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The synthesis and structural charact...

Texas Christian University., College of Science and Engineering.

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The synthesis and structural characterization of main group and transition metal complexes supported by nitrogen based ligands.

Record Type:	Electronic resources : Monograph/item
Title/Author:	The synthesis and structural characterization of main group and transition metal complexes supported by nitrogen based ligands./
Author:	Lesikar, Leslie Anne.
Description:	217 p.
Notes:	Adviser: Anne F. Richards.
Contained By:	Dissertation Abstracts International69-11B.
Subject:	Chemistry, Inorganic. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3336481
ISBN:	9780549898634

The synthesis and structural characterization of main group and transition metal complexes supported by nitrogen based ligands.
Lesikar, Leslie Anne.

The synthesis and structural characterization of main group and transition metal complexes supported by nitrogen based ligands. - 217 p.

Adviser: Anne F. Richards.

Thesis (Ph.D.)--Texas Christian University, 2008.

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 beta-diketimine, beta-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.

ISBN: 9780549898634Subjects--Topical Terms:

517253
Chemistry, Inorganic.

The synthesis and structural characterization of main group and transition metal complexes supported by nitrogen based ligands.
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020 $a 9780549898634
035 $a (UMI)AAI3336481
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040 $a UMI $c UMI
100 1 $a Lesikar, Leslie Anne. $3 1058658
245 1 4 $a The synthesis and structural characterization of main group and transition metal complexes supported by nitrogen based ligands.
300 $a 217 p.
500 $a Adviser: Anne F. Richards.
500 $a Source: Dissertation Abstracts International, Volume: 69-11, Section: B, page: 6793.
502 $a Thesis (Ph.D.)--Texas Christian University, 2008.
520 $a 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 beta-diketimine, beta-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.
520 $a beta-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.
520 $a Additionally, beta-ketiminato ligands, [RN(H)(C(Me))2C(Me)=O] where R = Dipp, and [RN(H)C(Me)CHC(Me)=O] where R = C2H4NEt 2, 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.
520 $a 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 catalysts, the smaller ligand backbone is capable of N,N'-chelation analogously to the beta-diketiminates and beta-ketiminato ligands, as well as a variety of other coordination modes. The stoichiometric ratio of ligand to the metal alkyl was emphasized for these reactions affording aluminum and zinc formamidinate complexes exhibiting monodentate, bidentate, and bridging coordination modes.
520 $a Lastly, the coordination of group 13 metal halides was investigated employing the pyridineselenolate, [HSe-2-NC5H4], and pyrazinecarboxamide, [(C4H3N2)CONH2], ligands. The research focused on the individual synthetic methods in the preparation of group 13 complexes.
590 $a School code: 0229.
650 4 $a Chemistry, Inorganic. $3 517253
690 $a 0488
710 2 $a Texas Christian University. $b College of Science and Engineering. $3 1029121
773 0 $t Dissertation Abstracts International $g 69-11B.
790 $a 0229
790 1 0 $a Hanna, Tracy A. $e committee member
790 1 0 $a Minter, David E. $e committee member
790 1 0 $a Neilson, Robert H. $e committee member
790 1 0 $a Richards, Anne F., $e advisor
791 $a Ph.D.
792 $a 2008
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3336481