This paper covers the use of calixarenes as complexing agents for uraniumvi. Calixarenes are excellent macro cyclic platforms that can be functionalized with numerous organic moieties to show cooperative binding towards anions. An attempt has also been made to critically evaluate the synthesis procedures for different lowerrim substituted calixarenes. This invention relates to a process for stabilizing a phenolic resin containing a mixture of linear phenolic resins and calixarenes and a demulsifier composition comprising the stabilized phenolic resins prepared from the process. Chemotherapy occupies a pivotal position in the treatment of cancer, and its significance in terms of cure and regression of various types of cancer should not be underestimated. Chapter 2 synthesis and characterization of calix4arene. Calixarenes are a well known class of macrocyclic compounds 1, obtained in very high yield through a onestep condensation of formaldehyde with ptert butyl phenol.
The present paper describes some recent developments made with platinum metal complexes attached to calix phosphine ligands, that is, calixarenes substituted with phosphino groups. Calixarene chemistry, at the turn of the millennium, is a field approaching true. The number n enclosed in brackets, which separates calix and arene, indicates the number of aromatic ring units in the macrocycle, for example, calix4arene, calix6arene and calix8arene. The synthesis and characterization of giant calixarenes.
Lowerrim substituted calixarenes and their applications core. Resource recovery and waste treatment with calixarenes. Conformations and stereodynamics of calixarenes cheminform abstract. Calixarenes represent a wellknown family of macrocyclic molecules with broad range of potential applications in chemical, analytical, and engineering materials fields. Us9580536b2 process for stabilizing phenolic resins.
In particular, the role of the calixnarenes in the detection. Their characteristic structural features with the ease of functionalization offers the way to tune the size of receptor cavity. The aromatic components are derived from phenol, resorcinol, or pyrogallol to give, respectively, calixarenes, resorcinarenes, and pyrogallolarenes. The complex formation between watersoluble calixarenes psulfonatocalixnarenes, n 4, 6, 8, calxsn and dodecylpyridinium chloride dpc has been studied by the potentiometric titration method using a surfactantselective electrode, at calxsn 1. Calixarenes are versatile macromolecules in the field of supramolecules because of its synthetic feasibility and extensive analytical applications. They are sparingly soluble and high melting solids. For phenol, the aldehyde most often used is simple formaldehyde, while larger aldehydes, like acetaldehyde, are usually required in condensation reactions with resorcinol and pyrogallol to facilitate formation of the c4v symmetric vase.
Their interaction with various substances of interest in pharmacy, engineering, and medicine is also described. Biopharmaceutical applications of calixarenes sciencedirect. This book that deals with a special class of hostguest chemistry, recognized by the 1987 nobel chemistry prize awards, should appeal to almost all chemists. Sciotti, and uwe pieles school of life sciences, institute of chemistry and bioanalytics, university of applied sciences northwestern switzerland, gru.
Calixarenes are cyclic oligomers obtained by condensation of suitable pfunctionalised phenols with formaldehyde, usually allowing for the synthesis. It emphasizes on selectivity, the design principles of the host molecules, and the type of. Noncovalent calixareneamino acid complexes formed by maldims. Due to the expansion of the cavity after substitution, the lower rim can facilitate the complexation with bigger moieties like heavy metals and also organic molecules. Calixarenes have hydrophobic cavities that can hold smaller molecules or ions and belong to the class of. An introduction 2nd edition provides a concise overview of the field with particular attention to the historical development of calixarenes. Conformations and stereodynamics of calixarenes thondorf, iris 20011030 00. This book contains extensive references to recent literature, offering the reader a valid. Investigations that explore the use of calixarenes for amino acid recognition are. Mar 28, 2007 the lower rim of calixarenes is less subjected to modification, but the applications of calixarenes substituted at the lower rim are far greater than substituted at the upper rim. Calixarenes 2001 this page intentionally left blank calixarenes 2001 edited by zouhair asfari ecpmulpcnrs, strasbourg, france volker bohmer johannes gutenberguniversitat, mainz, germany jack harrowfield unaecpm, perth, australia and jacques vicens ecpmulpcnrs, strasbourg, france. Request pdf calixarenes 2001 calixarene chemistry, at the turn of the millennium, is a field approaching true maturity. The binding of these functional particles with regard to various serum albumins bovine serum albumin, human serum albumin, porcine serum albumin and sheep serum albumin has been studied by variable temperature fluorescence spectroscopy.
Davis and viviane boyer dyson perrins laboratory, university of oxford, south parks road, oxford, uk ox1 3qy. Comparison of binding affinities of watersoluble calixarenes with. Murakami, in studies in surface science and catalysis, 2001. To access a cheminform abstract of an article which was.
Calixarenes 2001 edited by zouhair asfari ecpmulpcnrs. Appendices calixarenes rsc publishing c david gutsche. Jan 10, 2019 calixarenes are cyclic oligomers obtained by condensation of suitable pfunctionalised phenols with formaldehyde, usually allowing for the synthesis of the well known small calixarenes including. It provides a fascinating and lively account of the history, development and applications of calixarenes, which are probably the worlds most readily available. Unmodified calixarene frameworks show no affinity for anionic guests, functionalized calixarenes have been shown to be capable of binding anions. Entrapment of toxic anions using calixarenes framework. Us201701983a1 process for stabilizing phenolic resins. The properties and characteristics of calixnarenes are described, as well as their capacity to form amphiphilic assemblies by means of the design of synthetic macrocycles with a hydrophilic head and a hydrophobic tail. Calixarene chemistry, at the turn of the millennium, is a field approaching true maturity.
