首页> 外文OA文献 >Synthesis and characterization of novel organometallic chromium hexacarbonyl derivatives via ligand (L) substitution, where L = tris (3-methylphenyl) arsine, tris (M-fluorophenyl) phosphine and tris 3, 5-Bis (trifluoromethyl) phenyl phosphine
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Synthesis and characterization of novel organometallic chromium hexacarbonyl derivatives via ligand (L) substitution, where L = tris (3-methylphenyl) arsine, tris (M-fluorophenyl) phosphine and tris 3, 5-Bis (trifluoromethyl) phenyl phosphine

机译:通过配体(L)取代合成和表征新型有机金属六羰铬铬,其中L =三(3-甲基苯基)a,三(M-氟苯基)膦和三3,5-双(三氟甲基)苯基膦

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摘要

The aim of the research study is to substitute the carbonyl ligand on chromium complexes in order to result in novel organometallic monocrystal compounds for crystal structure elucidation followed by physical and chemical characterization. Derivatives of Chromium Carbonyl are prepared by reaction with a number of tertiary phosphines and arsenic ligands which have the potential to result in novel organometallic compounds. Three different ligands were used to produce novel organornetallic monocrystal compounds which are Tris(3-methylphenyl)Arsine, udTris(m-flurophenyl)Phosphine, and Tris[3 ,5-bis(trifluoromethyl)phenyl]Phosphine. Of these, the substitution reaction using Tris(m-fluorophenyl)Phosphine resulted in the formation of crystals with pale yellow colour. Monocrystal x-ray diffraction on a resulted in the novel crystal structure determined as trans-Tetracarbonylbis[tris(3fluorophenyl)phosphane]chromium(0) with molecular formula Cr(C 1 8H12F3P)2(CO)4. udInfrared Spectroscopy (IR) and Nuclear Magnetic Resonance (NMR) further compliment the X-ray diffraction results. In this novel structure, the Cr atom is octahedrally coordinated by four carbonyl ligands and two tertiary phosphanes, which are located trans to each other with a fluorine atom in the meta-position on each phenyl ring. The compound crystalises in the monoclinic system with space udgroup P2 1 /c and with an average Cr-P bond length of 2.3327 A and average Cr-CO bond length of 1.8869 A. This final year project meets international standards and led to an International Union of Crystallography (1UCr) journal publication, specifically in Acta Crystallographica Section E; (2011) with the title trans-Tetracarbonylbis [tris(3-fluorophenyl) phosphane]chromium(0).
机译:该研究的目的是取代铬络合物上的羰基配体,以便产生新颖的有机金属单晶化合物,以阐明晶体结构,然后进行物理和化学表征。羰基铬的衍生物是通过与许多叔膦和砷配体反应制得的,这些叔膦和砷配体有可能产生新型有机金属化合物。使用了三种不同的配体来生产新颖的有机金属单晶化合物,即Tris(3-甲基苯基)砷化氢, udTris(间氟苯基)膦和Tris [3,5-双(三氟甲基)苯基]膦。其中,使用三(间氟苯基)膦进行的取代反应导致形成浅黄色晶体。在上进行单晶X射线衍射,得到了新颖的晶体结构,确定为分子式为Cr(C 1 8H12F3P)2(CO)4的反式四羰基双[三(3氟苯基)膦]铬(0)。红外光谱(IR)和核磁共振(NMR)进一步补充了X射线衍射结果。在这种新颖的结构中,Cr原子由四个羰基配体和两个叔膦八面体配位,它们在每个苯环的间位与氟原子相互反位。该化合物在单斜系统中结晶,空间为 udgroup P2 1 / c,平均Cr-P键长为2.3327 A,平均Cr-CO键长为1.8869A。该最后一年的项目符合国际标准,导致了国际化。晶体学联盟(1UCr)期刊出版物,特别是《晶体学报》 E节; (2011),标题为反式-四羰基双[三(3-氟苯基)膦]铬(0)。

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