Coordination chemistry of the sulfur analog of tricatechol siderophores

被引：7

作者：

Birkmann, Birgit ^{[1
]}

Seidel, Wolfram W. ^{[1
]}

Pape, Tania ^{[1
]}

Ehlers, Andreas W. ^{[2
]}

Lammertsma, Koop ^{[2
]}

Hahn, F. Ekkehardt ^{[1
]}

机构：

[1] Univ Munster, Inst Anorgan & Analyt Chem, D-48149 Munster, Germany

[2] Vrije Univ Amsterdam, Dept Chem & Pharmaceut Sci, NL-1081 HV Amsterdam, Netherlands

来源：

DALTON TRANSACTIONS | 2009年 / 36期

关键词：

TRIPLE-STRANDED HELICATE; RAY MOLECULAR-STRUCTURE; CRYSTAL-STRUCTURE; STRUCTURAL-CHARACTERIZATION; OCTAHEDRAL COORDINATION; SEQUESTERING AGENTS; BUILDING-BLOCKS; COMPLEXES; ENTEROBACTIN; LIGAND;

D O I：

10.1039/b911014n

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Reaction of the siderophore analog tris(benzene-o-dithiol) ligand H-6-1 with Ti(OPr)(4) in methanol leads to the formation of the siderophore analog complex (Ph4As)(2)[Ti(1)(3)] exhibiting exclusively thiolato coordination to the metal center.

引用

页码：7350 / 7352

页数：3

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