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100   $a20080207d2008      uy             0
101 0 $aeng
135   $aur|n|---|||||
181   $ctxt
182   $cc
183   $acr
200 10$aCalixarenes$b[electronic resource] $ean introduction /$fC. David Gutsche
205   $a2nd ed.
210   $aCambridge $cRSC Publishing$dc2008
215   $a1 online resource (291 p.)
225 0 $aMonographs in supramolecular chemistry
300   $aRev. ed. of: Calixarenes. 1989.
311   $a0-85404-258-X 
320   $aIncludes bibliographical references and index.
327   $a""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""
330   $aCalixarenes belong to a family of macrocyclic compounds based on a hydrozyalkylation product of a phenol and an aldehyde, and are probably the world's most readily available synthetic molecular basket. The word calixarene is derived from calyx, Greek for chalice and arene in reference to the presence of aryl groups in the cyclic array. Calixarenes are appealing subjects for research since they can be functionalized in myriad ways to provide interesting and useful materials. As a result of their ease of synthesis they have attracted worldwide attention. Calixarenes An Introduction provides a co
410  0$aMonographs in Supramolecular Chemistry
606   $aCalixarenes
606   $aPhenols
615  0$aCalixarenes.
615  0$aPhenols.
676   $a547.632
700   $aGutsche$b C. David$g(Carl David),$f1921-$066140
701   $aGutsche$b C. David$g(Carl David),$f1921-$066140
712 02$aRoyal Society of Chemistry (Great Britain)
801  0$bMiAaPQ
801  1$bMiAaPQ
801  2$bMiAaPQ
906   $aBOOK
912   $a9910778312903321
996   $aCalixarenes$91020237
997   $aUNINA