Synthesis and Properties of Tetraarylmethanes Having Nitrogen-Containing Heteroaromatics
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- MATSUMOTO Kouzou
- Graduate School of Science, Osaka University
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- KANNAMI Masaki
- Graduate School of Science, Osaka University
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- INAGAKI Takuya
- Graduate School of Science, Osaka University
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- INOKUCHI Daisuke
- Graduate School of Science, Osaka University
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- MIKI Kaori
- Graduate School of Science, Osaka University
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- NEHIRA Tatsuo
- Graduate School of Integrated Arts and Sciences
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- Gennaro Pescitelli
- Department of Chemistry, University of Pisa
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- KURATA Hiroyuki
- Graduate School of Science, Osaka University
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- KAWASE Takeshi
- Graduate School of Science, Osaka University
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- KUBO Takashi
- Graduate School of Science, Osaka University
Bibliographic Information
- Other Title
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- 含窒素複素芳香環を置換基に有するテトラアリールメタン類の合成と性質
Abstract
In the course of studies on tetrakis(heteroaryl)methanes, we have synthesized tetrakis(4-pyridylmethane (2) from tris(4-pyridyl)methyl anion and 4-chloropyridine. It should be noted that the crystal structure of the silver(I) complex of 2, prepared from an equimolar mixture of 2 and AgBF4, is featured by three-dimensional, non-interpenetrated diamondoid network structure. We have also synthesized phenyl-(2-pyridyl)-(3-pyridyl)-(4-pyridyl)methane (3) as a prototypal chiral molecule based on tetraarylmethane framework. The optical signs expected for a pair of enantiomers. The calculated CD curve for (R)-3 based on time-dependent density functional theory (TDDFT) reproduces one of the experimantal CD spectra of 3, and suggests that the absolute configuration of the first-eluted fraction is R-isomer.
Journal
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- Abstracts of Symposium on Physical Organic Chemistry
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Abstracts of Symposium on Physical Organic Chemistry 37 (0), 36-36, 2007
The Society of Physical Organic Chemistry, Japan
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Keywords
Details 詳細情報について
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- CRID
- 1390282680532618880
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- NII Article ID
- 130004646270
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- Text Lang
- ja
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed