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|Title:||NEW PI-ELECTRON DONORS FOR ORGANIC METALS - SYNTHESIS OF SUBSTITUTED TETRATHIAFULVALENES WITH 8-MEMBERED AND 9-MEMBERED DITHIAHETEROCYCLES - CRYSTAL-STRUCTURE OF 5,6,7,8-TETRAHYDRO-1,3-DITHIOLO[4,5-B][1,4]DITHIOCINE-2-THIONE|
|Publisher:||ROYAL SOC CHEMISTRY|
|Citation:||JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (12), 3341-3347|
|Abstract:||Reaction of the dimercapto disodium salt 2 with 1,4-dibromobutane, dibromo-o-xylene, 1,8-bis(bromomethyl)naphthalene and 1,2,4,5-tetrakis(bromomethyl)benzene gave the thiones 3, 5, 8 and 11 respectively. The thiones 5 and 8 were oxidised to give the oxo derivatives 6 and 9. Coupling of the thiones 3, 5 and 8 or their oxo derivatives 6 and 9 in neat triethyl phosphite afforded new pi-donors 4, 7 and 10 respectively. Reaction of 2 with dimethyltellurium dichloride gave di-(dithiolo)tetrathiocinedithione 15. The oxidation potentials of the donors 4, 7 and 10 are reported along with the preparation and electrical conductivity measurements of their charge-transfer complexes with 7,7,8,8-tetracyano-p-quinodimethane and 2,3-dichloro-5,6-dicyano-p-benzoquinone. The crystal structure of 5,6,7,8-tetrahydro-1,3-dithiolo[4,5-b][1,4]dithiocine-2-thione 3 was determined by single-crystal X-ray diffraction. Compound 3 crystallizes in the monoclinic space group P2(1)/n with unit-cell dimensions a = 4.8048(6) angstrom, b = 9.029(1) angstrom, c = 23.250 angstrom, beta = 93.22(1), V = 1028.0(2) angstrom3, Z = 4 and R = 0.046.|
|Appears in Collections:||Article|
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