29959-92-0Relevant academic research and scientific papers
Robust Cooperative Photo-oxidation of Sulfides without Sacrificial Reagent under Air Using a Dinuclear RuII–CuII Assembly
Chao, Duobin,Zhao, Mengying
, p. 3358 - 3362 (2017)
A molecular chromophore–catalyst assembly containing a chromophore ruthenium(II) center (RuIIchro) and a catalytic copper(II) center (CuIIcat) has been prepared easily. The assembly was employed for photocatalyt
Flow Electrosynthesis of Sulfoxides, Sulfones, and Sulfoximines without Supporting Electrolytes
Amri, Nasser,Wirth, Thomas
, p. 15961 - 15972 (2021/07/20)
An efficient electrochemical flow process for the selective oxidation of sulfides to sulfoxides and sulfones and of sulfoxides toN-cyanosulfoximines has been developed. In total, 69 examples of sulfoxides, sulfones, andN-cyanosulfoximines have been synthesized in good to excellent yields and with high current efficiencies. The synthesis was assisted and facilitated through a supporting electrolyte-free, fully automated electrochemical protocol that highlights the advantages of flow electrolysis.
Sulfoxide and Sulfone Synthesis via Electrochemical Oxidation of Sulfides
Lee, Sunwoo,Park, Jin Kyu
, p. 13790 - 13799 (2021/10/12)
The oxidation of diaryl sulfides and aryl alkyl sulfides to the corresponding sulfoxides and sulfones under electrochemical conditions is reported. Sulfoxides are selectively obtained in good yield under a constant current of 5 mA for 10 h in DMF, while sulfones are formed as the major product under a constant current of 10 or 20 mA for 10 h in MeOH. The oxygen of both the sulfoxide and sulfone function is derived from water.
Lanthanide complexes based on an anthraquinone derivative ligand and applications as photocatalysts for visible-light driving photooxidation reactions
Zhu, Ting-Ting,Tao, Yu-Tong,Sun, Yue,Wang, Xue,Zhang, Xiao-Wen,Chai, Jia-Lu,Han, Jie,Zhao, Xiao-Li,Chen, Xu-Dong
, (2021/04/05)
Four isostructural lanthanide coordination complexes based on 3,7-diamino-9,10-anthraquinone-2,6-disulfonate (dianionic, L) have been synthesized by hydrothermal method, namely [Er(L)(H2O)6]?[Er(H2O)8]?2L?8H2O (Er-L), [Tm(L)(H2O)6]?[Tm(H2O)8]?2L?8.5H2O (Tm-L), [Yb(L)(H2O)6]?[Yb(H2O)8]?2L?9H2O (Yb-L), [Lu(L)(H2O)6]?[Lu(H2O)8]?2L?9H2O (Lu-L). Single-crystal X-ray analysis reveals the existence of both coordinated and free ligand L in the crystal structure. Versatile sulfonate groups on these distinct L ligands, together with very rich coordinated and lattice water molecules, form a lot of hydrogen-bonding motifs that contribute to the stabilization of the crystal packing. It is interesting that the ligands stack into columns through strong π-π interactions and the centroid-centroid distances are between 3.281 and 3.331 ?. These ligands are stacked in an alternate off-set mode to avoid the steric hindrance between the bulky sulfonate groups, generating a repeated structural unit involving six stacked ligands. These lanthanide complexes proved to be good heterogeneous photocatalyst for promoting the visible-light driving photooxidation reactions of diarylacetylenes and thioethers. The Er-L complex exhibited the best catalytic activity and showed good catalytic efficiency over a wide range of substrates for both reaction systems. The Er-L photocatalyst can be easily isolated by simple filtration as crystalline material upon completion of the photooxidation reaction without structure change, and can be recycled for at least five catalytic cycles with persistent catalytic efficiency without any need of activation or regeneration. This family of lanthanide complexes represent a category of promising heterogeneous photocatalysts in terms of green chemistry, with the potential of promoting organic transformations highly efficiently under the irradiation of visible light.
