صفحه اعضای هیئت علمی - دانشکده علوم
Professor
Update: 2025-03-03
Arash Mouradzadegun
دانشکده علوم / گروه شیمی
P.H.D dissertations
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طراحی، سنتز و شناسایی ساختارهای کربنی متخلخل دوپ شده با هترواتم مشتق شده از پلیمرهای آلی متخلخل بر پایه کلیکس [4] رزورسین آرن و بررسی فعالیت واکنش احیای اکسیژن و واکنش تولید اکسیژن
شیرین نری میسا 1403 -
سنتز و شناسایی کامپوزیت های دارای شبکه سه بعدی متخلخل بر پایه کلیکس[4] رزورسین آرن و بررسی فعالیت فتوکاتالیستی و جذب برخی آلاینده ها
اسیه شیخ زاده تك ابی 1401 -
طراحی، سنتز و شناسایی مشتقات پورفیرین متصل شده کوالانسی بر بستر شبکه سه بعدی پلیمر متخلخل بر پایه کلیکس [4]رزورسین آرن و بررسی فعالیت کاتالیستی آنها
شیدا حمید 1399 -
طراحی، سنتز و بررسی برخی کاربردهای کاتالیزوری و غیر کاتالیزوری پلیمر جدید نانو متخلخل دارای اتصالات عرضی فراوان، عامل دار شده با گروه های آمینی
مصطفوی-مهساالسادات 1396In this thesis first step, it was tried to produce an efficient magnetic phase-transfer catalyst on the basis of calix[4]resorcinarene through the addition of Fe3O4 nanoparticles for being used in the nucleophilic substitution of aryl halides. Successful catalyst formation was confirmed using various analytical techniques including: Infrared Spectroscopy (IR), X-ray diffraction (XRD), vibrating sample magnetometer (VSM) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and thermal gravimetric analysis (TGA). The prepared catalyst was successfully used in nucleophilic substitution reaction of aryl halides to produce benzyl cyanides and benzyl azides.
In fact, calixarene units in the polymeric matrix may provide stable bowl-shaped tetraphenolic structures which serve as the anionic host molecules for the incorporation of cations into the cavity by the electrostatic interactions. Moreover, the hydrophobic tail and hydrophilic upper rim of this readily accessible supramolecule make it suitable for standing in the organic-aqueous interfacial layer. The recoverability of the catalyst is in accordance with the aromatic-rich nature of this system, which makes it essentially insoluble in water.
In the project continuation, the addition of amine functionalities to the polymeric network on the basis of calix[4]resorcinarene and then the addition of other functionalities to this resulted structure and also its catalytic and noncatalytic applications were investigated.
In the second step of the project, a new and convenient approach for the functionalization of 3D-network polymer based on calix[4]resorcinarene was developed. According to this method, –NH2 moieties were grafted onto the polymeric surface ligand-functionalized organosilanes. The formation of polym-NH2 was confirmed using elemental analysis (CHN), atomic force microscope (AFM) and thermal gravimetric analysis (TGA). The remarkable advantages offered by this methodology are simple implementation, one-pot procedure and high loading of organic functional groups. Importantly, the reactions proceeded without the need for any additives such as acidic or basic catalysts.
In order to develop an efficient catalytic system for being applied in click reactions, it was tried to add Cu(Ӏ) moieties to the NH2-functionalized polymer. Successful synthesis of the catalyst was proved using various methods such as: Infrared Spectroscopy (IR), energy-dispersive X-ray spectroscopy (EDS) and atomic absorption spectroscopy (AAS). In addition, efficient synthesis of 1,2,3-triazole derivatives in the presence of this catalyst was another reason which proved that the catalyst was prepared in the right way. This environmentally friendly methodology offers several advantages including ease of manipulation and workup and also better control on copper ions toxicity through the easy isolation and reusability of the catalyst.
