7783-62-2Relevant articles and documents
Wilkens, C. J.,Haendler, H. M.
, (1965)
Polymorphism of the mixed tin fluoride Sn2F6
Grannec, J.,Fournes, L.,Lagassie, P.,Hagenmuller, P.,Cousseins, J. C.
, p. 815 - 820 (1990)
The mixed tin fluoride SnIISnIVF6 undergoes two phase transitions which have been unambiguously characterized by X-ray diffraction and micro-DTA. They occur at 385 ± 15 K and 470 ± 15 K. Evidence of the α ? β transition has also been given from a Mossbauer resonance investigation carried out over the temperature range 77 6-type.
Structural investigation and 119Sn Mossbauer study of graphite/SnF4 intercalation compound
Fournes,Roisnel,Grannec,Tressaud,Hagenmuller,Imoto,Touhara
, p. 79 - 87 (1990)
The intercalation of tin tetrafluoride into graphite has been carried out in fluorinated anhydrous HF. For long reaction times, a stage-2 compound has been obtained with an identity period of 11.53 angstrom. The structural characteristics of the intercala
The BaF2-SnF4 System
Lukiyanchuk,Fedorov
, p. 826 - 827 (2008/10/08)
The BaF2-SnF4 system is studied up to 55 mol % SnF4 by DTA and X-ray powder diffraction. The compound BaSnF6, which crystallizes congruently at 1120°C and undergoes phase transformations at 755 and 850°C, forms in the system. Another compound, hypothetically, Ba3SnF10, is formed peritectically at 900±5°C. The eutectic coordinates are 810±5°C, 35.5±2 mol % SnF4.
Synthesis, solution and magic angle spinning tin-119 nuclear magnetic resonance studies and crystal structures of dithioether complexes of tin(IV) halides
Dann, Sandra E.,Genge, Anthony R. J.,Levason, William,Reid, Gillian
, p. 4471 - 4478 (2007/10/03)
The compounds SnX4 reacted with 1 molar equivalent of dithioether, L-L, in dry CHCl3 solution to give the six-co-ordinate species [SnX4(L-L)] [X = Cl, L-L = MeS(CH2)nSMe, o-C6H4(SMe)2 or PhS(CH2)nSPh (n = 2 or 3); X = Br, L-L = MeS(CH2)nSMe or o-C6H4(SMe)2] in high yield as white or pale yellow powdered solids. Using SnBr4 and PhS(CH2)nSPh or SnI4 with MeS(CH2)nSMe did not produce isolable products, although solution 119Sn-{1H} NMR spectroscopy provided evidence for their existence at low temperatures. X-Ray structural studies on [SnCl4{MeS(CH2)2SMe}], [SnCl4{MeS(CH2)3SMe}], [SnCl4{o-C6H4(SMe)2}], [SnCl4{PhS(CH2)3SPh}] and [SnBr4{MeS(CH2)3SMe}] confirmed an S2X4 donor set with the dithioether acting as a bidentate chelate. Variable-temperature solution 1H and 119Sn-{1H} NMR spectroscopic studies showed that the complexes are extremely labile and ligand dissociation and pyramidal inversion are fast except at low temperatures. Magic angle spinning 119Sn NMR data for [SnCl4(L-L)] are reported. The crystal structure of cis-[SnI4{MeS(O)(CH2)3SMe}2], obtained as a decomposition product from the SnI4-MeS(CH2)3SMe reaction, shows monodentate sulfoxide (O) co-ordination.