Reaction of FvW(2)(H)(2)(CO)(6) with 2/8S(8) in THF results in rapid and quantitative formation of FvW(2)(SH)(2)(CO)(6). The crystal structure of this complex is reported and shows that the two tungsten-hydrosulfide groups are on opposite faces of the fulvalene ligand in an anti configuration. Nevertheless, treatment of FvW(2)(SH)(2)(CO)(6) (1) with PhN[double bond]NPh produces FvW(2)(mu-S(2))(CO)(6) (2) and Ph(H)NN(H)Ph. The crystal structure of the bridging disulfide, which cocrystallizes with 1 in a 2:1 ratio, is also described. Exposure of 2 equiv of *CrCp*(CO)(3) to 1 effects similar H atom transfers yielding 2 HCrCp*(CO)(3) and 2. Attempts to obtain crystals of the latter from solutions derived from this reaction mixture furnished a third product, FvW(2)(mu-S)(CO)(6) (3), which was analyzed crystallographically. The enthalpy of sulfur atom insertion into FvW(2)(H)(2)(CO)(6), yielding 1, has been measured by solution calorimetry.
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http://dx.doi.org/10.1021/ic025590b | DOI Listing |
Chem Sci
June 2020
Department of Chemistry , School of Life Sciences , University of Sussex, Brighton , BN1 9QR , UK . Email:
The dinucleating fulvalenyl ligand [1,1',3,3'-(C BuH)] (Fv) was used to synthesize the dimetallic dysprosocenium cation [{Dy(η-Cp*)}(μ-BH)(η:η-Fv)] () as the salt of [B(CF)] (Cp* = CMe). Compound [][B(CF)] was obtained using a method in which the double half-sandwich complex [{Dy(BH)(THF)}(Fv)] () was reacted with KCp* to give the double metallocene [{Dy(Cp*)(μ-BH)}(Fv)] (), followed by removal of a bridging borohydride ligand upon addition of [(EtSi)(μ-H)][B(CF)]. The dimetallic fulvalenyl complexes give rise to single-molecule magnet (SMM) behaviour in zero applied field, with the effective energy barriers of 154(15) cm, 252(4) cm and 384(18) cm, respectively, revealing a significant improvement in performance across the series.
View Article and Find Full Text PDFInorg Chem
May 2019
Institut für Anorganische Chemie , Technische Universität Graz, Stremayrgasse 9 , 8010 Graz , Austria.
A number of paramagnetic silylated d group 4 metallates were prepared by reaction of potassium tris(trimethylsilyl)silanide with group 4 metallates of the type K[CpMCl] (M = Ti, Zr, Hf). The outcomes of the reactions differ for all three metals. While for the hafnium case the expected complex [CpHf{Si(SiMe)}] was obtained, the analogous titanium reaction led to a product with two Si(H)(SiMe) ligands.
View Article and Find Full Text PDFDalton Trans
July 2018
J. Heyrovský Institute of Physical Chemistry, Czech Academy of Sciences, v.v.i., Dolejškova 3, 182 23 Prague 8, Czech Republic.
Reactions following the addition of dihydrogen under maximum atmospheric pressure to bis(trimethylsilyl)acetylene (BTMSA) complexes of titanocenes, [(η5-C5H5-nMen)2Ti(η2-BTMSA)] (n = 0, 1, 3, and 4) (1A-1D), and zirconocenes, [(η5-C5H5-nMen)2Zr(η2-BTMSA)] (n = 2-5) (4A-4D), proceeded in diverse ways and, depending on the metal, afforded different products. The former complexes lost, in all cases, their BTMSA ligand via its hydrogenation to bis-1,2-(trimethylsilyl)ethane when reacted at 80 °C for a prolonged reaction time. For n = 0, 1, and 3, the titanocene species formed in situ dimerised via the formation of fulvalene ligands and two bridging hydride ligands, giving known green dimeric titanocenes (2A-2C).
View Article and Find Full Text PDFTwo CuI complexes based on the π-conjugated tetrathiafulvalene-annulated phenanthroline ligands (TTF-Phen, L1 and L2), [CuI(Xantphos)(L1)]BF4 (1, Xantphos = 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene) and [CuI(Binap)(L2)]BF4 (2, Binap = 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl), have been synthesized. They have been fully characterized, and their photophysical and electrochemical properties are reported together with those of L1 and L2 for comparison. Both CuI complexes show metal-to-ligand charge transfer (MLCT) absorption bands, whereas the 3MLCT luminescence is strongly quenched.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
May 2016
Department of Inorganic Chemistry, Ukrainian State University of Chemical Technology, Gagarin Ave. 8, Dnipropetrovsk 49005, Ukraine.
The asymmetric unit of the title salt, (C10H8S8)[Re2Br6(CH3COO)]·0.5C2H3Cl3, contains one bis-(ethyl-enedi-thio)-tetra-thia-fulvalene (ET) radical cation, one μ2-acetato-bis-[tri-bromido-rhenate(III)] anion and a 1,1,2-tri-chloro-ethane mol-ecule with half-occupancy disordered about a twofold rotation axis. The tetra-thia-fulvalene fragment adopts an almost planar configuration typical of the ET radical cation.
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