Salen ligand

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.[1] These metal salen complexes primarily find use as catalysts.[2]

Salen ligand
Names
Other names
2,2′-Ethylenebis(nitrilomethylidene)diphenol, N,N′-Ethylenebis(salicylimine)
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.002.161
EC Number
  • 202-376-3
UNII
Properties
C16H16N2O2
Molar mass 268.32
Melting point 126 °C (259 °F; 399 K)
Hazards
GHS pictograms
GHS Signal word Warning
H315, H319, H335
P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references
This article is about Salen. For Complexes of salen and related ligands, see Metal salen complexes.

Synthesis and properties

H2salen may be synthesized by the condensation of ethylenediamine and salicylaldehyde.[3]

Salcomine, a complex of salen with cobalt
Jacobsen's salen-Mn catalyst

Complexes of salen with metal cations may be made without isolating it from the reaction mixture.[4][5] This is possible because the stability constant for the formation of the metal complexes are very high, due to the chelate effect.

H2L + Mn+ → ML(n−2)+ + 2 H+

where L stands for the ligand. The pyridine adduct of the cobalt(II) complex Co(salen)(py) (salcomine) has a square-pyramidal structure; it can act as a dioxygen carrier by forming a labile, octahedral O2 complex.[6][7]

The name “salen ligands” is used for tetradentate ligands which have similar structures. For example, in salpn there is a methyl substituent on the bridge. It is used as a metal deactivation additive in fuels.[8] The presence of bulky groups near the coordination site may enhance the catalytic activity of a metal complex and prevent its dimerization. Salen ligands derived from 3,5-di-tert-butylsalicylaldehyde fulfill these roles, and also increase the solubility of the complexes in non-polar solvents like pentane. Chiral “salen” ligands may be created by proper substitution of the diamine backbone, the phenyl ring, or both.[5] An example is the ligand obtained by condensation of the C2-symmetric trans-1,2-diaminocyclohexane with 3,5-di-tert-butylsalicylaldehyde. Chiral ligands may be used in asymmetric synthesis reactions, such as the Jacobsen epoxidation:[9][10]

Synthesis and complexation of Jäger's ligand.[11]

A class of tetradentate ligands with the generic name acacen are obtained by the condensation of derivatives of acetylacetone and ethylenediamine.[11] Cobalt complexes [Co(acacen)L2]+, selectively inhibit the activities of histidine-containing proteins through exchange of the axial ligands. These compounds show promise for the inhibition of oncogenesis.[12]

The salan and salalen ligands are similar in structure to salen ligands, but have one or two saturated nitrogen-aryl bonds (amines rather than imines). They tend to be less rigid and more electron rich at the metal center than the corresponding salen complexes.[13][14] Salans can be synthesized by the alkylation of an appropriate amine with a phenolic alkyl halide. The “half-salen” ligands have only one salicylimine group. They are prepared from a salicylaldehyde and a monoamine.[15]

The name “salen” or “salen-type” may be used for other ligands that have similar environment around the chelating site, namely two acidic hydroxyls and two Schiff base (aryl-imine) groups. These include the ligands abbreviated as salph, from the condensation of 1,2-phenylenediamine and salicylaldehyde, and salqu, from the condensation of salicylaldehyde and 2-quinoxalinol.[16]

