Lewis acids and bases

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File:Lewis bases and acids.jpg

Diagram of some Lewis Template:Font color and Template:Font color

{{#invoke:Sidebar|sidebar | titlestyle = background:#d3d3d3; | title = Acids and bases |image = Diagrammatic representation of the dissociation of acetic acid in aqueous solution to acetate and hydronium ions. |imagestyle = background:light-dark(transparent,#999); | headingstyle = background:#e5e5e5; | contentclass = hlist | contentstyle = padding:0.2em 0 0.75em;

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• Acceptor number
• Acid
• Acid–base reaction
• Acid–base homeostasis
• Acid strength
• Acidity function
• Amphoterism
• Base
• Buffer solutions
• Dissociation constant
• Donor number
• Equilibrium chemistry
• Extraction
• Hammett acidity function
• pH
• Proton affinity
• Self-ionization of water
• Titration
• Lewis acid catalysis
• Frustrated Lewis pair
• Chiral Lewis acid
• ECW model

| heading3 = Acid types | content3 =

• Brønsted–Lowry
• Lewis
• Mineral
• Organic
• Oxide
• Strong
• Superacids
• Weak
• Solid

| heading4 = Base types | content4 =

• Brønsted–Lowry
• Lewis
• Organic
• Oxide
• Strong
• Superbases
• Non-nucleophilic
• Weak

}} A Lewis acid (named for the American physical chemist Gilbert N. Lewis) is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct. A Lewis base, then, is any species that has a filled orbital containing an electron pair which is not involved in bonding but may form a dative bond with a Lewis acid to form a Lewis adduct. For example, NH₃ is a Lewis base, because it can donate its lone pair of electrons. Trimethylborane [(CH₃)₃B] is a Lewis acid as it is capable of accepting a lone pair. In a Lewis adduct, the Lewis acid and base share an electron pair furnished by the Lewis base, forming a dative bond.<ref name="Gold Book Lewis acid L03508">Template:GoldBookRef</ref> In the context of a specific chemical reaction between NH₃ and Me₃B, a lone pair from NH₃ will form a dative bond with the empty orbital of Me₃B to form an adduct NH₃•BMe₃. The terminology refers to the contributions of Gilbert N. Lewis.<ref name = lewisvalence>Template:Cite book From p. 142: "We are inclined to think of substances as possessing acid or basic properties, without having a particular solvent in mind. It seems to me that with complete generality we may say that a basic substance is one which has a lone pair of electrons which may be used to complete the stable group of another atom, and that an acid substance is one which can employ a lone pair from another molecule in completing the stable group of one of its own atoms. In other words, the basic substance furnishes a pair of electrons for a chemical bond, the acid substance accepts such a pair."</ref>

The terms nucleophile and electrophile are sometimes interchangeable with Lewis base and Lewis acid, respectively. These terms, especially their abstract noun forms nucleophilicity and electrophilicity, emphasize the kinetic aspect of reactivity, while the Lewis basicity and Lewis acidity emphasize the thermodynamic aspect of Lewis adduct formation.<ref>Template:Cite bookTemplate:Page needed</ref>

Depicting adducts

In many cases, the interaction between the Lewis base and Lewis acid in a complex is indicated by an arrow indicating the Lewis base donating electrons toward the Lewis acid using the notation of a dative bond — for example, Template:Chem2←Template:Chem2. Some sources indicate the Lewis base with a pair of dots (the explicit electrons being donated), which allows consistent representation of the transition from the base itself to the complex with the acid:

Template:Chem2

A center dot may also be used to represent a Lewis adduct, such as Template:Chem2. Another example is boron trifluoride diethyl etherate, Template:Chem2. In a slightly different usage, the center dot is also used to represent hydrate coordination in various crystals, as in Template:Chem2 for hydrated magnesium sulfate, irrespective of whether the water forms a dative bond with the metal.

