In chemistry, crystallography, and materials science, the coordination number, also called ligancy, of a central atom in a molecule or crystal is the number of atoms, molecules or ions bonded to it. The ion/molecule/atom surrounding the central ion/molecule/atom is called a ligand. This number is determined somewhat differently for molecules than for crystals.
For molecules and polyatomic ions the coordination number of an atom is determined by simply counting the other atoms to which it is bonded (by either single or multiple bonds). For example, [Cr(NH3)2Cl2Br2]− has Cr3+ as its central cation, which has a coordination number of 6 and is described as hexacoordinate. The common coordination numbers are 4, 6 and 8.
In chemistry, coordination number, defined originally in 1893 by Alfred Werner, is the total number of neighbors of a central atom in a molecule or ion. The concept is most commonly applied to coordination complexes.
The most common coordination number for d-block transition metal complexes is 6. The coordination number does not distinguish the geometry of such complexes, i.e. octahedral vs trigonal prismatic.
For transition metal complexes, coordination numbers range from 2 (e.g., AuI in Ph3PAuCl) to 9 (e.g., ReVII in [ReH9]2−). Metals in the f-block (the lanthanoids and actinoids) can accommodate higher coordination number due to their greater ionic radii and availability of more orbitals for bonding. Coordination numbers of 8 to 12 are commonly observed for f-block elements. For example, with bidentate nitrate ions as ligands, CeIV and ThIV form the 12-coordinate ions [Ce(NO3)6]2− (ceric ammonium nitrate) and [Th(NO3)6]2−. When the surrounding ligands are much smaller than the central atom, even higher coordination numbers may be possible. One computational chemistry study predicted a particularly stable PbHe152+ ion composed of a central lead ion coordinated with no fewer than 15 helium atoms. Among the Frank–Kasper phases, the packing of metallic atoms can give coordination numbers of up to 16.
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Ce cours présente les fondements du droit foncier et les apports des principaux instruments de gestion foncière pour la mise en œuvre du développement territorial.
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 chemistry, trigonal planar is a molecular geometry model with one atom at the center and three atoms at the corners of an equilateral triangle, called peripheral atoms, all in one plane. In an ideal trigonal planar species, all three ligands are identical and all bond angles are 120°. Such species belong to the point group D3h. Molecules where the three ligands are not identical, such as , deviate from this idealized geometry. Examples of molecules with trigonal planar geometry include boron trifluoride (), formaldehyde (), phosgene (), and sulfur trioxide ().
In crystallography, the cubic (or isometric) crystal system is a crystal system where the unit cell is in the shape of a cube. This is one of the most common and simplest shapes found in crystals and minerals. There are three main varieties of these crystals: Primitive cubic (abbreviated cP and alternatively called simple cubic) Body-centered cubic (abbreviated cI or bcc) Face-centered cubic (abbreviated cF or fcc) Note: the term fcc is often used in synonym for the cubic close-packed or ccp structure occurring in metals.
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.
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