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A typical triple bond, for example in acetylene (HC≡CH), consists of one sigma bond and two pi bonds in two mutually perpendicular planes containing the bond axis. Two pi bonds are the maximum that can exist between a given pair of atoms. Quadruple bonds are extremely rare and can be formed only between transition metal atoms, and consist of ...
In organic chemistry, neighbouring group participation (NGP, also known as anchimeric assistance) has been defined by the International Union of Pure and Applied Chemistry (IUPAC) as the interaction of a reaction centre with a lone pair of electrons in an atom or the electrons present in a sigma or pi bond contained within the parent molecule but not conjugated with the reaction centre.
In chemistry, π-effects or π-interactions are a type of non-covalent interaction that involves π systems.Just like in an electrostatic interaction where a region of negative charge interacts with a positive charge, the electron-rich π system can interact with a metal (cationic or neutral), an anion, another molecule and even another π system. [1]
As a result, pi–pi and cation–pi interactions are important factors in rational drug design. [24] One example is the FDA-approved acetylcholinesterase (AChE) inhibitor tacrine which is used in the treatment of Alzheimer's disease. Tacrine is proposed to have a pi stacking interaction with the indolic ring of Trp84, and this interaction has ...
The central carbon atom of allenes forms two sigma bonds and two pi bonds. The central carbon atom is sp-hybridized, and the two terminal carbon atoms are sp 2-hybridized. The bond angle formed by the three carbon atoms is 180°, indicating linear geometry for the central carbon atom.
Pi bonds are created by the “side-on” interactions of the orbitals. [3] Once again, in molecular orbitals, bonding pi (π) electrons occur when the interaction of the two π atomic orbitals are in-phase. In this case, the electron density of the π orbitals needs to be symmetric along the mirror plane in order to create the bonding ...
Furthermore, the M–CO bond length is shortened. The weakening of the C–O bond is indicated by a decrease in the wavenumber of the ν CO band(s) from that for free CO (2143 cm −1), for example to 2060 cm −1 in Ni(CO) 4 and 1981 cm −1 in Cr(CO) 6, and 1790 cm −1 in the anion [Fe(CO) 4] 2−. [3]
In chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they are Lewis bases. Nucleophilic describes the affinity of a nucleophile to bond with positively charged ...