Synthesis and Structural Properties of Some Novel Quadridentate Schiff Base Ligands, Their Transition Metal Complexes and Precursor 1,5-diaryl-2,4-pentanediones PDF Download
Are you looking for read ebook online? Search for your book and save it on your Kindle device, PC, phones or tablets. Download Synthesis and Structural Properties of Some Novel Quadridentate Schiff Base Ligands, Their Transition Metal Complexes and Precursor 1,5-diaryl-2,4-pentanediones PDF full book. Access full book title Synthesis and Structural Properties of Some Novel Quadridentate Schiff Base Ligands, Their Transition Metal Complexes and Precursor 1,5-diaryl-2,4-pentanediones by Juha Pulkkinen. Download full books in PDF and EPUB format.
Author: Juha Pulkkinen
Publisher:
ISBN: 9789517810807
Category :
Languages : en
Pages : 47
Get Book Here
Book Description
Author: Juha Pulkkinen
Publisher:
ISBN: 9789517810807
Category :
Languages : en
Pages : 47
Get Book Here
Book Description
Author: Sali Nabeel Hanna Jabrou
Publisher:
ISBN:
Category : Actinide elements
Languages : en
Pages : 191
Get Book Here
Book Description
Over recent years a great deal of interest has developed in new transition metal complexes of Schiff base ligand. The preparation of new ligand is the most important step in the development of metal complexes that exhibit unique properties and novel reactivity. The electron donor and electron acceptor properties of the ligand, the structural function groups and the position of the ligand in the coordination sphere, together with the reactivity of coordination compounds may be the factor for different studies. The synthesis and structural investigations of Schiff bases and their metal complexes are a considerable center of attention because of their potentially beneficial pharmacological properties and a wide variation in their mode of bonding. Metal coordination complexes have a wide variety of technological and industrial application, ranging from catalysis to anticancer drugs. In these compounds the metal atom itself may have a number of roles, based on its coordination geometry, oxidation state, and magnetic electronic and photochemical behaviors. This study presents the synthesis, characterization, and structural studies of different series of Copper and Uranium complexes of salicylaldehyde Schiff base derivatives with various organic amine compounds. The Schiff bases act as neutral and bidentate ligands, which can attach the metal through the azomethine nitrogen and furfural oxygens. These Schiff bases are prepared by iii reacting salicylaldehyde with various organic amines. In the case of most complexation reactions, highly colored precipitates were formed immediately. The complexes were found to have composition ML2 and M2L2, where M is the metal and L the organic ligand. This implies "mononuclear" structures with one metal + 2 ligands, and "binuclear" where the ligands hold two metal atoms in close proximity. The interesting molecular and crystal structural features of the Schiff base ligand called E-2-((benzo[d]thiazol-2-ylimino)methyl)phenol and its Cu(II) complex are presented in Chapter 2. Further investigations on the coordination chemistry of the Schiff base ligands are made by reacting these ligands with copper and uranium, described in Chapter 3. Another series of dicopper(II) complexes and diuranium complex of the Schiff base ligands, containing azomethine nitrogen and furfural oxygen donor group are investigated to evaluate the role of alkoxo bridge on the structures. Making the compounds with two uranium atoms leads to very high molecular weight, as a path to the highest molecular weight liquid crystal. This lays the pathway to future work for making those crystals. These dinuclear complexes are presented in chapter 4. The objective of the present study is to investigate the coordination chemistry of these ligands with Copper and Uranium. For the ligands this was done by a combination of nuclear magnetic resonance spectroscopy, infrared spectroscopy, ultraviolet-visible spectroscopy and single X-ray crystallography. The metal complexes were analyzed by the same techniques, except that in the case of uranium, all efforts to obtain single crystal for X-ray crystallography proved unsuccessful, so the molecular structure had to be ascertained from the other techniques.
