Hydrosulfide complexes of the transition elements: diverse roles in bioinorganic, cluster, coordination, and organometallic chemistry

被引:52
|
作者
Pluth, Michael D. [1 ]
Tonzetich, Zachary J. [2 ]
机构
[1] Univ Oregon, Dept Chem & Biochem, Mat Sci Inst, Inst Mol Biol, Knight Campus Accelerating Sci Impact, Eugene, OR 97403 USA
[2] Univ Texas San Antonio, Dept Chem, San Antonio, TX 78249 USA
基金
美国国家科学基金会;
关键词
X-RAY CRYSTAL; DERIVATIVES; MOLECULAR-STRUCTURES; IRON-SULFUR CLUSTERS; HYDROGEN-SULFIDE OXIDATION; MIXED-METAL SULFIDO; DINUCLEAR PALLADIUM(I) COMPLEXES; BRIDGED DIRUTHENIUM COMPLEXES; MERCAPTO-CARBONYL-COMPLEXES; GEM-DITHIOLATO COMPLEXES; CYTOCHROME-C-OXIDASE;
D O I
10.1039/c9cs00570f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Sulfur-based ligands are versatile donors that play important roles in a wide array of subdisciplines of inorganic chemistry including organometallic chemistry, bioinorganic chemistry, and cluster science. Despite the breadth of compounds containing sulfur-based ligands, those containing the simplest mercapto group, hydrosulfide ion (HS-), are significantly less developed. The acceptance of H2S/HS(-)as important biological signaling compounds during the last decade has engendered a renewed interest in the chemistry of these species. Bioinorganic reactivity of hydrosulfide, however, is only one aspect of its fascinating chemistry, much of which revolves around its interactions with transition metal ions. The coordination of HS(-)to d-block elements produces a unique class of substances that differ in significant ways from more ubiquitous metal thiolates. This review examines the preparation, structure, spectroscopy, and reactivity of such compounds and the roles they play across several fields of chemistry.
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页码:4070 / 4134
页数:65
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