Jump to content

Iptycene

From Wikipedia, the free encyclopedia
(Redirected from Iptycenes)
Chemical structure of triptycene, the simplest iptycene

An iptycene is an aromatic compound composed of varying number of arene subunits bound to a bridged bicyclo-octatriene core structure. They are formally derivatives of barrelene. The first and simplest iptycene molecule is triptycene.[1]

The first iptycene was reported in 1931 by Erich Clar.[2] Paul Bartlett's research group developed Clar's method and made the first triptycene.[3] Following Bertlett's work on triptycene, Hart et al., with acknowledgement to Professor Joel F. Liebman, proposed the trivial name iptycene for this class of molecules.[4]

References

[edit]
  1. ^ Chen, Chuan-Feng; Ma, Ying-Xian (Dec 2, 2012). Iptycenes Chemistry: From Synthesis to Applications. Springer Science & Business Media. ISBN 9783642328886.
  2. ^ Clar, E. (1931). "Über die Konstitution des Anthracens (Zur Kenntnis mehrkerniger aromatischer Kohlenwasserstoffe und ihrer Abkömmlinge, IX. Mitteil.)". Berichte der Deutschen Chemischen Gesellschaft. 64 (7): 1676–1688. doi:10.1002/cber.19310640722.
  3. ^ Bartlett, Paul D.; Ryan, M. Josephine; Cohen, Saul G. (1942). "Triptycene (9,10-o-benzenoanthracene)". J. Am. Chem. Soc. 64 (11): 2649–2653. doi:10.1021/ja01263a035.
  4. ^ Hart, Harold; Shamouilian, Shamouil; Takehira, Yoshikazu (1981). "Generalization of the triptycene concept. Use of diaryne equivalents in the synthesis of iptycenes". The Journal of Organic Chemistry. 46 (22): 4427–4432. doi:10.1021/jo00335a021. ISSN 0022-3263.


pFad - Phonifier reborn

Pfad - The Proxy pFad of © 2024 Garber Painting. All rights reserved.

Note: This service is not intended for secure transactions such as banking, social media, email, or purchasing. Use at your own risk. We assume no liability whatsoever for broken pages.


Alternative Proxies:

Alternative Proxy

pFad Proxy

pFad v3 Proxy

pFad v4 Proxy