Pyridinium chloride (PC) is examined as a selective, fluorescence quenching agent for alternant as opposed to nonalternant polycyclic aromatic hydrocarbons (PAHs) in two polar solvents - water and acetonitrile. Nine alternant and 13 nonalternant PAHs were dissolved in water and acetonitrile and a total of 0.2 M of pyridinium chloride was added. The resulting change in fluorescence intensity was observed and reported as the Stern-Volmer quenching constant. Results show that PC is a selective quencher in both polar solvents. It selectively quenches the fluorescence emission intensity of alternant PAHs while leaving the nonalternant PAH fluorescence emission virtually unchanged. These results agree with the selective quenching behavior seen for PC surfactant analogs, cetylpyridinium chloride (CPC) and dodecylpyridinium chloride (DDPC). Furthermore, these results illustrate that the presence of a surfactant or micelle is not a requirement for selective quenching. The selective quencher PC is applicable to situations where a surfactant is not desirable or soluble.
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http://dx.doi.org/10.1016/s0039-9140(00)00527-0 | DOI Listing |
This 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 PDFActa Crystallogr E Crystallogr Commun
October 2024
Carlson School of Chemistry and Biochemistry, Clark University, 950 Main St., Worcester, MA 01610, USA.
Reaction of 2-amino-5-iodo-pyridine (5IAP) with concentrated HBr at room temperature yielded 2-amino-5-iodo-pyridinium bromide, CHIN ·Br or (5IAPH)Br. The complex formed pale-yellow crystals, which exhibit significant hydrogen bonding between the amino and pyridinium N-H donors and bromide ion acceptors. Halogen bonding is also observed.
View Article and Find Full Text PDFMacromol Biosci
January 2025
Department of Chemistry, Paderborn University, Warburger Str. 100, 33098, Paderborn, Germany.
The complex distribution of functional groups in carbohydrates, coupled with their strong solvation in water, makes them challenging targets for synthetic receptors. Despite extensive research into various molecular frameworks, most synthetic carbohydrate receptors have exhibited low affinities, and their interactions with sugars in aqueous environments remain poorly understood. In this work, we present a simple pyridinium-based hydrogen-bonding receptor derived from a subtle structural modification of a well-known tetralactam macrocycle.
View Article and Find Full Text PDFTalanta
March 2025
School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, People's Republic of China; Collaborative Innovation Center of Yellow River Basin Pharmaceutical Green Manufacturing and Engineering Equipment, University of Jinan, Jinan 250022, People's Republic of China. Electronic address:
Drug-induced liver injury (DILI) has emerged as among of the undesirable drug effects, posing significant threats to human health. However, in clinical practice, there remains a shortage of dependable and pre-diagnosis tools for DILI. Numerous studies indicated that the elevated intrahepatic viscosity levels were closely linked to the onset and progression of DILI.
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