{{short description|Lasting attraction between dissolved cations and anions in solution}}
In chemistry, the '''intimate ion pair''' concept, introduced by Saul Winstein, describes the interactions between a cation, anion and surrounding solvent molecules.<ref>{{cite journal|last=Winstein|first=S.|author2=Clippinger, E. |author3=Fainberg, A. H. |author4=Heck, R. |author5= RobinsonG. C. |year=1956|title=''Salt Effects and Ion Pairs in Solvolysis and Related Reactions. III.1 Common Ion Rate Depression and Exchange of Anions during Acetolysis''|volume=78|issue=2|pages=328–335|doi=10.1021/ja01583a022|journal=Journal of the American Chemical Society}}</ref> In ordinary aqueous solutions of inorganic salts, an ion is completely solvated and shielded from the counterion. In less polar solvents, two ions can still be connected to some extent. In a ''tight'', ''intimate'', or ''contact'' ion pair, there are no solvent molecules between the two ions. When solvation increases, ionic bonding decreases and a ''loose'' or ''solvent-shared'' ion pair results. The ion pair concept explains stereochemistry in solvolysis.
500px|center
The concept of intimate ion pairs is used to explain the slight tendency for inversion of stereochemistry during an S{{sub|N}}1 reaction. It is proposed that solvent or other ions in solution may assist in the removal of a leaving group to form a carbocation which reacts in an S{{sub|N}}1 fashion; similarly, the leaving group may associate loosely with the cationic intermediate. The association of solvent or an ion with the leaving group effectively blocks one side of the incipient carbocation, while allowing the backside to be attacked by a nucleophile. This leads to a slight excess of the product with inverted stereochemistry, whereas a purely S{{sub|N}}1 reaction should lead to a racemic product. Intimate ion pairs are also invoked in the S{{sub|N}}i mechanism. Here, part of the leaving group detaches and attacks from the same face, leading to retention.<ref>{{Cite book |last1=Smith |first1=Michael |url=https://onlinelibrary.wiley.com/doi/book/10.1002/0470084960 |title=March's Advanced Organic Chemistry : Reactions, Mechanisms, and Structure. |last2=March |first2=Jerry |date=2007 |publisher=Wiley |isbn=978-1-61583-842-4 |edition=6th |location= |pages=468–469 |chapter=Aliphatic Substitution: Nucleophilic and Organometallic |doi=10.1002/9780470084960.ch10 |oclc= |chapter-url=https://onlinelibrary.wiley.com/doi/10.1002/9780470084960.ch10}}</ref>
== See also == *Ion association *Asymmetric ion-pairing catalysis
== References == {{reflist}}
Category:Chemical bonding