Chemistry:Tetradentate ligand

From HandWiki
Revision as of 22:05, 5 February 2024 by TextAI (talk | contribs) (linkage)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Short description: Ligand which binds 4 donor atoms in a coordination complex

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.

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 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

name abbreviation formula shape type charge MW central atoms pic
Chlorin ring NNNN –2 312.3678 Mg Chlorin.svg
Corrin ring NNNN –1 306.40 Co Corrin.svg
1,4,7,10-tetraoxacyclododecane 12-crown-4 (C2H4O)4 ring OOOO 0 176.21 Li 12-crown-4 skeletal.svg
1,4,8,11-tetraazacyclotetradecane cyclam (NHCH2CH2NHCH2CH2CH2)2 ring NNNN 200.33 transition metals Cyclam.svg
1,4,7,10-tetraazacyclododecane cyclen ring N4 172.271 Zn Cyclen.svg
Dibenzotetramethyltetraaza[14]annulene[10] tmtaa ring NNNN 2- UO2
N,N-ethylenediaminediacetic acid NH2C2H4N(CH2COOH)2 tripodal NNO2 2–
N,N'-ethylenediaminediacetic acid (-CH2NHCH2COOH)2 linear ONNO 2–
N-hydroxyimino-2,2'-dipropionic acid H3HIDPA HON(CH(CH3)CO2H)2 linear ONOO 3– V4+ HIDPA.svg
diethylenetriamineacetic acid DTMA[1] NH2C2H4NHC2H4NHCH2COOH linear NNNO 1– Co
iso-diethylenetriamineacetic acid i-DTMA[1] (NH2C2H4)2NCH2COOH tripodal NN2NO 1– Co
Jäger's N2O2 ligand linear acacen ONNO N2O2 Ni
Naphthalocyanine C48H26N8 ring NNNN 714.79 Naphthalocyanine.svg
Nitrilotriacetic acid NTA N(CH2CO2H)3 tripodal NO3 3– 191.14 Ca2+, Cr, Cu2+, and Fe3+, Ni Nitrilotriacetic acid 200.svg
Phthalocyanine H2Pc C32H18N8 ring NNNN 2– Cu, Co Phthalocyanine.svg
Porphyrin[11] ring NNNN Mg, V, Fe, Ni Porphyrin.svg
Rhodotorulic acid C14H24N4O6 I shape OOOO 344.36 Fe3+ Rhodotorulic acid.svg
Salen ligand linear ONNO N2O2 268.31 Salen structure.svg
salpn ligand salpn linear ONNO 2− 282.34 Cr, Cu, Fe, Ni Salpn.svg
tetars (meso and racemic isomers)[12] [(CH3)2As(CH2)3As(C6H5)CH2]2 linear AsAsAsAs 0 Co2+
1,1,4,7,10,10-hexaphenyl-1,4,7,10-tetraphosphadecane
tetraphos 		tet-1 linear PPPP 0 670.68 Fe+ Ru+ Os+ Re3+[2] Pd2+ Pt2+
1,4,7,10-tetrathiadodecane[13] [12]-ane-S4 ring SSSS 0 Cu2+
1,4,7,10-tetrathiatridecane[13] [13]-ane-S4 ring SSSS 0 Cu2+
1,4,8,11-tetrathiatetradecane[13] [14]-ane-S4 ring SSSS 0 Cu2+
1,4,8,12-tetrathiapentadecane[13] [15]-ane-S4 ring SSSS 0 Cu2+
1,5,9,13-tetrathiahexadecane[13] [14]-ane-S4 ring SSSS 0 Cu2+
2,5,8-trithia[9](2,5)thiophenophane [13] ring SSSS 0 Cu2+
Triethylene glycol dimethyl ether TG3 CH3(OCH2CH2)3OCH3 linear OOOO 0 178.23 neutral Na, K[14] Triglyme.svg
Triethylenetetramine TETA
trien 		[CH2NHCH2CH2NH2]2 linear NNNN 146.24 Cu2+ 180px
tris-(dimethylarsinopropyl)-arsine[15] As[CH2CH2CH2As(CH3)2]3 tripod AsAs3 0 Fe2+ Ni2+ Co3+ oct
Ni3+ tbp
tris-(o-dimethylarsinophenyl)-arsine[15] As[o-C6H4As(CH3)2]3 tripod AsAs3 0 Pt2+ Pd2+ Ni2+ tbp
Ru2+ oct
tris-(o-diphenylarsinophenyl)-arsine[15] As[o-C6H4As(C6H5)2]3 tripod AsAs3 0 Pt2+ Pd2+ Ru0 Rh+ Ni2+ tbp
Re2+ Ru2+ Os2+ Rh3+ Pd4+ Pt4+ oct
CH3[As(CH3)o-C6H4]3AsCH(3)2[15] linear As4 0 Pd2+ square pyramydal
[As(C6H5)2o-C6H4As(C6H5)CH2]2[15] linear As4 0 Ni2+ 4 coordinate
Ni2+ Co2+ five coordinate
tris-(o-diphenylphosphinophenyl)-phosphine[15] tripod tetraphosphine of Venanzi P[o-C6H4P(C6H5)2]3 tripod PP3 0 Pd2+ Pt2+ Ru0 Ru2+ Os2+ Cr0 Cr+ Cr3+ Mn+ Co3+ oct
Ni2+ Fe2+ Co+ Co2+ tbp
Tris(2-pyridylmethyl)amine TPA tripodal NN3 290.37 Cu Tris(pyridylmethyl)amine (structural diagram).png
2,2′-bi-1,10-phenanthroline[16] BIPHEN linear N4 0 Cd Sm Am
Quaterpyridine[17] qtpy linear N4 0 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.

