42967-62-4Relevant articles and documents
Heavy alkali metal arenedithiocarboxylates: A facile synthesis, dimeric structure, and nonbonding interaction between the metals and aromatic ring carbons
Kato, Shinzi,Kitaoka, Nobuyuki,Niyomura, Osamu,Kitoh, Yuka,Kanda, Takahiro,Ebihara, Masahiro
, p. 496 - 506 (2008/10/08)
Dithiocarboxylic acids and their trimethylsilyl esters were found to readily react with potassium, rubidium, and cesium fluorides to give the corresponding alkali metal dithiocarboxylates 3-5 in moderate to good yields. A series of tetramethylammonium dithiocarboxylates 8 have been prepared in good yields by the reaction of sodium dithiocarboxylates 7 with tetramethylammonium chloride. The structures of potassium (3b), rubidium (4g), cesium (5f), and tetramethylammonium 4-methylbenzenecarbodithioates (8e) and tetramethylammonium 2-methoxybenzenecarbodithioate (8f) were characterized crystallographically. These heavier alkali metal salts (3b, 4g, 5f) have a dimeric structure [(RCSSM)2, M = K, Rb, Cs] in which the two dithiocarboxylate groups are chelated to the metal cations which are located on the upper and lower sides of the plane involving the two opposing dithiocarboxylate groups. The K+ cations interact with the tolyl fragment of a neighboring molecule, while the Rb+ and Cs+ cations interact with two neighboring tolyl fragments, in which the ipso and ortho carbons are positioned close to the metals. The interaction number of the metals with surrounding atoms is 8 for K+ and Rb+ and 12 for Cs+. The C-S distances of the dithiocarboxylate group are different for the potassium salt 3b. In contrast, those of the rubidium salt 4g and cesium salt 5f are equal. Similarly, the chelating sulfur-metal bond distances of 3b are different, while those of 4g and 5f are almost equal. The dihedral angles of the phenyl ring and dithiocarboxylate plane increase in the order of the K, Rb, and Cs salts. The structural analysis of sodium 4-methylbenzenecarbodithioate (7g) revealed the presence of 4-CH3C6H4CS2Na0.36. In contrast, the tetramethylammonium salts 8 are monomeric where the cation moieties are located out of the dithiocarboxylate plane. The potassium 3, rubidium 4, and cesium dithiocarboxylates 5 readily reacted with methyl iodide or triorganotin chlorides at room temperature to give the corresponding methyl 9 and triorganotin dithioesters 10 in good yields. At 0 °C, the reactivity of the rubidium 4 and cesium salts 5 to methyl iodides decreases dramatically compared with those of the sodium salts 7 and potassium salts 3.
The Preparation and Some Reactions of Unsymmetrical Acyl Thioacyl Sulfides
Kato, Shinzi,Sugino, Katsumi,Matsuzawa, Yukihiko,Katada, Tomonori,Noda, Ippei,et al.
, p. 1798 - 1811 (2007/10/02)
A number of unsymmetrical acyl thioacyl sulfides have been prepared and characterized by the reaction of piperidinium or sodium dithiocarboxylates with acyl chlorides or by desulfurization reaction of acyl thioacyl disulfides with triphenylphosphine.They are deep blue oils or light green crystals and very unstable thermally and for moisture.The n --> ?* transitions of the thiocarbonyl group of 1 appear in higher wave length region than those of the corresponding symmetrical bis(thioacyl) sulfides .Some reactions with nucleophiles are discussed.It was found that the symmetricallization reaction of these unsymmetrical acyl thioacyl sulfides occurs in the presence of base such as lithium ethanethiolate to give the symmetrical bis(thioacyl) disulfides in fair yield.
