Photochemistry of nitrogen-bridged cyclophanes: 2,11-Diaza[3 2]anthracenoparacyclophane and 2,11-diaza[32] paracyclophane systems

Hideki Okamoto, Minoru Yamaji, Kyosuke Satake

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

This account provides an overview of the photochemical properties of cyclophanes possessing nitrogen atoms in the bridge chains, namely 2,11-diaza[32]anthracenoparacyclophane and 2,11-diaza[3 2]paracyclophane systems. Although the photoreactions of aromatic molecules that are bound by a linker or fixed in a cyclophane structure have been widely investigated, much less attention has been paid to the photochemistry of aromatic rings incorporated in a nitrogen-bridged cyclophane. During the course of our work on the photoreactions of cyclophanes possessing nitrogen atoms in their bridge chains, the nitrogen-bridged cyclophanes were found to display photoproperties significantly different from those of the nonbridged aromatic chromophores or the corresponding carbonbridged cyclophane analogues. The 2,11-diaza[32]anthracenoparacyclophane system displayed an efficient photochemical cycloaddition-adiabatic cycloreversion cycle in the excited singlet state, while in the triplet state, the photoisomer underwent a novel rearrangement and adiabatic cycloreversion. Upon photolysis of the 2,11-diaza[32]paracyclophane system, an octahedrane cage was formed. This is the first reported octahedrane formation to occur by the photochemical dimerization of benzene. Thus, the title cyclophane systems display a variety of photoprocesses involving cycloaddition, adiabatic cycloreversion accompanied by photoinduced chemiluminescence, novel rearrangements, and previously unknown benzene dimerization. 1 Introduction 2 Photochemistry of the 2,11-Diaza[32]anthracenoparacyclophane System 2.1 General Comments on the Photochemical Cycloaddition and Cycloreversion of Aromatic Molecules in the Singlet State 2.2 Intramolecular Photochemical Cycloaddition and Cycloreversion of the 2,11-Diaza[32] anthracenoparacyclophane System 2.3 General Introduction to the Photochemistry of Aromatic Molecules in the Triplet State 2.4 Photoproperties of the 2,11-Diaza[32]anthracenoparacyclo-phane System in the Triplet State 3 Photochemistry of the 2,11-Diaza[32]paracyclophane System 3.1 General Remarks on the Photoreactions of Cyclophanes Containing Two Benzene Rings 3.2 Construction of the 2,11-Diaza[32]paracyclophane Skeleton 3.3 Photoreactions of the 2,11-Diaza[32]paracyclophane System 4 Summary.

Original languageEnglish
Pages (from-to)1931-1945
Number of pages15
JournalSynlett
Issue number13
DOIs
Publication statusPublished - Aug 1 2008

Fingerprint

Cycloaddition
Photochemical reactions
Nitrogen
Benzene
Dimerization
Molecules
Atoms
Chemiluminescence
Photolysis
Chromophores
Excited states
cyclophane 2
octahedrane

Keywords

  • Chromophores
  • Cycloadditions
  • Cyclophanes
  • Photochemistry
  • Rearrangements

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Photochemistry of nitrogen-bridged cyclophanes : 2,11-Diaza[3 2]anthracenoparacyclophane and 2,11-diaza[32] paracyclophane systems. / Okamoto, Hideki; Yamaji, Minoru; Satake, Kyosuke.

In: Synlett, No. 13, 01.08.2008, p. 1931-1945.

Research output: Contribution to journalArticle

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