Although there have been attempts to use computational and experimental energetic criteria to distinguish dative bonding from non-dative covalent bonds,<ref>Template:Cite journal</ref> for the most part, the distinction merely makes note of the source of the electron pair, and dative bonds, once formed, behave simply as other covalent bonds do, though they typically have considerable polar character. Moreover, in some cases (e.g., sulfoxides and amine oxides as Template:Chem2 and Template:Chem2), the use of the dative bond arrow is just a notational convenience for avoiding the drawing of formal charges. In general, however, the donor–acceptor bond is viewed as simply somewhere along a continuum between idealized covalent bonding and ionic bonding.<ref name="March"/>

Lewis acids

File:NH3-BF3-adduct-bond-lengthening-2D.png

Major structural changes accompany binding of the Lewis base to the coordinatively unsaturated, planar Lewis acid BF₃

Lewis acids are diverse and the term is used loosely. Simplest are those that react directly with the Lewis base, such as boron trihalides and the pentahalides of phosphorus, arsenic, and antimony.

In the same vein, Template:Chem2 can be considered to be the Lewis acid in methylation reactions. However, the methyl cation never occurs as a free species in the condensed phase, and methylation reactions by reagents like CH₃I take place through the simultaneous formation of a bond from the nucleophile to the carbon and cleavage of the bond between carbon and iodine (S_N2 reaction). Textbooks disagree on this point: some asserting that alkyl halides are electrophiles but not Lewis acids,<ref>Template:Cite book</ref> while others describe alkyl halides (e.g. CH₃Br) as a type of Lewis acid.<ref>Template:Cite book</ref> The IUPAC states that Lewis acids and Lewis bases react to form Lewis adducts,<ref name="Gold Book Lewis acid L03508"/> and defines electrophile as Lewis acids.<ref>Template:GoldBookRef</ref>

Simple Lewis acids

Some of the most studied examples of such Lewis acids are the boron trihalides and organoboranes:<ref>Template:Cite journal</ref>

BF₃ + F⁻ → Template:Chem2

In this adduct, all four fluoride centres (or more accurately, ligands) are equivalent.

BF₃ + OMe₂ → BF₃OMe₂

Both BF₄⁻ and BF₃OMe₂ are Lewis base adducts of boron trifluoride.

Many adducts violate the octet rule, such as the triiodide anion:

I₂ + I⁻ → Template:Chem2

The variability of the colors of iodine solutions reflects the variable abilities of the solvent to form adducts with the Lewis acid I₂.

Some Lewis acids bind with two Lewis bases, a famous example being the formation of hexafluorosilicate:

SiF₄ + 2 F⁻ → Template:Chem2

Complex Lewis acids

Most compounds considered to be Lewis acids require an activation step prior to formation of the adduct with the Lewis base. Complex compounds such as Et₃Al₂Cl₃ and AlCl₃ are treated as trigonal planar Lewis acids but exist as aggregates and polymers that must be degraded by the Lewis base.<ref>Greenwood, N. N.; & Earnshaw, A. (1997). Chemistry of the Elements (2nd Edn.), Oxford:Butterworth-Heinemann. Template:ISBN.Template:Page needed</ref> A simpler case is the formation of adducts of borane. Monomeric BH₃ does not exist appreciably, so the adducts of borane are generated by degradation of diborane:

B₂H₆ + 2 H⁻ → 2 Template:Chem2

In this case, an intermediate Template:Chem2 can be isolated.

Many metal complexes serve as Lewis acids, but usually only after dissociating a more weakly bound Lewis base, often water.

[Mg(H₂O)₆]²⁺ + 6 NH₃ → [Mg(NH₃)₆]²⁺ + 6 H₂O

H⁺ as Lewis acid

The proton (H⁺) <ref name="hydron"/> is one of the strongest but is also one of the most complicated Lewis acids. It is convention to ignore the fact that a proton is heavily solvated (bound to solvent). With this simplification in mind, acid-base reactions can be viewed as the formation of adducts:

• H⁺ + NH₃ → Template:Chem2
• H⁺ + OH⁻ → H₂O

Applications of Lewis acids

A typical example of a Lewis acid in action is in the Friedel–Crafts alkylation reaction.<ref name=March>March, J. “Advanced Organic Chemistry” 4th Ed. J. Wiley and Sons, 1992: New York. Template:ISBN.Template:Page needed</ref> The key step is the acceptance by AlCl₃ of a chloride ion lone-pair, forming Template:Chem2 and creating the strongly acidic, that is, electrophilic, carbonium ion.

