Wednesday, May 15, 2019
Mixed metal and mixed ligand for tri-nuclear complexes Research Proposal
Mixed metal and mixed ligand for tri-nuclear complexes - Research Proposal ExampleThe first oddball involves trinuclear Au (I) pulls 3, 5-(CF3)2Pz Au3.6 (Bowmaker et al, 2014). Complexes involving synthesis of silver(I) and copper color(I) exist exhibiting the structures 3,5-(CF3)2PzAg3 and 3,5-(CF3)2PzCu3. The resultant effect is a copper complex that has a mixed vallent structure of 3, 5-(CF3)2Pz5Cu(II)2Cu(I).Cu2 dimer becomes available through treatment of 3,5-(CF3)2PzCu3 with 2,4,6- collidine which is of an appropriate amount. Bis(pyrazolyl)borate adduct Cu1 is a byproduct that originates from the synthesis of collidine, CuOTf and H2B(3,5-(CF3)2Pz)2K (Lalinde et al, 2014)The equivalent related adducts of Silver Ag1 and Ag2 underwent analogous procedures during their preparations. Various methods characterized their differing complexes which include roentgen ray crystallography. Cu1 and Cu2 have trigonal planar sites of copper (Miyake et al, 2014.In contrast to the feature, Ag 2 consists of Ag(u-N-N)2Ag unit that is found in half-boat conformation. The intermolecular distance between the Ag***Ag molecules is 3.5618A. Other crystals exist which feature Ag2 molecules comprising of flattened and boat hold in conformations (Beziau et al, 2013). It becomes important to observe that bis(pyrazolyl)borato components and complexes such as Ag1 are rare due to their ease of decomposition on silver metal (Zhou et al, 2014). Therefore, unique photophysical properties are highlighted for the mononuclear and dinuclear silver(I) and copper(I) complexes.Biswas, S., Saha, R., & Ghosh, A. (2012). Copper (II)Mercury (II) Heterometallic Complexes Derived from a Salen-Type Ligand A saucy Coordination Mode of the Old Schiff Base Ligand. Organometallics, 31(10), 3844-3850.Bowmaker, G. A., Hanna, J. V., King, S. P., Marchetti, F., Pettinari, C., Pizzabiocca, A., ... & White, A. H. (2014). Complexes of Copper (I) Thiocyanate with Monodentate
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