From Wikipedia, the không tính tiền encyclopedia
![]() | |||
| |||
Names | |||
---|---|---|---|
IUPAC name
| |||
Other names
| |||
Identifiers | |||
CAS Number Bạn đang xem: scl2 |
| ||
3D model (JSmol) |
| ||
ChemSpider |
| ||
ECHA InfoCard | 100.031.014 ![]() | ||
EC Number |
| ||
PubChem CID |
| ||
RTECS number |
| ||
UNII |
| ||
UN number | 1828 | ||
CompTox Dashboard (EPA) |
| ||
InChI
| |||
SMILES
| |||
Properties | |||
Chemical formula |
SCl2 | ||
Molar mass | 102.96 g·mol−1 | ||
Appearance | Cherry-red liquid | ||
Odor | Pungent | ||
Density | 1.621 g/cm3 | ||
Melting point | −121.0 °C (−185.8 °F; 152.2 K) | ||
Boiling point | 59 °C (138 °F; 332 K) (decomposes) | ||
Solubility in water |
Insoluble, reacts slowly | ||
Magnetic susceptibility (χ) |
−49.4·10−6 cm3/mol | ||
Refractive index (nD) |
1.5570 | ||
Structure | |||
Coordination geometry |
C2v | ||
Molecular shape |
Bent | ||
Hazards | |||
GHS labelling: | |||
Pictograms |
![]() ![]() ![]() | ||
Signal word Xem thêm: máu loãng |
Danger | ||
Hazard statements |
H314, H335, H400 | ||
Precautionary statements |
P260, P261, P264, P271, P273, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P363, P391, P403+P233, P405, P501 | ||
NFPA 704 (fire diamond) | ![]() 3 1 1 | ||
Autoignition |
234 °C (453 °F; 507 K) | ||
Safety data sheet (SDS) | ICSC 1661 | ||
Related compounds | |||
Related |
| ||
Related compounds |
| ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
Sulfur dichloride is the chemical compound with the formula SCl2. This cherry-red liquid is the simplest sulfur chloride and one of the most common, and it is used as a precursor to tướng organosulfur compounds. It is a highly corrosive and toxic substance, and it reacts on liên hệ with water to tướng size chlorine-containing acids.
Chlorination of sulfur[edit]
SCl2 is produced by the chlorination of either elemental sulfur or disulfur dichloride.[1] The process occurs in a series of steps, some of which are:
- S8 + 4 Cl2 → 4 S2Cl2; ΔH = −58.2 kJ/mol
- S2Cl2 + Cl2 ↔ 2 SCl2; ΔH = −40.6 kJ/mol
The addition of Cl2 to tướng S2Cl2 has been proposed to tướng proceed via a mixed valence intermediate Cl3S−SCl. SCl2 undergoes even further chlorination to tướng give SCl4, but this species is unstable at near room temperature. It is likely that several SnCl2 exist where n > 2.
Disulfur dichloride, S2Cl2, is the most common impurity in SCl2. Separation of SCl2 from S2Cl2 is possible via distillation with PCl3 to tướng size an azeotrope of 99% purity, however sulfur dichloride loses chlorine slowly at room temperature and reverts to tướng disulfur dichloride. Pure samples may be stored in sealed glass ampules which develop a slight positive pressure of chlorine, halting the decomposition.
Use of SCl2 in chemical synthesis[edit]
SCl2 is used in organic synthesis. It adds to tướng alkenes to tướng give chloride-substituted thioethers. Illustrative is its addition to tướng 1,5-cyclooctadiene to tướng give a bicyclic thioether[2] A well tested method for the production of the mustard gas bis(2-chloroethyl)sulfide, is the addition of ethylene to tướng sulfur dichloride:[3]
Xem thêm: cây trồng thuộc nhóm nguồn gốc nào thích hợp trồng trong vụ đông ở miền bắc việt nam
- SCl2 + 2 C2H4 → (ClC2H4)2S
SCl2 is also a precursor to tướng several inorganic sulfur compounds. Treatment with fluoride salts gives SF4 via the decomposition of the intermediate sulfur difluoride. With H2S, SCl2 reacts to tướng give "lower" sulfanes such as S3H2.
Reaction with ammonia affords sulfur nitrides related to tướng S4N4. Treatment of SCl2 with primary amines gives sulfur diimides. One example is di-t-butylsulfurdiimide.[4]
Safety considerations[edit]
SCl2 hydrolyzes with release of HCl. Old samples contain Cl2.[citation needed]
References[edit]
- ^ F. Fehér "Dichloromonosulfane" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 370.
- ^ Bishop, Roger (1992). "9-Thiabicyclo[3.3.1]nonane-2,6-dione". Organic Syntheses. 70: 120.; Collective Volume, vol. 9, p. 692
- ^ R. J. Cremlyn “An Introduction to tướng Organosulfur Chemistry” John Wiley and Sons: Chichester (1996). ISBN 0-471-95512-4.
- ^ Kresze, G.; Wucherpfennig, W. (1967). "New Methods of Preparative Organic Chemistry V: Organic Syntheses with Imides of Sulfur Dioxide". Angewandte Chemie International Edition in English. 6 (2): 149–167. doi:10.1002/anie.196701491. PMID 4962859.
Bình luận