Cyclometalated Iridium(III) Complex with Substituted Benzimidazole: pH Directed Organelle‐Specific Localization Within Lysosome

We report the synthesis and pH dependent emission spectral behaviour of four emissive iridium(III) complexes (Ir1-Ir4) with two isomeric pairs of bis-trifluoromethyl appended benzimidazole ligands. The imidazolyl hydrogen(N-H) has been replaced by phenyl groups (N-Ph) in two ligands to understand the impact of hydrogen bonding on the photophysical properties of the complexes and it indeed plays interesting role in the charge-transfer dynamics. The pH dependent electronic spectral change is observed for two of the complexes. The enhancement of emission intensity is observed at different wavelength for pH<7 and pH>7 for Ir1 and Ir3. The emission sensing of biogenic amines with pk<sub>a</sub> values ranging from 5.80-9.74 is reported along with cellular imaging. The complex Ir1 specifically localizes within lysosome (pH=4.5-5) and thus image this organelle with great precision. The detail electronic spectra and electrochemical behaviour were reported here along with TDDFT results.

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Publication Details

Journal
ChemBioChem
Published
2024-09-17
DOI
https://doi.org/10.1002/cbic.202400597
Citations
3
Primary Topic
Organic Light-Emitting Diodes Research
Type
article
Field-Weighted Citation Impact
0.63

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article

Cyclometalated Iridium(III) Complex with Substituted Benzimidazole: pH Directed Organelle‐Specific Localization Within Lysosome

Parna Gupta, S. Sil, Jayasri Das Sarma, Afaq Hussain
3 citations
ChemBioChem
Organic Light-Emitting Diodes Research
0.63
article

Cyclometalated Iridium(III) Complex with Substituted Benzimidazole: pH Directed Organelle‐Specific Localization Within Lysosome

Parna Gupta, S. Sil, Jayasri Das Sarma, Afaq Hussain
article en
3 citations

Abstract

We report the synthesis and pH dependent emission spectral behaviour of four emissive iridium(III) complexes (Ir1-Ir4) with two isomeric pairs of bis-trifluoromethyl appended benzimidazole ligands. The imidazolyl hydrogen(N-H) has been replaced by phenyl groups (N-Ph) in two ligands to understand the impact of hydrogen bonding on the photophysical properties of the complexes and it indeed plays interesting role in the charge-transfer dynamics. The pH dependent electronic spectral change is observed for two of the complexes. The enhancement of emission intensity is observed at different wavelength for pH<7 and pH>7 for Ir1 and Ir3. The emission sensing of biogenic amines with pk<sub>a</sub> values ranging from 5.80-9.74 is reported along with cellular imaging. The complex Ir1 specifically localizes within lysosome (pH=4.5-5) and thus image this organelle with great precision. The detail electronic spectra and electrochemical behaviour were reported here along with TDDFT results.

ChemBioChemVol. 25(24)
Indian Institute of Science Education and Research Kolkata (IN), Indian Institute of Science Education and Research, Bhopal (IN)
Indian Institute of Science Education and Research Mohali, Indian Institute of Science Education and Research Kolkata
Clean water and sanitation
Openalex Percentile: Top 31%
Organic Light-Emitting Diodes Research
0.63
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