Tetradentate ligand

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In chemistry, tetradentate ligands are ligands that bind four donor atoms to a central atom to form a coordination complex. This number of donor atoms that bind is called denticity and is a method of classifying ligands.

Contents

Tetradentate ligands are common in nature in the form of chlorophyll, which has a core ligand called chlorin, and heme, which has a core ligand called porphyrin. They are responsible for the colour observed in plants and humans. Phthalocyanine is an artificial macrocyclic tetradentate ligand that is used to make blue and green pigments.

Shape

Tetradentate ligands can be classified by the topology of the connections between donor atoms. Common forms are linear (also called sequential), ring or tripodal. A tetrapodal ligand that is also tetradentate has four legs with donor atoms and a bridgehead that is not a donor. Upon binding with a central atom, there are several arrangements possible (known as geometric isomers).

Linear ligands

A linear tetradentate ligand has the four donor atoms in a line and each subsequent donor is connected by one of three bridges. Such a ligand bound to a metal in tetrahedral coordination can only connect in one way, though if the ligand is unsymmetrical then there are two chiral arrangements. A linear tetradentate ligand can also bind to a metal in square planar coordination in one way, where anticlockwise or clockwise arrangements are equivalent.

Linear ligands in octahedral coordination

linear tetradentate ligand in three isomers in the right hand column. From top to bottom a, b, trans Linear2-4Chelate.png
linear tetradentate ligand in three isomers in the right hand column. From top to bottom α, β, trans

A linear tetradentate ligand has its donor atoms arranged along or in a chain so that each adjacent donor atom has to be adjacent on the central atom. This arrangement leads to three stereochemical outcomes, and the four donor groups can be co-equatorial. This geometry is called trans because the remaining unoccupied positions on the octahedron are mutually trans (opposite). [1] [2] [3] When the two internal donor atoms are pyramidal (such as the secondary amines in trien or EDDA), two diastereomers for the trans arrangement are determined by the relative stereochemistry of these centers. Typically these donors are mutually trans, resulting in a chiral complex of C2-symmetric complexes. This arrangement is illustrated by complexes of the Trost ligand.

The ligand can bend so that one donor atom is at the pole and the remaining three are on the equator of the central atom. This is called cis-β (beta). The remaining octahedral positions are cis (adjacent) to each other. The triangles of coordinating atoms and the central atom have two coplanar atoms, and one perpendicular atom. This arrangement is chiral, so there are two possible mirror images. The arrangement where the chain goes down and clockwise is termed lambda, Λ, and where it goes down and anticlockwise is called delta, Δ. [2] If the chain is not symmetrical, then different isomers can be produced by the end of the ligand that has the bend. If three donor atoms are the same at one end of the chain, the mer- and fac- prefixes used for tridentate ligands can be used. If the three donor atoms are arranged on a meridian, β-mer- is used; if the three donor atoms are arranged on the face of an octahedron, β-fac is used. [1]

The chain can have two bends, with one donor at a pole, two on the equator and one at the opposite pole. None of the triangles of coordinating atoms and the central atom are coplanar. This is termed cis-alpha (α). This arrangement is chiral, so there are two possible mirror images. The arrangement where the chain goes down and clockwise and down is termed lambda, Λ, and where is goes down and anticlockwise and down is called delta (Δ). [4] [2]

Tripodal ligands

Tripodal tetradentate ligands have a donor atom connected via three chains to other donor atoms. The top of the tripod is called the apex, and a donor atom in that position is apical, or also known as the bridging atom. The other three donor atoms are on the "feet" of the tripod. Tripodal tetradentate ligands can have three identical chains attached to an atom (such as nitrogen, phosphorus, or arsenic) in tertiary arrangement. Molecules containing phosphorus, or arsenic donor atoms remain stiff at the P or As and can hold their shape, unlike nitrogen compounds which rapidly racemize. If all the feet of the tripod are symmetrical and identical to each other, there will be only one way to attach in an octahedral coordination. However, there are two non-equivalent positions left on the central atom, so if two different monodentate ligands or an unsymmetrical bidentate ligand attaches, there will be two possible isomers. If the feet differ, there are more isomers. When two feet are the same, and one is different there are three arrangements, two of which are enantiomers of each other. When there are three different legs, there are six possible isomers, but two are enantiomers of another pair and two are symmetric. [5]