In the third step, the reaction of NH2-functionalized polymer with chlorosulfonic acid resulted in the synthesis of an efficient acidic catalyst for being used in multi-component reactions. The resulting catalyst was applied in the synthesis of various heterocycles including: 14-aryl-14H-dibenzo[a,j]xanthenes, 1,8-dioxo-octahydro-xanthenes, 2H-indazolo[2,1-b]phthalazine-triones and 2,4,6-triarylpyridines. The results revealed that the products were successfully obtained in high yields and short reaction times. As a matter of fact, the porosity of the polymeric support and also covalently anchored acidic moieties might indeed provide a synergistic means for the efficient approach of the starting materials to acidic sites, enough space for the reactants concentration and products preparation.
The cheapness and readily available starting materials, simple procedure coupled with easy catalyst isolation and reusability make this new and viable route attractive to both research and pharmaceutical development endeavors.
In the fourth step, it was tried to improve the NH2-functionalized porous polymer properties from the viewpoints of mechanical stability and electrical conductivity through the addition of nano-structured graphene oxide and graphene agents for the future purposes. The formation of these composites was examined via different spectroscopic techniques such as: Infrared Spectroscopy (IR), energy-dispersive X-ray spectroscopy (EDS), raman spectroscopy, atomic force microscope (AFM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and and thermal gravimetric analysis (TGA).
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طراحی و سنتز هتروسیکل های فعال بیولوژیک با استفاده از واکنشهای چند جزئی ایزوسیانید محور
شیما السادات دیانت 1394The aim of this thesis has been designing and synthesizing some new heterocycle derivatives with remarkable biological properties via isocyanide based multi component reactions (IMCRs). Some of them were investigated for their anti-inflammatory and anti-cancer activities.
In the first step of this project a series of 2-chloro-quinoline-based imidazopyridines and imidazothiazoles bearing a bulky alkylamine side chain were synthesized as 15-LOX inhibitors. The target compounds were prepared via one-pot reaction of 2-chloroquinoline-3-carbaldehyde, heteroaromatic amidine, and alkyl isocyanides in the presence of NH4Cl. All compounds showed significant anti-15-LOX activity (IC50 values ≤40 µM).
In the second section, the synthesized compounds in the first part were synthesized again in the presence of catalytic amounts of sulfamic acid-functionalized γ -Fe2O3 nanoparticles encapsulated by hydroxyapatite (denoted as [γ -Fe2O3-HAp-(CH2)3-NHSO3H]) under solvent-free conditions. The mentioned compounds were obtained in high to excellent yields using a mild and environmentally benign protocol by applying [γ -Fe2O3-HAp-(CH2)3-NHSO3H]) as an efficient magnetically recoverable Brønsted acid catalyst. It is notable that the catalyst could be easily recovered and reused without any significant loss of its performance and activity.
In the third section, 2-Chloro-3-formyl quinoline has been applied as an aldehyde moiety in the Groebke–Blackburn–Bienaymé multi-component reaction with isocyanides,
2-aminoazines, and 2-aminoazole to afford the desired adducts which are amenable for further cyclization on the basis of Ullmann-type coupling. The copper iodide-mediated intramolecular C–N bond formation in the second step gave an easy access to a series of imidazo[4',5':4,5]pyrrolo[2,3-b]quinoline derivatives in moderate to good yields.
In the fourth section, Groebke-Blackburn-Bienayme reaction (GBB) has been utilized for the synthesis of new imidazo[1,2-a]pyrimidine derivatives as novel anticancer agents. The cytotoxic activities of compounds were evaluated against human cancer cell lines including MCF-7, T-47D and MDA-MB-231, and compared with etoposide as the standard drug. Among the tested compounds, hydroxy- and/or methoxy-phenyl derivatives with IC50 values of 6.7-14.4 µM were more potent than etoposide against all cell lines. In particular, the 3-hydroxy-4-methoxyphenyl derivative with IC50 value of 6.7 µM was 5-fold more potent than etoposide against T-47D cells. The acridine-orange/ethidium bromide double staining and DNA-fragmentation studies demonstrated that the cytotoxic effect of promising compound associated with apoptosis in cancer cells.