Author: Dr. S. N. Battin
Publisher: Lulu.com
ISBN: 0359913911
Category :
Languages : en
Pages : 282
Get Book Here
Book Description
Author: Takashiro Akitsu
Publisher: BoD – Books on Demand
ISBN: 1803556781
Category : Science
Languages : en
Pages : 210
Get Book Here
Book Description
A Schiff base (imine -N=CH-) is a part of a popular group of organic compounds prepared form primary amines and aldehyde. Many studies have been carried out on Schiff bases not only as organic compounds but also as ligands for metal complexes. In this context, this book provides a comprehensive, interdisciplinary review of Schiff base compounds, with an emphasis on the latest advances. It compiles research results, commentary, reviews, and more dealing with preparation, spectroscopy, crystallography, (asymmetric) synthetic roles, physical properties (magnets, optics, etc.), computational chemistry, and theoretical chemistry. The book focuses on Schiff base and its strong connection to organic chemistry, biochemistry, and polymer materials chemistry. It covers three topics: Schiff base of organic chemistry, Schiff base of inorganic chemistry, and Schiff base of functional or biological materials.
Author: Diane A. Dickie
Publisher:
ISBN:
Category :
Languages : en
Pages : 44
Get Book Here
Book Description
Author: Khalil Khalaf Abid
Publisher:
ISBN:
Category :
Languages : en
Pages :
Get Book Here
Book Description
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :
Get Book Here
Book Description
Nitrogen based monodentate and bidentate chelating ligands have captured a significant interest due to their ability to coordinate to a wide variety of elements. The â-diketimine, â-ketoiminato, formamidine, pyridineselenolate, and pyrazinecarboxamide ligands have all been employed in this study to further investigate the coordination preferences among main group and transition metals. Steric and electronic properties of these ligands can easily be altered by manipulating the substituents attached, thus leading to predictable structures with potential for many useful and significant applications. Investigations have shown that temperature, solvent, and metal halide employed are all key factors in the reaction outcomes. All of the complexes obtained throughout these studies have been characterized by X-ray crystallography along with other spectroscopic techniques, including NMR, IR, UV/Vis, and M/S. â-diketiminato ligands, [{N(R)C(Me)}2C(H)] where R = Dipp, Mes, commonly referred to as nacnac, have played an important role in the synthesis of novel pnictogenium complexes. Results show that through manipulation of the halide precursor, reaction stoichiometry, and the R substituent on the nacnac both N, N'- and N, C'-metal chelated complexes can be achieved. Additionally, â-ketiminato ligands, [RN(H)(C(Me))2C(Me)=O] where R = Dipp, and [RN(H)C(Me)CHC(Me)=O] where R = C2H4NEt2, have been studied. Both ligands were investigated with a range of d and p block metal halides and alkyls in order to compare and contrast the bulky, flexible, and even multi-dentate nature of each ligand. The preferred metal geometry remains constant for products with either ligand, but the steric protection offered by the individual ligands governs the nuclearity of the products, ranging from tetrameric cages to simple adducts. The formamidinate ligand, [RN(H)C(H)NR] where R = Dipp, was employed in synthesizing several aluminum and zinc complexes. In addition to their numerous applications as cata.
Author: Fatimah Alqahtani
Publisher:
ISBN:
Category :
Languages : en
Pages :
Get Book Here
Book Description
Author: Habu Nuhu Aliyu
Publisher:
ISBN: 9789785451733
Category :
Languages : en
Pages : 16
Get Book Here
Book Description
Author: Saikat Sarkar
Publisher:
ISBN:
Category : Electronic books
Languages : en
Pages : 0
Get Book Here
Book Description
The fabulous advancement of a large section of modern coordination chemistry depends upon different kinds of strategically designed and functionally tuned ligand systems; Schiff base ligands play a pivotal role among them. Such Schiff bases become more motivating when they are designed to be synthesized using very simple organic molecules. This paper reviews our work on a family of three functionally different types of Schiff base ligands, derived from diacetylmonoxime, which have been employed to synthesize mononuclear metal complexes with various binding modes of ligands and topologies around the metal centers. Such Schiff base ligands have been synthesized by reacting diacetylmonoxime with diethylenetriamine, 1,3-diaminopropane-2-ol, and morpholine N-thiohydrazide. The synthesized Schiff bases and the metal complexes of such ,Äúprivileged ligands,Äù show many interesting supramolecular coordination architectures involving different weak forces, e.g., H-bonding, C,ÄìH¬∑¬∑¬∑œÄ interactions, etc.