References

  1. ↑ 1.0 1.1 1.2 1.3 Schneider, Peter W.; Collman, James P. (October 1968). "Complexes of cobalt(III) with the two isomeric diethylenetriamineacetic acids". Inorganic Chemistry 7 (10): 2010–2015. doi:10.1021/ic50068a010. 
  2. ↑ 2.0 2.1 2.2 2.3 Bautista, Maria Teresa; Earl, Kelly Anne; Maltby, Patricia Anne; Morris, Robert Harold; Schweitzer, Caroline Theresia (March 1994). "New dihydrogen complexes: the synthesis and spectroscopic properties of iron(II), ruthenium(II), and osmium(II) complexes containing the meso-tetraphos-1 ligand". Canadian Journal of Chemistry 72 (3): 547–560. doi:10.1139/v94-078. 
  3. ↑ Sloan, Thomas E.; Busch, Daryle H. (27 May 1980). "Stereochemical Description and Notation for Coordination Systems". Stereochemistry of Optically Active Transition Metal Compounds. ACS Symposium Series. 119. p. 401. doi:10.1021/bk-1980-0119.ch021. ISBN 9780841205383. 
  4. ↑ "Coordination Chemistry I Structures and Isomers". p. 51. http://www.chem.ccu.edu.tw/~bct/IC-pdf%20files/Coordination%20Chemistry%20I%20-%20Structures%20and%20Isomers%20(9).pdf. 
  5. ↑ KOINE, Norio; YAMAGUCHI, Hiroyuki; TANIGAKI, Teiichi; HIDAKA, Jinsai; SHIMURA, Yoichi (1974). "PREPARATION AND STRUCTURAL ASSIGNMENT OF ISOMERS OF POTASSIUM TRANS(N)- (C-METHYL SUBSTITUTED AMMONIATRIACETATO) (β-ALANINATO) COBALTATE(III)". Chemistry Letters 3 (9): 993–996. doi:10.1246/cl.1974.989.  open access
  6. ↑ 6.0 6.1 6.2 Ambundo, Edna A.; Yu, Qiuyue; Ochrymowycz, L. A.; Rorabacher, D. B. (August 2003). "Electron-Transfer Kinetics of Copper(II/I) Tripodal Ligand Complexes". Inorganic Chemistry 42 (17): 5267–5273. doi:10.1021/ic030176c. PMID 12924898. 
  7. ↑ 7.0 7.1 7.2 Lindoy, Leonard F. (1989). The chemistry of macrocyclic ligand complexes (1. publ., transferred to digital print. ed.). Cambridge [England]: Cambridge University Press. p. 4. ISBN 052125261X. https://archive.org/details/chemistrymacrocy00lind. 
  8. ↑ Chomitz, WayneA.; Arnold, John (16 February 2009). "Use of Tetradentate Monoanionic Ligands for Stabilizing Reactive Metal Complexes". Chemistry - A European Journal 15 (9): 2020–2030. doi:10.1002/chem.200801069. PMID 19160435. 
  9. ↑ Collins, Terrence J.; Kostka, Kimberly L.; Munck, Eckard; Uffelman, Erich S. (July 1990). "Stabilization of mononuclear five-coordinate iron(IV)". Journal of the American Chemical Society 112 (14): 5637–5639. doi:10.1021/ja00170a037. 
  10. ↑ Pedrick, Elizabeth A.; Assefa, Mikiyas K.; Wakefield, Megan E.; Wu, Guang; Hayton, Trevor W. (15 May 2017). "Uranyl Coordination by the 14-Membered Macrocycle Dibenzotetramethyltetraaza[14]annulene". Inorganic Chemistry 56 (11): 6638–6644. doi:10.1021/acs.inorgchem.7b00700. PMID 28504885. 
  11. ↑ Numerous derivatives of porpyrin are known. See the list in Buchler, J. W.; Dreher, C.; Kunzel, F. M. (1995). Buchler, J. W.. ed. Metal complexes with tetrapyrrole ligands III. Berlin: Springer. p. 5. ISBN 978-3-540-59281-5. 
  12. ↑ Bosnich, B.; Jackson, W. G.; Wild, S. B. (December 1973). "Metal complexes of dissymmetric arsines. Stereochemistry, topological stability, and spectra of cobalt(III) complexes containing a linear quadridenate tetra-tert-arsine ligand". Journal of the American Chemical Society 95 (25): 8269–8280. doi:10.1021/ja00806a012. 
  13. ↑ 13.0 13.1 13.2 13.3 13.4 13.5 Zanello, P. (1990). "ELECTROCHEMISTRY OF MONONUCLEAR COPPER COMPLEXES. STRUCTURAL REORGANIZATIONS ACCOMPANYING REDOX CHANGES". in Bernal, Ivan. Stereochemical control, bonding, and steric rearrangements. Amsterdam: Elsevier. p. 208. ISBN 0444888411. 
  14. ↑ Down, J. L.; Lewis, J.; Moore, B.; Wilkinson, G. (1959). "The solubility of alkali metals in ethers". Journal of the Chemical Society: 3767. doi:10.1039/JR9590003767. 
  15. ↑ 15.0 15.1 15.2 15.3 15.4 15.5 McAuliffe, C. A. (1973). Transition Metal Complexes of Phosphorus, Arsenic and Antimony Ligands. Macmillan Ecucation. pp. 282–285. ISBN 9780333136287. 
  16. ↑ Tucker, Lyndsay E.; Littman, Galen C.; Uritis, Stuart; Nugent, Joseph W.; Thummel, Randolph P.; Reibenspies, Joseph H.; Jones, S. Bart; Lee, Hee-Seung et al. (2020-09-08). "Fluorescence and Metal-Binding Properties of the Highly Preorganized Tetradentate Ligand 2,2′-Bi-1,10-phenanthroline and Its Remarkable Affinity for Cadmium(II)" (in en). Inorganic Chemistry 59 (18): 13117–13127. doi:10.1021/acs.inorgchem.0c00361. ISSN 0020-1669. PMID 32897701. https://pubs.acs.org/doi/10.1021/acs.inorgchem.0c00361. 
  17. ↑ Gorczyński, Adam; Harrowfield, Jack M.; Patroniak, Violetta; Stefankiewicz, Artur R. (14 December 2016). "Quaterpyridines as Scaffolds for Functional Metallosupramolecular Materials". Chemical Reviews 116 (23): 14620–14674. doi:10.1021/acs.chemrev.6b00377. PMID 27960268. 



Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:Tetradentate_ligand&oldid=3325863"