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سنتز کاتالیزورها و نانوکاتالیزورهای اسیدی چندعاملی جدید بر پایه رزورسین آرن و ملامین و کاربرد آنها جهت تهیه ترکیبات هتروسیکل ویژه پراستخلاف
هادی عصاره 1393In this project, the synthesis of some triarylpyridines containing electron-donor and withdrawing groups in the para position of substituted phenyl rings in solvent and solvent-free conditions were investigated.
In this dissertation the main activities have investigated to four parts:
Part 1:
a novel approach for the synthesis of calix[4]resorcinarene were introduced. According to the low cost, ease of handling, remarkably low toxicity of metal solid acids compared with mineral acids, the catalytic role of zinc hydrogen sulfate are reported
Part 2:
3-Dimentional Network polymer based on cis-tetra benzyle calix[4]resorcinarene with nanoprous was obtained of resol polycondensation resorcinarene with benzaldehyde. The porosity of the polymer was confirmed by AFM and SEM images. this porous polymer contains both hydrophilic and hydrophobic layer in their structure that increases their potential for heterogenous and phase transfer catalyst. This catalyst was used in the ring opening of epoxides with azide and thiocyanide in water and corresponding β-hydroxy products were separated in good to excellent isolated yields.
Part 3:
In order to improve the ability of network polymer and Attempts to synthesize catalysts with high acidity nature, polymer was functionalized with trimethoxysilylpropanethiol and by addition of chloro sulfonic acid under suitable pH in which a new acid catalysts obtained. This catalyst was used in the ring opening of epoxides with azide in water, The results show that the use of this acidic polymer leads to increasing the efficiency and better reaction times.
Part 4:
hydroxyl groups on the upper rim of calix[4]resorcinarene were functionalized with trimethoxysilylpropanethiol. The Fe3O4 nano particles were prepared by co-pricipitation reaction of Fe+2 and Fe+3 in the alkaline condition and this nano particles coated with tetraortosilicate . The hydroxyl groups on magnetic nanoparticles were grafted on the functionalized resorcinarene. By addition of chloro sulfonic acid under controled conditions, resorcinarenes functionalized magnetic nano solid acid was prepared and it,s formation was confirmed by SEM images. The amount of magnetic property of the resulting compound was determined by VSM. This compound was used as acidic and phase transfer catalyst in the ring opening of epoxides.
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روش های نوین حلقه گشایی و انقباض هتروسیکلی جهت سنتز مشتقات جدید فوران و سیانودی اِن اُن و عامل دار کردن شبکه های پلیمری متخلخل بر پایه کلیکس[4]رزورسین آرن
فاطمه عبادست 1393First step of thesis was established based on new and direct pathway for the synthesis of several new 2-furyl acetonitrile derivatives from the reaction of pyrylium salts with sodium cyanide. The cheapness and readily available starting materials coupled with simple procedure make this new and viable route attractive to both research and pharmaceutical development endeavors. In the second section, the reaction of cyanide-containing resin with some of the triarylpyrylium salts carrying electron-donor and withdrawing groups in the para position of substituted phenyl rings for the synthesis of new 2-aroylfuran derivatives was investigated. The results revealed that the products successfully obtained in high yields and short reaction times. This environmentally friendly methodology offers several advantages including ease of manipulation and workup, better control of hazardous cyanide, and minimization of byproducts. These aspects point to a green and efficient protocol which could be useful in academic research and in pharmaceutical development. In the third section, for the first time, the performance of water-insoluble tetraphenolate C-methylcalix[4]resorcinarene as a heterogeneous phase transfer catalyst at room temperature was investigated. This tetraanion structure adopts a stable bowl-shaped conformation with four intramolecular OH…O- hydrogen bonds which serve as the anionic host molecule for the incorporation of cations into the cavity by the electrostatic interactions. Moreover, the hydrophobic tail and hydrophilic upper rim of this readily accessible supramolecule make