Cyclam

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Cyclam
Cyclam.png
Names
Preferred IUPAC name
1,4,8,11-Tetraazacyclotetradecane
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.005.491 Edit this at Wikidata
UNII
  • InChI=1S/C10H24N4/c1-3-11-7-9-13-5-2-6-14-10-8-12-4-1/h11-14H,1-10H2 checkY
    Key: MDAXKAUIABOHTD-UHFFFAOYSA-N checkY
  • N1CCNCCCNCCNCCC1
Properties
C10H24N4
Molar mass 200.330 g·mol−1
Melting point 185 to 188 °C (365 to 370 °F; 458 to 461 K)
5 g/100 mL (20 °C)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Cyclam (1,4,8,11-tetraazacyclotetradecane) is an organic compound with the formula (NHCH2CH2NHCH2CH2CH2)2. Classified as an aza-crown ether, it is a white solid that is soluble in water. As a macrocyclic ligand, it binds strongly to many transition metal cations.[1] The compound was first prepared by the reaction of 1,3-dibromopropane and ethylenediamine.[2]

Structure of one isomer of trans-Ni(cyclam)Cl2.[3]

The compound features four secondary amines. Its complexes therefore can exist as several diastereomers, depending on the relative orientation of the N–H centres. Its complexes feature alternating five- and six-membered chelate rings. The closely related ligand cyclen ((CH2CH2NH)4) forms only five-membered C2N2M chelate rings and tends not to form square-planar complexes.

N-Alkyl derivatives[edit]

Metal-cyclam complexes are prone to oxidative degradation, which is initiated by deprotonation of the secondary amine. This flaw led to the development of cyclam derivatives wherein the NH centres are replaced by tertiary amines. For example, the tetramethyl derivatives are readily prepared by methylation using formaldehyde and formic acid.[1] These oxidatively robust derivatives of cyclam have enabled a number of metal–O2 complexes.[4]

Isomers of a square planar metal cyclam complex.

See also[edit]

References[edit]

  1. ^ a b Barefield, E. Kent (2010). "Coordination chemistry of N-tetraalkylated cyclam ligands—A status report". Coord. Chem. Rev. 254 (15–16): 1607–1627. doi:10.1016/j.ccr.2010.03.007.
  2. ^ Van Alphen, J. (1937). "On Aliphatic Polyamines IV". Recl. Trav. Chim. Pays-Bas. 56 (4): 343–350. doi:10.1002/recl.19370560405.
  3. ^ Ito, T.; Kato, M.; Ito, H. (1984). "The Structures of trans-Dichloro- and trans-Bis(isothiocyanato)nickel(II) Complexes with 1,4,8,11-Tetraazacyclotetradecane, 1,4,8,12-Tetraazacyclopentadecane, and 1,5,9,13-Tetraazacyclohexadecane. The Negative Correlation between the Axial and In-plane Coordination Bond Lengths in Tetragonal Ni(II) Complexes of the trans-NiX2N4 Type". Bull. Chem. Soc. Jpn. 57 (9): 2641. doi:10.1246/bcsj.57.2641.
  4. ^ Cho, J.; Sarangi, R.; Nam, W. (2012). "Mononuclear Metal–O2 Complexes Bearing Macrocyclic N-Tetramethylated Cyclam Ligands". Acc. Chem. Res. 45 (8): 1321–1330. doi:10.1021/ar3000019. PMC 3627547. PMID 22612523.