TY - JOUR
T1 - Chemiluminescence of polyhydroxyphenol linked-calix[4]arenes
AU - Nakazono, Manabu
AU - Ohba, Yoshihito
AU - Zaitsu, Kiyoshi
N1 - Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 1999/4
Y1 - 1999/4
N2 - Pyrogallol cyclic tetramers, tetrasulfonated pyrogallol cyclic tetramers and 25,27-di(3,4,5-trihydroxybenzoyloxy)dihydroxy-calix[4]arene were synthesized. The calix[4]arenes emit light in the presence of hydrogen peroxide in an alkaline medium. Of three calix[4]arenes, 25,27-di(3,4,5- trihydroxybenzoyloxy)dihydroxy-calix[4]arene gave the highest chemiluminescence intensity, and the intensity of the calix[4]arene was 190- fold greater than that of gallic acid in the same solvent.
AB - Pyrogallol cyclic tetramers, tetrasulfonated pyrogallol cyclic tetramers and 25,27-di(3,4,5-trihydroxybenzoyloxy)dihydroxy-calix[4]arene were synthesized. The calix[4]arenes emit light in the presence of hydrogen peroxide in an alkaline medium. Of three calix[4]arenes, 25,27-di(3,4,5- trihydroxybenzoyloxy)dihydroxy-calix[4]arene gave the highest chemiluminescence intensity, and the intensity of the calix[4]arene was 190- fold greater than that of gallic acid in the same solvent.
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U2 - 10.1248/cpb.47.569
DO - 10.1248/cpb.47.569
M3 - Article
AN - SCOPUS:0032921427
SN - 0009-2363
VL - 47
SP - 569
EP - 570
JO - Chemical and Pharmaceutical Bulletin
JF - Chemical and Pharmaceutical Bulletin
IS - 4
ER -