Date published: 2025-10-15

1-800-457-3801

SCBT Portrait Logo
Seach Input

1,4,8,11-Tetrathiacyclotetradecane (CAS 24194-61-4)

0.0(0)
Write a reviewAsk a question

Alternate Names:
14-Ane-S4
Application:
1,4,8,11-Tetrathiacyclotetradecane is a sulfur crown-ether analog used in liquid-liquid metal ion extraction
CAS Number:
24194-61-4
Purity:
95%
Molecular Weight:
268.53
Molecular Formula:
C10H20S4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

1,4,8,11-Tetrathiacyclotetradecane is a cyclic sulfur compound that functions as a complexing agent in various experimental applications. It has the ability to form stable complexes with metal ions, particularly with transition metals such as copper, nickel, and zinc. 1,4,8,11-Tetrathiacyclotetradecane′s mechanism of action involves the formation of coordination bonds with metal ions, leading to the stabilization of these complexes. In development applications, it is utilized for its capacity to chelate metal ions, which is relevant in the study of metal ion coordination chemistry and the development of metal-based materials. Its molecular structure allows it to effectively interact with metal ions, which may be useful for investigating the behavior of metal complexes in various experimental systems. 1,4,8,11-Tetrathiacyclotetradecane′s role in experimental applications involves its ability to form stable complexes with metal ions, contributing to the study and manipulation of metal coordination chemistry.


1,4,8,11-Tetrathiacyclotetradecane (CAS 24194-61-4) References

  1. Effect of conformational constraints on gated electron-transfer kinetics. 3. Copper(II/I) complexes with cis- and trans-cyclopentanediyl-1,4,8,11-tetrathiacyclotetradecane.  |  Wijetunge, P., et al. 2000. Inorg Chem. 39: 2897-905. PMID: 11232830
  2. Direct evidence for a geometrically constrained 'entatic state' effect on copper(II/I) electron-transfer kinetics as manifested in metastable intermediates.  |  Yu, Q., et al. 2001. J Am Chem Soc. 123: 5720-9. PMID: 11403604
  3. Arsenic(III) halide complexes with acyclic and macrocyclic thio- and selenoether coligands: synthesis and structural properties.  |  Hill, NJ., et al. 2002. Inorg Chem. 41: 2070-6. PMID: 11952360
  4. 1lambda(4),4lambda(4),8lambda(4),11lambda(4)-Tetrathiacyclotetradecane-1,4,7,10-tetraylidenetetraaminium tetrakis(2,4,6-trimethylbenzenesulfonate).  |  Dale, SH., et al. 2005. Acta Crystallogr C. 61: o411-3. PMID: 15930699
  5. Effect of constrained donor atom orientations on the stabilities, complexation kinetics, redox potentials, and structures of macrocyclic polythiaether Complexes. Copper(II) complexes with cyclopentanediyl derivatives of [14]aneS4 in 80% methanol.  |  Kakos, SH., et al. 2006. Inorg Chem. 45: 923-34. PMID: 16411732
  6. Ruthenium complexes containing 2-(2-nitrosoaryl)pyridine: structural, spectroscopic, and theoretical studies.  |  Chan, SC., et al. 2011. Inorg Chem. 50: 11636-43. PMID: 22023038
  7. Influence of crown thioether ligands in the structures and of perhalophenyl groups in the optical properties of complexes with argentoaurophilic interactions.  |  Blake, AJ., et al. 2014. Inorg Chem. 53: 10471-84. PMID: 25216233
  8. Syntheses and investigation of metal complexes with macrocyclic polythioether ligands.  |  Rotärmel, T., et al. 2022. Faraday Discuss. 234: 70-85. PMID: 35171171

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1,4,8,11-Tetrathiacyclotetradecane, 200 mg

sc-251603
200 mg
$255.00