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Metal ions can serve as a centre of molecular motions due to their coordination geometry, reversible bonding nature and external stimuli responsiveness. Such essential features of metal ions have been utilized for metal-mediated molecular machines with the ability to motion switch via metallation/demetallation or coordination number variation at the metal centre; however, motion switching based on the change in coordination geometry remain largely unexplored. Herein, we report a Pt-centred molecular gear that demonstrates control of rotor engagement and disengagement based on photo- and thermally driven cis-trans isomerization at the Pt centre. This molecular rotary motion transmitter has been constructed from two coordinating azaphosphatriptycene rotators and one Pt ion as a stator. Isomerization between an engaged cis-form and a disengaged trans-form is reversibly driven by ultraviolet irradiation and heating. Such a photo- and thermally triggered motional interconversion between engaged/disengaged states on a metal ion would provide a selector switch for more complex interlocking systems.
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http://dx.doi.org/10.1038/ncomms14296 | DOI Listing |
Small
December 2024
College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou, 310018, People's Republic of China.
The conversion of biomass into chemical fuels is exciting but quite challenging in the development of an effective conversion strategy to generate easily-separated products without energy consumption. Herein, a lignocellulosic biomass-to-H conversion system via photo-thermal catalysis over MoC hierarchical nanotube catalysts in an acidic solution, in which the lignocellulose is hydrolyzed to small organic molecules (such as glucose, etc) by dilute HSO, and then the resulting glucose is oxidized by MoC catalyst to generate H are reported. During the photo-thermal catalytic processes, the carbon vacancy in MoC catalysts results in the generation of undercoordinated Mo sites, which act as active sites for both biomass oxidation and H generation reactions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Key Labs for Advanced Materials, Institute of Fine Chemicals, East China University of Science and Technology, Meilong Road 130, 200237, Shanghai, CHINA.
High-performance polymers based on dynamic chemistry have been widely explored for multi-field advanced applications. However, noncovalent sacrifice bond mediated energy dissipation mechanism causes a trade-off between mechanical toughness and resilience. Herein, we achieved the synchronous boost of seemingly conflicting material properties including mechanical robustness, toughness and elasticity via the incorporation of mechanical chemistry into traditional semi-crystalline networks.
View Article and Find Full Text PDFSmall Methods
December 2024
Hefei National Research Center for Physical Sciences at the Microscale, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, 230026, China.
The stabilization and structural integrity of DNA architectures remain significant challenges in their biomedical applications, particularly when inserting functional units into the genome using long single-stranded DNA (lssDNA). To address these challenges, a site-specific photo-cross-linking method is employed. Single-stranded oligonucleotides, containing one or two photosensitive cyanovinylcarbazole nucleoside (K) molecules, are precisely incorporated and cross-linked at the specific sites of ssDNA through base-pairing, followed by rapid UV irradiation at 365 nm.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
School of Environment, South China Normal University, Guangzhou 510006, China; MOE Key Laboratory of Theoretical Chemistry of Environment, South China Normal University, Guangzhou 510006, China; Guangdong Provincial Key Lab of Functional Materials for Environmental Protection, Guangzhou 510006, China. Electronic address:
We report here a BiWO/TiCT@Ag (BT@Ag) photothermal photocatalyst for efficient CO reduction with tunable CH selectivity. Incorporation of TiCT MXene creates well-defined heterointerfaces between BiWO and TiCT and converts thermal energy upon light illumination via photothermal effect, which contributes to a mitigation of the recombination of photo-induced charge carries for a high electron mobility. Density functional theory calculations substantiate that TiCT functions as the adsorption site and active center where the transferred electrons are effectively involved in CO reduction for enhanced CH selectivity.
View Article and Find Full Text PDFAdv Colloid Interface Sci
December 2024
School of Materials Science and Engineering, Shaanxi Key Laboratory of Green Preparation and Functionalization for Inorganic Materials, Shaanxi University of Science and Technology, Xi'an, Shaanxi 710021, China.
Photothermal conversion materials (PCMs) are crucial component in solar-thermal energy technologies. Although various PCMs with excellent sunlight harvesting have been developed for colorful solar-thermal applications, uniform and large-scale production of PCMs remains a challenge, and the PCMs prepared through the conventional methods are often non-site specific. Laser processing technology (LPT), as an efficient, convenient, green and sustainable technology, can directly create micro/nano structures and patterns at specific locations on materials surface, attracting widespread attention in photo-to-thermal applications.
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