TY - JOUR
T1 - Preparation and properties of octa-substituted phthalocyanines peripherally substituted with phenyl derivatives
AU - Sugimori, Tamotsu
AU - Torikata, Masaharu
AU - Nojima, Jun
AU - Tominaka, Shinobu
AU - Tobikawa, Kaori
AU - Handa, Makoto
AU - Kasuga, Kuninobu
N1 - Funding Information:
This work was supported by Grant-in-Aids for Scientific Research from Ministry of Education, Culture, Sports, Science and Technology.
PY - 2002/12/1
Y1 - 2002/12/1
N2 - 2,3,9,10,16,17,23,24-Octa-substituted phthalocyanines modified with phenyl, tolyl, tert-butylphenyl, and trifluoromethylphenyl groups and their nickel(II) complexes were prepared and characterized. The phthalonitriles with the phenyl derivatives, which are precursors of the phthalocyanines, were synthesized from 4,5-dichlorophthalonitrile and phenyl boronic acids by use of Suzuki-coupling reaction.
AB - 2,3,9,10,16,17,23,24-Octa-substituted phthalocyanines modified with phenyl, tolyl, tert-butylphenyl, and trifluoromethylphenyl groups and their nickel(II) complexes were prepared and characterized. The phthalonitriles with the phenyl derivatives, which are precursors of the phthalocyanines, were synthesized from 4,5-dichlorophthalonitrile and phenyl boronic acids by use of Suzuki-coupling reaction.
KW - Octa-substituted phthalocyanines
KW - Solubility
KW - Spectroscopy
KW - Suzuki-coupling
UR - http://www.scopus.com/inward/record.url?scp=0036891812&partnerID=8YFLogxK
U2 - 10.1016/S1387-7003(02)00636-6
DO - 10.1016/S1387-7003(02)00636-6
M3 - 学術論文
AN - SCOPUS:0036891812
SN - 1387-7003
VL - 5
SP - 1031
EP - 1033
JO - Inorganic Chemistry Communications
JF - Inorganic Chemistry Communications
IS - 12
ER -