Enantiopure Radical Cation Salt Based on Tetramethyl-Bis(ethylenedithio)-Tetrathiafulvalene and Hexanuclear Rhenium Cluster

نویسندگان

  • Flavia Pop
  • Patrick Batail
  • Narcis Avarvari
چکیده

Electrocrystallization of the (S,S,S,S) enantiomer of tetramethyl-bis(ethylenedithio)tetrathiafulvalene donor 1 in the presence of the dianionic hexanuclear rhenium (III) cluster [Re6S6Cl8]2 ́ affords a crystalline radical cation salt formulated as [(S)-1]2 ̈Re6S6Cl8, in which the methyl substituents of the donors adopt an unprecedented all-axial conformation. A complex set of intermolecular TTF ̈ ̈ ̈TTF and cluster ̈ ̈ ̈TTF interactions sustain an original tridimensional architecture.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Regioselective synthesis of chiral dimethyl-bis(ethylenedithio)tetrathiafulvalene sulfones

Enantiopure (R,R) and (S,S)-dimethyl-bis(ethylenedithio)tetrathiafulvalene monosulfones have been synthesized by the aerial oxidation of the chiral dithiolates generated from the propionitrile-protected precursors. Both enantiomers crystallize in the orthorhombic chiral space group P212121. They show a boat-type conformation of the TTF moiety, a rather rigid dithiin sulfone ring and the methyl ...

متن کامل

Chemo- and enantioselective sulfoxidation of bis(ethylenedithio)-tetrathiafulvalene (BEDT-TTF) into chiral BEDT-TTF-sulfoxide.

Selective sulfoxidation of BEDT-TTF (bis(ethylenedithio)-tetrathiafulvalene) with enantiopure (camphoryl-sulfonyl)oxaziridine derivatives provided the inner monosulfoxide, as demonstrated using single crystal X-ray analysis, with an enantiomeric excess of 44% (up to 74% after recrystallization).

متن کامل

Synthesis of bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) derivatives functionalised with two, four or eight hydroxyl groups.

Short synthetic routes to a range of BEDT-TTF derivatives functionalised with two, four or eight hydroxyl groups are reported, of interest because of their potential for introducing hydrogen bonding between donor and anion into their radical cation salts. The cycloaddition of 1,3-dithiole-2,4,5-trithione with alkenes to construct 5,6-dihydro-1,3-dithiolo[4,5-b]1,4-dithiin-2-thiones is a key ste...

متن کامل

Rsc_nj_c1nj20034h 1..7

A chiral tetrathiafulvalene (1) bearing a binaphtholdimethylene moiety on one side, an ethylenedithio substituent on the other side, is prepared from atropoisomeric (R)-, (S)and racemic (R,S)-binaphthol. Its oxidation potential (0.49 V vs. SCE) allows for its oxidation with TCNQF4. Crystal structures of the neutral racemic (R,S)-1 and enantiopure (R)-1 were determined together with those of the...

متن کامل

Synthesis and Properties of Bis-(phenylenedithio)-tetrathiafulvalene (BPhDT-TTF): a New ;r-Donor for Organic Metals

The new 7r-donor bis-(phenylenedithio)-tetrathiafulvalene (5), synthesized via phosphite coupling o f 2-oxo-l,3-dithiolo-[4,5b][l,4]-benzodithiin (4), has been prepared in 5 steps start­ ing from 1,2-dimercaptobenzene and chloroacetyl chloride. Spectroscopic and electrochemical data point to a close similarity o f 5 and dibenzo-tetrathiafulvalene (DB-TTF). 5 forms a highly conducting radical-ca...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2016