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  • Royal Society of Chemistry (RSC)  (4)
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  • Royal Society of Chemistry (RSC)  (4)
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  • 1
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Chemical Science Vol. 13, No. 36 ( 2022), p. 10824-10835
    In: Chemical Science, Royal Society of Chemistry (RSC), Vol. 13, No. 36 ( 2022), p. 10824-10835
    Abstract: Achieving long-lived symmetry-broken charge-separated states in chromophoric assemblies is quintessential for enhanced performance of artificial photosynthetic mimics. However, the occurrence of energy trap states hinders exciton and charge transport across photovoltaic devices, diminishing power conversion efficiency. Herein, we demonstrate unprecedented excimer formation in the relaxed excited-state geometry of bichromophoric systems impeding the lifetime of symmetry-broken charge-separated states. Core-annulated perylenediimide dimers (SC-SPDI2 and SC-NPDI2) prefer a near-orthogonal arrangement in the ground state and a π-stacked foldamer structure in the excited state. The prospect of an excimer-like state in the foldameric arrangement of SC-SPDI2 and SC-NPDI2 has been rationalized by fragment-based excited state analysis and temperature-dependent photoluminescence measurements. Effective electronic coupling matrix elements in the Franck–Condon geometry of SC-SPDI2 and SC-NPDI2 facilitate solvation-assisted ultrafast symmetry-breaking charge-separation (SB-CS) in a high dielectric environment, in contrast to unrelaxed excimer formation (Ex*) in a low dielectric environment. Subsequently, the SB-CS state dissociates into an undesired relaxed excimer state (Ex) due to configuration mixing of a Frenkel exciton (FE) and charge-separated state in the foldamer structure, downgrading the efficacy of the charge-separated state. The decay rate constant of the FE to SB-CS ( k FE→SB–CS ) in polar solvents is 8–17 fold faster than that of direct Ex* formation ( k FE→Ex* ) in non-polar solvent ( k FE→SB–CS ≫ k FE→Ex* ), characterized by femtosecond transient absorption (fsTA) spectroscopy. The present investigation establishes the impact of detrimental excimer formation on the persistence of the SB-CS state in chromophoric dimers and offers the requisite of conformational rigidity as one of the potential design principles for developing advanced molecular photovoltaics.
    Type of Medium: Online Resource
    ISSN: 2041-6520 , 2041-6539
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2559110-1
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  • 2
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2023
    In:  Chemical Society Reviews Vol. 52, No. 19 ( 2023), p. 6664-6679
    In: Chemical Society Reviews, Royal Society of Chemistry (RSC), Vol. 52, No. 19 ( 2023), p. 6664-6679
    Abstract: Fundamental understanding of the supramolecular assemblies of organic chromophores and the development of design strategies have seen endless ripples of interest owing to their exciting photophysical properties and optoelectronic applications. The independent discovery of dye aggregates by Jelley and Scheibe was the commencement of the remarkable advancement in the field of aggregate photophysics. Subsequent research warranted an exceptional model for defining the exciton interactions in aggregates, proposed by Davydov, Kasha and co-workers, independently, based on the long-range Coulombic coupling. Fascinatingly, the orthogonally cross-stacked molecular transition dipole arrangement was foretold by Kasha to possess null exciton interaction leading to spectroscopically uncoupled molecular assembly, which lacked an experimental signature for decades. There have been several attempts to identify and probe atypical molecular aggregates for decoding their optical behaviour. Herein, we discuss the recent efforts in experimentally verifying the unusual exciton interactions supported with quantum chemical computations, primarily focusing on the less explored null exciton splitting. Exciton engineering can be realized through synthetic modifications that can additionally offer control over the assorted non-covalent interactions for orchestrating precise supramolecular assembly, along with molecular editing. The task of attaining a minimal excitonic coupling through an orthogonally cross-stacked crystalline architecture envisaged to offer a monomer-like optical behaviour was first reported in 1,7-dibromoperylene-3,4,9,10-tetracarboxylic tetrabutylester (PTE-Br 2 ). The attempt to stitch molecules covalently in an orthogonal fashion to possess null excitonic character culminated in a spiro-conjugated perylenediimide dimer exhibiting a monomer-like spectroscopic signature. The computational and experimental efforts to map the emergent properties of the cross-stacked architecture are also discussed here. Using the null aggregates formed by the interference effects between CT-mediated and Coulombic couplings in the molecular array is another strategy for achieving monomer-like spectroscopic properties in molecular assemblies. Moreover, identifying supramolecular assemblies with precise angle-dependent properties can have implications in functional material design, and this review can provide insights into the uncharted realm of null exciton splitting.
    Type of Medium: Online Resource
    ISSN: 0306-0012 , 1460-4744
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2197419-6
    detail.hit.zdb_id: 1472875-8
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  • 3
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Chemical Science Vol. 13, No. 30 ( 2022), p. 8860-8870
    In: Chemical Science, Royal Society of Chemistry (RSC), Vol. 13, No. 30 ( 2022), p. 8860-8870
    Abstract: The discovery of vibrant excited-state dynamics and distinctive photochemistry has established nitrated polycyclic aromatic hydrocarbons as an exhilarating class of organic compounds. Herein, we report the atypical photorearrangement of nitro-perylenediimide (NO2-PDI) to nitrito-perylenediimide (ONO-PDI), triggered by visible-light excitation and giving rise to linkage isomers in the polar aprotic solvent acetonitrile. ONO-PDI has been isolated and unambiguously characterized using standard spectroscopic, spectrometric, and elemental composition techniques. Although nitritoaromatic compounds are conventionally considered to be crucial intermediates in the photodissociation of nitroaromatics, experimental evidence for this has not been observed heretofore. Ultrafast transient absorption spectroscopy combined with computational investigations revealed the prominence of a conformationally relaxed singlet excited-state (SCR1) of NO2-PDI in the photoisomerization pathway. Theoretical transition state (TS) analysis indicated the presence of a six-membered cyclic TS, which is pivotal in connecting the SCR1 state to the photoproduct state. This article addresses prevailing knowledge gaps in the field of organic linkage isomers and provides a comprehensive understanding of the unprecedented photoisomerization mechanism operating in the case of NO2-PDI.
    Type of Medium: Online Resource
    ISSN: 2041-6520 , 2041-6539
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2559110-1
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  • 4
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2018
    In:  Physical Chemistry Chemical Physics Vol. 20, No. 28 ( 2018), p. 19120-19128
    In: Physical Chemistry Chemical Physics, Royal Society of Chemistry (RSC), Vol. 20, No. 28 ( 2018), p. 19120-19128
    Type of Medium: Online Resource
    ISSN: 1463-9076 , 1463-9084
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2018
    detail.hit.zdb_id: 1476283-3
    detail.hit.zdb_id: 1476244-4
    detail.hit.zdb_id: 1460656-2
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