Synthesis and properties of bis-corannulenes

Corannulenecarbaldehyde and corannulenylmethyl triphenylphosphonium bromide are combined through the Wittig olefination reaction to furnish dicorannulenylethene with 70% yield. A subsequent oxidative photocyclization leads to annulation of the corannulene nuclei to produce a C42H18 nanographene stru...

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Main Authors: Halilovic, Dzeneta, Rajeshkumar, Venkatachalam, Stuparu, Mihaiela Corina
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2022
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Online Access:https://hdl.handle.net/10356/160360
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1603602023-12-11T15:34:51Z Synthesis and properties of bis-corannulenes Halilovic, Dzeneta Rajeshkumar, Venkatachalam Stuparu, Mihaiela Corina School of Physical and Mathematical Sciences Science::Chemistry Bis-Corannulenes Bicorannulene System Corannulenecarbaldehyde and corannulenylmethyl triphenylphosphonium bromide are combined through the Wittig olefination reaction to furnish dicorannulenylethene with 70% yield. A subsequent oxidative photocyclization leads to annulation of the corannulene nuclei to produce a C42H18 nanographene structure in 59% yield. Interestingly, only the trans isomer of the dicorannulenylethene forms cocrystals with fullerene C60 through concave-convex and convex-convex π-π stacking interactions. The Mallory photocyclization could be extended to a phenanthrene-based diarylethene precursor to yield a large bicorannulene system. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Nanyang Technological University Financial support from the Ministry of Education Singapore under the AcRF Tier 1 (2019-T1-002-066) (RG106/19) (2018-T1-001-176) (RG18/18); Agency for Science, Technology and Research (A* STAR)-AME IRG A1883c0006; and NTU (04INS000171C230) is gratefully acknowledged. 2022-07-20T01:55:20Z 2022-07-20T01:55:20Z 2021 Journal Article Halilovic, D., Rajeshkumar, V. & Stuparu, M. C. (2021). Synthesis and properties of bis-corannulenes. Organic Letters, 23(4), 1468-1472. https://dx.doi.org/10.1021/acs.orglett.1c00146 1523-7060 https://hdl.handle.net/10356/160360 10.1021/acs.orglett.1c00146 33534592 2-s2.0-85101923732 4 23 1468 1472 en 2019-T1-002-066 RG106/19 2018-T1-001-176 RG18/18 A1883c0006 04INS000171C230 Organic Letters © 2021 American Chemical Society. All rights reserved. This article may be downloaded for personal use only. Any other use requires prior permission of the copyright holder. The Version of Record is available online at http://doi.org/10.1021/acs.orglett.1c00146. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry
Bis-Corannulenes
Bicorannulene System
spellingShingle Science::Chemistry
Bis-Corannulenes
Bicorannulene System
Halilovic, Dzeneta
Rajeshkumar, Venkatachalam
Stuparu, Mihaiela Corina
Synthesis and properties of bis-corannulenes
description Corannulenecarbaldehyde and corannulenylmethyl triphenylphosphonium bromide are combined through the Wittig olefination reaction to furnish dicorannulenylethene with 70% yield. A subsequent oxidative photocyclization leads to annulation of the corannulene nuclei to produce a C42H18 nanographene structure in 59% yield. Interestingly, only the trans isomer of the dicorannulenylethene forms cocrystals with fullerene C60 through concave-convex and convex-convex π-π stacking interactions. The Mallory photocyclization could be extended to a phenanthrene-based diarylethene precursor to yield a large bicorannulene system.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Halilovic, Dzeneta
Rajeshkumar, Venkatachalam
Stuparu, Mihaiela Corina
format Article
author Halilovic, Dzeneta
Rajeshkumar, Venkatachalam
Stuparu, Mihaiela Corina
author_sort Halilovic, Dzeneta
title Synthesis and properties of bis-corannulenes
title_short Synthesis and properties of bis-corannulenes
title_full Synthesis and properties of bis-corannulenes
title_fullStr Synthesis and properties of bis-corannulenes
title_full_unstemmed Synthesis and properties of bis-corannulenes
title_sort synthesis and properties of bis-corannulenes
publishDate 2022
url https://hdl.handle.net/10356/160360
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