02569nam 2200613Ia 450 991077831290332120200520144314.01-84755-819-4(CKB)1000000000791471(EBL)1185233(OCoLC)854960786(SSID)ssj0000578390(PQKBManifestationID)12207860(PQKBTitleCode)TC0000578390(PQKBWorkID)10578778(PQKB)10689908(MiAaPQ)EBC1185233(Au-PeEL)EBL1185233(CaPaEBR)ebr10618735(CaONFJC)MIL872435(PPN)198468849(EXLCZ)99100000000079147120080207d2008 uy 0engur|n|---|||||txtccrCalixarenes[electronic resource] an introduction /C. David Gutsche2nd ed.Cambridge RSC Publishingc20081 online resource (291 p.)Monographs in supramolecular chemistryRev. ed. of: Calixarenes. 1989.0-85404-258-X Includes bibliographical references and index.""9780854042586""; ""i_iv""; ""v_vii""; ""viii_xiv""; ""001_026""; ""027_060""; ""061_076""; ""077_115""; ""116_146""; ""147_163""; ""164_207""; ""208_237""; ""238_243""; ""244_260""; ""261_276""Calixarenes belong to a family of macrocyclic compounds based on a hydrozyalkylation product of a phenol and an aldehyde, and are probably the world's most readily available synthetic molecular basket. The word calixarene is derived from calyx, Greek for chalice and arene in reference to the presence of aryl groups in the cyclic array. Calixarenes are appealing subjects for research since they can be functionalized in myriad ways to provide interesting and useful materials. As a result of their ease of synthesis they have attracted worldwide attention. Calixarenes An Introduction provides a coMonographs in Supramolecular ChemistryCalixarenesPhenolsCalixarenes.Phenols.547.632Gutsche C. David(Carl David),1921-66140Gutsche C. David(Carl David),1921-66140Royal Society of Chemistry (Great Britain)MiAaPQMiAaPQMiAaPQBOOK9910778312903321Calixarenes1020237UNINA