355117-89-4Relevant academic research and scientific papers
Functionalised organosulfur donor molecules: Synthesis of racemic hydroxymethyl-, alkoxymethyl- and dialkoxymethyl-bis(ethylenedithio)tetrathiafulvalenes
Saygili, Nezire,Brown, R.James,Day, Peter,Hoelzl, Robert,Kathirgamanathan, Poopathy,Mageean, Eileen R,Ozturk, Turan,Pilkington, Melanie,Qayyum, Mohammed M.B,Turner, Scott S,Vorwerg, Lars,Wallis, John D
, p. 5015 - 5026 (2001)
Short synthetic routes to racemic derivatives of bis(ethylenedithio)tetrathiafulvalene carrying one hydroxymethyl (HMET), alkoxymethyl or dialkoxymethyl side chain are reported along with cyclic voltammetry measurements and conversion of HMET to (2:1) radical cation salts.
Novel organosulfur donors containing hydroxy functionalities: Synthesis of bis[2,2-bis(hydroxymethyl)propane-1,3-diyldithio]-tetrathiafulvalene and related materials
Ozturk, Turan,Saygili, Nezire,Ozkara, Serife,Pilkington, Melanie,Rice, Craig R.,Tranter, Deborah A.,Turksoy, Figen,Wallis, John D.
, p. 407 - 414 (2007/10/03)
A report on the synthesis of novel organosulfur donors with two or more hydroxymethyl groups were presented. Achiral hydroxy-substituted derivatives of tetrathiafulvalene and some tetrathiafulvalene carrying alternative hydrogen bond donors were studied. Cyclic sulfate esters of vic-diols in the preparation of substituted bis(ethylenedithio)tetrathiafulvalene derivative were used by performing substitution reactions with the thiolate.
