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The geometry is prevalent for transition metal complexes with d 8 configuration, which includes Rh(I), Ir(I), Pd(II), Pt(II), and Au(III). Notable examples include the anticancer drugs cisplatin, [PtCl 2 (NH 3) 2], and carboplatin. Many homogeneous catalysts are square planar in their resting state, such as Wilkinson's catalyst and Crabtree's ...
Molecular geometry influences several properties of a substance including its reactivity, polarity, phase of matter, color, magnetism and biological activity. [1] [2] [3] The angles between bonds that an atom forms depend only weakly on the rest of molecule, i.e. they can be understood as approximately local and hence transferable properties.
The seesaw geometry occurs when a molecule has a steric number of 5, with the central atom being bonded to 4 other atoms and 1 lone pair (AX 4 E 1 in AXE notation). An atom bonded to 5 other atoms (and no lone pairs) forms a trigonal bipyramid with two axial and three equatorial positions, but in the seesaw geometry one of the atoms is replaced ...
In effect, they considered nitrogen dioxide as an AX 2 E 0.5 molecule, with a geometry intermediate between NO + 2 and NO − 2. Similarly, chlorine dioxide (ClO 2) is an AX 2 E 1.5 molecule, with a geometry intermediate between ClO + 2 and ClO − 2. [citation needed] Finally, the methyl radical (CH 3) is predicted to be trigonal pyramidal ...
The bonding mode depends on the electrophilicity and basicity of the metal centre. [2] Most common is the η 2-CO 2 coordination mode as illustrated by Aresta's complex, Ni(CO 2)(PCy 3) 2, which was the first reported complex of CO 2. [3] [4] This square-planar compound is a derivative of Ni(II) with a reduced CO 2 ligand.
S + 4CoF 3 → SF 4 + 4CoF 2. SF 4 is industrially produced by the reaction of SCl 2 and NaF with acetonitrile as a catalyst [6] 3 SCl 2 + 4 NaF → SF 4 + S 2 Cl 2 + 4 NaCl. At higher temperatures (e.g. 225–450 °C), the solvent is superfluous. Moreover, sulfur dichloride may be replaced by elemental sulfur (S) and chlorine (Cl 2). [7] [8]
In the natural bond orbital viewpoint of 3c–4e bonding, the triiodide anion is constructed from the combination of the diiodine (I 2) σ molecular orbitals and an iodide (I −) lone pair. The I − lone pair acts as a 2-electron donor, while the I 2 σ* antibonding orbital acts as a 2-electron acceptor. [12]
In agreement with this description the photoelectron spectrum for water shows a sharp peak for the nonbonding 1b 1 MO (12.6 eV) and three broad peaks for the 3a 1 MO (14.7 eV), 1b 2 MO (18.5 eV) and the 2a 1 MO (32.2 eV). [29] The 1b 1 MO is a lone pair, while the 3a 1, 1b 2 and 2a 1 MO's can be localized to give two O−H bonds and an in-plane ...