In coordination chemistry, a bridging ligand is a ligand that connects two or more atoms, usually metal ions. The ligand may be atomic or polyatomic. Virtually all complex organic compounds can serve as bridging ligands, so the term is usually restricted to small ligands such as pseudohalides or to ligands that are specifically designed to link two metals.
In naming a complex wherein a single atom bridges two metals, the bridging ligand is preceded by the Greek letter mu, μ, with a subscript number denoting the number of metals bound to the bridging ligand. μ2 is often denoted simply as μ. When describing coordination complexes care should be taken not to confuse μ with η ('eta'), which relates to hapticity. Ligands that are not bridging are called terminal ligands.
Virtually all ligands are known to bridge, with the exception of amines and ammonia. Common bridging ligands include most of the common anions.
Many simple organic ligands form strong bridges between metal centers. Many common examples include organic derivatives of the above inorganic ligands (R = alkyl, aryl): , , , (imido), (phosphido, note the ambiguity with the preceding entry), (phosphinidino), and many more.
File:Ru-Cl.png|In this ruthenium complex ([[(cymene)ruthenium dichloride dimer|(benzene)ruthenium dichloride dimer]]), two [[chloride]] ligands are terminal and two are μ2 bridging.
File:Creutz-Taube-Ion.svg|[[Pyrazine]] is a bridging ligand in this diruthenium compound, called the [[Creutz–Taube complex]].
File:Mu3 compound.svg|In the cobalt cluster {{chem2|Co3(CO)9(C^{''t''}Bu)}}, the {{chem2|link=Alkylidyne complex|C^{''t''}Bu}} ligand is triply bridging, although this aspect is typically not indicated in the formula.
File:Fe3(CO)12lessFe-Fe.png|In [[triiron dodecacarbonyl]], two CO ligands are bridging and ten are terminal ligands. The terminal and bridging CO ligands interchange rapidly.
File:Niobium-pentachloride-dimer-2D.png|In [[Niobium pentachloride|NbCl5]], there are two bridging and eight terminal chloride ligands.
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The course will provide a synopsis of the chemistry of f elements (lanthanides and actinides) covering structure, bonding, redox and spectroscopic properties and reactivity. The coordination and organ
In coordination chemistry, denticity () refers to the number of donor groups in a given ligand that bind to the central metal atom in a coordination complex. In many cases, only one atom in the ligand binds to the metal, so the denticity equals one, and the ligand is said to be monodentate (sometimes called unidentate). Ligands with more than one bonded atom are called polydentate or multidentate. The denticity of a ligand is described with the Greek letter κ ('kappa').
In coordination chemistry, hapticity is the coordination of a ligand to a metal center via an uninterrupted and contiguous series of atoms. The hapticity of a ligand is described with the Greek letter η ('eta'). For example, η2 describes a ligand that coordinates through 2 contiguous atoms. In general the η-notation only applies when multiple atoms are coordinated (otherwise the κ-notation is used). In addition, if the ligand coordinates through multiple atoms that are contiguous then this is considered denticity (not hapticity), and the κ-notation is used once again.
In chemistry, a polyoxometalate (abbreviated POM) is a polyatomic ion, usually an anion, that consists of three or more transition metal oxyanions linked together by shared oxygen atoms to form closed 3-dimensional frameworks. The metal atoms are usually group 6 (Mo, W) or less commonly group 5 (V, Nb, Ta) transition metals and Tc in their high oxidation states. Polyoxometalates are often colorless, orange or red diamagnetic anions.
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Octahedral coordination cages of the general formula Pd6L1212 were obtained by combining Pd(CH3CN)42 with heteroditopic N-donor ligands. Four different ligands were employed. These ligands have 3-pyridyl donor groups at one end and 4-pyridyl, ...
2024
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A dinuclear metal-organic cage with four acrylate side chains was prepared by self-assembly. Precipitation polymerization of the cage with N-isopropylacrylamide yielded a thermoresponsive nanogel. The host properties of the cage were retained within the ge ...
One of the main goals of organometallic chemistry in the last decades was the activation of small molecule in mild reaction conditions. Even though multiple examples of catalytic cycles able to produce fine chemicals from cheap and abundant sources using t ...