RCl +AlCl₃ → R⁺ + Template:Chem2

Lewis bases

A Lewis base is an atomic or molecular species where the highest occupied molecular orbital (HOMO) is highly localized. Typical Lewis bases are conventional amines such as ammonia and alkyl amines. Other common Lewis bases include pyridine and its derivatives. They are nucleophilic in nature.

Some of the main classes of Lewis bases are:

• amines of the formula NH_3−xR_x where R = alkyl or aryl. Related to these are pyridine and its derivatives.
• phosphines of the formula PR_3−xAr_x.
• compounds of O, S, Se and Te in oxidation state −2, including water, ethers, ketones

The most common Lewis bases are anions. The strength of Lewis basicity correlates with the Template:Var of the parent acid: acids with high Template:Var's give good Lewis bases. As usual, a weaker acid has a stronger conjugate base.

• Examples of Lewis bases based on the general definition of electron pair donor include:
  • simple anions, such as H⁻ and F⁻
  • other lone-pair-containing species, such as H₂O, NH₃, HO⁻, and CH₃⁻
  • complex anions, such as sulfate
  • electron-rich Template:Pi-system Lewis bases, such as ethyne, ethene, and benzene

The strength of Lewis bases have been evaluated for various Lewis acids, such as I₂, SbCl₅, and BF₃.<ref>Christian Laurence and Jean-François Gal "Lewis Basicity and Affinity Scales : Data and Measurement" Wiley, 2009. Template:ISBN.Template:Page needed</ref>

Heats of binding of various bases to BF₃

Lewis base	Donor atom	Enthalpy of complexation (kJ/mol)
Quinuclidine	N	150
Et3N	N	135
Pyridine	N	128
Acetonitrile	N	60
DMA	O	112
DMSO	O	105
THF	O	90.4
Et2O	O	78.8
Acetone	O	76.0
EtOAc	O	75.5
Trimethylphosphine	P	97.3
Tetrahydrothiophene	S	51.6

Applications of Lewis bases

{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}} Nearly all electron pair donors that form compounds by binding transition elements can be viewed ligands. Thus, a large application of Lewis bases is to modify the activity and selectivity of metal catalysts. Chiral Lewis bases, generally multidentate, confer chirality on a catalyst, enabling asymmetric catalysis, which is useful for the production of pharmaceuticals. The industrial synthesis of the anti-hypertension drug mibefradil uses a chiral Lewis base (R-MeOBIPHEP), for example.<ref name="CompAsymmetricCatalysis">Template:Cite book</ref>

File:Partial Roche Synthesis of Mibefradil.tif

Hard and soft classification

{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}} Lewis acids and bases are commonly classified according to their hardness or softness. In this context hard implies small and nonpolarizable and soft indicates larger atoms that are more polarizable.

• typical hard acids: H⁺, alkali/alkaline earth metal cations, boranes, Zn²⁺
• typical soft acids: Ag⁺, Mo(0), Ni(0), Pt²⁺
• typical hard bases: ammonia and amines, water, carboxylates, fluoride and chloride
• typical soft bases: organophosphines, thioethers, carbon monoxide, iodide

For example, an amine will displace phosphine from the adduct with the acid BF₃. In the same way, bases could be classified. For example, bases donating a lone pair from an oxygen atom are harder than bases donating through a nitrogen atom. Although the classification was never quantified it proved to be very useful in predicting the strength of adduct formation, using the key concepts that hard acid—hard base and soft acid—soft base interactions are stronger than hard acid—soft base or soft acid—hard base interactions. Later investigation of the thermodynamics of the interaction suggested that hard—hard interactions are enthalpy favored, whereas soft—soft are entropy favored.Template:Citation needed

Quantifying Lewis acidity

Many methods have been devised to evaluate and predict Lewis acidity. Many are based on spectroscopic signatures such as shifts NMR signals or IR bands e.g. the Gutmann-Beckett method and the Childs<ref>Template:Cite journal</ref> method.