See also

References
  1. Cozzi, Pier Giorgio (2004). "Metal–Salen Schiff base complexes in catalysis: practical aspects". Chem. Soc. Rev. 33 (7): 410–421. doi:10.1039/B307853C. PMID 15354222.
  2. Shaw, Subrata; White, James D. (11 June 2019). "Asymmetric Catalysis Using Chiral Salen–Metal Complexes: Recent Advances". Chemical Reviews. 119 (16): 9381–9426. doi:10.1021/acs.chemrev.9b00074. PMID 31184109.
  3. Tsumaki, T. (1938). "Nebenvalenzringverbindungen. IV. Über einige innerkomplexe Kobaltsalze der Oxyaldimine". Bulletin of the Chemical Society of Japan (in German). 13 (2): 252–260. doi:10.1246/bcsj.13.252.
  4. Diehl, Harvey; Hach, Clifford C. (1950). Bis(N,N′-Disalicylalethylenediamine)-μ-Aquodicobalt(II). Inorg. Synth. Inorganic Syntheses. 3. pp. 196–201. doi:10.1002/9780470132340.ch53. ISBN 978-0-470-13234-0.
  5. Pier Giorgio Cozzi (2004). "Metal-Salen Schiff base complexes in catalysis: Practical aspects". Chem. Soc. Rev. 33 (7): 410–421. doi:10.1039/B307853C. PMID 15354222.
  6. Appleton, T. G. (1977). "Oxygen Uptake by a Cobalt(II) Complex". J. Chem. Educ. 54 (7): 443. doi:10.1021/ed054p443.
  7. Yamada, Shoichiro (1999). "Advancement in stereochemical aspects of Schiff base metal complexes". Coordination Chemistry Reviews. 190–192: 537–555. doi:10.1016/S0010-8545(99)00099-5.
  8. Dabelstein, W.; Reglitzky A.; Schutze A.; Reders, K. "Automotive Fuels". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a16_719.pub2.CS1 maint: multiple names: authors list (link)
  9. Larrow, J. F.; Jacobsen, E. N. (2004). "(R,R)-N,N'-Bis(3,5-Di-tert-Butylsalicylidene)-1,2-Cyclohexanediamino Manganese(III) Chloride, A Highly Enantioselective Epoxidation Catalyst". Organic Syntheses.; Collective Volume, 10, p. 96
  10. Yoon, TP; Jacobsen, EN (2003). "Privileged Chiral Catalysts". Science. 299 (5613): 1691–1693. Bibcode:2003Sci...299.1691Y. doi:10.1126/science.1083622. PMID 12637734. S2CID 27416160.
  11. Weber, Birgit; Jäger, Ernst-G. (2009). "Structure and Magnetic Properties of Iron(II/III) Complexes with N
    2    O2–
    2    -Coordinating Schiff Base-Like Ligands". Eur. J. Inorg. Chem.: 455. doi:10.1002/ejic.200990003.
  12. Bajema, Elizabeth A.; Kaleigh F. Roberts; Meade, Thomas J. (2019). "Chapter 11. Cobalt-Schiff Base Complexes:Preclinical Research and Potential Therapeutic Uses". In Sigel, Astrid; Freisinger, Eva; Sigel, Roland K. O.; Carver, Peggy L. (Guest editor) (eds.). Essential Metals in Medicine:Therapeutic Use and Toxicity of Metal Ions in the Clinic. Metal Ions in Life Sciences. 19. Berlin: de Gruyter GmbH. pp. 267–301. doi:10.1515/9783110527872-017. ISBN 978-3-11-052691-2. PMID 30855112.
  13. Atwood, David A.; Remington, Michael P.; Rutherford, Drew (1996). "Use of the Salan Ligands to Form Bimetallic Aluminum Complexes". Organometallics. 15 (22): 4763. doi:10.1021/om960505r.
  14. Berkessel, Albrecht; Brandenburg, Marc; Leitterstorf, Eva; Frey, Julia; Lex, Johann; Schäfer, Mathias (2007). "A Practical and Versatile Access to Dihydrosalen (Salalen) Ligands: Highly Enantioselective Titanium. In Situ Catalysts for Asymmetric Epoxidation with Aqueous Hydrogen Peroxide". Adv. Synth. Catal. 349 (14–15): 2385. doi:10.1002/adsc.200700221.
  15. Pang, Xuan; Duan, Ranlong; Li, Xiang; Sun, Zhiqiang; Zhang, Han; Wang, Xianhong; Chen, Xuesi (2014). "Synthesis and characterization of half-salen complexes and their application in the polymerization of lactide and ε-caprolactone". Polymer Chemistry. 5 (23): 6857–6864. doi:10.1039/C4PY00734D.
  16. Wu, Xianghong, Gorden, A. V. E. (2009). "2-Quinoxalinol Salen Copper Complexes for Oxidation of Aryl Methylenes". Eur. J. Org. Chem. 2009 (4): 503–509. doi:10.1002/ejoc.200800928.CS1 maint: multiple names: authors list (link)
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