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Phosphinoferrocene ligands with polar amide substituents
Charvátová, Hana ; Štěpnička, Petr (advisor) ; Trávníček, Zdeněk (referee) ; Jambor, Roman (referee)
Title: Phosphinoferrocene ligands with polar amide substituents Author: Hana Charvátová Department: Department of Inorganic Chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D. Abstract: This thesis is focused on phosphino-urea ferrocene ligands that are still rather neglected in the literature. It describes the synthesis of novel polar amides and hydrazides of 1'-(diphenylphosphino)ferrocene-1-carboxylic acid (Hdpf) with or without ethylene linker bearing various urea and guanidine terminal functional groups. Urea and guanidine derivatives with ethylene bridge can be prepared from Hdpf and appropriate amine with amidation agents. Phosphine ureas without the linker are accessible from reactions of primary amide of Hdpf with suitable acylation agents while analogical guanidine is obtained from guanylation of amide-amine generated from Hdpf acylbenzotriazole and ethylenediamine. Reaction of the acylbenzotriazole with free guanidine leads to [1-(diphenylphosphino)ferrocenecarbonyl]guanidine hydrochloride. These ferrocene ligands were used to prepare four types of palladium(II) complexes, viz. where L denotes the newly synthesized ligands and LNC is 2- [(dimethylamino)methyl]phenyl-C,N auxiliary chelating ligand. Catalytic efficiency of complexes with ethylene bridge was tested on reactions of aromatic...
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Preparation of titanium and zirconium metallocene complexes with pendant nitrile groups
Večeřa, Miloš ; Štěpnička, Petr (advisor) ; Vojtíšek, Pavel (referee)
Preparation of metallocene complexes of titanium and zirconium with pendant nitrile groups Miloš Večeřa bachelor thesis Abstract: Two cyclopentadienide salts with pendant nitrile groups were prepared in the form of their corresponding lithium salts and these salts were utilized for the preparation of titanium and zirconium metallocene complexes. One of the ligands was already described in the literature, while the other as well as all the prepared group 4 metallocene complexes are new compounds. Starting materials for these syntheses were 6,6-dimethylfulvene and spiro[2.4]hepta-4,6-diene which, upon a nucleophilic attack by 2-lithio-2-methylpropanenitrile, afforded the corresponding substituted lithium cyclopentadienides, which were characterized by 1 H and 13 C NMR spectroscopy and infrared spectroscopy. Then lithium salts were reacted with Cp*TiCl3 and Cp*ZrCl3 to give the corresponding metallocene dichlorides. Solid-state structures of the prepared titanocene dichlorides were elucidated by means of single crystal X-ray diffraction analysis. The obtained structures allowed a comparison with the known structures of the previously prepared homologous derivative. Unfortunately the corresponding zirconocene dichlorides did not crystallize. Moreover, all the newly prepared metallocenes were characterized by 1...
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Synthesis, characterization and catalytic application of novel zeolites
Eliášová, Pavla ; Čejka, Jiří (advisor) ; Štěpnička, Petr (referee) ; Mintova, Svetlana (referee)
The PhD thesis concerns the synthesis of novel zeolite materials, investigation of their properties and their possible use in catalytic application. The work was focused on the two- dimensional zeolites. The thesis was worked out at the Department of Synthesis and Catalysis at J. Heyrovský Institute of Physical Chemistry, AS CR. Germanosilicate UTL (Si/Ge molar ratio 4.0-6.5) was found to undergo unique structural changes in the neutral or acid environment leading to transformation of its three-dimensional framework into two-dimensional layered material denoted IPC-1P. The UTL degradation, so called top-down synthesis, was enabled due to a presence of double-four-units (D4Rs), which can be seen as supporting units/pillars between the rigid layers. The preferential location of Ge in D4Rs makes the units an ideal target for their selective degradation. The interlayer space in lamellar IPC-1P was modified by swelling with long-organic chain surfactant (material IPC-1SW). To keep the interlayer space permanently expanded (up to 3.3 nm) the silica amorphous pillars were subsequently introduced (material IPC-1PI). The integrity of the layers and their preserved UTL character was confirmed in all members of IPC-1 family by HRTEM and electron diffraction measuring. The layers of IPC-1P were condensed back...
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Salts of 2-aminoethanol and ferrocene-based acids
Zábranský, Martin ; Štěpnička, Petr (advisor) ; Němec, Ivan (referee)
Combination of the compact but sterically flexible ferrocene scaffold with intermolecular binding potential and conformational variability of (2-hydroxyethyl)ammonium structural motif was utilised in the construction of solid crystalline materials. Crystallisation in systems containing ferrocenecarboxylic, 2-ferrocenylacetic, 3-ferrocenylpropionic, 3-ferrocenyl- acrylic, 3-ferrocenylacrylic, 3-ferrocenylpropiolic, ferrocene-1,1'-dicarboxylic or ferrocene- sulfonic acid with 2-aminoethanol afforded crystals of the corresponding salts. The resulting crystalline products were characterised with the usual methods (proton nuclear magnetic resonance, infrared spectroscopy, elemental analysis) and their crystal structures were determined by means of single-crystal X-ray diffraction analysis. The crystal structures of the salts mentioned above usually contain rather complicated two dimensional networks of charge-assisted hydrogen bonds. With the aim of studying potentially more simple hydrogen-bonded structures, additional crystallisation experiments were conducted in systems of ferrocenecarboxylic acid and 2-(methylamino)ethanol or 2-(dimethylamino)ethanol. These experiments yielded simple salt of the former amine and adducts of salts of both bases with ferrocenecarboxylic acid in the ratio of 1:1. The...
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Orgonophosphorus analogues of triphosphate
Šrein, Jakub ; Kubíček, Vojtěch (advisor) ; Štěpnička, Petr (referee)
Two substances were prepared in this work, both with PCPCP structure motif. The motif is similar to ATP molecule, although the oxygen bridges are replaced with methylene groups. Both compounds were characterized by mass spectrometry and NMR spectroscopy. Since bis(methylenephosphonato)phosphinate is soluble in water, four pKa values were determined. Both prepared compounds have potential to serve as chelating ligands. Powered by TCPDF (www.tcpdf.org)
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Polar ligands derived from a phosphinoferrocene hydrazide
Vašíček, Tomáš ; Štěpnička, Petr (advisor) ; Schulz, Jiří (referee)
Title: Polar ligands derived from a phosphinoferrocene hydrazide Author: Tomáš Vašíček Institution: Faculty of Science, Charles University in Prague, Department of Inorganic Chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D. This thesis describes the syntheses of three new ligands derived from a phosphinoferrocene hydrazide, namely 1'-(diphenylphosphino)ferrocene-1-carbohydrazide. The reaction conditions were optimized by varying the reaction time and temperature in order to achieve high yields and purity of the products. Newly prepared compounds that bear extended polar groups were characterized by NMR spectroscopy, mass spectrometry, infrared spectroscopy and by elemental analysis. Additionally, the molecular structure of 1'-(diphenylphosphino)-1- {[2-(aminocarbonyl)hydrazino]-carbonyl}ferrocene (8) was determined by X-ray diffraction analysis. Key words: Ferrocene, Phosphines, Hydrazides
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Synthesis of a ferrocenyl-substituted bicyclic phosphite
Bárta, Ondřej ; Štěpnička, Petr (advisor) ; Kubíček, Vojtěch (referee)
Title: Synthesis of a ferrocenyl-substituted bicyclic phosphite Author: Ondřej Bárta Institution: Faculty of Science, Charles University in Prague, Department of Inorganic Chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D. This thesis describes the synthesis of a novel bicyclic phosphite ester, {N-(2,6,7-trioxa-1-phosphabicyclo[2.2.2]oct-4-yl)carbamoyl}ferrocene (3). This compound was obtained by the reaction of phosphorus trichloride with the appropriate tris(hydroxymethyl)methyl-amide in the presence of triethylamine or pyridine. The reaction conditions were optimized by varying the solvent, reaction temperature and the base to achive the highest possible yield of the product and to enable its easy and effective chromatographic purification. A new compound, 2-ferrocenyl-4,4-bis(chloromethyl)-4,5-dihydro-1,3-oxazol (4), was isolated as the by-product of this reaction. Compound 3 was further used to prepare the carbonyl complex cis-[W(CO)4(3-κP)2] (5). All the newly prepared compounds were characterized by NMR spectroscopy, mass spectrometry, infrared spectroscopy and by elemental analysis, and their molecular structures were determined by X-ray diffraction analysis. Hydrogen bonds are cooperating to form one-dimensional chains in the crystals of phosphite 3 and solvate 4 × ½ H2O or...
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Synthesis and characterization of ferrocenylated amidophosphine
Horký, Filip ; Štěpnička, Petr (advisor) ; Kubíček, Vojtěch (referee)
Title: Synthesis and characterization of ferrocenylated amidophosphine. Author: Filip Horký Department: Department of Inorganic chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D. Abstract: Complexes with amidophosphine donors have found interesting applications in catalysis and in medicinal chemistry. This led us to synthesize {[(2-(diphenylphosphino) ethyl)]-amino]carbonyl}ferrocene (compound 1) and the corresponding phosphine oxide (compound 2). This work describes three new synthetic routes to the target amidophosphine 1. The first one is a simple reaction of ferrocenecarboxylic acid with 2-(diphenylphosphino)ethylamine with reagents mediating amide bond formation. The second approach is based on the reaction of the mentioned amine with the respective acylbenzotriazole. Finally, the third way makes use of the reaction between the amine and an active ester, pentafluorophenyl ferrocencarboxylate. All products and intermediates were characterized by NMR spectra. The newly prepared phosphine oxide 2 was further characterized by infrared spectroscopy, elemental analysis, mass spectrometry and its crystal structure was determined by single-crystal X-ray crystallography. Keywords: ferrocene ligands, ferrocene, phosphine, amide, phosphineoxide, synthesis.
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