In chemistry, ÃÂ-effects or ÃÂ-interactions are a type of non-covalent interaction that involves ÃÂ systems. Just like in an electrostatic interaction where a region of negative charge interacts with a positive charge, the electron-rich ÃÂ system can interact with a metal (cationic or neutral), an anion, another molecule and even another ÃÂ system. Non-covalent interactions involving ÃÂ systems are pivotal to biological events such as protein-ligand recognition.
The most common types of ÃÂ-interactions involve:
Graphite consists of stacked sheets of covalently bonded carbon. The individual layers are called graphene. In each layer, each carbon atom is bonded to three other atoms forming a continuous layer of sp<sup>2</sup> bonded carbon hexagons, like a honeycomb lattice with a bond length of 0.142 nm, and the distance between planes is 0.335 nm.
Cation-ÃÂ interactions are important for the acetylcholine (Ach) neurotransmitter. The structure of acetylcholine esterase includes 14 highly conserved aromatic residues. The trimethyl ammonium group of Ach binds to the aromatic residue of tryptophan (Trp). The indole site provides a much more intense region of negative electrostatic potential than benzene and phenol residue of Phe and Tyr.
PiâÂÂpi and cationâÂÂpi interactions are important in rational drug design. 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 been exploited in the rational design of novel AChE inhibitors.
<chem>\pi - \pi </chem>, <chem>CH-\pi </chem> and <chem>\pi -cation</chem> interactions are widely observed motifs in supramolecular assembly and recognition.
<chem>\pi-\pi</chem> concerns the direct interactions between two -systems; and <chem>cation-\pi </chem> interaction arises from the electrostatic interaction of a cation with the face of the -system. Unlike these two interactions, the <chem>CH-\pi </chem> interaction arises mainly from charge transfer between the CâÂÂH orbital and the -system.
àsystems contribute to supramolecular assembly. Some catenanes feature ÃÂâÂÂàinteractions. The major challenge for the synthesis of catenane is to interlock molecules in a controlled fashion. Stoddart and co-workers developed a series of systems utilizing the strong ÃÂâÂÂàinteractions between electron-rich benzene derivatives and electron-poor pyridinium rings. [2]Catanene was synthesized by reacting bis(pyridinium) (A), bisparaphenylene-34-crown-10 (B), and 1, 4-bis(bromomethyl)benzene (C) (Fig. 2). The ÃÂâÂÂàinteraction between A and B directed the formation of an interlocked template intermediate that was further cyclized by substitution reaction with compound C to generate the [2]catenane product.
A combination of tetracyanoquinodimethane (TCNQ) and tetrathiafulvalene (TTF) forms a strong charge-transfer complex referred to as TTF-TCNQ. The solid shows almost metallic electrical conductance. In a TTF-TCNQ crystal, TTF and TCNQ molecules are arranged independently in separate parallel-aligned stacks, and an electron transfer occurs from donor (TTF) to acceptor (TCNQ) stacks.
Anion and ÃÂâÂÂaromatic systems (typically electron-deficient) create an interaction that is associated with the repulsive forces of the structures. These repulsive forces involve electrostatic and anion-induced polarized interactions. This force allows for the systems to be used as receptors and channels in supramolecular chemistry for applications in the medical (synthetic membranes, ion channels) and environmental fields (e.g. sensing, removal of ions from water).
The first X-ray crystal structure that depicted anionâÂÂàinteractions was reported in 2004. In addition to this being depicted in the solid state, there is also evidence that the interaction is present in solution.
ÃÂ-effects have an important contribution to biological systems since they provide a significant amount of binding enthalpy. Neurotransmitters produce most of their biological effect by binding to the active site of a protein receptor. Cation-ÃÂ interactions are important for the acetylcholine (Ach) neurotransmitter. The structure of cholinesterase includes 14 highly conserved aromatic residues. The trimethyl ammonium group of Ach binds to the aromatic residue of tryptophan (Trp). The indole site provides a much more intense region of negative electrostatic potential than benzene and phenol residue of Phe and Tyr.
systems are important building blocks in supramolecular assembly because of their versatile noncovalent interactions with various functional groups. Particularly, <chem>\pi - \pi </chem> , <chem>CH-\pi </chem> and <chem>\pi -cation</chem> interactions are widely used in supramolecular assembly and recognition.
<chem>\pi-\pi</chem> concerns the direct interactions between two -systems; and <chem>cation-\pi </chem> interaction arises from the electrostatic interaction of a cation with the face of the -system. Unlike these two interactions, the <chem>CH-\pi </chem> interaction arises mainly from charge transfer between the CâÂÂH orbital and the -system.