In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Product Details of 27148-03-4, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 27148-03-4, name is Benzo[d]isothiazole-3(2H)-thione 1,1-dioxide. In an article£¬Which mentioned a new discovery about 27148-03-4
Zn thiosacharinates: From ionic to polymeric structures. Synthesis, characterization and cell proliferation inhibition studies
A series of Zn thiosacharinates complexes with nitrogen donor co-ligands were synthesized: [Zn(tsac)2(o-phen)], [Zn(tsac)2(TMDP)]n, [(4,4?-bipy)H2][Zn(tsac)4] [Zn(tsac)2(2,2?-bipy)], [Zn(tsac)2(2,2?-bquin)], (tsac, thiosaccharinate anion: 1,1-dioxo-1,2-benzisothiazole-3-thiolato, C7H4NO2S2?, o-phen: 1,10?-phenantroline, TMDP: trimethylenedipyridine, 2,2?-bipy: 2,2?-bipyridine, 4,4?-bipy: 4,4?-bipyridine, 2,2?-bquin: 2,2?-biquinoline). They were fully characterized by means of FTIR, 13C and 1H NMR, elemental analysis and conductivity measurements. Three of them, [Zn(tsac)2(o-phen)], [(4,4?-bipy)H2][Zn(tsac)4], [Zn(tsac)2(TMDP)]n were also characterized by X-ray single crystal diffractometry and their crystal structures are described herein. DFT geometry optimization for the [Zn(tsac)2(o-phen)] complex was performed and its vibrational spectra was predicted. Moreover, we studied the effects of the five complexes on cell proliferation, thus providing preliminary evidence for their therapeutic potential as anti-cancer drugs.
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Reference£º
Isothiazole – Wikipedia,
Isothiazole – ScienceDirect.com