Lanthanide complexes of anthraquinone-1,8-disulfonate: Syntheses, structures and catalytic studies
Cao, Fu-Yu,Chen, Xu-Dong,Gao, Hui-Lei,Han, Jie,Huang, Meng-Ping,Zhao, Xiao-Li
, (2021/06/07)
Two isostructural series of four lanthanide coordination complexes have been synthesized by hydrothermal method with anthraquinone-1,8-disulfonate as the anionic ligand. The complexes also comprise K+ ions that participate into coordination to
Assembly of a Hexameric Cluster of Polyoxomolybdotriphosphonate Builts from [Zn(H2O){TeMo6O21}{N(CH2PO3)3}]6-Subunits and Its Optical and Catalytic Properties
Kong, Hui,Li, Keli,Liu, Siyu,Ma, Pengtao,Niu, Jingyang,Wang, Jingping,Wang, Yaqiong,Xu, Qian
, p. 15759 - 15767 (2021/10/20)
The crown-shaped organotriphosphonate-modified 36-molybdenum cluster (NH4)18Na7H11[Zn(H2O)TeMo6O21{N(CH2PO3)3}]6·23H2O (1) has been synthesized, which is the largest zinc-containing organophosphonate-based polyoxometalate to date. Compound 1 was prepared in buffer solution (pH 5.5) with heptamolybdate and amino trimethylene phosphonic acid (ATMP) as the organic ligand. The polyanion constructed from a hexmeric assembly of [Zn(H2O){TeMo6O21}{N(CH2PO3)3}]6- subunits has been fully investigated by a few characterization methods. In this work, we discovered that 1 exhibited reversible photochromism and it changed from white to reddish brown upon UV irradiation. In addition, compound 1, as a catalyst, can oxidize sulfides to sulfoxides, showing a high yield/conversion and a good selectivity.
Alloxan-catalyzed biomimetic oxidations with hydrogen peroxide or molecular oxygen
Zhang, Shiqi,Li, Guangxun,Li, Ling,Deng, Xiongfei,Zhao, Gang,Cui, Xin,Tang, Zhuo
, p. 245 - 252 (2019/12/24)
Inspired by biological flavin catalysis, the nonionic alloxan derivatives were applied as the biomimetic catalysts for various oxidations, catalyzing oxidations of sulfides and amines with hydrogen peroxide or molecular oxygen under mild conditions with high yields in a short time. The whole catalytic cycle has been verified to be a biomimetic approach through the formation of the alloxan hydroperoxide reactive intermediate. Additionally, encouraging asymmetric catalytic results have been obtained with an easily prepared chiral alloxan in a sulfoxidation reaction.
Emodinas a novel organic photocatalyst for selective oxidation of sulfides under mild conditions
Li, Min,Lou, Jiangli,Rao, Yijian,Yuan, Zhenbo,Zhang, Yan
, p. 19747 - 19750 (2020/06/04)
Herein, we have developed naturally-occurringEmodin, which is commercially available at low-cost, as a novel organic photocatalyst for the first time.Emodinwas successfully employed in the selective oxidation of sulfides promoted by visible-light, deliver
A Lacunary Polyoxovanadate Precursor and Transition-Metal-Sandwiched Derivatives for Catalytic Oxidation of Sulfides
Wan, Rong,He, Peipei,Liu, Zhen,Ma, Xinyi,Ma, Pengtao,Singh, Vikram,Zhang, Chao,Niu, Jingyang,Wang, Jingping
, p. 8760 - 8766 (2020/05/25)
A SeO3-centered lacunary Keggin-type heteropolyoxovanadate (hetero-POV) K6H2[SeV10O28(SeO3)3]?14 H2O (1) was isolated by one-pot reaction of KVO3 and SeOsu
Visible-Light-Responsive Anthraquinone Functionalized Covalent Organic Frameworks for Metal-Free Selective Oxidation of Sulfides: Effects of Morphology and Structure
An, Guangyu,Bai, Guoyi,Lan, Xingwang,Li, Qing,Ricardez-Sandoval, Luis,Wang, Zhenguang
, p. 6664 - 6675 (2020/07/16)
Visible-light-responsive covalent organic frameworks (COFs) as photocatalysts for metal-free organic reactions are highly desirable due to their structural controllability and molecular functionality. In this study, we describe the fabrication of an anthr
