Xerogel-Derived Bis-Imidazole Semiconductors: Chain-Length-Controlled Gelation and Polycrystalline Blue OLED Emission

The development of efficient and stable blue-light emissive organic materials that retain long-range structural order remains a key challenge for optoelectronic applications. Soft materials are a wonderful platform for fabricating various optoelectronic materials as they offer a unique opportunity to combine molecular tunability with a polycrystalline nature. Herein, we report a series of alkyl-substituted 1,4-bis(imidazolyl)benzene gelators designed to investigate the effect of side-chain modulation on supramolecular assembly, xerogel formation, and electroluminescent behavior. Systematic gelation studies reveal that molecules with alkyl chains longer than butyl form robust organogels through a balance of van der Waals and hydrogen-bonding interactions, with xerogels exhibiting polycrystalline features confirmed by X-ray powder diffraction. Structural analyses and computational studies establish that alkylation increases molecular nonplanarity, disrupts face-to-face π···π stacking, and induces pronounced blue shifts in emission relative to the nonalkylated analogue. Incorporation of selected derivatives into the emissive layer of organic light-emitting diodes (OLEDs) demonstrates a clear evolution from bluish-green to pure blue emission, with the butyl and octyl-substituted compound delivering high color purity (CIE 0.16, 0.07; 0.16,0.13), narrow emission bandwidth, and intrinsic electrical and morphological robustness of the xerogel-derived polycrystalline emissive layers. Notably, the butyl derivative exhibits an operational threshold voltage of only 2.8 V, which ranks among the lowest values reported for undoped pristine small-molecule OLEDs. These finding highlights side chain-length-directed supramolecular packing as a powerful design strategy for controlling emission color and accessing ordered soft-material electroluminescence, positioning bis-imidazole xerogels as promising candidates for emerging flexible optoelectronic technologies.

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Journal
ACS Applied Materials & Interfaces
Published
2026-02-06
DOI
https://doi.org/10.1021/acsami.5c23337
Primary Topic
Supramolecular Self-Assembly in Materials
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article
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article

Xerogel-Derived Bis-Imidazole Semiconductors: Chain-Length-Controlled Gelation and Polycrystalline Blue OLED Emission

Subhajit Saha, Shaona Bose, Kumar Biradha, Samit K. Ray et al.
ACS Applied Materials & Interfaces
Supramolecular Self-Assembly in Materials
article

Xerogel-Derived Bis-Imidazole Semiconductors: Chain-Length-Controlled Gelation and Polycrystalline Blue OLED Emission

Subhajit Saha, Shaona Bose, Kumar Biradha, Samit K. Ray, Priya Paul, Vladimir V. Chernyshev
article en

Abstract

The development of efficient and stable blue-light emissive organic materials that retain long-range structural order remains a key challenge for optoelectronic applications. Soft materials are a wonderful platform for fabricating various optoelectronic materials as they offer a unique opportunity to combine molecular tunability with a polycrystalline nature. Herein, we report a series of alkyl-substituted 1,4-bis(imidazolyl)benzene gelators designed to investigate the effect of side-chain modulation on supramolecular assembly, xerogel formation, and electroluminescent behavior. Systematic gelation studies reveal that molecules with alkyl chains longer than butyl form robust organogels through a balance of van der Waals and hydrogen-bonding interactions, with xerogels exhibiting polycrystalline features confirmed by X-ray powder diffraction. Structural analyses and computational studies establish that alkylation increases molecular nonplanarity, disrupts face-to-face π···π stacking, and induces pronounced blue shifts in emission relative to the nonalkylated analogue. Incorporation of selected derivatives into the emissive layer of organic light-emitting diodes (OLEDs) demonstrates a clear evolution from bluish-green to pure blue emission, with the butyl and octyl-substituted compound delivering high color purity (CIE 0.16, 0.07; 0.16,0.13), narrow emission bandwidth, and intrinsic electrical and morphological robustness of the xerogel-derived polycrystalline emissive layers. Notably, the butyl derivative exhibits an operational threshold voltage of only 2.8 V, which ranks among the lowest values reported for undoped pristine small-molecule OLEDs. These finding highlights side chain-length-directed supramolecular packing as a powerful design strategy for controlling emission color and accessing ordered soft-material electroluminescence, positioning bis-imidazole xerogels as promising candidates for emerging flexible optoelectronic technologies.

ACS Applied Materials & InterfacesVol. 18(6)
Indian Institute of Technology Kharagpur (IN), Lomonosov Moscow State University (RU)
Industry, innovation and infrastructure
Openalex Percentile: Top 68%
Supramolecular Self-Assembly in Materials
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