35112-74-4Relevant articles and documents
Vlasova et al.
, (1975)
Design of heterogeneous catalysts via multiple active site positioning in organic-inorganic hybrid materials
Dufaud, Veronique,Davis, Mark E.
, p. 9403 - 9413 (2003)
Catalytic materials bearing multiple sulfonic acid functional groups and positioned at varying distances from one another on the surface of mesoporous solids are prepared to explore the effects that the spatial arrangement of active sites have on catalytic activity and selectivity. A series of organosiloxane precursors containing either disulfide or sulfonate ester functionalities (synthons of the eventual sulfonic acid groups) are synthesized. From these molecular precursors, a variety of organic - inorganic hybrid, mesostructured SBA-15 silica materials are prepared using a postsynthetic grafting procedure that leads to disulfide and sulfonate ester modified silicas: [Si]CH2CH2CH2SS-pyridyl, 2·SBA, [Si]CH2CH2CH2SSCH2 CH2CH2[Si], 3·SBA, [Si]CH2CH2(C6H4) (SO2)OCH2CH3, 4·SBA, and [Si]CH2CH2(C6H4) (SO2)OC6H4O(SO2) (C6H4)CH2CH2[Si], 6·SBA ([Si] = (≡SiO)x(RO)3-xSi, where x = 1, 2). By subsequent chemical derivatization of the grafted species, thiol and sulfonic acid modified silicas are obtained. The materials are characterized by a variety of spectroscopic (13C and 29Si CP MAS NMR, X-ray diffraction) and quantitative (TGA/DTA, elemental analysis, acid capacity titration) techniques. In all cases, the organic fragment of the precursor molecule is grafted onto the solid without measurable decomposition, and the precursors are, in general, attached to the surface of the mesoporous oxide by multiple siloxane bridges. The disulfide species 2·SBA and 3·SBA are reduced to the corresponding thiols 7·SBA and 8·SBA, respectively, and 4·SBA and 6· SBA are transformed to the aryl sulfonic acids 11·SBA and 12·SBA, respectively. 7·SBA and 8·SBA differ only in terms of the level of control of the spatial arrangement of the thiol groups. Both 7·SBA and 8·SBA are further modified by oxidation with hydrogen peroxide to produce the alkyl sulfonic acid modified materials 9·SBA and 10·SBA, respectively. The performances of the sulfonic acid containing SBA-15 silica materials (with the exception of 12·SBA) are tested as catalysts for the condensation reaction of phenol and acetone to bisphenol A. The alkyl sulfonic acid modified material 10·SBA derived from the cleavage and oxidation of the dipropyl disulfide modified material 3·SBA is more active than not only its monosite analogue 9· SBA, but also the presumably stronger acid aryl sulfonic acid material 11·SBA. It appears that a cooperative effect between two proximal functional groups may be operating in this reaction.
Iridium-Catalyzed Hydrosilylation of Sulfur-Containing Olefins
Srinivas, Venu,Nakajima, Yumiko,Sato, Kazuhiko,Shimada, Shigeru
supporting information, p. 12 - 15 (2018/01/12)
Hydrosilylation of various sulfur-containing olefins with (RO)3SiH has been achieved using iridium catalysts [IrX(cod)]2 (X = Cl, SPh). The catalysis is applicable to the chemoselective hydrosilylation of thioacetate, which enables the preparation of an industrially important silane coupling agent.
CpMn(CO)3-catalyzed photoconversion of thiols into disulfides and dihydrogen
Tan, Kheng Yee Desmond,Kee, Jun Wei,Fan, Wai Yip
experimental part, p. 4459 - 4463 (2011/01/10)
The UV photolysis of CpMn(CO)3 with thiols at room temperature effected the following catalytic transformation: 2 RSH → R 2S2 + H2. This reaction is a cleaner and greener way toward making disulfides, as it produces dihydrogen as the only side-product. The manganese system exhibits high chemoselectivity as the transformation proceeds efficiently even in the presence of numerous functional groups. A manganese dicarbonyl complex, CpMn(CO)2RSH, and cyclopentadiene have also been detected using FTIR and NMR spectroscopic techniques, respectively. Based on our experimental data, a mechanism has been proposed to account for the catalysis.