Atoms with five coordinate positions are usually trigonal bipyramidal or square pyramid geometry. A symmetric tripodal tetradentate ligand can form two isomers on a square pyramid, depending on whether the bridging donor is on the apex or the base of the pyramid. The extra vacant position on the square pyramid is on the base. Square pyramidal coordination tends to occur where a six-member ring is formed with the bridgehead, bridge, feet donor atom and central atom. The longer leg (with three bridging atoms) connects to the apex of the pyramid, and symmetry is lost. [6]

For the trigonal bipyramid, the tripod shaped ligand has its most symmetrical position with the bridging donor at one of the apexes, and the feet of the tripod are arranged around the base, leaving a vacant position at the opposite apex, resulting in C3v symmetry. Trigonal bipyramidal coordination tends to occur where five member rings are formed with the bridgehead, bridge, feet donor atoms and central atom. [6]

In four coordination a tripodal ligand would fill all the positions available, the geometry is trigonal pyramid. The shape is distorted from the tetrahedron due to the non-symmetry of the tripod. [6]

Classification

In addition to shape, tetradentate ligands can be classified by the ligating atoms on the ligand. For linear ligands the order can be given. The ligand may have a negative charge when it is in a complex with the central atom. This may develop through the loss of hydrogen ions when the substance is dissolved.

One further characteristic is the size of the rings formed by the central metal with two donor atoms and the intervening chain of the ligand. Usually these rings have five or six members, but sometimes seven atoms. [7] For ring shaped ligands, the total number of atoms in the ring is important, as it is a determiner of the hole size for the central atom. [7] Each additional atom in the ring enlarges the hole radius from 0.1 to 0.15 Å. [7]

Ligands are also characterized by charge. Tetradentate ligands can be neutral so that the charge of the whole complex is the same as the central atom. A tetradentate monoanionic (TMDA) ligand has one donor atom with a negative charge. [8] A tetradentate dianionic ligand has a double negative charge, and tetradentate trianionic ligands have a triple negative charge. The maximal charge is on tetradentate tetraanionic ligands, which can stabilize metals in high oxidation states, however such ligands also have to resist oxidation by the highly oxidizing metal centre. [9]

