253178-48-2Relevant academic research and scientific papers
Synthesis of p-benzylcalix[4]arene and its sulfonated water soluble derivative
Makha,Raston
, p. 2470 - 2471 (2007/10/03)
p-Benzylcalix[4]arene is formed in good yield by a direct one pot reaction involving p-benzylphenol and formaldehyde, selectively converted to the corresponding chlorosulfonyl and sulfonate analogues.
Convergent synthesis of p-benzylcalix[7]arene: Condensation and UHIG of p-benzylcalix[6 or 8]arenes
Atwood, Jerry L.,Hardie, Michaele J.,Raston, Colin L.,Sandoval, Christian A.
, p. 1523 - 1526 (2008/02/09)
(matrix presented). p-Benzylcalix[5]arene and p-benzylcalix[7]arene are formed on ultrahigh intensity grinding (UHIG) of p-benzylcalix[6 or 8]arenes in the presence of KOH and molecular sieves (4 ?), and the same calix[7]arene is also formed on condensation of p-benzylphenol and formaldehyde (15-20% yield), under more forcing conditions, along with p-benzylcalix[10]arene.
Complexation of a hexameric uranium(VI) cluster by p-benzylcalix[7]arene
Thuery, Pierre,Nierlich, Martine,Souley, Bahari,Asfari, Zouhair,Vicens, Jacques
, p. 2589 - 2594 (2007/10/03)
The reaction of uranyl nitrate hexahydrate with p-benzylcalix[7]arene (H7L) in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO) resulted in the formation of the compound (UO22+)6(L7-)2
ISOLATION AND CHARACTERIZATION OF P-BENZYLCALIXARENES (N=5,6 AND 8) FROM p-BENZYLPHENOL AND FORMALDEHYDE
Souley, B.,Asfari, Z.,Vicens, J.
, p. 959 - 961 (2007/10/02)
The condensation of p-benzylphenol and formaldehyde in tetraline in the presence of potassium hydroxide affords, in addition to the "easy" calixarenes (n=6 and 8), the cyclopentamer (n=5) in 33percent yield.