it suitable for the standing in the organic-aqueous interfacial layer. The recoverability of the catalyst is in accordance with the aromatic-rich nature of this system, which makes it essentially insoluble in water. In the fourth section, a new, highly selective chemosensor for the naked-eye colorimetric sensing of cyanide anion was designed based on a hybrid pyrylium/alumina probe. The synergistic incorporation of organic-inorganic can play pivotal role in the convenient field-usable determination of this toxic anion in water. The simplicity and portability of the analysis coupled with low cost of the starting materials suggests that this new method may find application in a variety of different environments where easy and rapid determination of cyanide anion might be required. In the fifth step, a new and convenient approach for the functionalization of 3D-network polymer based on calix[4]resorcinarene was developed. According to this method, a variety of organic functional groups such as –SH and –NH2 was grafted onto the surface of polymer using ligand-functionalized organosilanes. The formation of polym-SH and polym-NH2 was confirmed by elemental analysis (CHNS), atomic force microscope (AFM), thermal gravimetric analysis (TGA) techniques. The remarkable advantages offered by this methodology are simple implementation, one-pot procedure and high loading of organic functional group. Importantly, the reactions proceeded without the need for any additives such as acidic or basic catalysts. In the following, the removal of mercury (II) from wastewaters using polym-SH was investigated. The results revealed the removal of 48% Hg2+ from 10 ppm solution. The concentrations of Hg2+ remaining in the solutions were analyzed by an inductively coupled plasma optical emission spectroscopy (ICP-OES) technique.
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طراحی، سنتز و کاربرد سوپرامولکول های جدید انبرمانند و پلیمرهای متخلخل تزیین شده با آویزهای کاتیونی بر پایه کلیکس[4]رزورسین آرن
سمیه الهی 1393In the first step of this project, direct incorporation of ionic liquid (1-methyl-3-(trimethylsilylpropyl) imidazolium chloride) onto the upper rim of calix[4]resorcinarene led to the formation of tweezer-like cationic calix[4]resorcinarene. The formation of this cationic supramolecular structure was confirmed by 1HNMR, 13CNMR, CHNS, TGA and DTA techniques. A survey of the literatures indicates that, this is the first report on the functionalization of calix[4]resorcinarene via one pot strategy without the use of acidic or basic catalyst. Hence, the procedure opens a novel entry to the convenient synthesis of a number of functionalized supramolecular structures based on calix[4]resorcinarene. Following the synthetic strategy, the application of this novel tweezer-like structure as a heterogeneous phase transfer catalyst for the preparation of some azidohydrins in water was investigated. The catalytic activity of this valuable compound could be attributed to the synergetic effect of the hydrophobic central cavity and hydrophilic cationic arms. In the second step, a convenient and straightforward route for the synthesis of novel three dimensional pyridinium salt via covalently anchored ionic liquid containing pyridinium moiety onto calix[4]resorcinarene was reported. The bactericidal action of this cationic supramolecular structure was evaluated against Gram-positive and Gram-negative bacteria. Surprisingly, this compound exhibited selective antibacterial effect on Gram-positive bacteria which is very important from the industrial and medicinal point of view. To the best of our knowledge, this is the first effort to assess the antibacterial activity of cationic supramolecular structure based on calix[4]resorcinarene. These preliminary results are attractive for the development of new antibacterial agent. In the next step, for the first time, cationic polymer containing pendant pyridinium groups was synthesized via post-functionalization of polymeric backbone based on calix[4]resorcinarene and characterized by AFM, TEM, CHNS, TGA and DTG techniques. The functionalized polymer conveniently loaded with desired anions, thereby providing a novel and recyclable polymer supported reagents for achieving synthetic goals. Thermal stability of this cationic polymer (up to 250 °C by TGA), allows thermally demanding ring