List

nameabbreviationformulashapetypechargeMWcentral atomspic
Chlorin ringNNNN–2312.3678Mg Chlorin.svg
Corrin ringNNNN–1306.40Co Corrin.svg
1,4,7,10-tetraoxacyclododecane 12-crown-4 (C2H4O)4ringOOOO0176.21Li 12-crown-4 skeletal.svg
1,4,8,11-tetraazacyclotetradecane cyclam (NHCH2CH2NHCH2CH2CH2)2ringNNNN200.33 transition metals Cyclam.svg
1,4,7,10-tetraazacyclododecane cyclen ringN4172.271Zn Cyclen.svg
Dibenzotetramethyltetraaza[14]annulene [10] tmtaaringNNNN2-UO2
N,N-ethylenediaminediacetic acidNH2C2H4N(CH2COOH)2tripodalNNO22–
N,N'-ethylenediaminediacetic acid(-CH2NHCH2COOH)2linearONNO2–
N-hydroxyimino-2,2'-dipropionic acidH3HIDPAHON(CH(CH3)CO2H)2linearONOO3–V4+ HIDPA.svg
diethylenetriamineacetic acidDTMA [1] NH2C2H4NHC2H4NHCH2COOHlinearNNNO1–Co
iso-diethylenetriamineacetic acidi-DTMA [1] (NH2C2H4)2NCH2COOHtripodalNN2NO1–Co
Jäger's N2O2 ligandlinear acacenONNO N2O2Ni
Naphthalocyanine C48H26N8ringNNNN714.79 Naphthalocyanine.svg
Nitrilotriacetic acid NTAN(CH2CO2H)3tripodalNO33–191.14Ca2+, Cr, Cu2+, and Fe3+, Ni Nitrilotriacetic acid 200.svg
Phthalocyanine H2PcC32H18N8ringNNNN2–Cu, Co Phthalocyanine.svg
Porphyrin [11] ringNNNNMg, V, Fe, Ni Porphyrin.svg
Rhodotorulic acid C14H24N4O6I shapeOOOO344.36Fe3+ Rhodotorulic acid.svg
Salen ligand linearONNO N2O2268.31 Salen structure.svg
salpn ligand salpnlinearONNO2−282.34Cr, Cu, Fe, Ni Salpn.svg
tetars (meso and racemic isomers) [12] [(CH3)2As(CH2)3As(C6H5)CH2]2linearAsAsAsAs0Co2+
1,1,4,7,10,10-hexaphenyl-1,4,7,10-tetraphosphadecane
tetraphos
tet-1linearPPPP0670.68Fe+ Ru+ Os+ Re3+ [2] Pd2+ Pt2+
1,4,7,10-tetrathiadodecane [13] [12]-ane-S4ringSSSS0Cu2+
1,4,7,10-tetrathiatridecane [13] [13]-ane-S4ringSSSS0Cu2+
1,4,8,11-tetrathiatetradecane [13] [14]-ane-S4ringSSSS0Cu2+
1,4,8,12-tetrathiapentadecane [13] [15]-ane-S4ringSSSS0Cu2+
1,5,9,13-tetrathiahexadecane [13] [14]-ane-S4ringSSSS0Cu2+
2,5,8-trithia[9](2,5)thiophenophane [13] ringSSSS0Cu2+
Triethylene glycol dimethyl ether TG3CH3(OCH2CH2)3OCH3linearOOOO0178.23neutral Na, K [14] Triglyme.svg
Triethylenetetramine TETA
trien
[CH2NHCH2CH2NH2]2linearNNNN146.24Cu2+ N1,N1'-(ethane-1,2-diyl)bis(ethane-1,2-diamine) 200.svg
tris-(dimethylarsinopropyl)-arsine [15] As[CH2CH2CH2As(CH3)2]3tripodAsAs30Fe2+ Ni2+ Co3+ oct
Ni3+ tbp
tris-(o-dimethylarsinophenyl)-arsine [15] As[o-C6H4As(CH3)2]3tripodAsAs30Pt2+ Pd2+ Ni2+ tbp
Ru2+ oct
tris-(o-diphenylarsinophenyl)-arsine [15] As[o-C6H4As(C6H5)2]3tripodAsAs30Pt2+ Pd2+ Ru0 Rh+ Ni2+ tbp
Re2+ Ru2+ Os2+ Rh3+ Pd4+ Pt4+ oct
CH3[As(CH3)o-C6H4]3AsCH(3)2 [15] linearAs40Pd2+ square pyramydal
[As(C6H5)2o-C6H4As(C6H5)CH2]2 [15] linearAs40Ni2+ 4 coordinate
Ni2+ Co2+ five coordinate
tris-(o-diphenylphosphinophenyl)-phosphine [15] tripod tetraphosphine of VenanziP[o-C6H4P(C6H5)2]3tripodPP30Pd2+ Pt2+ Ru0 Ru2+ Os2+ Cr0 Cr+ Cr3+ Mn+ Co3+ oct
Ni2+ Fe2+ Co+ Co2+ tbp
Tris(2-pyridylmethyl)amine TPAtripodalNN3290.37Cu Tris(pyridylmethyl)amine (structural diagram).png
2,2′-bi-1,10-phenanthroline [16] BIPHENlinearN40Cd Sm Am
Quaterpyridine [17] qtpylinearN40 2,2' 6',2 6,2-quaterpyridine.svg

Biomolecules

Heme is a heterocyclic macrocycle ring shaped tetradentate ligand. It is an important molecule in red blood cells.

Chlorophyll comes in several forms and is important in plant photosynthesis. Bacteria may use variants called bacteriochlorophylls.

Related Research Articles

<span class="mw-page-title-main">Coordination complex</span> Molecule or ion containing ligands datively bonded to a central metallic atom

A coordination complex is a chemical compound consisting of a central atom or ion, which is usually metallic and is called the coordination centre, and a surrounding array of bound molecules or ions, that are in turn known as ligands or complexing agents. Many metal-containing compounds, especially those that include transition metals, are coordination complexes.

<i>Cis</i>–<i>trans</i> isomerism Pairs of molecules with same chemical formula showing different spatial orientations

Cistrans isomerism, also known as geometric isomerism or configurational isomerism, is a term used in chemistry that concerns the spatial arrangement of atoms within molecules. The prefixes "cis" and "trans" are from Latin: "this side of" and "the other side of", respectively. In the context of chemistry, cis indicates that the functional groups (substituents) are on the same side of some plane, while trans conveys that they are on opposing (transverse) sides. Cistrans isomers are stereoisomers, that is, pairs of molecules which have the same formula but whose functional groups are in different orientations in three-dimensional space. Cis-trans notation does not always correspond to EZ isomerism, which is an absolute stereochemical description. In general, cistrans stereoisomers contain double bonds that do not rotate, or they may contain ring structures, where the rotation of bonds is restricted or prevented. Cis and trans isomers occur both in organic molecules and in inorganic coordination complexes. Cis and trans descriptors are not used for cases of conformational isomerism where the two geometric forms easily interconvert, such as most open-chain single-bonded structures; instead, the terms "syn" and "anti" are used.