The ECW model is a quantitative model that describes and predicts the strength of Lewis acid base interactions, −ΔH. The model assigned E and C parameters to many Lewis acids and bases. Each acid is characterized by an E_A and a C_A. Each base is likewise characterized by its own E_B and C_B. The E and C parameters refer, respectively, to the electrostatic and covalent contributions to the strength of the bonds that the acid and base will form. The equation is

−ΔH = E_AE_B + C_AC_B + W

The W term represents a constant energy contribution for acid–base reaction such as the cleavage of a dimeric acid or base. The equation predicts reversal of acids and base strengths. The graphical presentations of the equation show that there is no single order of Lewis base strengths or Lewis acid strengths.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> and that single property scales are limited to a smaller range of acids or bases.

History

File:Dative covalent bond2.png

MO diagram depicting the formation of a dative covalent bond between two atoms

The concept originated with Gilbert N. Lewis who studied chemical bonding. In 1923, Lewis wrote An acid substance is one which can employ an electron lone pair from another molecule in completing the stable group of one of its own atoms.<ref name="lewisvalence"/><ref name="lewis_1">Miessler, L. M., Tar, D. A., (1991) p. 166 – Table of discoveries attributes the date of publication/release for the Lewis theory as 1923.</ref> The Brønsted–Lowry acid–base theory was published in the same year. The two theories are distinct but complementary. A Lewis base is also a Brønsted–Lowry base, but a Lewis acid does not need to be a Brønsted–Lowry acid. The classification into hard and soft acids and bases (HSAB theory) followed in 1963. The strength of Lewis acid-base interactions, as measured by the standard enthalpy of formation of an adduct can be predicted by the Drago–Wayland two-parameter equation.

Reformulation of Lewis theory

Lewis had suggested in 1916 that two atoms are held together in a chemical bond by sharing a pair of electrons.<ref>Template:Cite journal</ref> When each atom contributed one electron to the bond, it was called a covalent bond. When both electrons come from one of the atoms, it was called a dative covalent bond or coordinate bond. The distinction is not very clear-cut. For example, in the formation of an ammonium ion from ammonia and hydrogen the ammonia molecule donates a pair of electrons to the proton;<ref name="hydron">Traditionally, but not precisely, H⁺ ions are referred as "protons". See Template:GoldBookRef</ref> the identity of the electrons is lost in the ammonium ion that is formed. Nevertheless, Lewis suggested that an electron-pair donor be classified as a base and an electron-pair acceptor be classified as acid.

A more modern definition of a Lewis acid is an atomic or molecular species with a localized empty atomic or molecular orbital of low energy. This lowest-energy unoccupied molecular orbital (LUMO) can accommodate a pair of electrons.

Comparison with Brønsted–Lowry theory

A Lewis base is often a Brønsted–Lowry base as it can donate a pair of electrons to H⁺;<ref name="hydron"/> the proton is a Lewis acid as it can accept a pair of electrons. The conjugate base of a Brønsted–Lowry acid is also a Lewis base as loss of H⁺ from the acid leaves those electrons which were used for the A—H bond as a lone pair on the conjugate base. However, a Lewis base can be very difficult to protonate, yet still react with a Lewis acid. For example, carbon monoxide is a very weak Brønsted–Lowry base but it forms a strong adduct with BF₃.

In another comparison of Lewis and Brønsted–Lowry acidity by Brown and Kanner,<ref>Template:Cite journal</ref> 2,6-Di-tert-butylpyridine reacts to form the hydrochloride salt with HCl but does not react with BF₃. This example demonstrates that steric factors, in addition to electron configuration factors, play a role in determining the strength of the interaction between the bulky di-t-butylpyridine and tiny proton.

See also

• Acid
• Base (chemistry)
• Acid–base reaction
• Brønsted–Lowry acid–base theory
• Chiral Lewis acid
• Frustrated Lewis pair
• Gutmann–Beckett method
• ECW model
• Philosophy of chemistry

Further reading

• Template:Cite book
• Template:Cite book