transformation and expansion of triarylthiopyrylium salts on its side chains and polymeric backbone without decomposition and leaching of active species in the reaction media. This green method furnished a straightforward route for the synthesis of valuable 2,4,6-triarylpyridine along with novel 2,5,7-triaryl-[1,3]thiazepine derivatives which are widely present as motifs in an assortment of biologically active molecules. In the fourth step, an acidic 3D-network polymer was synthesized via two post-functionalization steps. Initially, the active homogeneous catalyst was chemically immobilized onto a polymeric support based on calix[4]resorcinarene by silylation of the hydroxyl groups to form a cationic polymer that contains imidazolium moieties. The formation of this cationic polymer was confirmed by CHNS, SEM, TGA and DTG techniques. Subsequently, HSO4 anion was incorporated into the polymer along the imidazolium pendant groups via a well-known ion exchange reaction. Elemental analysis data revealed that the cationic polymer was conveniently loaded with the desired Bronsted acid anion; therefore, it provides a novel heterogeneous acid catalyst for achieving synthetic goals. The immobilized acidic ionic liquid effectively catalyzed the one-pot synthesis of symmetrical bisamides by the multicomponent condensation of two moles of amides with aldehydes. Interestingly, the catalyst exhibited a high turnover number (TON) and turnover frequency (TOF), which were even comparable with that of H2SO4. The porosity of the polymeric support and covalently anchored acidic ionic liquid might indeed provide a synergistic means for the efficient approach of the starting materials to acidic sites, enough space for the preparation of product and a suitable hydrophobicity to drive out the water formed during the reaction from the support. The unique features of this catalyst, such as superior thermal stability, recyclability, excellent catalytic activity in terms of yield and reaction time, high turnover number and turnover frequency, are potentially important for the applications of this catalyst in the industry. In the fifth step of this thesis, by combining the advantages of 3D-network polymer with ionic liquids, the first functionalized polymers based on calix[4]resorcinarene under solvent free conditions was developed. The remarkable advantages offered by this approach are operational simplicity, functionalization via one-pot one-step procedure, no use of organic solvent and acidic or basic catalysts, ease of isolation and purification of functionalized polymer.
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: بررسی روشهای سنتزی و کاربردهای جدید رزورسینارن ها
پگاه كاظمیانفر 1391
Master Theses
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جداسازی و شناسایی اجزا مهم اسانس جعفری ایرانی(Petroselinum Crispum )با تاكید بر میریستیسین، آپیول با استفاده از روش فراصوت
رعنا كیانی 1403 -
بروماسیون مشتقات فنلی و اكسیداسیون الكل های بنزیلی در حضور شبكههای نانو متخلخل آلییونی (NIONs) بر پایه كلیكس رزورسین آرن
سیدحمزه تفاخ 1401 -
: اکسایش کارا و انتخابی الکل های بنزیلی نوع اول و دوم در حضور شبکه نانو متخلخل آلی یونی (NIONs) بر پایه کلیکس [4]رزورسین آرن/ H2O2
امل منشدی 1401 -
طراحی، سنتز و کاربرد شبکه نانو متخلخل آلی یونی (NIONS) حاوی برخی آنیون ها نظیر برمات در اکسایش الکل های بنزیلی
مهرناز نهاوندی 1399 -
بررسی واکنش نمک های تری آریل پیریلیوم با c-نوکلئوفیل نیترومتان
سیده الهام میرنجفی نیاكی 1399 -
طراحی و بررسی مطالعه شبکه پلیمری حافظه شکلی بر پایه سلولز
آمنه نواصر 1396A thermally induced shape memory polymer (SMP) was designed based on Ethyl cellulose and Poly(ε-caprolactone)(PCL). Ethyl cellulose and PCL are well known for being biodegradable and biocompatible. However, Ethyl cellulose was used as backbone of the network and PCL was grafted to it by Ring opening polymerization of the ε-caprolactone. PCL chains were end-functionalized with Diels-Alder adducts, Furan and Maleimide, by two step esterification. PCL was employed to play the role of the soft segment of the polymer network. Furthemore, The hard segment was achieved by cross-linking the polymer using Diels-Alder reaction between Furan and Maleimide. However, the polymer network was proved by FT-IR. Then, the thermo-responsive synthesized polymer was programed to fix a certain temporary shape above transition temperature. Subsequently, the polymer was recovered to its permanent shape upon heating to 41 °C. Thermal and mechanical analysis and shape memory effect of the network were studied by DSC and DMTA techniques. The SMP demonstrated the R_(r,tot) = 87.85% and R_f= 89.95% after two cycles. Moreover, the synthesized polymer was recyclable and re-processable which was due to the fact that the Diels-Alder reaction is thermally reversible, therefore a .new memory (permanent shape) was developed in the polymer
