Cyclic tetramer of a metalloporphyrin based on a quadruple hydrogen bond

Haruki Ohkawa, Akihiro Takayama, Satoshi Nakajima, Hiroyuki Nishide

研究成果: Article

49 引用 (Scopus)

抜粋

This paper describes the selective formation of a cyclic tetramer from a readily synthesized metalloporphyrin with two self-complementary quadruple hydrogen-bonding units. The extremely strong quadruple hydrogen-bonding unit, 2-ureido-4[1H]-pyrimidinone, enabled the formation of a stable cyclic tetramer based on a tetraphenylporphyrin derivative over a wide concentration range. This hydrogen-bonded tetramer is a new functional unit for use in a higher-ordered architecture of a supramolecular porphyrin assembly.

元の言語English
ページ(範囲)2225-2228
ページ数4
ジャーナルOrganic Letters
8
発行部数11
DOI
出版物ステータスPublished - 2006 5 25

    フィンガープリント

ASJC Scopus subject areas

  • Molecular Medicine

これを引用

Ohkawa, H., Takayama, A., Nakajima, S., & Nishide, H. (2006). Cyclic tetramer of a metalloporphyrin based on a quadruple hydrogen bond. Organic Letters, 8(11), 2225-2228. https://doi.org/10.1021/ol060488u