TTF based charge transfer salts of [Cr(NCS)4(phen)]-: Bulk magnetic order and crystal structures of the TTF, TMTTF (tetramethyltetrathiafulvalene) and TMTSF (tetramethyltetraselenafulvalene) derivatives
Turner, SS, Pevelen, DL, Day, P and Prout, K (2000) TTF based charge transfer salts of [Cr(NCS)4(phen)]-: Bulk magnetic order and crystal structures of the TTF, TMTTF (tetramethyltetrathiafulvalene) and TMTSF (tetramethyltetraselenafulvalene) derivatives Journal of the Chemical Society, Dalton Transactions (16). pp. 2739-2744.
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Abstract
A series of new charge transfer salts of electron donors based on tetrathiafulvalene, TTF, with the anion [Cr(NCS)4(phen)]~ (phen = 1,10-phenanthroline) have been prepared. Single crystal X-ray diffraction provided structures for salts with donors TTF, TMTTF, tetramethyltetrathiafulvalene, and TMTSF, tetramethyltetraselenafulvalene. The salts were found to be [TTF][Cr(NCS)(phen)] at 293 K, [TMTTF][Cr(NCS)(phen)]-CHCl2 at 250 K and rrMTSF][Cr(NCS)(phen)]2-0.5CHCl at 293 K. For the TMTSF compound the solvent is disordered at 293 K so the structure was also solved at 120 K when the solvent becomes ordered. All of the salts have multiple S ⋯S or S ⋯Se close contacts between the anions and cations. The TTF salt is a bulk ferrimagnet with Tc = 9 K and is an insulator whereas the TMTTF salt is an antiferromagnetic (TN = 3.0 K) insulator. Both have close atomic interactions of the phen-donor n-stacking type, but the TMTTF salt also contains close anion-anion contacts and dimerised cations whereas the TTF salt consists of stacks of alternating cations and anions. The TMTSF salt is a paramagnetic semiconductor and does not display n stacking but has close inter-donor Se ⋯Se contacts and isolated anions which afford the magnetic and transport properties. © The Royal Society of Chemistry 2000.
Item Type: | Article |
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Divisions : | Surrey research (other units) |
Authors : | Turner, SS, Pevelen, DL, Day, P and Prout, K |
Date : | 2000 |
DOI : | 10.1039/b004140h |
Depositing User : | Symplectic Elements |
Date Deposited : | 28 Mar 2017 13:22 |
Last Modified : | 24 Jan 2020 12:10 |
URI: | http://epubs.surrey.ac.uk/id/eprint/802876 |
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