TY - JOUR
T1 - Basic Photophysical Properties of meso-Bis(pyren-2-yl)porphyrin
T2 - An Isomer of Pyrene-Substituted Porphyrins
AU - Tomita, Shohei
AU - Hirabayashi, Kazunori
AU - Shimizu, Toshio
AU - Goto, Kenta
AU - Sugiura, Ken ichi
N1 - Funding Information:
This work was supported in part by the Tokyo Kasei Chemical Promotion Foundation, the Cooperative Research Program of ‘Network Joint Research Center for Materials and Devices: Dynamic Alliance for Open Innovation Bridging Human, Environment and Materials’, and the Priority Research Program sponsored by the Asian Human Resources Fund of Tokyo Metropolitan Government (TMG). We appreciate the technical assistance provided by the Service Centre of the Elementary Analysis of Organic Compounds at Kyushu University.
Publisher Copyright:
© Georg Thieme VerlagStuttgart · New York.
PY - 2017/5/17
Y1 - 2017/5/17
N2 - The Suzuki-Miyaura coupling reaction of pyren-2-yl boronic acid ester with a meso-dibromodiphenylporphyrin derivative was carried out to give another pyrene-substituted porphyrin. The electrophilic substitution reaction occurred selectively on the porphyrin nucleus of this molecule. The introduced pyrenes acted as a light-harvesting antenna.
AB - The Suzuki-Miyaura coupling reaction of pyren-2-yl boronic acid ester with a meso-dibromodiphenylporphyrin derivative was carried out to give another pyrene-substituted porphyrin. The electrophilic substitution reaction occurred selectively on the porphyrin nucleus of this molecule. The introduced pyrenes acted as a light-harvesting antenna.
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U2 - 10.1055/s-0036-1588715
DO - 10.1055/s-0036-1588715
M3 - Article
AN - SCOPUS:85014538787
VL - 49
SP - 2182
EP - 2186
JO - Synthesis
JF - Synthesis
SN - 0039-7881
IS - 10
M1 - ss-2016-f0878-op
ER -