抄録
A triply bridged capped hexahomotrioxacalix[3]arene 4 with C3-symmetry was synthesized by treatment of hexahomotrioxacalix[3]arene tricarboxylic acid 3 with 1,3,5-tris(bromomethyl)benzene in the presence of Na2CO3 in DMF. The complexation modes of 4 with cations differed according to the ionic size and properties of the guest cations, as was clearly elucidated by 1H NMR titration spectra. Conformational studies on 4 in solution and in the solid state are also described.
| 元の言語 | 英語 |
|---|---|
| ページ（範囲） | 1069-1075 |
| ページ数 | 7 |
| ジャーナル | European Journal of Organic Chemistry |
| 発行部数 | 6 |
| DOI | |
| 出版物ステータス | 出版済み - 1 1 2001 |
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All Science Journal Classification (ASJC) codes
- Physical and Theoretical Chemistry
- Organic Chemistry
これを引用
Synthesis and inclusion properties of C3-symmetrically capped hexahomotrioxacalix[3]arenes with ester groups on the lower rim. / Yamato, Takehiko; Zhang, Fenglei; Tsuzuki, Hirohisa; Miura, Yoshinori.
：: European Journal of Organic Chemistry, 番号 6, 01.01.2001, p. 1069-1075.研究成果: ジャーナルへの寄稿 › 記事
}
TY - JOUR
T1 - Synthesis and inclusion properties of C3-symmetrically capped hexahomotrioxacalix[3]arenes with ester groups on the lower rim
AU - Yamato, Takehiko
AU - Zhang, Fenglei
AU - Tsuzuki, Hirohisa
AU - Miura, Yoshinori
PY - 2001/1/1
Y1 - 2001/1/1
N2 - A triply bridged capped hexahomotrioxacalix[3]arene 4 with C3-symmetry was synthesized by treatment of hexahomotrioxacalix[3]arene tricarboxylic acid 3 with 1,3,5-tris(bromomethyl)benzene in the presence of Na2CO3 in DMF. The complexation modes of 4 with cations differed according to the ionic size and properties of the guest cations, as was clearly elucidated by 1H NMR titration spectra. Conformational studies on 4 in solution and in the solid state are also described.
AB - A triply bridged capped hexahomotrioxacalix[3]arene 4 with C3-symmetry was synthesized by treatment of hexahomotrioxacalix[3]arene tricarboxylic acid 3 with 1,3,5-tris(bromomethyl)benzene in the presence of Na2CO3 in DMF. The complexation modes of 4 with cations differed according to the ionic size and properties of the guest cations, as was clearly elucidated by 1H NMR titration spectra. Conformational studies on 4 in solution and in the solid state are also described.
UR - http://www.scopus.com/inward/record.url?scp=0035081619&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0035081619&partnerID=8YFLogxK
U2 - 10.1002/1099-0690(200103)2001:6<1069::AID-EJOC1069>3.0.CO;2-R
DO - 10.1002/1099-0690(200103)2001:6<1069::AID-EJOC1069>3.0.CO;2-R
M3 - Article
AN - SCOPUS:0035081619
SP - 1069
EP - 1075
JO - Liebigs Annalen der Chemie
JF - Liebigs Annalen der Chemie
SN - 1434-193X
IS - 6
ER -