846571-61-7

Upstream product

• 846571-59-3 4-(2-cyanoethyl)thio-5-ethylthio-1,3-dithiole-2-thione 
• 250687-28-6 5-tosyl-[1,3]dithiolo[4,5-c]pyrrol-2-one 
• 250687-25-3 4,6-dihydro-N-tosyl-(1,3)-dithiolo[4,5-c]pyrrole-2-thione 
• 186826-01-7 4,5-bis(hydroxymethyl)-2-thioxo-1,3-dithiole 
• 159223-12-8 4,5-Bis(hydroxymethyl)-1,3-dithiole-2-thione 
• 7396-41-0 4,5-bis(methoxycarbonyl)-1,3-dithiole-2-thione 
• 250687-26-4 4,6-dihydro-N-tosyl-(1,3)-dithiolo[4,5-c]pyrrole-2-one 
• 132765-35-6 4,5-bis((2-cyanoethyl)thio)-1,3-dithiole-2-thione 

Downstream Products

• 846571-63-9 2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5-(toluene-4-sulfonyl)-5H-[1,3]dithiolo[4,5-c]pyrrole 
• 877032-14-9 5-(3,5-di-tert-butyl-benzyl)-2-{4-ethylsulfanyl-5-[2-(2-methoxy-ethoxy)-ethylsulfanyl]-[1,3]dithiol-2-ylidene}-5H-[1,3]dithiolo[4,5-c]pyrrole 
• 877032-12-7 C₂₂H₂₅NO₄S₇ 
• 1357295-19-2 2-[4-(3,5-di-t-butylbenzylthio)-5-(ethylthio)-1,3-dithiole-2-ylidene]-[1,3]dithiolo[4,5-c]pyrrole 
• 1357295-20-5 2-[4-(3,5-di-t-butylbenzylthio)-5-(ethylthio)-1,3-dithiole-2-ylidene]-5-{2-[2-(2-iodoethoxy)ethoxy]ethyl}-[1,3]dithiolo[4,5-c]pyrrole 
• 1357295-10-3 C₄₆H₆₃NO₅S₁₃ 
• 1357295-18-1 C₃₂H₃₇NO₂S₇ 
• 1357295-12-5 N-tosyl-2-[4-(ethylthio)-5-(2-(2-(2-methoxyethoxy)ethoxy)ethylthio)-(1,3)-dithiole-2-ylidene]-(1,3)-dithiolo[4,5-c]pyrrole 
• 1443384-36-8 C₄₀H₅₃NO₇S₆ 
• 1443384-41-5 C₃₂H₄₅NO₃S₆ 

Relevant academic research and scientific papers

Evidence of strong hydration and significant tilt of amphiphilic [2]rotaxane molecules in Langmuir films studied by synchrotron X-ray reflectivity

Surface sensitive X-ray techniques have been used to elucidate the structures of amphiphilic [2]rotaxane and dumbbell monolayers at the air/water interface. The [2]rotaxanes were found to adopt highly hydrated tilted and/or folded conformations on the wat

Advances in the synthesis of functionalised pyrrolotetrathiafulvalenes

The electron-donor and unique redox properties of the tetrathiafulvalene (TTF, 1) moiety have led to diverse applications in many areas of chemistry. Monopyrrolotetrathiafulvalenes (MPTTFs, 4) and bispyrrolotetrathiafulvalenes (BPTTFs, 5) are useful struc

Ground-state equilibrium thermodynamics and switching kinetics of bistable [2]rotaxanes switched in solution, polymer gels, and molecular electronic devices

We report on the kinetics and ground-state thermodynamics associated with electrochemically driven molecular mechanical switching of three bistable [2]rotaxanes in acetonitrile solution, polymer electrolyte gels, and molecular-switch tunnel junctions (MST