Quadruple Decker [3.3][3.3][3.3]orthocyclophane acetal - An orthocyclophane ladder

Shuntaro Mataka; Kouichiro Shigaki; Tsuyoshi Sawada; Yoshihara Mitoma; Masahiko Taniguchi; Thies Thiemann; Kazuya Ohga; Naoyoshi Egashira

doi:10.1002/(SICI)1521-3773(19981002)37:18<2532::AID-ANIE2532>3.0.CO;2-R

Quadruple Decker [3.3][3.3][3.3]orthocyclophane acetal - An orthocyclophane ladder

Shuntaro Mataka, Kouichiro Shigaki, Tsuyoshi Sawada, Yoshihara Mitoma, Masahiko Taniguchi, Thies Thiemann, Kazuya Ohga, Naoyoshi Egashira

Research output: Contribution to journal › Article › peer-review

24 Citations (Scopus)

Abstract

Through clever bridging of orthocyclophanes (in this case by acetalization), molecules such as 1 can be formed with four benzene rings in a stacked face-to-face arrangement. UV/Vis spectroscopic and electrochemical properties of 1 are governed by π-π through-space interactions within the molecule.

Original language	English
Pages (from-to)	2532-2534
Number of pages	3
Journal	Angewandte Chemie - International Edition
Volume	37
Issue number	18
DOIs	https://doi.org/10.1002/(SICI)1521-3773(19981002)37:18<2532::AID-ANIE2532>3.0.CO;2-R
Publication status	Published - Oct 2 1998
Externally published	Yes

Keywords

Cations
Cyclic voltammetry
Cyclophanes
Stacking interactions

ASJC Scopus subject areas

Catalysis
General Chemistry

Access to Document

10.1002/(SICI)1521-3773(19981002)37:18<2532::AID-ANIE2532>3.0.CO;2-R

Cite this

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abstract = "Through clever bridging of orthocyclophanes (in this case by acetalization), molecules such as 1 can be formed with four benzene rings in a stacked face-to-face arrangement. UV/Vis spectroscopic and electrochemical properties of 1 are governed by π-π through-space interactions within the molecule.",

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year = "1998",

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T1 - Quadruple Decker [3.3][3.3][3.3]orthocyclophane acetal - An orthocyclophane ladder

AU - Mataka, Shuntaro

AU - Shigaki, Kouichiro

AU - Sawada, Tsuyoshi

AU - Mitoma, Yoshihara

AU - Taniguchi, Masahiko

AU - Thiemann, Thies

AU - Ohga, Kazuya

AU - Egashira, Naoyoshi

PY - 1998/10/2

Y1 - 1998/10/2

N2 - Through clever bridging of orthocyclophanes (in this case by acetalization), molecules such as 1 can be formed with four benzene rings in a stacked face-to-face arrangement. UV/Vis spectroscopic and electrochemical properties of 1 are governed by π-π through-space interactions within the molecule.

AB - Through clever bridging of orthocyclophanes (in this case by acetalization), molecules such as 1 can be formed with four benzene rings in a stacked face-to-face arrangement. UV/Vis spectroscopic and electrochemical properties of 1 are governed by π-π through-space interactions within the molecule.

KW - Cations

KW - Cyclic voltammetry

KW - Cyclophanes

KW - Stacking interactions

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Quadruple Decker [3.3][3.3][3.3]orthocyclophane acetal - An orthocyclophane ladder

Abstract

Keywords

ASJC Scopus subject areas

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