealed two geometric isomers and a distinct impurity after thermal treatment, characterized by different UV maxima.
  • Chiral separation on AS-H columns resolved Flrpic enantiomers, enabling enantiomeric excess determination crucial for circularly polarized emission studies.
  • Single-run separation of four Flrpic isomers (two geometric × two optical) demonstrated comprehensive profiling capability.
  • Semi-preparative SFC achieved preparative isolation of pure Flrpic isomers under mild conditions, minimizing further isomerization.


Benefits and Practical Applications


  • Enables rapid QC of OLED emitters post-sublimation to ensure high purity and device performance.
  • Combines geometric and optical isomer separation in a single analytical run, saving time and resources.
  • Scalable method transfer from analytical UPC2 to preparative SFC supports material production workflows.
  • Improved control of isomer composition translates to enhanced device efficiency and longevity.


Future Trends and Applications


Integration of SFC-based purity checks into OLED manufacturing, expansion to diverse phosphorescent complexes, and coupling with mass spectrometry for real-time monitoring are expected. Innovations in stationary phases and convergence chromatography will likely drive faster analysis and superior chiral separations.

Conclusion


Supercritical fluid chromatography on the ACQUITY UPC2 platform offers a fast, high-resolution, and gentle approach for isomeric separations of cyclometalated iridium complexes. This methodology addresses critical purity challenges in OLED material processing and provides a viable alternative to thermal sublimation for both analytical and preparative applications.

Instrumental Setup


  • Waters ACQUITY UPC2 System with Empower 3 Software
  • Waters Investigator SFC System with ChromScope Software
  • Columns: BEH and 2-Ethylpyridine (3.0×100 mm, 1.7 µm); CHIRALPAK AS-H (4.6×150 mm, 5 µm)


References


  1. Kappaun S, Slugovc C, List EJW. Phosphorescent organic light-emitting devices: Working principle and iridium based emitter materials. Int J Mol Sci. 2008;9:1527-1547.
  2. Tamayo B et al. Synthesis and characterization of facial and meridional tris-cyclometalated iridium(III) complexes. J Am Chem Soc. 2003;125(24):7377-7387.
  3. McDonald AR et al. Probing meridional to facial isomerization of tris-cyclometallated (C,N)3 iridium(III) complexes. Inorg Chem. 2008;47:6681-6691.
  4. Coughlin FJ et al. Separation and circularly polarized luminescence of iridium(III) enantiomers. Inorg Chem. 2008;47:2039-2048.
  5. Baranoff E et al. Sublimation not an innocent technique: Case of bis-cyclometalated iridium emitter for OLED. Inorg Chem. 2008;47:6575-6577.
  6. Baranoff E et al. Influence of iridium(III) isomer on OLED efficiency. Dalton Trans. 2010;39:8914-8918.

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