Synthesis and Characterizations of a Porphyrin Dimer Having a 2,6-diacylpyridyl Group as a Spacer between Two Porphyrin Units.
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- SUGA Yasuhiro
- National Insititute of Materials and Chemical Research, COE laboratory
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- ARIMURA Takashi
- National Insititute of Materials and Chemical Research, COE laboratory
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- IDE Seiji
- National Insititute of Materials and Chemical Research, COE laboratory
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- SUGIWARA Hideki
- National Insititute of Materials and Chemical Research, COE laboratory
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- MURATA Shigeo
- National Insititute of Materials and Chemical Research, COE laboratory
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- TACHIYA Masanori
- National Insititute of Materials and Chemical Research, COE laboratory
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Abstract
The synthesis of a porphyrin dimer with a 2,6-diacylpyridyl group as a recognition site was accomplished by the coupling of 2,6-diaminopyridine and two porphyrins with a 4’-ethoxycarbonylbiphenyl substitutent at a meso -position of the porphyrin ring. By comparing the absorption spectrum of the obtained porphyrin dimer in CH2Cl2 with that of the corresponding porphyrin monomer, no remarkable interaction between two zinc porphyrin units was indicated. 1H NMR studies revealed that hydrogen bonding interactions of the 2,6-diacylpyridyl group in the porphyrin dimer serve to form a novel supramolecular assembly in the presence of naphthalenediimide compound.
Journal
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- Journal of Oleo Science
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Journal of Oleo Science 50 (3), 165-171, 2001
Japan Oil Chemists' Society
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Keywords
Details 詳細情報について
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- CRID
- 1390001204092937984
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- NII Article ID
- 10006788944
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- NII Book ID
- AA11503337
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- COI
- 1:CAS:528:DC%2BD3MXhsVamur8%3D
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- ISSN
- 13473352
- 13458957
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- NDL BIB ID
- 5912119
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed