Abstract – In this Research paper a new Schiff base ligands like HMAPPTH (p-Toulic hydrazone and 2-hydroxy, 4-methoxy acetophenone Schiff base), and RAPPTH (p-Toulic hydrazone and Resacetophone Schiff base) and its vanadium metal complexes have been synthesized and characterized by various physio chemical techniques & methods like FT-IR, H1-NMR, UV-Visible, ESR, VSM, Molar conductance, XRD and micro analytical data and biological activity studies. Key words - Schiff base, antibacterial activity, Vanadium (IV), HMAPPTH and RAPPTH. I.INTRODUCTION Schiff bases are very important today because its play an important role in chemistry and all interdisciplinary subjects. Schiff base and their metal complexes have been found to posses important …show more content…
The whole mixture was transferred into 250 ml round bottom flask. The mixture was refluxed about 2 hours on water bath. When the reaction mixture was allowed to cool yellow crystals were obtained. The compound was recrystalized from ethanol. The % of yield was 78% and melting point of the compound was 190 - 192 0C. Scheme 2: Synthesis of p-toluic hydrazide and 2-hydroxy-4 mehoxy Acetophenone Schiff base B. Synthesis of RAPPTH & HMAPPTH - V (IV) Schiff base Metal Complexes: The reagent p-Toluic hydrazide and Resacetophenone (2,4 Dihydroxyacetophenone) Schiff base was dissolved in 40ml of 50% methanol and V (IV) metal ions dissolved in 20ml of distilled water, this compounds mixture was stirred for 6 hours in the presence of sodium acetate. Orange red color metal complex (RAPPTH) was formed with good yield. This product washed several times with hot water and cold methanol to free from un reacted metal slats and ligand respectively and finally with ether and dried in vacuo over calcium chloride …show more content…
The thermo analytical data is summarized in Table.1. The thermal decomposition proceeds in three stages. The RAPPTH & HMAPPTH-V (IV) metal complexes are thermally stable up to 66 and 720C respectively. In the first stage loss of two water molecules occur in the temperature range 60-130oc and 72-110oC respectively for RAPPTH & HMAPPTH (IV) complexes by decomposition corresponds to endothermic dehydration. The intermediates are stable up to 230 and 2100c.The second decomposition with exothermic peak by the loss of ligand moiety occurs in the temperature range 230-583oc and 210-550oC. The solid residues above 600, and 5500C were recognized as vanadium metal oxides respectively for RAPPTH & HMAPPTH-V (IV). The final products are metal oxides in all the metal complexes.The molar conductance data of complexes which was carried out in DMF at10-3. The molar conductance values are 6.00 and 6.48 ohm-1 cm2 mol-1 respectively for RAPPTH & HMAPPTH-V (IV).These values suggest non-electrolytic nature of the present
There were four steps, or reactions, where we measured the change in enthalpy. Step 1: Mg(OH)2(s) Mg(OH)2(slurry) Step 2:2H3C6H5O7(s) +Mg(OH)2(slurry)Mg3(C6H5O7)2 (aq) + 6H2O (l) Step 3:H3C6H5O7(s)H3C6H5O7(aq) Step 4:2H3C6H5O7(aq)
Al(s) wire was placed in the solution from the last step and 5 drops of HCl along with a stir bar was added to the beaker and this was stirred on the hot plate. Cu(s) precipitate formed on the wire and the solution turned from clear to cloudy until it eventually become a brownish red color. When the reaction was complete the Al(s) wire was scraped with the stirring rod to get off any residual Copper product. All of the reactions except for reaction 3 were exothermic. This is because each reaction gave
Diels-Alder Reaction: Synthesis of 9, 10 dihydroanthraceno-9, 10-endo-α,β-succinic anhydride Introduction: For this experiment, a Diels-Alder reaction was performed. The concept of this reaction involves two compounds, one of which is an electron donating group and the other is an electron withdrawing group (Weldegirma). These two compounds are referred to as the diene and dienophile respectively (Weldegirma). The conditions for this reaction to take place generally require a fair amount of heat and the reaction is also stereoselective (Diels-Alder).
In the empirical data above the mean percentage of water in the iron salt crystal was 6.27%. The mean percentage of the potassium ion was determined to be 17.81%. For the iron ion the mean percentage was 12.20% and the average percent for oxalate was 57.20%. The total percentage of the mean adds up to 97.28%. The empirical formula using the means provided created the formula K2Fe(C2O4)3
During this last semester in American Literature, I unequivocally believe that I deserve a solid A. (claim) From the consistent punctuality of assignments, to the effort of sustained attention to class, I have reached an educational pursuit within your classroom, strengthening my writing capabilities. I have grown not only as a student but as a person, exploring the different parts of literature such as transcendentalism (Thoreau/Emerson and Into the Wild), American tragedies (The Crucible), dramas (The Miracle Worker), and even a picaresque novel (The Adventures of Huckleberry Finn). I have accomplished many things this year, gained some of my best grades yet, and produced deep insight regarding multiple topics throughout. Since the beginning
There are several different reactions that can be used to synthesize an alkene product, however the main reaction being utilized for this experiment is the Wittig reaction and the Horner-Wadsworth-Emmons modification. The Wittig reaction involves a reaction between an aldehyde or ketone and ylid, which is also referred to as the Wittig reagent. The Wittig reagent is synthesized from a phosphonium salt and a strong base (Wittig Reaction, 2006). The reaction between the Wittig reagent and the ketone or aldehyde is a nucleophilic substitution; the carbon double bonded to the oxygen in the carbonyl is replaced with a carbon double bonded to another carbon (University of Liverpool, 2008).
Purpose: The purpose of this experiment was to determine the molar mass of unknown #43 using the derived freezing point depression. To obtain the freezing point depression, t-butyl alcohol was placed in a cold-water bath and frozen solid for a total of two runs. Then, unknown #43 was dissolved in t-butyl alcohol and placed in a cold-water bath until frozen solid. This process was repeated for a total of three runs, with the first two runs containing half of the unknown, and the last run containing the full amount of unknown.
Standard N is connected to synthesis 3-4, because we wrote a story about a song that had to include all of the standards points. The assignment that I wrote was to write a story about a song of my choice so I had to create a setting, situation, problem, one or more points of view, and introducing characters. This standard helped me understand how to write correctly and to show my strong and weak points. Therefore, It will help me grow in my literary knowledge and my writing skills for a job interview. I think that I did fairly well on this standard, but I need to work on my punctuation skills, and my tense usage.
The purpose of this experiment is to perform a two step reductive amination using o-vanillin with p-toluidine to synthesize an imine derivative. In this experiment, 0.386 g of o-vanillin and 0.276 g of p-toluidine were mixed into an Erlenmeyer flask. The o-vanillin turned from a green powder to orange layer as it mixed with p-toludine, which was originally a white solid. Ethanol was added as a solvent for this reaction. Sodium borohydride was added in slow portion as the reducing agent, dissolving the precipitate into a yellowish lime solution.
The purpose of this experiment is to perform a Friedel-Crafts reaction of ferrocene. Friedel-Crafts reactions are examples of electrophilic aromatic substitution reactions in which the electrophile is a carbocation or an acylium ion. These reactions form a carbon-carbon bond and allows for either an alkyl or acyl group to be substituted onto an aromatic ring. Figure 1 shows the general mechanism for the Friedel-Crafts acylation of benzene. First, the alkyl halide reacts with a strong Lewis Acid catalyst, usually aluminum chloride, to form a complex, which will then lose the halide to the Lewis acid to give the electrophilic acylium ion.
Next, the oxygen is protonated from the 3-nitrobenzaldehyde, which is then followed by an elimination reaction where this acts as a leaving group. The product is the trans-alkene present in the product. After the reaction was completed, purification of the product was conducted using semi-microscale recrystallization.
Introduction The purpose of this week’s lab was to enhance our understanding of the Grignard reagents that were examined in lecture. In this lab, a Grignard reagent will be prepared through the reaction of magnesium turnings and bromobenzene. Instead of isolating the product it will then be combined with benzophenone, which will give the final product of triphenylmethanol. Procedure
For this lab we performed an electrophilic aromatic substitution through the nitration of methyl benzoate. Aromatic compounds can and do react with electrophiles under vigorous reaction conditions and in a presence of a catalyst. The stability of aromatic compounds is a result of resonance. Aromatic compounds only react with powerful electrophilic reagents and elevated temperatures because aromatic electrons are less reactive in addition reactions as formation of a carbocation intermediate entails loss of resonance stabilization. The nitration of methyl benzoate to synthesize methyl m-nitrobenzoate is an example of an electrophilic aromatic substitution because a nitro group is substituted for a proton on the aromatic ring.
As humans we live for our dreams and aspirations, yet we know so little about their biological purpose and function. The neural basis of dreaming is an enigma that many scientists have pondered over for centuries. From Plato and Aristotle’s theory of consciousness to Sigmund Freud’s hypothesis that dreaming is essentially a safety valve for our unconscious desires, numerous theories have made their way into the medical journals. Today, however, scientists tend to generally support one of these two surprisingly contrasting theories; activation synthesis and threat simulation. Activation Synthesis describes that (insert definition of activation synthesis).
This MMT was used as such without any further purification. Tri-Octyl Amine(TOA) was the product of Tokyo Chemical Industry Co., Ltd. Japan, which had a purity of about 98% and was procured from Sigma Aldrich. The molecular formula of TOA was C24H51N. It was used without any further purification. Copper sulphate solution was prepared by dissolving CuSO4 unhydrated in distilled water. Hexane, Hydrochloric acid, Methaol, Ammonium Chloride, Ammonia were used from laboratory.