Enhancement of a Catalysis-Based Fluorometric Detection Method for Palladium through Rational Fine-Tuning of the Palladium Species

被引:154
作者
Garner, Amanda L. [1 ]
Song, Fengling [1 ]
Koide, Kazunori [1 ]
机构
[1] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
基金
美国国家科学基金会;
关键词
PLASMA-MASS-SPECTROMETRY; PI-ALLYLPALLADIUM COMPLEXES; ACTIVE PHARMACEUTICAL INGREDIENTS; CROSS-COUPLING REACTIONS; ALLYLIC ALKYLATION; FLUORESCENT SENSORS; PLATINUM; REMOVAL; RHODIUM; CONVERTERS;
D O I
10.1021/ja808385a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal analyses in chemistry, materials science, and environmental science are currently performed using techniques such as inductively coupled plasma mass spectrometry and X-ray fluorescence, which require expensive instrumentation and are not high-throughput. Although fluorescent probes are known for their sensitivity and specificity and are amenable to high-throughput analyses, the robustness of such analyses are typically limited due to their binding-based nature. Herein we report an improvement of our previously reported catalysis-based fluorescent probe for palladium by rationally fine-tuning the redox and coordination chemistries of the palladium species involved in the O-deallylation reaction. This method now rivals current analytical methods with respect to sensitivity. We demonstrate palladium detection in various active pharmaceutical ingredients, spent catalytic converter materials, and a metal scavenger resin. Thus, fluorescent methods may have the potential for substituting the current instrument-intensive techniques.
引用
收藏
页码:5163 / 5171
页数:9
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