110431-65-7

Usage

Uses

Used in Environmental Remediation:
HEXA-SODIUM-BENZENE-HEXATHIOLATE is used as a chelating agent for the purpose of environmental remediation. It effectively binds with heavy metals, aiding in the detoxification of contaminated sites and the removal of harmful substances from the environment.
Used in Metal Extraction Processes:
In the industry of metal extraction, HEXA-SODIUM-BENZENE-HEXATHIOLATE serves as a chelating agent to facilitate the separation and purification of metals. Its strong binding capacity with heavy metals enhances the efficiency of metal extraction processes.
Used in Chemical Synthesis:
HEXA-SODIUM-BENZENE-HEXATHIOLATE is utilized as a reagent in chemical synthesis due to its unique chemical properties. It contributes to the creation of new compounds and the advancement of chemical research.
Used in Environmental Protection Efforts:
HEXA-SODIUM-BENZENE-HEXATHIOLATE is employed in environmental protection initiatives as a means to mitigate the impact of heavy metal pollution. Its application helps in the development of strategies to safeguard ecosystems and human health from the detrimental effects of heavy metal contamination.
It is important to handle HEXA-SODIUM-BENZENE-HEXATHIOLATE with care due to its potential toxicity and reactivity, ensuring safety measures are in place during its use in various applications.

Upstream product

• 127022-77-9 hexakis(benzylthio)benzene 
• 74542-72-6 hexakis(isopropylthio)benzene 

Downstream Products

• 127022-77-9 hexakis(benzylthio)benzene 
• 134172-95-5 4,5,6,7-Tetrakis-benzylsulfanyl-benzo[1,3]dithiole-2-thione 
• 62968-45-0 hexamercaptobenzene 
• 119449-12-6 C₂₇H₁₅N₃S₆ 

Relevant academic research and scientific papers

Benzenehexathiol as a Template Rim for a Golden Wheel: Synthesis and Structure of 6>

The reaction of benzenehexathiol, C6(SH)6, with in the presence of triethylamine gave the hexanuclear gold(I) compound 6> whose structure has been determined; the hexagon of the central benzene carbon atoms is surrounded by a hexagon of sulfur atoms, followed by a hexagon of gold atoms and the wheel-like structure is completed by six peripheral phosphine ligands with interlocked aryl groups.

A Theoretical and Structural Investigation of Thiocarbon Anions

Density functional theory energies, geometries, and population analyses as well as nucleus-independent chemical shifts (NICS) have been used to investigate the structural and magnetic evidence for cyclic CnS n2- and CnSn (n = 3-6) electron delocalization. Localized molecular orbital contributions to NICS, computed by the individual gauge for localized orbitals method, dissect π effects from the σ single bonds and lone pair influences. CnS n2- (n = 3-5) structures in Dnh symmetry are minima. Their aromaticity decreases with increasing ring size. C 3S32- is both σ and π aromatic, while C4S42- and C5S5 2- are much less aromatic. NICS(0)π, the C-C(π) contribution to NICS(0) (i.e., at the ring center), decreases gradually with ring size. In contrast, cyclic C6S62- prefers D2h symmetry due to the balance between aromaticity, strain energy, and the S-S bond energies and is as aromatic as benzene. The theoretical prediction that C6S66- has D6h minima was confirmed by X-ray structure analysis. Comparisons between thiocarbons and oxocarbons based on dissected NICS analysis show that CnSn 2- (n = 3-5) and C6S66- are less aromatic in Dnh symmetry than their oxocarbon analogues.