98%
921
2 minutes
20
Fluorescent flippers are twisted push-pull mechanophores that report planarization with red-shifted absorption and an increase in fluorescence intensity and lifetime. Until today, their planarization by physical forces has focused on compression to visualize physical forces in biology. Here, we show that planarization can also be achieved by stretching of flipper probes that are equipped with tethers in their core and to visualize mechanical stress in polymeric materials. The synthesis of dithieno-[3,2-:2',3'-]-thiophene dimers with alcohols extending from their twisted core is accomplished in 17 steps. Covalently integrated into polyurethanes, these core-substituted flippers exhibit an excitation-wavelength-dependent fluorescence enhancement upon polymer stretching, validating their mode of action. Noncovalently interfaced flipper controls are much less responsive. In light of the importance their fluorogenic compression has reached in biology, synthetic access to flippers that can be stretched rather than compressed and use in materials rather than life sciences opens up significant, fundamentally new perspectives for flipper research.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12381726 | PMC |
http://dx.doi.org/10.1021/jacsau.5c00579 | DOI Listing |
JACS Au
August 2025
Department of Organic Chemistry, University of Geneva, 1211 Geneva, Switzerland.
Fluorescent flippers are twisted push-pull mechanophores that report planarization with red-shifted absorption and an increase in fluorescence intensity and lifetime. Until today, their planarization by physical forces has focused on compression to visualize physical forces in biology. Here, we show that planarization can also be achieved by stretching of flipper probes that are equipped with tethers in their core and to visualize mechanical stress in polymeric materials.
View Article and Find Full Text PDFJ Phys Chem A
August 2025
School of Chemistry and Chemical Engineering, Hainan University, Haikou 570228, China.
Although cationic units show great promise as building blocks for functional aggregation-induced emission (AIE) materials, their underlying working mechanisms have not been sufficiently elucidated. Here, we present a comprehensive theoretical investigation into the AIE behavior of cationic fluorophores, employing density functional theory (DFT) and time-dependent DFT (TD-DFT). Our findings reveal that methylation of cationic fluorophores substantially lowers their lowest unoccupied molecular orbital (LUMO) levels and narrows the energy gaps.
View Article and Find Full Text PDFJ Phys Chem B
August 2025
Department of Chemistry & Toxicology, University of Guelph, Guelph, Ontario N1G 2W1, Canada.
Fluorogenic probes that undergo excited-state proton transfer (ESPT) and twisted intramolecular charge transfer (TICT) offer tunable fluorescence properties for bioimaging and sensing applications. However, the relationship between ESPT and TICT remains poorly understood in push-pull chromophores. Despite extensive research on photoacids, photobases remain underutilized as fluorescence modulators, and the roles of solvent polarity, acidity, and donor-acceptor strength in governing photobasicity and TICT activation are not well established.
View Article and Find Full Text PDFJ Chem Phys
June 2025
Faculty of Chemistry, University of Warsaw, Pasteura 1, Warsaw, Poland.
Light-driven rotary molecular motors convert light energy into unidirectional rotational movement. In overcrowded alkene-based molecular motors, rotary motion is accomplished through consecutive cis-trans photoisomerization reactions and thermal helix inversion steps. To date, a complete understanding of the photoisomerization reactions of overcrowded alkene motors has not been achieved yet.
View Article and Find Full Text PDFJ Am Chem Soc
April 2025
Department of Chemistry and Pharmacy and Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-University Erlangen-Nuremberg, Egerlandstraße 3, 91058 Erlangen, Germany.
Graphene nanoribbons (NRs) constitute a versatile platform for developing novel materials, where their structure governs their optical, electronic, and magnetic properties while also shaping their excited-state dynamics. Here, we investigate a set of three twisted N-doped molecular NRs of increasing length, obtained by linearly fusing perylene diimide to pyrene and pyrazino- or thiadiazolo-quinoxaline residues. By employing various temperature-dependent time-resolved spectroscopy techniques, we reveal how the flexible twisted NR geometry promotes the formation of a mixed electronic state with varying contributions from locally excited and charge-transfer (CT) states.
View Article and Find Full Text PDF