𝜈 | Molecule 1 : 1 Host | ||
Ka = | 340.0 | ± 22.0 | M-1 |
Kd = | |||
logKa = | |||
T | 25.0 °C | ||
Energy | kJ mol-1 | kcal mol-1 | |||
---|---|---|---|---|---|
ΔG | = | -14.45 | ± 0.16 | -3.45 | ± 0.04 |
Detection Method: | Direct | |||
Assay Type: | Direct Binding Assay | |||
Technique: | Fluorescence | |||
𝛌ex | = | 520.0 nm | ||
𝛌em | = | 549.0 nm | ||
Ibound⁄Ifree | = | 1.18 |
Solvent System | Buffer System | acetate pH-5.0 |
Solvents | water | |
Additives | Sodium acetate | |
acetic acid | ||
Source of Concentration | ||
pH | 5.0 |
Citation: |
X. ZHU, J. SUN, J. WU, SupraBank 2024, Study on the inclusion interactions of β-cyclodextrin and its derivative with dyes by spectrofluorimetry and its analytical application (dataset). https://doi.org/10.34804/supra.20210928302 |
Link: | https://doi.org/10.34804/supra.20210928302 |
Export: | BibTex | RIS | EndNote |
Citation: |
X. ZHU, J. SUN, J. WU, Talanta 2007, 72, 237–242. |
Link: | https://doi.org/10.1016/j.talanta.2006.10.016 |
Export: | BibTex | RIS | EndNote |
The plot depicts the binding isotherm simulation of a 1:1 interaction of Erythrosin B (0.058823529411764705 M) and heptakis-O-(2-hydroxypropyl)-β Cyclodextrin (0 — 0.11764705882352941 M).