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The collective self-assembly of colloidal particles can be influenced by the composition of the suspending medium, the bulk material of the particles themselves and, importantly, by their surface chemistry. This can be inhomogeneous or patchy to give an orientational dependence to the interaction potential between the particles. These additional constraints to the energy landscape then steer the self-assembly towards configurations of fundamental or applicational interest. We present a novel approach to modify the surface chemistry of colloidal particles to give them two polar patches, using gaseous ligands. In particular, we synthesize polar inverse patchy colloids, i.e., charged particles with two (fluorescent) patches of the opposite charge on their poles. We characterize the dependence of these charges on the pH of the suspending solution.
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http://dx.doi.org/10.1088/1361-648X/acbddc | DOI Listing |
Angew Chem Int Ed Engl
September 2025
Deutsches Elektronen-Synchrotron DESY, Notkestr. 85, 22607, Hamburg, Germany.
The cluster growth behavior of CO and CH on an aromatic ligand has been studied through the unambiguous identification of complex structures of 1,2,3-trifluorobenzene-(CO) and -ß(CH) using broadband rotational spectroscopy in conjunction with extensive theoretical calculations. The results reveal a contrast in the thermodynamically favorable ligand-gas binding sites and noncovalent interactions of the two gaseous molecules on the ligand. The observation of a tunneling splitting and large centrifugal distortions indicates that CH molecules bind to the fluorinated π system via three weak hydrogen bonds without CH self-interactions, resulting in an effective structure displaced toward the dissociation limit.
View Article and Find Full Text PDFInorg Chem
July 2025
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, Jiangsu, People's Republic of China.
Reaction of AuCN with a PNN-type ligand dppmaphen (-(diphenylphosphanylmethyl)-2-amino-1,10-phenanthroline) yielded a novel monoprotonated trinuclear Au(I) complex [AuH(dppmaphen)(CN)] (). Upon excitation at 368 nm, compound emitted phosphorescence at 524 nm at room temperature and an additional phosphorescent band around 610 nm at lower temperatures and may function as a low-temperature thermometer. Compound also exhibited reversible PL changes from green to yellow upon grinding and exposure to organic solvents, which is attributed to the destruction and rebuilding of voids in its crystal structure.
View Article and Find Full Text PDFInorg Chem
June 2025
Laboratory of Nuclear Energy Chemistry, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China.
The clusters have garnered widespread interest owing to their captivating structures and their potential applications in diverse scientific disciplines. Within this study, we synthesized two uranyl clusters, (UO)(DMF)(CO)(bmpd)·DMF () and (UO)(O)(OH)(CO)(btpd) (), by the utilization of 1,10-phenanthroline derivative ligands in conjunction with uranyl cations through solvothermal synthesis techniques. Both clusters are characterized by a V-shaped [(UO)(CO)] unit, whose configuration strikingly differs from the typical triangular [(UO)(O)]/[(UO)(OH)] structures.
View Article and Find Full Text PDFRSC Adv
May 2025
Department of Physical Chemistry and Nanochemistry, Faculty of Chemistry, Alzahra University P.O. Box 1993893973 Tehran Iran.
In this work, a metal-organic nickel framework (Ni-MOF) modified with a biological ligand (asparagine) (Ni-Bio-MOF) was synthesized by a hydrothermal method. Asparagine is believed to create defects on the surface of the MOF, thereby increasing its electrocatalytic activity. Then, a Diclofenac (DCF) polymer imprinted with l-methionine (PL-Met) was electrodeposited on a carbon paste electrode (CPE)/Ni-Bio-MOF and used as a new electrochemical sensor for highly selective and sensitive detection of DCF in biological and pharmaceutical samples.
View Article and Find Full Text PDFNat Commun
May 2025
Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, Liaoning, China.
The catalytic conversion of carbon monoxide (CO) provides an enormous opportunity to construct carbonyl-containing molecules. Among them, the direct carbonylation of C-H bonds on gaseous hydrocarbon feedstocks provides a straightforward approach to access industrially important short-chain carboxylic acid derivatives. Here, we report a general and mild direct carbonylation of methane, ethane, and propane under blue LED irradiation at ambient temperature, enabling the direct formation of short-chain carboxylic acid derivatives.
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