The dynamics of chemically powered sphere dimers at the micro- and nano-scales confined in a quasi-two-dimensional geometry are investigated. The dimer consists of a Janus particle and a non-catalytic sphere. A chemical reaction taking place on the catalytic surface of the Janus particle creates asymmetric concentration gradients that give rise to the self-propulsion of both rotation and translation of the dimer. Due to the chemical interactions, ensembles of dimers spontaneously form anti-parallel aligned doublets that exhibit the same rotation direction and lose translational motion. The chirality of the dimer plays an important role in the process of doublet formation. The study displays new collective dynamics and structures when both translational and rotational self-propulsion occur.
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http://dx.doi.org/10.1039/d0nr06368a | DOI Listing |
Inorg Chem
December 2024
Department of Chemistry, Inorganic Chemistry Section, Jadavpur University, Kolkata 700032, India.
In the present study, we have synthesized and thoroughly characterized two Ru(II) dimers with compositions [(ttpy)Ru(tpvpt')Ru(ttpy)](ClO) and [(ttpy)Ru(t'pvpvpt')Ru(ttpy)](ClO) incorporating phenylene-vinylene-substituted terpyridine bridging ligands capable of coordinating in both an NNN- and cyclometalated NNC-fashion. The complexes display strong absorption across the entire UV-vis spectral domain and exhibit luminescence in the NIR region (820-850 nm). The N atoms in the outer coordination sphere were employed for alteration of the photoredox behaviors of the complexes via acid-base equilibria.
View Article and Find Full Text PDFJ Chem Theory Comput
December 2024
College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018, China.
The propulsion mechanisms and collective dynamics of chemically powered Janus sphere dimers at the micro- and nanoscales, confined in a quasi-two-dimensional geometry, are investigated using a coarse-grained microscopic dynamical model. These active Janus dimers consist of two identical Janus spheres, featuring a catalytic cap on one hemisphere. The chemical reaction taking place on the catalytic surface generates asymmetric concentration gradients of product molecules around the Janus sphere, leading to the self-propulsion of the dimers.
View Article and Find Full Text PDFMolecules
October 2024
Institute of Chemistry and Biochemistry, Freie Universität Berlin, Fabeckstr. 34/36, 14195 Berlin, Germany.
2,6-Dipicolinoylbis(-dialkylthioureas), HL, readily react with uranyl salts under formation of monomeric or dimeric complexes of the compositions [UO(L)(solv)] (solv = donor solvents such as HO, MeOH or DMF) or [{UO(L)(µ-OMe)}] (). In such complexes, the uranyl ions are exclusively coordinated by the "hard" ,, or donor atom sets of the central ligand unit and the lateral sulfur donor atoms do not participate in the coordination. Different conformations have been found for the dimeric anions.
View Article and Find Full Text PDFOrganometallics
October 2024
Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
The catalytic activity of an NHC-pyridonate-supported nickel(0) complex for Suzuki-Miyaura coupling of aryl halides was evaluated. Product formation was observed in the absence of a basic additive. However, low turnover numbers resulted from competitive catalyst deactivation.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
November 2024
Department of Chemistry, The Pennsylvania State University, University Park, PA 16802.
Elucidating details of biology's selective uptake and trafficking of rare earth elements, particularly the lanthanides, has the potential to inspire sustainable biomolecular separations of these essential metals for myriad modern technologies. Here, we biochemically and structurally characterize () LanD, a periplasmic protein from a bacterial gene cluster for lanthanide uptake. This protein provides only four ligands at its surface-exposed lanthanide-binding site, allowing for metal-centered protein dimerization that favors the largest lanthanide, La.
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