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سنتز معرف سدیم بور هیدرید تثبیت شده بر پلمیر متخلخل بر پایه رزورسین آرن جهت احیاء برخی نمکهای شالکوژ نو پیریلیوم پرکلرات
فاطمه خسروی بابادی 1396Due to the growing importance of using fixed Reagents on porous polymeric bases as active compounds with increased efficiency and also their high selectivity in different fields of study specially in organic synthesis, herein it is tried to investigate the efficiency of polymeric reagents on the basis of calix[4]resorcinarene as hydride donors for the one-pot regioselective reduction of some chalcogenopyrylium perchlorate salts.
In the first step, two methods are applied to examine for the preparation of borohydride containing polymeric supports on the basis of calix[4]resorcinarene through the post functionalization processes. In the first method, addition of BH4- to the mentioned polymeric support will result in producing the desired reagent. The second method is consisted of the initial addition of pyridinium site containing ionic liquids to the cationic polymer on the basis of calix[4]resorcinarene and then the anion exchange process of the structure will create the desired product. In order to investigate the efficiency of these reagents, their application as highly regioselective reducing agents for some chalcogeno pyrylium salts’ reduction has been examined.
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بررسی انجام واکنش های چند جزیی تک ظرف تهیه برخی زانتن ها و فتالازین ها در حضور کاتالیزور پلیمری متخلخل بر پایه رزورسین آرن باآویزهای مایع یونی اسید برونستد
نادیه ناصری 1395In this thesis, an acidic 3D-network polymer was synthesis via two post- functionlized steps. Initially, the active homogneous catalyst was chemically immobilized onto a polymeric support based on calix[4]resorcinarene by silylation of the hydroxyl groups to form a cationic polymer that contains imidazolium moieties. The formation of this cationic polymer was confirmed by CHNS, SEM, TGA, and DTG techniques. Subsequently, HSO4 anion was incorporated into the polymer along the imidazolium pendant groups via a well- known ion exchange reaction. Elemental analysis data revealed that the cationic polymer was conveniently loaded with the desired Bronsted acid anion; therefore, it provides a novel heterogeneous acid catalyst for achieving synthesis goals. The catalytic ability of acidic polyme as a novel environmentally safe heterogeneous catalyst for the preparation of 2H-indazolo [1,2-b]Phthalazine trione and Xanthene derivatives via a one-pot multicomponent method under solvent-free conditions has been described.
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شناسایی کمی و کیفی عصاره آبی-الکلی تفاله زیتون و بررسی نقش احتمالی آللوپاتیک آن
فهیمه جوكار 1395Increasing global population is a threat to food security and agricultural sustainability. Since the emergence of agriculture, weed control was serious concern has been the main problem for mankind. Cereal is the most important crop on earth, and the diversity and production in human nutrition have the greatest contribution and among these are wheat as the main part of this group special importance to account for, so weed control in wheat fields always serious and challenging issues facing agriculture. The use of chemical herbicides and synthetic pesticides to weeds control is increasing nowadays, increased use of these compounds have been caused harmful environmental effects. Allelopathy has offered a pragmatic approach in association with the natural weed control. Plant secondary metabolites that enter the environment and their most important role is to defend the plant against environmental stresses, called allelochemical. The purpose of allelopathy in weeds control is using of these compounds to control of weeds. Use of plants that have significant allelopathic effects is the perfect option for achieving this goal.
