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An intramolecular force (from Latin intra-'within') is any force that binds together the atoms making up a molecule. [1] Intramolecular forces are stronger than the intermolecular forces that govern the interactions between molecules. [2]
Otherwise-intermolecular reactions can be made temporarily intramolecular by linking both reactants by a tether with all the advantages associated to it. Popular choices of tether contain a carbonate ester , boronic ester , silyl ether , or a silyl acetal link ( silicon tethers ) [ 9 ] [ 10 ] which are fairly inert in many organic reactions yet ...
Intermolecular forces observed between atoms and molecules can be described phenomenologically as occurring between permanent and instantaneous dipoles, as outlined above. Alternatively, one may seek a fundamental, unifying theory that is able to explain the various types of interactions such as hydrogen bonding , [ 22 ] van der Waals force ...
A 1,2-rearrangement is an organic reaction where a substituent moves from one atom to another atom in a chemical compound. In a 1,2 shift the movement involves two adjacent atoms but moves over larger distances are possible. Skeletal isomerization is not normally encountered in the laboratory, but is the basis of large applications in oil ...
The strength of intermolecular hydrogen bonds is most often evaluated by measurements of equilibria between molecules containing donor and/or acceptor units, most often in solution. [21] The strength of intramolecular hydrogen bonds can be studied with equilibria between conformers with and without hydrogen bonds.
In molecular mechanics, several ways exist to define the environment surrounding a molecule or molecules of interest. A system can be simulated in vacuum (termed a gas-phase simulation) with no surrounding environment, but this is usually undesirable because it introduces artifacts in the molecular geometry, especially in charged molecules.
Ligation is complicated by the fact that the reaction can involve both inter- and intra-molecular reactions, but the desired ligation products in many ligation reactions (e.g. ligating a DNA fragment into a vector) needed first to be inter-molecular, i.e. between two different DNA molecules, followed by an intra-molecular reaction to seal and ...
Steric hindrance is the slowing of chemical reactions due to steric bulk. It is usually manifested in intermolecular reactions, whereas discussion of steric effects often focus on intramolecular interactions. Steric hindrance is often exploited to control selectivity, such as slowing unwanted side-reactions.