70165-72-9

Usage

Uses

Used in Organic Synthesis:
Tricyclohexyl(dithiocarboxylato)phosphonium is used as a reagent in organic synthesis for its ability to catalyze various reactions, enhancing the efficiency and selectivity of the processes.
Used in Coordination Chemistry:
In the field of coordination chemistry, tricyclohexyl(dithiocarboxylato)phosphonium is employed as a ligand or a catalyst, contributing to the formation of complex structures and compounds.
Used in Materials Science:
Tricyclohexyl(dithiocarboxylato)phosphonium is utilized in materials science for its potential applications in the synthesis and modification of materials with specific properties.
Used in Industrial Catalysis:
tricyclohexyl(dithiocarboxylato)phosphonium is studied for its potential use in industrial catalysis, where it could improve the efficiency of chemical processes in large-scale manufacturing.
Used in Polymerization Reactions:
Tricyclohexyl(dithiocarboxylato)phosphonium is used as a stabilizing agent in polymerization reactions, helping to control the reaction kinetics and produce polymers with desired characteristics.

InChI:InChI=1/C19H33PS2/c21-19(22)20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h16-18H,1-15H2/p+1

Upstream product

• 75-15-0 carbon disulfide 
• 1605-53-4 diethyl-phenyl-phosphine 
• 2622-14-2 tricyclohexylphosphine 

Downstream Products

• 123086-25-9 ethyltricyclohexylphosphonium bromide 
• 123086-30-6 C₂₂H₃₈OP⁽¹⁺⁾*Br^(1-) 
• 123086-27-1 ((E)-3-Bromo-3-trimethylsilanyl-allyl)-tricyclohexyl-phosphonium; bromide 
• 2622-14-2 tricyclohexylphosphine 
• 57441-10-8 benzyltricyclohexylphosphonium bromide 
• 80697-67-2 RuH(CO)(S₂CP(C₆H₁₁)3)(P(C₆H₁₁)3)2⁽¹⁺⁾*B(C₆H₅)4^(1-)=RuH(CO)(S₂CP(C₆H₁₁)3)(P(C₆H₁₁)3)2B(C₆H₅)4 
• 82999-55-1 2Ni*2CS₂*2P(C₆H₁₁)3=[Ni(CS₂)(P(C₆H₁₁)3)]2 

Relevant academic research and scientific papers

Assessing the potential of zwitterionic NHOCS2 adducts for probing the stereoelectronic parameters of N-heterocyclic carbenes

Five imidazol(in)ium-2-dithiocarboxylates bearing cyclo-hexyl, mesityl, or 2,6-diisopropylphenyl substituents on their nitrogen atoms were prepared from the corresponding N-heterocyclic carbenes (NHCs) by reaction with carbon disul-fide. They were charact

Synthesis of Cationic Palladium(II) and Platinum(II) Complexes with a Monodentate Trialkylphosphoniumditiocarboxylate Ligand: Molecular Structure of trans-ClO4*CHCl3

Reaction of trans- with the zwitterion S2C-PR'3 affords the complexes trans-ClO4 (M= Pd; R3=R'3= Et3, Bu3 or Et2Ph; R= Bu, R'= cyclo-C6H11; R= Ph, R'= Et or cyclo-C6H11; M= Pt, R=R'= Et or Bu). trans-ClO4 is also given by reaction of ClO4 with CS2.Reaction of (bipy= 2,2'-bipyridyl) with S2C-PR'3 affords ClO4 (M=Pd or Pt; R'=Et, Bu, or cyclo-C6A11).A crystallographic study of trans-ClO4 (as its 1:1 chloroform solvate) shows that the cation contains a unidentate triethylphosphoniumdithiocarboxylate ligand, and 31P n.m.r. spectra of all products with two terminal phosphine ligands are consistent with trans stereochemistries.Crystals of trans-ClO4*CHCl3 are monoclinic, space group P21/a, with a=14.596 5(18), b=15.356(3), c=19.324 2(16) angstroem, β=109.257(8) deg, and Z=4.Using 4 093 amplitudes the structure has been refined to R=0.1049.The non-bonding Pd...S distance is 3.644(4) angstroem.