56423-74-6

Usage

Uses

Used in Organic Electronics:
[1,2]dithiolo[4,3-c]-1,2-dithiole-3,6-dithione is used as a conductive and semiconductive material for its potential in enhancing the performance of electronic devices.
Used in Energy Storage and Conversion Devices:
DTDT is used as a component in the development of new materials for energy storage and conversion devices, capitalizing on its unique electronic properties to improve efficiency and performance.
Used in Materials Science:
[1,2]dithiolo[4,3-c]-1,2-dithiole-3,6-dithione is used as a subject of interest in the field of materials science for its potential to contribute to the development of advanced materials for various technological applications.
Used in Research and Development:
DTDT is used as a candidate for further research, particularly in the areas of electronic and energy storage applications, due to its unique structure and properties.

Upstream product

• 87-68-3 Hexachlorobutadiene 

Downstream Products

• 130626-82-3 3H,6H-3-(p-N,N-Dimethylaminophenyl-imino)1,2-dithiolo<4,3-c>1,2-dithiol-6-thion 
• 130626-81-2 3H,6H-2,5-Bis-(p-N,N-dimethylaminophenyl)-1,2-thiazolino<5,4-d>1,2-thiazolin-3,6-dithion 
• 116967-37-4 3H,6H-2,5-bisphenyl-1,2-thiazolino<5,4-d>1,2-thiazoline-3,6-dithione 
• 116967-34-1 3H,6H-3-phenylimino-1,2-dithiolo<4,3-c>1,2-dithiole-6-thione 
• 116967-32-9 3H,6H-3,6-bisphenylimino-1,2-dithiolo<4,3-c>1,2-dithiole 
• 116967-36-3 3H,6H-3-p-methoxyphenylimino<1,2>dithiolo<4,3-c><1,2>dithiole-6-thione 
• 160593-30-6 3H,6H-3-(p-N,N-diethylamino)phenylimino<1,2>dithiolo<4,3-c><1,2>dithiole-6-thione 
• 116967-33-0 3H,6H-3,6-bis(p-methoxy-phenylimino)-1,2-dithiolo<4,3-c>1,2-dithiole 
• 116967-36-3 3H,6H-3-p-methoxy-phenylimino-1,2-dithiolo<4,3-c>1,2-dithiole-6-thione 
• 116967-39-6 3H,6H-2,5-bis(p-methoxy-phenyl)-1,2-thiazolino<5,4-d>1,2-thiazoline-3,6-dithione 
• 116967-31-8 3H,6H-3,6-bis(p-methyl-phenylimino)-1,2-dithiolo<4,3-c>1,2-dithiole 
• 116967-35-2 3H,6H-3-p-methyl-phenylimino-1,2-dithiolo<4,3-c>1,2-dithiole-6-thione 
• 116967-38-5 3H,6H-2,5-bis(p-methyl-phenyl)-1,2-thiazolino<5,4-d>1,2-thiazoline-3,6-dithione 

Relevant academic research and scientific papers

DONATORSUBSTITUIERTE POLYACETYLENE UND ANALOGA II. NOTIZ UEBER DIE SYNTHESE EINFACHER DERIVATE DES NEUEN HETEROBICYCLISCHEN GRUNDKOERPERS 3H,6H-1,2-DITHYOLO(1,2)-DITHIOL

Sulfuration of 2,3-di-tert-butylthio-fumarates with phosphorus-pentasulfide leads to 3H,6H-1,2-dithiolo(1,2)-dithiol-3,6-dithione.Desulfuration gives the mono-thione and di-one, respectively.

EINKRISTALL-MOLEKUELSTRUKTUREN 55 DITHIOLO-DITHIOL-DITHION C4S6 UND DITHIOL-DITHIOL-DION C4O2S4

The two iso(valence)electronic molecules, the violet-blue 3H,6H-1,2-Dithiolo-1,2-dithiol-3,6-dithione and its yellow oxygen analogue, the corresponding dione, are characterized by single crystal structure determinations and quantum chemical calculations to gain information on similarities and differences.The molecular structures are comparable except for the O perturbation, which causes short C=O and long (O)C-S bonds; the carbon chain CC bond lengths alternate between 143 and 134 pm.The crystal lattices are both monoclinic (P21/c), but with moleculesarranged differently in β-type and γ-type layered staples due to 293 pm short (S...O)2 dimer contacts.The color differences can be rationalized by extensive PM3/Cl-calculations.Accordingly, both molecules exhibit long wavelength ? ?*-transitions (1Ag) (1Bu), with the one of the sulfur derivative further lowered by a strong ns? nss* admixture.In addition, structural changes are discussed, which are expected for potentially conducting polymers containing disulfide-bridged chains on doping with suitable acceptors.Key words: Sulfur heterocycles C4H6 and C4O2S4, single crystal structures, quantum chemical calculations.

Addition Compounds of Nucleophiles and 3-Ethylthio-6-oxo-6H-1,2-dithiolo1,2-dithiolium Tetrafluoroborate. Synthesis of 3H,6H-1,2-Dithiolo1,2-dithiole-3-one-6-thione

A smooth method of synthesizing 3H,6H-1,2-dithiolo1,2-dithiole-3,6-dithione (3),and also its partial desulfuration to yield 3H,6H-1,2-dithiolo1,2-dithiole-3-one-6-thione (4) is presented.The ethylation product 5 of the monothione 4 reacts wi