Although many promising aspects of the chemistry of calix arenes have been highlighted in recent years, relatively little attention has been paid to the coordination chemistry of these macrocyclic molecules. Their unique topology offers not only the potential for designed cavities, through selective functionalisation, but also the fine tuning of binding due to the hydrophobic nature of the cavity. Calixarenes are used in commercial applications as sodium selective electrodes for the measurement of sodium levels in blood. Calixarenes also form complexes with cadmium, lead, lanthanides and actinides. Some of the least studied calixarenes are those that consist of azulene rings bridged by ch 2 groups. Selfassembly and interactions with dna aminosubstituted. All structured data from the file and property namespaces is available under the creative commons cc0 license. Applications of calixarenes in cancer chemotherapy. Energetics of the inclusion of organic molecules by rigidified cone calix4arenes in carbon tetrachloride. Water soluble calixarenes in molecular recognition.
In many areas, applications are real and important, and the arsenal of structures based on calixarenes provides tools effective in numerous areas of supramolecular. Calix5arene and the c 70 fullerene in pxylene form a ballandsocket supramolecular complex. The anionic calixarenes parasulphonatocalix4arene and 1,3diophosphonatocalix 4arene, have been used to cap silver nanoparticles. Calixarenes article about calixarenes by the free dictionary. This has led to finely tune the binding site and central hydrophobic cavity for the specified anions. Biocatalysis and enzymes in organic synthesis benjamin g. Applications of calixarenes as extractants and sensors 2. The synthesis, characterization, and properties of the. University of wisconsin 19471951 under william summer johnson warf postdoctoral fellow at u. Study of calixarenes thin films as chemical sensors for the detection of. A calixarene is a macrocycle or cyclic oligomer based on a hydroxyalkylation product of a phenol and an aldehyde the word calixarene is derived from calix or chalice because this type of molecule resembles a vase and from the word arene that refers to the aromatic building block. Calixarenes are macrocyclic oligomers, formed from phenolformaldehyde condensation. Antonio carlos 6627, 31270901 belo horizonte, mg, brazil.
David gutsche macromolecular people aman imani macalester college, mn 2. The beginning born march 21, 1921 in oak park, il family. Calixarenes for biochemical recognition and separation. Author links open overlay panel mohamed makha a colin l raston b. The calixarene and the related resorcinarenes represent an. Calixarenes we are interested in the application of multidentate aryloxide ligands to prepare reactive metal complexes that may emulate aspects of heterogeneous catalyst surfaces. Calixarenes are cyclic oligomers obtained by condensation of suitable pfunctionalised phenols with formaldehyde, usually allowing for the synthesis of the well known small calixarenes including. Since lash and colbys discovery of a simple and convenient method for producing the parent allhydrocarbon calix4azulene, there have been two other allhydrocarbon calix4azulenes which have been synthesized in good yields by their method. In many areas, applications are real and important, and the arsenal of structures based on calixarenes provides tools effective in numerous areas of supramolecular chemistry. Entrapment of toxic anions using calixarenes framework medcrave. Lowerrim substituted calixarenes and their applications. Some calixarenes are efficient sodium ionophores and are potentially useful in chemical sensors.
The journal of organic chemistry 2001, 66 4, 14731479. Files are available under licenses specified on their description page. Davis and others published calixarenes find, read and cite all the research you need on researchgate. Download hires image download to mspowerpoint cite this. Calixarenes can be used as ion sensitive electrodes or sensors4, optical sensors5, chiral recognition devices for solid phase extraction, as a stationary phase and modifiers6.
The lower rim of calixarenes is less subjected to modification, but the applications of calixarenes substituted at the lower rim are far greater than substituted at the upper rim. V arious analytical applications of calixarenes are discussed. Screening of anion activators reveals best synergism for amphiphilic carboxylates fullerene. Besides classical calixarenes, also calixarenes containing modified meso bridges are known,22 they are calixradialenes,23 ketocalixarenes24 and homocalixarenes. Design and synthesis of calixarene y k agrawal j p pancholi and j m v yas institute of research and development, gujarat forensic sciences university, sector 18a, gandhinagar 382 007, india. We report that the efflux of 56carboxyfluorescein anions from neutral egg yolk phosphatidylcholine vesicles is mediated by oligopolyarginines only in the presence of activating amphiphilic anions. The process comprises contacting the phenolic resin with an alkylene carbonate, in the presence of a base catalyst, to at least partially alkoxylate the phenolic. Application of calixarenes as macrocyclic ligands for.
Chirality in calixarenes and calixarene assemblies cheminform abstract. Volume 42, issue 35, 27 august 2001, pages 62156217. It provides a fascinating and lively account of the history, development and applications of calixarenes, which are probably the worlds most readily available synthetic molecular baskets. Download hires imagedownload to mspowerpointcite this. Selfassembly and interactions with dna patrick shahgaldian, michel a. The development of platinocalixarenes johnson matthey. Chirality in calixarenes and calixarene assemblies vysotsky, myroslav. Direct synthesis of calixarenes with extended arms.
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