In this research project used the folin-Ciocalteu assay to determination of allelopathic compound such as phenolics and reducing power assay to study of antioxidant activity of olive pomace extract. To study of allelopathic properties of olive pomace, the effects of pomace examined on biological, physiological and morphological factors of avena fatua which is considered one of the most important weeds in wheat fields. Ethanolic and n-hexane extract in different concentrations of different methods were applied on the seeds of avena fatua.
According to the results obtained can be stated that pomace containing antioxidant and phenolic compounds show significant allelopathic effects on avena fatua seeds and in specific concentrations causes inhibition of germination and growth of this weed.
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استخراج،جداسازی و شناسایی ترکیبات مؤثره موجود در جلبک هیپنا بورگسنی و بررسی خواص بیواکتیویته آنها
لیلا حیدری زاده 1395Algae have multiple biological properties therefore; the natural products that isolated from them have been interested for elimination of harmful microorganism and the preservation of foods from toxic effects of oxidants.
In this research project, the study has been made on, ” Hypnea boergesenii” a Red algae from Chabahar sea against Several species of pathogens, including bacteria on Escherichia coli, Staphylococcus aureus, Proteus vulgaris, Klebsiella pneumoniae, Pseudomonas aeruginosa, Salmonella Enteritidis and three species of fungus including, Candida albicans and Two species of dermatophytes including Microsporum canis and Microsporum gypseum and As well as to compare the effects with standard antibiotics, including Streptomycin, Methicillin, Meropenem, Gentamicin, Imipenem, Vancomycin, Trimethoprim and Ciprofloxacin for the bacterias and Miconazole, Metronidazole and Canazole for fungus at in vitro.
Antibacterial properties of the extracts was evaluated by disk diffusion method and anti funguls properties was done by well diffusion method and the inhibitory zoon was determined. The result shows that all of the microorganisms were sensitive to the extracts. In this study, the minimum inhibitory concentration (MIC) for bacterial and fungal growth was determined in addition, the minimum bactericidal concentration was determined.
This researches also, including measures of antioxidant activity by the ferric reducing antioxidant power (FRAP) method and DPPH assay.
Determination of total phenolic and total flavonoid content also was done. The total phenolic content was determined by using the Folin-Ciocalteu assay and the Total flavonoid content was measured by the aluminum chloride colorimetric assay.
This study was an experimental that including the extracting of algae powder by just ethanol 70% and the other extracting was done by four solvent consecutively (Hexane, petroleum ether, dichloromethane and methanol) and then all of then the extracts were dried by using freeze dryer.
The results of this study show that, all the extracts have a good anti-microbial and anti-oxidant potential
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سنتزپلیمرمتخلخل عامل دارجدیدبرپایه کلیکس[4]رزورسین آرن حاوی آنیون بورهیدریدبه عنوان یک واکنشگرموثربرای احیاء ناحیه گزین نمکهای تری آریلپیریلیوم
سعیده ساكی 1394Abstract:
In this research, for the first time, a 3D-network polymer-supported borohydride anion was synthesized via two post-functionalization steps.
Initially, the homogeneous ionic liquid was chemically immobilized onto a polymeric support based on calix[4]resorcinarene by silylation of the hydroxyl groups to form a cationic polymer that contains pyridinium moieties. The formation of this cationic polymer was confirmed by atomic force microscopy (AFM), thermal gravimetric analysis (TGA) and derivative thermogravimetric (DTG) analysis. Subsequently, borohydride anion was incorporated into the polymer along the pyridinium pendant groups via a well-known ion exchange reaction.
It is noteworthy that the synthesized polymer supported reagent is insoluble in various solvents, including water, methanol, ethanol, ethylacetate, acetonitrile, dichloromethane, and chloroform. These features render its suitable for using as a solid-supported reagent in various reaction media.
