Keto–enol at play: regioisomerism regulated switching in indole-naphthyl Schiff bases

Indole-naphthyl Schiff bases studied in this work show the importance of hydroxyl positions on enol (E)-keto (K) emissions, aggregation-induced emission (AIE), and viscosity-dependent emission properties. Single-crystal X-ray diffraction and computational studies provide insights into the structural properties of the tautomeric species. INpOH-1 and INpOH-2 demonstrated potential for distinguishing normal and cancer cells based on their polarity and viscosity sensitivity.

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Publication Details

Journal
Physical Chemistry Chemical Physics
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cp01939g
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
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article

Keto–enol at play: regioisomerism regulated switching in indole-naphthyl Schiff bases

Adarash Kumar Shukla, Anupam Bhattacharya, Ashutosh Mahale, Onkar P. Kulkarni et al.
Physical Chemistry Chemical Physics
Axial and Atropisomeric Chirality Synthesis
article

Keto–enol at play: regioisomerism regulated switching in indole-naphthyl Schiff bases

Adarash Kumar Shukla, Anupam Bhattacharya, Ashutosh Mahale, Onkar P. Kulkarni, Pravinkumar Vipparthi, Savita Choudhary, Sanjana Panyala
article en

Abstract

Indole-naphthyl Schiff bases studied in this work show the importance of hydroxyl positions on enol (E)-keto (K) emissions, aggregation-induced emission (AIE), and viscosity-dependent emission properties. Single-crystal X-ray diffraction and computational studies provide insights into the structural properties of the tautomeric species. INpOH-1 and INpOH-2 demonstrated potential for distinguishing normal and cancer cells based on their polarity and viscosity sensitivity.

Physical Chemistry Chemical PhysicsVol. 27(39)
Birla Institute of Technology and Science - Hyderabad Campus (IN), Birla Institute of Technology and Science, Pilani (IN)
Openalex Percentile: Top 83%
Axial and Atropisomeric Chirality Synthesis
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