<span class="mw-page-title-main">Ligand</span> Ion or molecule that binds to a central metal atom to form a coordination complex

In coordination chemistry, a ligand is an ion or molecule with a functional group that binds to a central metal atom to form a coordination complex. The bonding with the metal generally involves formal donation of one or more of the ligand's electron pairs, often through Lewis bases. The nature of metal–ligand bonding can range from covalent to ionic. Furthermore, the metal–ligand bond order can range from one to three. Ligands are viewed as Lewis bases, although rare cases are known to involve Lewis acidic "ligands".

<span class="mw-page-title-main">VSEPR theory</span> Model for predicting molecular geometry

Valence shell electron pair repulsion (VSEPR) theory, is a model used in chemistry to predict the geometry of individual molecules from the number of electron pairs surrounding their central atoms. It is also named the Gillespie-Nyholm theory after its two main developers, Ronald Gillespie and Ronald Nyholm.

<span class="mw-page-title-main">Chirality (chemistry)</span> Geometric property of some molecules and ions

In chemistry, a molecule or ion is called chiral if it cannot be superposed on its mirror image by any combination of rotations, translations, and some conformational changes. This geometric property is called chirality. The terms are derived from Ancient Greek χείρ (cheir) 'hand'; which is the canonical example of an object with this property.

<span class="mw-page-title-main">Scorpionate ligand</span> Tridentate ligand which "pinches" the central metal atom

In coordination chemistry, a scorpionate ligand is a tridentate (three-donor-site) ligand that binds to a central atom in a fac manner. The most popular class of scorpionates are the hydrotris(pyrazolyl)borates or Tp ligands. These were also the first to become popular. These ligands first appeared in journals in 1966 from the then little-known DuPont chemist of Ukrainian descent, Swiatoslaw Trofimenko. Trofimenko called this discovery "a new and fertile field of remarkable scope".

<span class="mw-page-title-main">Cyanate</span> Anion with formula OCN and charge –1

The cyanate ion is an anion with the chemical formula OCN. It is a resonance of three forms: [O−C≡N] (61%) ↔ [O=C=N] (30%) ↔ [+O≡C−N2−] (4%).

<span class="mw-page-title-main">Octahedral molecular geometry</span> Molecular geometry

In chemistry, octahedral molecular geometry, also called square bipyramidal, describes the shape of compounds with six atoms or groups of atoms or ligands symmetrically arranged around a central atom, defining the vertices of an octahedron. The octahedron has eight faces, hence the prefix octa. The octahedron is one of the Platonic solids, although octahedral molecules typically have an atom in their centre and no bonds between the ligand atoms. A perfect octahedron belongs to the point group Oh. Examples of octahedral compounds are sulfur hexafluoride SF6 and molybdenum hexacarbonyl Mo(CO)6. The term "octahedral" is used somewhat loosely by chemists, focusing on the geometry of the bonds to the central atom and not considering differences among the ligands themselves. For example, [Co(NH3)6]3+, which is not octahedral in the mathematical sense due to the orientation of the N−H bonds, is referred to as octahedral.

<span class="mw-page-title-main">Salen ligand</span> Chemical compound

Salen refers to a tetradentate C2-symmetric ligand synthesized from salicylaldehyde (sal) and ethylenediamine (en). It may also refer to a class of compounds, which are structurally related to the classical salen ligand, primarily bis-Schiff bases. Salen ligands are notable for coordinating a wide range of different metals, which they can often stabilise in various oxidation states. For this reason salen-type compounds are used as metal deactivators. Metal salen complexes also find use as catalysts.

<span class="mw-page-title-main">Tetrahedral molecular geometry</span> Central atom with four substituents located at the corners of a tetrahedron

In a tetrahedral molecular geometry, a central atom is located at the center with four substituents that are located at the corners of a tetrahedron. The bond angles are cos−1(−13) = 109.4712206...° ≈ 109.5° when all four substituents are the same, as in methane as well as its heavier analogues. Methane and other perfectly symmetrical tetrahedral molecules belong to point group Td, but most tetrahedral molecules have lower symmetry. Tetrahedral molecules can be chiral.

