1996-67-4Relevant articles and documents
Synthesis, nucleation, growth, structural, spectral, thermal, linear and nonlinear optical studies of novel organic NLO crystal: 4-fluoro 4-nitrostilbene (FONS)
Dinakaran, Paul M.,Kalainathan
, p. 509 - 515 (2013)
A novel organic nonlinear optical material 4-fluoro 4-nitrostilbene (FONS), with molecular formula (C14H10FNO2) has been synthesized. Using ethyl methyl ketone as solvent, the synthesized material has been repeatedly recrystallized to minimize the impurities and good optical quality single crystals were harvested by slow evaporation method. Single crystal X-ray diffraction analysis reveals that the grown FONS crystal belongs to monoclinic system with noncentrosymmetric space group P2 1 . The powder X-ray diffraction pattern of FONS has been recorded. Functional groups of the title compound were confirmed by FTIR and the molecular structure was confirmed by 1H NMR. The UV-vis-NIR absorption study reveals no absorption in the visible region and the cut-off wavelength was found to be at 408 nm. Optical band gap (Eg) of the grown crystal was found to be 3.27 eV and also the optical constants were determined. Thermal behaviour of the FONS has been studied by TGA/DTA analyses. From the mass spectrum, the ratio of compound formation of FONS was analyzed. The NLO property has been confirmed by Kurtz and Perry powder SHG technique and the SHG efficiency of FONS (262 mV) crystal was found to be 12 times greater than that of KDP (21.7 mV).
Immobilized Pd on Eggshell Membrane: A powerful and recyclable catalyst for Suzuki and Heck cross-coupling reactions in water
Wu, Shang,Jiang, Hongyan,Zhang, Hong,Zhao, Lianbiao,Yuan, Peilin,Zhang, Ying,Su, Qiong,Wang, Yanbin,Wu, Lan,Yang, Quanlu
, (2020/09/09)
A stable heterogeneous palladium catalysts, the waste eggshell membrane (ESM) anchored Pd complex, was synthesized by a simple and green technique. The catalyst obtained can display an outstanding catalytic activity for Suzuki and Heck coupling reactions in water media. The reactions of various aryl halides with aryl boronic acids and terminal alkenes provided the corresponding products in moderate to excellent yields. More importantly, this novel and efficient catalyst with high stability can be easily reused for at least twelve times with no decrease of the catalytic activity, performing an endurable and wide tolerance of the substrates. Facile synthesis, high catalytic activity, and recyclability make these catalysts interesting for further studies.
Heck, Sonogashira, and Hiyama reactions catalyzed by palladium nanoparticles stabilized by tris-imidazolium salt
Planellas, Marc,Moglie, Yanina,Alonso, Francisco,Yus, Miguel,Pleixats, Roser,Shafir, Alexandr
supporting information, p. 3001 - 3008 (2014/05/20)
Palladium nanoparticles, prepared by the hydrogenation of Pd(dba) 2 in the presence of a tris-imidazolium iodide as stabilizer, act as an efficient catalyst for Heck and copper-free Sonogashira reactions with a range of aryl iodides and bromides at 0.2 mol-% Pd loading. Moreover, we describe a convenient protocol for the fluoride-free Hiyama coupling of vinylsilanes with aryl iodides that involves the use of sodium hydroxide as promoter in a methanol/water mixture. Under the developed conditions, one-pot, double Heck and Hiyama-Heck reactions are successfully achieved.
