Literature DB >> 27897398

An Obtuse-angled Corner Unit for Fluctuating Carbon Nanohoops.

Zhe Sun1,2, Naoya Miyamoto3, Sota Sato1,4, Hidetoshi Tokuyama3, Hiroyuki Isobe1,2,4.   

Abstract

The invention of corner units was the key factor that allowed the synthesis of cyclo-para-phenylenes with strained curved π-systems. Despite only a few scarce instances of the development of corner units to date, a variety of structural congeners have been synthesized. These preceding corner units commonly possessed directing angles of ≤90°, which enabled the macrocyclization of multiple units, up to six. In this study, we introduce an obtuse-angled corner unit for the synthesis of cyclo-para-phenylene congeners. The corner unit with oxanorbornadiene possessed a directing angle of 126° and thus allowed for the macrocyclization of larger structures with up to seven units. Reductive aromatization was applicable to complete the cyclo-para-phenylene structures and afforded the congeners with multiple anthracenylene panels. Structural studies with experimental and theoretical methods revealed a fluctuating structure with an intrinsic non-belt shape.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  anthracenylene; carbon nanohoop; macrocycles; oxanorbornadiene; structure elucidation

Year:  2016        PMID: 27897398     DOI: 10.1002/asia.201601614

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  2 in total

1.  Chiral Dibenzopentalene-Based Conjugated Nanohoops through Stereoselective Synthesis.

Authors:  Mathias Hermann; Daniel Wassy; Julia Kohn; Philipp Seitz; Martin U Betschart; Stefan Grimme; Birgit Esser
Journal:  Angew Chem Int Ed Engl       Date:  2021-03-23       Impact factor: 15.336

Review 2.  Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero- or Polycyclic Aromatics.

Authors:  Mathias Hermann; Daniel Wassy; Birgit Esser
Journal:  Angew Chem Int Ed Engl       Date:  2021-03-22       Impact factor: 16.823

  2 in total

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