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Here the supramolecular liquid crystalline (LC) phase behavior of a series of fullerene block molecules was investigated regarding spacer length, alkyl tail length and temperature. These compounds exhibit several lamellar LC phases with different packings of self-organized fullerene two-dimensional (2D) crystals. With a short hexamethylene spacer, they form sandwich-like structures with triple or quadruple fullerene layers. By increasing the spacer length to 10 or 12 carbons, a composite layers-in-lamella superlattice structure with alternating soft hydrocarbon single layers and fullerene single or double layers was obtained. As the molecular configurational freedom between incompatible moieties was enhanced by the elongated spacer, the required cross-sectional fullerene-to-hydrocarbon ratio for the superlattice could be achieved despite of different volume fractions of the blocks. The superlattice phase range is efficiently widened by the design principle of constructing LC molecules with a long spacer, which also provides a facile way to tailor novel superstructures.
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http://dx.doi.org/10.1002/chem.202301015 | DOI Listing |
J Am Chem Soc
September 2025
Department of Chemistry, Stanford University, Stanford, California 94305, United States.
The potential of coding RNAs as a general therapeutic modality is limited by their short intracellular lifetime. Here, we investigate the effects of localized post-transcriptional RNA modification on protein expression over time. While 2'-OH acylation of GFP RNA with stable adducts in the protein-coding region strongly suppressed protein expression, acylation at the poly(A) tail extended translation duration, with protein output increased by up to 8-fold at 36 h.
View Article and Find Full Text PDFNat Chem
September 2025
The Institute for Advanced Studies, TaiKang Center for Life and Medical Sciences, State Key Laboratory of Metabolism and Regulation in Complex Organisms, Wuhan University, Wuhan, China.
Precision in site-selective functionalization of molecules bearing multiple potentially reactive positions is a longstanding challenge in organic synthesis. Although migratory difunctionalization offers a powerful strategy for programmed functional group installation along carbon chains, its implementation with multisubstituted alkenes has been impeded by the increased complexity of site-selectivity. Here we report a head-tail carboboration of multisubstituted alkenes with exceptional site-selectivity, enabled by ligand steric exclusion in a nickel-catalysed chain-walking system.
View Article and Find Full Text PDFChemistry
August 2025
Department of Bioproducts and Biosystems, Aalto University, Espoo, 0076 Aalto, Finland.
Directing the collective behavior of bacteria is important for various applications in chemical bioproduction, water treatment, and antibiofilm solutions. A potential approach to such control mechanisms lies in sequestering signal molecules (autoinducers) by macrocyclic host molecules that lower the effective concentration of the former, modulating bacterial signaling. Cyclodextrins (CD) - one of the best-established families of hosts - have been shown to bind homoserine lactones (HSL) acting as autoinducers, but with a focus limited to shorter (≤ 8 carbons) tailed molecules and β-CD.
View Article and Find Full Text PDFChemistry
August 2025
Department of Applied Chemistry, National Yang Ming Chiao Tung University, 1001 Ta Hsueh Road, Hsinchu, 30030, Taiwan.
We present herein a systematic study on the cyclodimerization of (trialkylsilyl)ethynyl-substituted derivatives of indeno[2.1-b]fluorene and fluoreno[2,3-b]fluorene, which incorporate an open-shell meta-quinodimethane (m-QDM) unit. Our investigation focuses on the influence of different alkyl groups (methyl, isopropyl, or cyclohexyl) attached to the silyl moiety.
View Article and Find Full Text PDFInt J Mol Sci
July 2025
Institute of Pharmacognosy, University of Szeged, Eötvös u. 6, H-6720 Szeged, Hungary.
Estradiol (E2) plays an important role in cell proliferation and certain brain functions. To reveal its mechanism of action, its detectability is essential. Only a few fluorescent-labeled hormonally active E2s exist in the literature, and their mechanism of action usually remains unclear.
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