Under this light and considering this fact that regioselective reduction is one of the most important classes of organic reactions from the academic, industrial and pharmaceutical points of views, we decided to investigate the application of this cationic polymer as a solid-supported reagent for an efficient and regioselective reducing reaction.
Reactivity and selectivity of the synthesized polymeric reagent were investigated in the regioselective reduction of some of the triarylpyrylium salts carrying electron-donor or electron-withdrawing groups on phenyl substituents of heterocyclic ring for synthesis of valuable dienone derivatives.
The remarkable advantages offered by this simple methodology are short reaction times, ease of product isolation and purification and good yields of the target products. Moreover, the reaction proceeded without the need for any additives such as catalysts.
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سنتز ترکیبات هتروسیکل زیست فعال از طریق واکنش آریل پیریلیوم ها با سدیم نیتریت در حضور مایعات یونی
عسكری كیا-ندا 1393In this thesis, the reaction of sodium nitrite with some of the triarylpyrylium salts carrying
electron-donor or electron-withdrawing groups on phenyl substituents of heterocyclic ring for
synthesis of bioactive heterocyclic compounds in the presence of ionic liquid were investigated.
According to the long reactions time for the reaction of pyrylium salts with sodium nitrite in the
solvent and in order to preceding the green chemistry aims, these reactions were performed in the
presence of ionic liquid as a solvent.
Using the ionic liquid as green and efficient solvent for the synthesis of isoxazole and furan
derivatives eliminates the toxic and hazardous solvents in chemical processes in addition to
accelerate the reaction. The results revealed that the products obtained in good yields and very short
reaction times.
-
بررسی واکنش نوکلئوفیلی تری آریل تیوپیریلیوم پرکلرات ها با آنیون آزید در حضور مایعات یونی
پرستو قنبرزاده 1392 -
بررسی واکنش آریل پیریلیوم ها با آمونیوم کاربامات به عنوان N - نوکلئوفیل کارآمد تحت شرایط بدون حلال
فاطمه بهزادی پشم 1392 -
سنتز نانو لایه های Fe3O4/SiO2 اصلاح شده با کاتالیزور انتقال فاز رزورسین آرن و بررسی برخی کاربرد های آن
سجاد برون 1391 -
اندازه گیری میزان تورم دینامیک شیل های سازنده ی پابده و گورپی در حضور سیال پایه آبی برای برخی از میادین جنوب
محمد بابایی 1390 -
سنتز رزورسین ارن ها با قابلیت انحلال بالا با استفاده ازکاتالیزور اسیدهای جامد
ندا خیراندیش 1390 -
احیاء ناحیه گزین تری آریل پیریلیوم پرکلرات در حضور مایع یونی کار ویژه
الهام صباغ 1389 -
استفاده ازبرخی اسید های جامد در تهیه 1و5-دی کتون های استخلافی
زهرا نجفی 1389 -
کاربرد مایعات یونی در واکنش های نوکلئوفیلی برخی از نمک های پیریلیوم وتیوپیریلیوم
زینب نجفی 1388 -
بررسی واکنشهای نوکلئوفیلی سیانید با برخی فوکهای تریآریل پیریلیوم پرکلات
فاطمه عبادست 1387 -
سنتز ترکیبات پلی آروماتیک تحت تابش مایکروویو
فاطمه قاسم هزاوه 1386 -
بررسی راههای جدید سنتز 2-آروئیل-3 و 5-دی آریل فوران تحت شرایط بدون حلال و تابش مایکروویو
فاطمه رحیمی 1386 -
واکنش برخی N- نوکلئوفیلها با ترکیبات پیریلیوم در فاز جامد و تحت تابش مایکروویو
مریم كریمی نیا 1386 -
بررسی واکنش برخی از نمکهای پیریلیوم پرکلرات با هیدروکسیل آمین هیدروکلراید در فاز جامد
شیما السادات دیانت 1385 -
سنتز و احیا برخی نمکهای شالکوژنوپیریلیوم در فاز جامد
نرگس قیطاسوند 1383