4.7 Article

Synthesis and Coordination Chemistry of a Phosphine-Decorated Fluorescein: Double Turn-On Sensing of Gold(III) Ions in Water

期刊

INORGANIC CHEMISTRY
卷 55, 期 12, 页码 5828-5835

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.6b00080

关键词

-

资金

  1. National Science Foundation [DGE-1252521, CHE-1300371]
  2. Welch Foundation [A-1423]
  3. Texas A&M University (Arthur E. Martell Chair of Chemistry)
  4. Division Of Chemistry
  5. Direct For Mathematical & Physical Scien [1300371] Funding Source: National Science Foundation

向作者/读者索取更多资源

Although phosphine ligands are ubiquitous in transition metal chemistry, few reports of fluorescent phosphines exist that explore the effect of metal coordination on the photophysical properties of a phosphine-bound fluorescent group. The coordination chemistry of a derivative of fluorescein decorated with an o-phenylene-linked phosphine group has been studied with late transition metals. An Au(I) complex of the phosphine-decorated fluorescein has been structurally characterized, showing that the metal center is held closely over the plane of the fluorophore. Despite the presence HO of the heavy metal center, however, the phosphine-gold complex displays greatly increased fluorescence compared to the free ligand, in which photoelectron transfer from the lone-pair-bearing phosphine causes low emission. The phosphine-decorated fluorescein ligand was tested in a simple sensing system for metal ions in aqueous solution and shows a turn-on response to Au, Ag, and Hg, with an especially dramatic response to Au(III) species. The selectivity for Au(III) was determined to be the result of a double turn-on response that is both reaction- and coordination-based.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据