Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Fluorescence correlation spectroscopy (FCS) has been extensively used to measure equilibrium binding constants (K) or association and dissociation rates in many reversible chemical reactions across chemistry and biology. For the majority of investigated reactions, the binding constant was on the order of ∼100 M , with dissociation constants faster or equal to 10  s , which ensured that enough association/dissociation events occur during the typical diffusion-determined transition time of molecules through the FCS detection volume. However, complexation reactions involving metal ions and chelating ligands exhibit equilibrium constants exceeding 10  M . In the present paper, we explore the applicability of FCS for measuring reaction rates of such complexation reactions, and apply it to binding of iron, europium and uranyl ions to a fluorescent chelating ligand, calcein. For this purpose, we exploit the fact that the ligand fluorescence becomes strongly quenched after binding a metal ion, which results in strong intensity fluctuations that lead to a partial correlation decay in FCS. We also present measurements for the strongly radioactive ions of Am , where the extreme sensitivity of FCS allows us to work with sample concentrations and volumes that exhibit close to negligible radioactivity levels. A general discussion of the applicability of FCS to the investigation of metal-ligand binding reactions concludes our paper.

Download full-text PDF

Source
http://dx.doi.org/10.1002/cphc.201900517DOI Listing

Publication Analysis

Top Keywords

metal ion
8
fluorescence correlation
8
correlation spectroscopy
8
complexation reactions
8
applicability fcs
8
fcs
6
binding
5
reactions
5
determining metal
4
ion complexation
4

Similar Publications

Ultra-High Zinc Utilization Enabled by MXene Anode for Flexible Dual-Plating Zn-Br Microbatteries.

J Phys Chem Lett

September 2025

College of Materials Science and Engineering, Sichuan University, No. 24 South Section 1, Yihuan Road, Chengdu 610065, P. R. China.

Aqueous zinc-ion microbatteries exhibit promising prospects for wearable devices due to their high safety and cost-effectiveness but face challenges such as low energy density and short cycle life. To address these challenges, a dual-plating flexible Zn-Br microbattery was developed using freestanding MXene films as a zinc metal free anode. The MXene anode retains no redundant Zn, as Zn from the electrolyte undergoes deposition/stripping reactions on its substrate, thereby eliminating the necessity for excess zinc.

View Article and Find Full Text PDF

Precise Modulation of Zeolite Acidity by Alkali Metal Ions for Enhancing Catalytic Performance in CO Cycloaddition Reactions.

Inorg Chem

September 2025

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130021, P. R. China.

The CO cycloaddition route is an effective way to achieve efficient conversion and utilization of CO. Zeolites with diverse topologies and tunable acidic sites can efficiently promote the cycloaddition reaction of CO with epoxides. The exchangeable cations in zeolites have a great influence on the performance of the CO cycloaddition, but there are few studies on it.

View Article and Find Full Text PDF

Towards durable photocatalytic seawater splitting: design strategies and challenges.

Chem Commun (Camb)

September 2025

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing & State Key Laboratory of Silicate Materials for Architectures & School of Chemistry, Chemical Engineering and Life Sciences & School of Materials Science and Engineering, Wuhan University of Technology, Wuhan, 430070

Photocatalytic seawater splitting (PSWS), which utilizes abundant solar and ocean resources, is one of the most promising technologies for sustainable hydrogen production. However, the complex composition of seawater significantly limits the durability and activity of photocatalysts. In this review, we first identify the primary factors that contribute to photocatalyst deactivation during PSWS, including chloride induced corrosion and loss of active sites, and light shielding caused by precipitation of metal cation salts.

View Article and Find Full Text PDF

The photocatalytic reduction of carbon dioxide (CO) to chemicals holds significant importance for mitigating the current energy crisis. Rational design of catalytic centers within well-defined structures can effectively enhance the reaction activity and selectivity. In this study, we constructed interrupted zeolitic boron imidazolate frameworks (BIFs) featuring unsaturated coordination at the central Co ion.

View Article and Find Full Text PDF

Chemically Lithiated Poly(vinylidene difluoride) with In Situ Generated LiF Nanofiller as Hybrid Artificial Layer for Stable Lithium Metal Anodes.

Small

September 2025

Key Laboratory of Electrochemical Power Sources of Hubei Province, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, China.

Hybrid artificial layer based on inorganic/polymer composite endows superior toughness and mechanical strength, which can achieve high stability of lithium metal anode. However, the large particle size and uneven distribution of inorganic fillers hinder the uniform flow of lithium ions across the membrane, making it difficult to achieve smooth lithium metal deposition/stripping. In this work, a chemical lithiation-induced defluorination strategy is proposed to engineer  poly(vinylidene difluoride) (PVDF)-based artificial layers, enabling in situ incorporation of highly dispersed LiF nanofiller within the polymer matrix and precise control over the LiF content.

View Article and Find Full Text PDF