Exploring Size-Controlled Exciton Evolution Using DNA Libraries

To investigate multichromophore phenomena, progress traditionally relies on model covalent dimers for spectroscopic interrogation. Integrating molecular semiconductors into nucleic acid libraries can enable rapid screening of multichromophore phenomena. Here, we report DNA-directed assembly of up to five π-conjugated chromophores that demonstrate charge separation and electronic delocalization phenomena. We integrate a range of porphyrins and perylene diimides (PDIs)─molecular semiconducting materials widely used in organic electronic devices─in DNA, encoding nearest-neighbor assembly through base-sequence programmed hybridization. In this way, we can assemble multicomponent stacks with tailored electronic properties from a central chromophore-DNA library. This allows dimer and multimer production on demand, within hours, from presynthesized DNA-chromophores for spectroscopic analysis. We demonstrate the library's ability to optimize for charge transfer, computationally prescreening for close π-stacking as a proxy for large orbital overlap and exchange energy. Our modular DNA assembly reveals opportunities for rapid development of simple, bespoke chromophore architectures with stoichiometric chromophore control and ordering.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-02-19
DOI
https://doi.org/10.1021/jacs.5c21113
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Exploring Size-Controlled Exciton Evolution Using DNA Libraries

Akshay Sridhar, Sarah R. E. Orsborne, Eugen Stulz, Seán T. J. Ryan et al.
Journal of the American Chemical Society
DNA and Nucleic Acid Chemistry
article

Exploring Size-Controlled Exciton Evolution Using DNA Libraries

Akshay Sridhar, Sarah R. E. Orsborne, Eugen Stulz, Seán T. J. Ryan, Florian Auras, Jake L. Greenfield, Richard Henry Friend, Peter Budden, J.A. Gorman, Simon Dowland, Yun Liu, Akshay Rao, Raj Pandya, Rosana Collepardo-Guevara, Hugo Bronstein, Jonathan R. Nitschke, Daniel G. Congrave
article en

Abstract

To investigate multichromophore phenomena, progress traditionally relies on model covalent dimers for spectroscopic interrogation. Integrating molecular semiconductors into nucleic acid libraries can enable rapid screening of multichromophore phenomena. Here, we report DNA-directed assembly of up to five π-conjugated chromophores that demonstrate charge separation and electronic delocalization phenomena. We integrate a range of porphyrins and perylene diimides (PDIs)─molecular semiconducting materials widely used in organic electronic devices─in DNA, encoding nearest-neighbor assembly through base-sequence programmed hybridization. In this way, we can assemble multicomponent stacks with tailored electronic properties from a central chromophore-DNA library. This allows dimer and multimer production on demand, within hours, from presynthesized DNA-chromophores for spectroscopic analysis. We demonstrate the library's ability to optimize for charge transfer, computationally prescreening for close π-stacking as a proxy for large orbital overlap and exchange energy. Our modular DNA assembly reveals opportunities for rapid development of simple, bespoke chromophore architectures with stoichiometric chromophore control and ordering.

Journal of the American Chemical SocietyVol. 148(8)
Agency for Science, Technology and Research (SG), University of St Andrews (GB), Durham University (GB), University of Cambridge (GB), Institute of High Performance Computing (SG), University of Warwick (GB), University of Oxford (GB), Cavendish Hospital (GB), Universitas Islam Syekh Yusuf (ID), University of Southampton (GB), Technische Universität Dresden (DE)
European Commission, Engineering and Physical Sciences Research Council
Affordable and clean energy
Openalex Percentile: Top 51%
DNA and Nucleic Acid Chemistry
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