Font Size: a A A

Synthesis, Structure And Properties Of Schiff Base Complexes And Ternary Complexes

Posted on:2007-10-12Degree:MasterType:Thesis
Country:ChinaCandidate:W ZhangFull Text:PDF
GTID:2121360185953925Subject:Inorganic Chemistry
Abstract/Summary:PDF Full Text Request
Schiff-base and its transition metal complexes have significant antiviral and antibacterial activities. Heteropolymetallic complexes are in the active fields of research encompassing life science and material science, especially the research on heteropolymetallic coupling complexes is the base of design of molecular material science. Much work has been devoted to study the Schiff-base complexes containing phenolic oxygens as bridges. The Schiff bases derived from 3-formyl-2-hydroxybenzoic acid and diamines are binucleating ligands with coordinative selectivity, their complexes MM'L·nH2O have been studied extensively. If a methyl group were added to 3-formyl-2-hydroxybenzoic acid, the alkalescence and field intensity of the base ligands should be enhanced obviously, thus, the electron spinning, magnetic behavior and catalytic property of the complexes maybe changed obviously.In view of reasons above, we designed and synthesized 5-methyl-3-carboxyl–salicylaldehyde, its Schiff-base ligands and corresponding complexes. These compounds were characterized by single-crystal X-ray analysis, 1H NMR, 13C NMR, IR, UV-vis, etc. The main contents are described as following:(1) The complex [Cu(OS)]·H2O, where H2OS is the N,N'-bis(salicylaldehyde) ethylenediamine, was obtained through selfassembly. Its crystal structure has been determined by X-ray analysis. The crystal belongs to trigonal system, space group R-3, a=3137.41(2)pm, b=3137.41(2)pm, c=918.100(10)pm,γ=120°, Z=18, R1=0.0425, wR2=0.1042. The copper atom is in a planar coordination site of [N2O2] and it devites from the mean plane by only 0.80 pm. Byπ-πstacking interactions, a alabastrine structure was obtained.(2)Schiff-base complex [Cu(HGS)(H2O)]·H2O, where H3GS is the 3-carboxyl -salicylidene glycine, was synthesized and characterized by elemental analysis, IR spectra and single-crystal analysis. The crystal belongs to monoclinic system, space group P2(1)/c, a=848.46(3)pm, b=681.54(3)pm, c=1967.16(8)pm,β=95.8210(10)°, Z=4, R1=0.0279, wR2=0.0724. The copper atom is in a square-pyramidal field with the base...
Keywords/Search Tags:Synthesis,
PDF Full Text Request
Related items
Green chemistry in pyrrole synthesis. I. Solvent effect in Barton-Zard pyrrole synthesis: An improved synthesis of 3,4-dialkyl-1H-pyrrole-2-carboxylates. II. A novel route for the synthesis of pharmaceutically important pyrrole derivatives
Part I: Design, synthesis, and reactivity of 1-hydrazinodienes for use in organic synthesis Part II: Studies toward a synthesis of the antibiotic platensimycin
Manganese(III)-based oxidative cyclizations: Formal synthesis of 15-acetoxypallescensin A. Synthesis of hindered guanidines. Completion of the total synthesis of martinellic acid
Synthesis, Characterization And Luminescence Properties Of Environmental Functional Material β-NaYF4 Doped With Rare Earth
Part I: The total synthesis of (+/-)-securinine and (+/-)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids and Part II: The use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and
New methods and strategies for heterocycle synthesis: Progress toward the total synthesis of upenamide and the total synthesis of (+)-5-epiindolizidine 167B and indolizidine 223AB
Synthesis of side chain-modified iodothyronines. Synthesis and structure-activity relationships (SARS) of galanthamine derivatives. Total synthesis of (+)-valyldetoxinine. Synthesis and mechanism of cyclic acetal and ketal formation in pentono-1,4-lactone
The application of asymmetric catalysis to the synthesis of natural products: A total synthesis of (-)-tubulosine, progress towards a total synthesis of (+)-reserpine, and a total synthesis of (+)-peloruside A
Cyclobutanes in organic synthesis: Lewis acid-promoted ketene-alkene [2+2] cycloadditions, total synthesis of gracilioether F, and collaborative total synthesis of hippolachnin A
10 A ring-closing metathesis/Diels-Alder approach to the synthesis of the eunicellin diterpenes: Application to the total synthesis of ophirin B and partial synthesis of astrogorgin