Calibrating the coordination chemistry tool chest: metrics of bi- and tridentate ligands

被引:34
作者
Aguila, David [1 ]
Escribano, Esther [1 ]
Speed, Saskia [1 ]
Talancon, Daniel [1 ]
Yerman, Luis [1 ]
Alvarez, Santiago [1 ]
机构
[1] Univ Barcelona, Dept Quim Inorgan, Barcelona 08028, Spain
关键词
TRANSITION-METAL-COMPLEXES; RHODIUM-CATALYZED HYDROFORMYLATION; MRI CONTRAST AGENTS; MOLECULAR-STRUCTURE; CRYSTAL-STRUCTURES; BIDENTATE LIGANDS; STRUCTURAL CHARACTERIZATION; CHELATING DIPHOSPHINES; ALKENE METATHESES; CARBON-MONOXIDE;
D O I
10.1039/b904938j
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Bi- and multidentate ligands form part of the tools commonly used for designing coordination and supramolecular complexes with desired stereochemistries. Parameters and concepts usually employed include the normalized bite of bidentate ligands, their cis- or trans-coordinating ability, their rigidity or flexibility, or the duality of some ligands that can act in chelating or dinucleating modes. In this contribution we present a structural database study of over one hundred bi- and tridentate ligands that allows us to parametrize their coordinating properties and discuss the relevance of such parameters for the choice of coordination polyhedron or coordination sites.
引用
收藏
页码:6610 / 6625
页数:16
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