The dynamics of the pyridinium cation in thiourea pyridinium nitrate inclusion compound has been studied using quasielastic neutron scattering in a wide temperature range (10-350 K). The elastic incoherent structure factor was determined from neutron backscattering and time-of-flight measurements and its analysis allows to describe in detail the geometry of the motions of the pyridinium cation. Our study reveals two types of motion having two different correlation times. The pyridinium cation reorients about the axis perpendicular to its molecular plane over inequivalent threefold potential energy barriers and also executes a faster out-of-plane motion about the axis passing through two opposite atoms of the ring.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1063/1.2833961 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Access to fluorinated dienes through hydrofluorination of 2-En-4-ynoates.
Org Chem Front
December 2024
Department of Chemistry, University of Pittsburgh Pittsburgh Pennsylvania 15260 USA
Article Synopsis
- The hydrofluorination of enynoates allows for the efficient synthesis of fluorinated dienoates using a pyridinium tetrafluoroborate salt.
- This method effectively converts various aryl-substituted enynoates into the desired fluorinated products with significant control over their stereochemistry and regioselectivity.
- Mechanistic studies were performed to understand the reaction process better and to optimize the outcomes based on different reaction conditions.
Charge-transfer complexation of coordination cages for enhanced photochromism and photocatalysis.
Nat Commun
January 2025
State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China.
Intensified host-guest electronic interplay within stable metal-organic cages (MOCs) presents great opportunities for applications in stimuli response and photocatalysis. Zr-MOCs represent a type of robust discrete hosts for such a design, but their host-guest chemistry in solution is hampered by the limited solubility. Here, by using pyridinium-derived cationic ligands with tetrakis(3,5-bis(trifluoromethyl)phenyl)borate (BAr) as solubilizing counteranions, we report the preparation of soluble Zr-MOCs of different shapes (1-4) that are otherwise inaccessible through a conventional method.
View Article and Find Full Text PDFThis study investigates the modulations in the optical properties of cationic surfactant cetylpyridinium chloride (CPC) and hydrazine-mediated copper nanoclusters (CuNCs). By employing a bottom-up approach, we demonstrate the formation of blue-emitting CuNCs facilitated by CPC and hydrazine, where hydrazine acts both as a reducing and stabilizing agent. The optical properties of the CuNCs were systematically tuned by varying the chain length of the diamine, resulting in emissions ranging from blue to yellow.
View Article and Find Full Text PDFTriclinic polymorph of bis-[2-methyl-3-(pyridin-2-yl)imidazo[1,5-]pyridin-2-ium] tetra-chloridocadmium(II).
Acta Crystallogr E Crystallogr Commun
October 2024
Department of Inorganic Chemistry and Technology, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana, Slovenia.
The crystal structure of the title organic-inorganic hybrid salt, (CHN)[CdCl], (I), has been reported with four mol-ecules in the asymmetric unit in a monoclinic cell [Vassilyeva (2021 ▸). , , 7713-7722]. While using two different aldehydes in the oxidative cyclization-condensation involving CHNH·HCl to prepare a new monovalent cation with the imidazo[1,5-]pyridinium skeleton, a new polymorph was obtained for (I) in space group 1 and a unit cell with approximately half the volume of the monoclinic form.
View Article and Find Full Text PDFGiant {Mo} polyoxometalate isolated with diverse organic cations: a systematic proton conductivity study.
Dalton Trans
December 2024
School of Chemistry, University of Hyderabad, Hyderabad - 500046, India.
The development of efficient and stable proton conductors is a pivotal area of research due to their transformative potential in alternative energy technologies. Recently, there has been a surge of interest in synthesizing proton conductors based on polyoxometalate (POM) materials, attributed to their highly negatively charged and oxygen-rich surfaces. In this study, we report on a highly water-soluble giant POM, (NH)[MoO(CHCOO)(HO)]·300HO·10CHCOONH (designated as {Mo}), which was rendered insoluble in water by exchanging its ammonium cations with larger organic cations, specifically histidinium, pyridinium, bipyridinium, and methyl viologen, resulting in His-Mo132, Py-Mo132, Bpy-Mo132 and MV-Mo132, respectively.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!