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The strong bonding of metals in liquid form demonstrates that the energy of a metallic bond is not highly dependent on the direction of the bond; this lack of bond directionality is a direct consequence of electron delocalization, and is best understood in contrast to the directional bonding of covalent bonds.
Covalent bonding corresponds to sharing of a pair of electrons between two atoms of essentially equal electronegativity (for example, C–C and C–H bonds in aliphatic hydrocarbons). As bonds become more polar, they become increasingly ionic in character. Metal oxides vary along the iono-covalent spectrum. [4]
A cyclopentadienyl complex is a coordination complex of a metal and cyclopentadienyl groups (C 5 H − 5, abbreviated as Cp −). Cyclopentadienyl ligands almost invariably bind to metals as a pentahapto (η 5-) bonding mode. The metal–cyclopentadienyl interaction is typically drawn as a single line from the metal center to the center of the ...
The bond results because the metal atoms become somewhat positively charged due to loss of their electrons while the electrons remain attracted to many atoms, without being part of any given atom. Metallic bonding may be seen as an extreme example of delocalization of electrons over a large system of covalent bonds, in which every atom ...
The other form of coordination π bonding is ligand-to-metal bonding. This situation arises when the π-symmetry p or π orbitals on the ligands are filled. They combine with the d xy, d xz and d yz orbitals on the metal and donate electrons to the resulting π-symmetry bonding orbital between them and the metal. The metal-ligand bond is ...
Mn 2 (CO) 10 is a simple and clear case of a metal-metal bond because no other atoms tie the two Mn atoms together. When several metals are linked by metal-metal bonds, the compound or ion is called a metal cluster. Many metal clusters contain several unsupported M–M bonds. Some examples are M 3 (CO) 12 (M = Ru, Os) and Ir 4 (CO) 12.
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On the left, a filled pi-orbital on C 2 H 4 overlaps with an empty d-orbital on the metal. On the right, an empty pi-antibonding orbital on C 2 H 4 overlaps with a filled d-orbital on the metal. The Dewar–Chatt–Duncanson model is a model in organometallic chemistry that explains the chemical bonding in transition metal alkene complexes.