In chemistry, a (redox) non-innocent ligand is a ligand in a metal complex where the oxidation state is not clear. Typically, complexes containing non-innocent ligands are redox active at mild potentials. The concept assumes that redox reactions in metal complexes are either metal or ligand localized, which is a simplification, albeit a useful one.

<span class="mw-page-title-main">Bite angle</span>

In coordination chemistry, the bite angle is the angle on a central atom between two bonds to a bidentate ligand. This ligand–metal–ligand geometric parameter is used to classify chelating ligands, including those in organometallic complexes. It is most often discussed in terms of catalysis, as changes in bite angle can affect not just the activity and selectivity of a catalytic reaction but even allow alternative reaction pathways to become accessible.

<span class="mw-page-title-main">Diphosphines</span>

Diphosphines, sometimes called bisphosphanes, are organophosphorus compounds most commonly used as bidentate phosphine ligands in inorganic and organometallic chemistry. They are identified by the presence of two phosphino groups linked by a backbone, and are usually chelating. A wide variety of diphosphines have been synthesized with different linkers and R-groups. Alteration of the linker and R-groups alters the electronic and steric properties of the ligands which can result in different coordination geometries and catalytic behavior in homogeneous catalysts.

<span class="mw-page-title-main">Tris(2-aminoethyl)amine</span> Chemical compound

Tris(2-aminoethyl)amine is the organic compound with the formula N(CH2CH2NH2)3. This colourless liquid is soluble in water and is highly basic, consisting of a tertiary amine center and three pendant primary amine groups. Tris(2-aminoethyl)amine is commonly abbreviated as tren or TREN. It is used a crosslinking agent in the synthesis of polyimine networks and a tripodal ligand in coordination chemistry.

<span class="mw-page-title-main">Tripodal ligand</span>

Tripodal ligands are tri- and tetradentate ligands. They are popular in research in the areas of coordination chemistry and homogeneous catalysis. Because the ligands are polydentate, they do not readily dissociate from the metal centre. Many tripodal ligands have C3 symmetry.

<span class="mw-page-title-main">Denticity</span> Number of atoms in a ligand that bond to the central atom of a coordination complex

In coordination chemistry, denticity refers to the number of donor groups in a given ligand that bind to the central metal atom in a coordination complex. In many cases, only one atom in the ligand binds to the metal, so the denticity equals one, and the ligand is said to be monodentate. Ligands with more than one bonded atom are called polydentate or multidentate. The denticity of a ligand is described with the Greek letter κ ('kappa'). For example, κ6-EDTA describes an EDTA ligand that coordinates through 6 non-contiguous atoms.

<span class="mw-page-title-main">Jacobsen's catalyst</span> Chemical compound

Jacobsen's catalyst is the common name for N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexane­diaminomanganese(III) chloride, a coordination compound of manganese and a salen-type ligand. It is used as an asymmetric catalyst in the Jacobsen epoxidation, which is renowned for its ability to enantioselectively transform prochiral alkenes into epoxides. Before its development, catalysts for the asymmetric epoxidation of alkenes required the substrate to have a directing functional group, such as an alcohol as seen in the Sharpless epoxidation. This compound has two enantiomers, which give the appropriate epoxide product from the alkene starting material.

<span class="mw-page-title-main">Tridentate ligand</span> Ligand with 3 acceptor atoms for a coordination complex

A tridentate ligand is a ligand that has three atoms that can function as donor atoms in a coordination complex.

<span class="mw-page-title-main">Hexadentate ligand</span> Class of chemical compounds

A hexadentate ligand in coordination chemistry is a ligand that combines with a central metal atom with six bonds. One example of a hexadentate ligand that can form complexes with soft metal ions is TPEN. A commercially important hexadentate ligand is EDTA.

In homogeneous catalysis, C2-symmetric ligands refer to ligands that lack mirror symmetry but have C2 symmetry. Such ligands are usually bidentate and are valuable in catalysis. The C2 symmetry of ligands limits the number of possible reaction pathways and thereby increases enantioselectivity, relative to asymmetrical analogues. C2-symmetric ligands are a subset of chiral ligands. Chiral ligands, including C2-symmetric ligands, combine with metals or other groups to form chiral catalysts. These catalysts engage in enantioselective chemical synthesis, in which chirality in the catalyst yields chirality in the reaction product.

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